102 results on '"Dellaripa, P"'
Search Results
2. Systemic sclerosis associated interstitial lung disease: a conceptual framework for subclinical, clinical and progressive disease.
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Roofeh, David, Brown, Kevin, Kazerooni, Ella, Tashkin, Donald, Assassi, Shervin, Martinez, Fernando, Wells, Athol, Raghu, Ganesh, Denton, Christopher, Chung, Lorinda, Hoffmann-Vold, Anna-Maria, Distler, Oliver, Johannson, Kerri, Allanore, Yannick, Matteson, Eric, Kawano-Dourado, Leticia, Pauling, John, Seibold, James, Volkmann, Elizabeth, Walsh, Simon, Oddis, Chester, White, Eric, Barratt, Shaney, Bernstein, Elana, Domsic, Robyn, Dellaripa, Paul, Conway, Richard, Rosas, Ivan, Bhatt, Nitin, Hsu, Vivien, Ingegnoli, Francesca, Kahaleh, Bashar, Garcha, Puneet, Gupta, Nishant, Khanna, Surabhi, Korsten, Peter, Lin, Celia, Mathai, Stephen, Strand, Vibeke, Doyle, Tracy, Steen, Virginia, Zoz, Donald, Ovalles-Bonilla, Juan, Rodriguez-Pinto, Ignasi, Shenoy, Padmanabha, Lewandoski, Andrew, Belloli, Elizabeth, Lescoat, Alain, Nagaraja, Vivek, Ye, Wen, Huang, Suiyuan, Maher, Toby, and Khanna, Dinesh
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connective tissue disease interstitial lung disease ,systemic sclerosis associated interstitial lung disease subsets ,systemic sclerosis interstitial lung disease ,Humans ,Lung Diseases ,Interstitial ,Scleroderma ,Systemic ,Vital Capacity ,Tomography ,X-Ray Computed ,Severity of Illness Index ,Lung - Abstract
OBJECTIVES: To establish a framework by which experts define disease subsets in systemic sclerosis associated interstitial lung disease (SSc-ILD). METHODS: A conceptual framework for subclinical, clinical and progressive ILD was provided to 83 experts, asking them to use the framework and classify actual SSc-ILD patients. Each patient profile was designed to be classified by at least four experts in terms of severity and risk of progression at baseline; progression was based on 1-year follow-up data. A consensus was reached if ≥75% of experts agreed. Experts provided information on which items were important in determining classification. RESULTS: Forty-four experts (53%) completed the survey. Consensus was achieved on the dimensions of severity (75%, 60 of 80 profiles), risk of progression (71%, 57 of 80 profiles) and progressive ILD (60%, 24 of 40 profiles). For profiles achieving consensus, most were classified as clinical ILD (92%), low risk (54%) and stable (71%). Severity and disease progression overlapped in terms of framework items that were most influential in classifying patients (forced vital capacity, extent of lung involvement on high resolution chest CT [HRCT]); risk of progression was influenced primarily by disease duration. CONCLUSIONS: Using our proposed conceptual framework, international experts were able to achieve a consensus on classifying SSc-ILD patients along the dimensions of disease severity, risk of progression and progression over time. Experts rely on similar items when classifying disease severity and progression: a combination of spirometry and gas exchange and quantitative HRCT.
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- 2023
3. POS0132 ASSOCIATIONS BETWEEN COMBINED ENVIRONMENTAL BURDEN AND SOCIAL VULNERABILITY AND CARE FRAGMENTATION AMONG INDIVIDUALS WITH RHEUMATIC CONDITIONS
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Feldman, C., primary, Santacroce, L., additional, Yang, S., additional, Valle, A., additional, and Dellaripa, P., additional
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- 2024
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4. POS1035 FORCED VITAL CAPACITY TRAJECTORIES AND RISK OF LUNG TRANSPLANT AND ILD-RELATED MORTALITY AMONG PATIENTS WITH RHEUMATOID ARTHRITIS-ASSOCIATED INTERSTITIAL LUNG DISEASE
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Venkat, R., primary, Hayashi, K., additional, Juge, P. A., additional, Mcdermott, G., additional, Paudel, M. L., additional, Vanni, K., additional, Kowalski, E., additional, Qian, G., additional, Bade, K., additional, Saavedra, A., additional, Mueller, K., additional, Chang, S. H., additional, Dellaripa, P., additional, Weinblatt, M. E., additional, Shadick, N. A., additional, Doyle, T., additional, Dieudé, P., additional, and Sparks, J. A., additional
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- 2024
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5. Effects of Social Vulnerability and Environmental Burden on Care Fragmentation and Social Needs Among Individuals With Rheumatic Conditions
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Santacroce, Leah, Yang, Sherry, Summit, Rebecca, Valle, Ana, Collins, Jamie E., Dellaripa, Paul F., and Feldman, Candace H.
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Environmental hazards and heightened neighborhood social vulnerability coexist and disproportionately affect minoritized populations. We investigated associations between exposure to adverse environmental burden concentrated in areas with high social vulnerability and care fragmentation (missed appointments, emergency department visits, and hospitalizations) and social needs (eg, food and housing insecurity) among individuals with rheumatic conditions. We identified adults receiving care in a Massachusetts multihospital system with at least two rheumatic disease codes and complete street addresses. Geocoded addresses were linked to the Centers for Disease Control and Prevention/Agency for Toxic Substances and Disease Registry Social–Environmental Ranking (SER), which combines census‐tract social vulnerability variables (eg, socioeconomic status) with environmental hazards (eg, air and water pollution). Social needs were obtained from self‐reported surveys. Multilevel, multinomial regression models estimated associations between SER quartiles and care fragmentation and social need burden, accounting for demographics and comorbidities. Among 16,856 individuals with rheumatic conditions, 70% were female, 6% were Black, 82% were White, and 7% resided in the highest combined social vulnerability and environmental burden (SER quartile 4) areas. Among 7,083 with social needs data, 19% experienced more than one challenge. Individuals in SER quartile 4 areas (vs quartile 1) had 2.02 (95% confidence interval [CI] 1.67–2.46) times greater odds of at least four care fragmentation occurrences (vs 0) and 2.37 (95% CI 1.73–3.25) times greater odds of at least two social needs (vs 0). Residence in areas of high combined adverse environmental burden and social vulnerability was associated with significantly greater odds of care fragmentation and social needs. Addressing structural factors and emerging environmental threats contributing to these adverse exposures is essential to reduce rheumatic disease care inequities.
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- 2025
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6. Rheumatoid Arthritis–Associated Interstitial Lung Disease: Current Update on Prevalence, Risk Factors, and Pharmacologic Treatment
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Huang, Sicong, Kronzer, Vanessa L., Dellaripa, Paul F., Deane, Kevin D., Bolster, Marcy B., Nagaraja, Vivek, Khanna, Dinesh, Doyle, Tracy J., and Sparks, Jeffrey A.
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- 2020
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7. 2023 American College of Rheumatology (ACR)/American College of Chest Physicians (CHEST) Guideline for the Screening and Monitoring of Interstitial Lung Disease in People with Systemic Autoimmune Rheumatic Diseases
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Johnson, Sindhu R., Bernstein, Elana J., Bolster, Marcy B., Chung, Jonathan H., Danoff, Sonye K., George, Michael D., Khanna, Dinesh, Guyatt, Gordon, Mirza, Reza D., Aggarwal, Rohit, Allen, Aberdeen, Assassi, Shervin, Buckley, Lenore, Chami, Hassan A., Corwin, Douglas S., Dellaripa, Paul F., Domsic, Robyn T., Doyle, Tracy J., Falardeau, Catherine Marie, Frech, Tracy M., Gibbons, Fiona K., Hinchcliff, Monique, Johnson, Cheilonda, Kanne, Jeffrey P., Kim, John S., Lim, Sian Yik, Matson, Scott, McMahan, Zsuzsanna H., Merck, Samantha J., Nesbitt, Kiana, Scholand, Mary Beth, Shapiro, Lee, Sharkey, Christine D., Summer, Ross, Varga, John, Warrier, Anil, Agarwal, Sandeep K., Antin‐Ozerkis, Danielle, Bemiss, Bradford, Chowdhary, Vaidehi, Dematte D'Amico, Jane E., Hallowell, Robert, Hinze, Alicia M., Injean, Patil A., Jiwrajka, Nikhil, Joerns, Elena K., Lee, Joyce S., Makol, Ashima, McDermott, Gregory C., Natalini, Jake G., Oldham, Justin M., Saygin, Didem, Lakin, Kimberly Showalter, Singh, Namrata, Solomon, Joshua J., Sparks, Jeffrey A., Turgunbaev, Marat, Vaseer, Samera, Turner, Amy, Uhl, Stacey, and Ivlev, Ilya
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We provide evidence‐based recommendations regarding screening for interstitial lung disease (ILD) and the monitoring for ILD progression in people with systemic autoimmune rheumatic diseases (SARDs), specifically rheumatoid arthritis, systemic sclerosis, idiopathic inflammatory myopathies, mixed connective tissue disease, and Sjögren disease. We developed clinically relevant population, intervention, comparator, and outcomes questions related to screening and monitoring for ILD in patients with SARDs. A systematic literature review was performed, and the available evidence was rated using the Grading of Recommendations, Assessment, Development, and Evaluation methodology. A Voting Panel of interdisciplinary clinician experts and patients achieved consensus on the direction and strength of each recommendation. Fifteen recommendations were developed. For screening people with these SARDs at risk for ILD, we conditionally recommend pulmonary function tests (PFTs) and high‐resolution computed tomography of the chest (HRCT chest); conditionally recommend against screening with 6‐minute walk test distance (6MWD), chest radiography, ambulatory desaturation testing, or bronchoscopy; and strongly recommend againstscreening with surgical lung biopsy. We conditionally recommend monitoring ILD with PFTs, HRCT chest, and ambulatory desaturation testing and conditionally recommend againstmonitoring with 6MWD, chest radiography, or bronchoscopy. We provide guidance on ILD risk factors and suggestions on frequency of testing to evaluate for the development of ILD in people with SARDs. This clinical practice guideline presents the first recommendations endorsed by the American College of Rheumatology and American College of Chest Physicians for the screening and monitoring of ILD in people with SARDs.
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- 2024
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8. 2023 American College of Rheumatology (ACR)/American College of Chest Physicians (CHEST) Guideline for the Treatment of Interstitial Lung Disease in People with Systemic Autoimmune Rheumatic Diseases
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Johnson, Sindhu R., Bernstein, Elana J., Bolster, Marcy B., Chung, Jonathan H., Danoff, Sonye K., George, Michael D., Khanna, Dinesh, Guyatt, Gordon, Mirza, Reza D., Aggarwal, Rohit, Allen, Aberdeen, Assassi, Shervin, Buckley, Lenore, Chami, Hassan A., Corwin, Douglas S., Dellaripa, Paul F., Domsic, Robyn T., Doyle, Tracy J., Falardeau, Catherine Marie, Frech, Tracy M., Gibbons, Fiona K., Hinchcliff, Monique, Johnson, Cheilonda, Kanne, Jeffrey P., Kim, John S., Lim, Sian Yik, Matson, Scott, McMahan, Zsuzsanna H., Merck, Samantha J., Nesbitt, Kiana, Scholand, Mary Beth, Shapiro, Lee, Sharkey, Christine D., Summer, Ross, Varga, John, Warrier, Anil, Agarwal, Sandeep K., Antin‐Ozerkis, Danielle, Bemiss, Bradford, Chowdhary, Vaidehi, Dematte D'Amico, Jane E., Hallowell, Robert, Hinze, Alicia M., Injean, Patil A., Jiwrajka, Nikhil, Joerns, Elena K., Lee, Joyce S., Makol, Ashima, McDermott, Gregory C., Natalini, Jake G., Oldham, Justin M., Saygin, Didem, Lakin, Kimberly Showalter, Singh, Namrata, Solomon, Joshua J., Sparks, Jeffrey A., Turgunbaev, Marat, Vaseer, Samera, Turner, Amy, Uhl, Stacey, and Ivlev, Ilya
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We provide evidence‐based recommendations regarding the treatment of interstitial lung disease (ILD) in adults with systemic autoimmune rheumatic diseases (SARDs). We developed clinically relevant population, intervention, comparator, and outcomes questions. A systematic literature review was then performed, and the available evidence was rated using the Grading of Recommendations, Assessment, Development, and Evaluation methodology. A panel of clinicians and patients reached consensus on the direction and strength of the recommendations. Thirty‐five recommendations were generated (including two strong recommendations) for first‐line SARD‐ILD treatment, treatment of SARD‐ILD progression despite first‐line ILD therapy, and treatment of rapidly progressive ILD. The strong recommendations were against using glucocorticoids in systemic sclerosis–ILD as a first‐line ILD therapy and after ILD progression. Otherwise, glucocorticoids are conditionally recommended for first‐line ILD treatment in all other SARDs. This clinical practice guideline presents the first recommendations endorsed by the American College of Rheumatology and American College of Chest Physicians for the treatment of ILD in people with SARDs.
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- 2024
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9. Connective tissue disease related interstitial lung diseases and idiopathic pulmonary fibrosis: provisional core sets of domains and instruments for use in clinical trials.
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Saketkoo, Lesley Ann, Mittoo, Shikha, Huscher, Dörte, Khanna, Dinesh, Dellaripa, Paul F, Distler, Oliver, Flaherty, Kevin R, Frankel, Sid, Oddis, Chester V, Denton, Christopher P, Fischer, Aryeh, Kowal-Bielecka, Otylia M, LeSage, Daphne, Merkel, Peter A, Phillips, Kristine, Pittrow, David, Swigris, Jeffrey, Antoniou, Katerina, Baughman, Robert P, Castelino, Flavia V, Christmann, Romy B, Christopher-Stine, Lisa, Collard, Harold R, Cottin, Vincent, Danoff, Sonye, Highland, Kristin B, Hummers, Laura, Shah, Ami A, Kim, Dong Soon, Lynch, David A, Miller, Frederick W, Proudman, Susanna M, Richeldi, Luca, Ryu, Jay H, Sandorfi, Nora, Sarver, Catherine, Wells, Athol U, Strand, Vibeke, Matteson, Eric L, Brown, Kevin K, Seibold, James R, and CTD-ILD Special Interest Group
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CTD-ILD Special Interest Group ,Humans ,Lung Diseases ,Interstitial ,Connective Tissue Diseases ,Registries ,Consensus ,International Cooperation ,Societies ,Medical ,Congresses as Topic ,Randomized Controlled Trials as Topic ,Idiopathic Pulmonary Fibrosis ,Connective tissue disease associated lung disease ,Idiopathic pulmonary fibrosis ,Interstitial Fibrosis ,Rheumatoid lung disease ,Systemic disease and lungs ,Lung Diseases ,Interstitial ,Societies ,Medical ,Respiratory System ,Clinical Sciences - Abstract
RationaleClinical trial design in interstitial lung diseases (ILDs) has been hampered by lack of consensus on appropriate outcome measures for reliably assessing treatment response. In the setting of connective tissue diseases (CTDs), some measures of ILD disease activity and severity may be confounded by non-pulmonary comorbidities.MethodsThe Connective Tissue Disease associated Interstitial Lung Disease (CTD-ILD) working group of Outcome Measures in Rheumatology-a non-profit international organisation dedicated to consensus methodology in identification of outcome measures-conducted a series of investigations which included a Delphi process including >248 ILD medical experts as well as patient focus groups culminating in a nominal group panel of ILD experts and patients. The goal was to define and develop a consensus on the status of outcome measure candidates for use in randomised controlled trials in CTD-ILD and idiopathic pulmonary fibrosis (IPF).ResultsA core set comprising specific measures in the domains of lung physiology, lung imaging, survival, dyspnoea, cough and health-related quality of life is proposed as appropriate for consideration for use in a hypothetical 1-year multicentre clinical trial for either CTD-ILD or IPF. As many widely used instruments were found to lack full validation, an agenda for future research is proposed.ConclusionIdentification of consensus preliminary domains and instruments to measure them was attained and is a major advance anticipated to facilitate multicentre RCTs in the field.
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- 2014
10. Association of rheumatoid arthritis-related autoantibodies with pulmonary function test abnormalities in a rheumatoid arthritis registry
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Huang, Sicong, He, Xintong, Doyle, Tracy J., Zaccardelli, Alessandra, Marshall, Allison A., Friedlander, H. Maura, Blaustein, Rachel B., Smith, Elisabeth A., Cui, Jing, Iannaccone, Christine K., Mahmoud, Taysir G., Weinblatt, Michael E., Dellaripa, Paul F., Shadick, Nancy A., and Sparks, Jeffrey A.
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- 2019
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11. Meta‐analysis of genetic polymorphisms in granulomatosis with polyangiitis (Wegener's) reveals shared susceptibility loci with rheumatoid arthritis
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Chung, Sharon A, Xie, Gang, Roshandel, Delnaz, Sherva, Richard, Edberg, Jeffrey C, Kravitz, Megan, Dellaripa, Paul F, Hoffman, Gary S, Mahr, Alfred D, Seo, Philip, Specks, Ulrich, Spiera, Robert F, St.Clair, E William, Stone, John H, Plenge, Robert M, Siminovitch, Katherine A, Merkel, Peter A, and Monach, Paul A
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Biological Sciences ,Biomedical and Clinical Sciences ,Genetics ,Epidemiology ,Health Sciences ,Clinical Sciences ,Arthritis ,Digestive Diseases ,Autoimmune Disease ,Clinical Research ,Prevention ,Lupus ,Human Genome ,Rheumatoid Arthritis ,Inflammatory Bowel Disease ,2.1 Biological and endogenous factors ,Aetiology ,Inflammatory and immune system ,Adolescent ,Adult ,Aged ,Aged ,80 and over ,Arthritis ,Rheumatoid ,Female ,Genetic Loci ,Genetic Predisposition to Disease ,Genotype ,Granulomatosis with Polyangiitis ,Humans ,Male ,Middle Aged ,Polymorphism ,Genetic ,Risk Factors ,Immunology ,Public Health and Health Services ,Arthritis & Rheumatology ,Clinical sciences - Abstract
ObjectiveTo examine the association of previously identified autoimmune disease susceptibility loci with granulomatosis with polyangiitis (Wegener's) (GPA), and to determine whether the genetic susceptibility profiles of other autoimmune diseases are associated with those of GPA.MethodsGenetic data from 2 cohorts were meta-analyzed. Genotypes for 168 previously identified single-nucleotide polymorphisms (SNPs) associated with susceptibility to different autoimmune diseases were ascertained in a total of 880 patients with GPA and 1,969 control subjects of European descent. Single-marker associations were identified using additive logistic regression models. Associations of multiple SNPs with GPA were assessed using genetic risk scores based on susceptibility loci for Crohn's disease, type 1 diabetes, systemic lupus erythematosus, rheumatoid arthritis (RA), celiac disease, and ulcerative colitis. Adjustment for population substructure was performed in all analyses, using ancestry-informative markers and principal components analysis.ResultsGenetic polymorphisms in CTLA4 were significantly associated with GPA in the single-marker meta-analysis (odds ratio [OR] 0.79, 95% confidence interval [95% CI] 0.70-0.89, P = 9.8 × 10(-5) ). The genetic risk score for RA susceptibility markers was significantly associated with GPA (OR 1.05 per 1-unit increase in genetic risk score, 95% CI 1.02-1.08, P = 5.1 × 10(-5) ).ConclusionRA and GPA may arise from a similar genetic predisposition. Aside from CTLA4, other loci previously found to be associated with common autoimmune diseases were not statistically significantly associated with GPA in this study.
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- 2012
12. POS1240 EFFICACY AND SAFETY OF ABATACEPT IN MYOSITIS ASSOCIATED INTERSTITIAL LUNG DISEASE
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Aggarwal, R., primary, Moghadam-Kia, S., additional, Koontz, D., additional, Saygin, D., additional, Bae, S., additional, Sullivan, D., additional, Marder, G., additional, Venuturupalli, S., additional, Dellaripa, P., additional, Danoff, S., additional, Doyle, T., additional, Hunninghake, G., additional, Lee, J. S., additional, Fischer, A., additional, Falk, J., additional, Kang, C. R., additional, Lin, Y., additional, Johnson, C., additional, Ascherman, D., additional, and Oddis, C. V., additional
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- 2023
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13. POS1055 ASSOCIATIONS AND MORTALITY IMPACT OF MACHINE LEARNING-DERIVED QUANTITATIVE PARENCHYMAL LUNG COMPUTED TOMOGRAPHY FEATURES IN RHEUMATOID ARTHRITIS AND NON-RA COMPARATORS IN A MULTICENTER PROSPECTIVE COHORT OF SMOKERS
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Mcdermott, G., primary, Hayashi, K., additional, Yoshida, K., additional, Moll, M., additional, Cho, M., additional, Doyle, T., additional, Dellaripa, P., additional, Kinney, G., additional, Wallace, Z., additional, Regan, E., additional, Hunninghake, G., additional, Silverman, E., additional, San Jose Estepar, R., additional, Ash, S., additional, Washko, G., additional, and Sparks, J., additional
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- 2023
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14. Correction to: Association of rheumatoid arthritis-related autoantibodies with pulmonary function test abnormalities in a rheumatoid arthritis registry
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Huang, Sicong, He, Xintong, Doyle, Tracy J., Zaccardelli, Alessandra, Marshall, Allison A., Friedlander, H. Maura, Blaustein, Rachel B., Smith, Elisabeth A., Cui, Jing, Iannaccone, Christine K., Mahmoud, Taysir G., Weinblatt, Michael E., Dellaripa, Paul F., Shadick, Nancy A., and Sparks, Jeffrey A.
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- 2020
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15. Short peripheral blood leukocyte telomere length in rheumatoid arthritis-interstitial lung disease
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Doyle, Tracy J, Juge, Pierre-Antoine, Peljto, Anna L, Lee, Seoyeon, Walts, Avram D, Esposito, Anthony Joseph, Poli, Sergio, Gill, Ritu, Hatabu, Hiroto, Nishino, Mizuki, Dellaripa, Paul F, Weinblatt, Michael E, Shadick, Nancy A, Demoruelle, M Kristen, Sparks, Jeffrey A, Rosas, Ivan O, Granger, Benjamin, Deane, Kevin D, Crestani, Bruno, Wolters, Paul J, Dieudé, Philippe, and Lee, Joyce S
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Shortened telomere lengths (TLs) can be caused by single nucleotide polymorphisms and loss-of-function mutations in telomere-related genes (TRG), as well as ageing and lifestyle factors such as smoking. Our objective was to determine if shortened TL is associated with interstitial lung disease (ILD) in individuals with rheumatoid arthritis (RA). This is the largest study to demonstrate and replicate that shortened peripheral blood leukocytes-TL is associated with ILD in patients with RA compared with RA without ILD in a multinational cohort, and short PBL-TL was associated with baseline disease severity in RA-ILD as measured by forced vital capacity percent predicted.
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- 2024
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16. Safety, tolerability, and efficacy of pirfenidone in patients with rheumatoid arthritis-associated interstitial lung disease: a randomised, double-blind, placebo-controlled, phase 2 study.
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Solomon, Joshua J, Danoff, Sonye K, Woodhead, Felix A, Hurwitz, Shelley, Maurer, Rie, Glaspole, Ian, Dellaripa, Paul F, Gooptu, Bibek, Vassallo, Robert, Cox, P Gerard, Flaherty, Kevin R, Adamali, Huzaifa I, Gibbons, Michael A, Troy, Lauren, Forrest, Ian A, Lasky, Joseph A, Spencer, Lisa G, Golden, Jeffrey, Scholand, Mary Beth, and Chaudhuri, Nazia
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INTERSTITIAL lung diseases ,VITAL capacity (Respiration) ,COMPUTED tomography ,RHEUMATOID arthritis - Abstract
Interstitial lung disease is a known complication of rheumatoid arthritis, with a lifetime risk of developing the disease in any individual of 7·7%. We aimed to assess the safety, tolerability, and efficacy of pirfenidone for the treatment of patients with rheumatoid arthritis-associated interstitial lung disease (RA-ILD). TRAIL1 was a randomised, double-blind, placebo-controlled, phase 2 trial done in 34 academic centres specialising in interstitial lung disease in four countries (the UK, the USA, Australia, and Canada). Adults aged 18–85 years were eligible for inclusion if they met the 2010 American College of Rheumatology and European Alliance of Associations for Rheumatology criteria for rheumatoid arthritis and had interstitial lung disease on a high-resolution CT scan imaging and, when available, lung biopsy. Exclusion criteria include smoking, clinical history of other known causes of interstitial lung disease, and coexistant clinically significant COPD or asthma. Patients were randomly assigned (1:1) to receive 2403 mg oral pirfenidone (pirfenidone group) or placebo (placebo group) daily. The primary endpoint was the incidence of the composite endpoint of a decline from baseline in percent predicted forced vital capacity (FVC%) of 10% or more or death during the 52-week treatment period assessed in the intention-to-treat population. Key secondary endpoints included change in absolute and FVC% over 52 weeks, the proportion of patients with a decline in FVC% of 10% or more, and the frequency of progression as defined by Outcome Measures in Rheumatoid Arthritis Clinical Trials (OMERACT) in the intention-to-treat population. This study is registered with ClinicalTrials.gov , NCT02808871. From May 15, 2017, to March 31, 2020, 231 patients were assessed for inclusion, of whom 123 patients were randomly assigned (63 [51%] to the pirfenidone group and 60 [49%] to the placebo group). The trial was stopped early (March 31, 2020) due to slow recruitment and the COVID-19 pandemic. The difference in the proportion of patients who met the composite primary endpoint (decline in FVC% from baseline of 10% or more or death) between the two groups was not significant (seven [11%] of 63 patients in the pirfenidone group vs nine [15%] of 60 patients in the placebo group; OR 0·67 [95% CI 0·22 to 2·03]; p=0·48). Compared with the placebo group, patients in the pirfenidone group had a slower rate of decline in lung function, measured by estimated annual change in absolute FVC (–66 vs –146; p=0·0082) and FVC% (–1·02 vs –3·21; p=0·0028). The groups were similar with regards to the decline in FVC% by 10% or more (five [8%] participants in the pirfenidone group vs seven [12%] in the placebo group; OR 0·52 [95% CI 0·14–1·90]; p=0·32) and the frequency of progression as defined by OMERACT (16 [25%] in the pirfenidone group vs 19 [32%] in the placebo group; OR 0·68 [0·30–1·54]; p=0·35). There was no significant difference in the rate of treatment-emergent serious adverse events between the two groups, and there were no treatment-related deaths. Due to early termination of the study and underpowering, the results should be interpreted with caution. Despite not meeting the composite primary endpoint, pirfenidone slowed the rate of decline of FVC over time in patients with RA-ILD. Safety in patients with RA-ILD was similar to that seen in other pirfenidone trials. Genentech. [ABSTRACT FROM AUTHOR]
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- 2023
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17. P1.06B.01 NSCLC in Patients with CTD-ILD: Apobec-Related Mutagenesis, Frequent TP53 Mutations and Paucity of Targetable Alterations
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Odintsov, I., Hammer, M.M., Awad, M.M., Dellaripa, P.F., and Sholl, L.M.
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- 2024
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18. ACUTE VASOREACTIVITY TESTING IN A MIXED COHORT OF GROUP-2 PULMONARY HYPERTENSION (PH) PATIENTS
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DELLARIPA, BENJAMIN, HARDER, EILEEN, and WAXMAN, AARON B
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- 2024
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19. Association of Area‐LevelHeat and Social Vulnerability With Recurrent Hospitalizations Among Individuals With Rheumatic Conditions
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Santacroce, Leah, Dellaripa, Paul F., Costenbader, Karen H., Collins, Jamie, and Feldman, Candace H.
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Climate and social vulnerability contribute to morbidity and health care utilization. We examined associations between the neighborhood Social Vulnerability Index (SVI) and the Heat Vulnerability Index (HVI) and recurrent hospitalizations among individuals with rheumatic conditions. Using a Massachusetts multihospital centralized clinical data repository, we identified individuals ≥18 years of age with a rheumatic condition who received rheumatology care within 3 years of April 2021. We defined the index date as 2 years before the last encounter and the baseline period as 1 year pre‐index date. Addresses were geocoded and linked by census tract to the SVI and the HVI. We used multilevel, multinomial logistic regression to examine the odds of 1–3 and ≥4 hospitalizations (reference = 0) over 2 years post index date by vulnerability index, adjusting for age, gender, race/ethnicity, insurance, and comorbidities. Among 14,401 individuals with rheumatic conditions, the mean ± age was 61.9 ± 15.7 years, 70% were female, 79% White, 7% Black, and 2% Hispanic. There were 8,251 hospitalizations; 11,649 individuals (81%) had 0 hospitalizations, 2,063 (14%) had 1–3, and 689 (5%) had ≥4. Adjusting for individual‐level factors, individuals living in the highest versus lowest SVI areas had 1.84 times higher odds (95% confidence interval [95% CI] 1.43–2.36) of ≥4 hospitalizations. Individuals living in the highest versus lowest HVI areas had 1.64 times greater odds (95% CI 1.17–2.31) of ≥4 hospitalizations. Individuals with rheumatic conditions living in areas with high versus low social and heat vulnerability had significantly greater odds of recurrent hospitalizations. Studies are needed to determine modifiable factors to mitigate risks.
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- 2023
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20. Demographic, Lifestyle, and Serologic Risk Factors for Rheumatoid Arthritis (RA)-associated Bronchiectasis: Role of RA-related Autoantibodies.
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McDermott, Gregory, Gill, Ritu, Gagne, Staci, Byrne, Suzanne, Weixing Huang, Xiaosong Wang, Prisco, Lauren C., Zaccardelli, Alessandra, Martin, Lily W., Masto, Lucy, Kronzer, Vanessa L., Shadick, Nancy, Dellaripa, Paul F., Doyle, Tracy J., Sparks, Jeffrey A., Huang, Weixing, and Wang, Xiaosong
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- 2022
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21. OP0115 EFFECT OF NINTEDANIB ON PROGRESSION OF INTERSTITIAL LUNG DISEASE (ILD) IN PATIENTS WITH AUTOIMMUNE DISEASE-RELATED ILDS: FURTHER DATA FROM THE INBUILD TRIAL
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Matteson, E., primary, Kelly, C., additional, Distler, J., additional, Hoffmann-Vold, A. M., additional, Seibold, J., additional, Mittoo, S., additional, Distler, O., additional, Dellaripa, P. F., additional, James, A., additional, Schlenker-Herceg, R., additional, Stowasser, S., additional, Quaresma, M., additional, and Flaherty, K. R., additional
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- 2020
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22. The Knowledge and Practices of Rheumatologists and Pulmonologists in Rheumatoid Arthritis-Associated Interstitial Lung Disease
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Solomon, J., primary, Kreuter, M., additional, Polke, M., additional, Aronson, K.I., additional, Hoffmann-Vold, A., additional, and Dellaripa, P., additional
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- 2020
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23. Significant Burden of Undiagnosed Emphysema in a Rheumatoid Arthritis Population
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Esposito, A.J., primary, Sparks, J., additional, Gill, R., additional, Hatabu, H., additional, Schmidlin, E., additional, Hota, P., additional, Fletcher, E., additional, Poli De Frias, S., additional, Xiong, W., additional, Frits, M., additional, Christine, I., additional, Dellaripa, P., additional, Weinblatt, M., additional, Shadick, N., additional, Rosas, I.O., additional, and Doyle, T.J., additional
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- 2020
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24. Differential Protein Expression in Rheumatoid Arthritis Interstitial Lung Disease
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Wu, X., primary, Poli De Frias, S., additional, Taheri, S., additional, Hoffman, K., additional, Easthausen, I., additional, Esposito, A.J., additional, Quesada Arias, L.D., additional, Ayaub, E., additional, Maurer, R., additional, Gill, R., additional, Hatabu, H., additional, Nishino, M., additional, Frits, M., additional, Iannaccone, C., additional, Weinblatt, M., additional, Shadick, N., additional, Dellaripa, P., additional, Rosas, I.O., additional, Martinez, F.J., additional, Choi, A.M.K., additional, and Doyle, T.J., additional
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- 2020
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25. Royal academy of medicine in Ireland international conference on homocysteine metabolism from basic science to clinical medicine: Proceedings of meeting held at Dromoland Castle, Co. Clare on July 2nd–6th, 1995
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Björkegren, K., Bergmark, C., de Faire, U., Mansoor, M. Azam, Svardal, A., Bostom, A. G., Roubenoff, R., Dellaripa, P., Nadeau, M. R., Sutherland, P., Wilson, P. W. F., Jacques, P. F., Selhub, J., Rosenberg, I. H., Bostom, A. G., Brosnan, J. T., Hall, B., Nadeau, M. R., Selhub, J., Bostom, A. G., Shemin, D., Lapane, K. L., Sutherland, P., Nadeau, M. R., Wilson, P. W. F., Selhub, J., Bostom, A. G., Shemin, D., Nadeau, M. R., Selhub, J., Bostom, A. G., Selhub, J., Jacques, P. F., Nadeau, M. R., Williams, R. R., Ellison, R. C., Cuskelly, G. J., McNulty, H., Strain, J. J., McPartlin, J. M., Scott, J. M., Chadefaux-Vekemans, B., Coudé, M., Aupetit, J., Kamoun, P., Coudé, M., Aral, B., Zabot, M. T., Aupetit, J., Kamoun, P., Chadefaux-Vekemans, B., Calaf, R., Ghiringelli, O., Barlatier, A., Charpiot, P., Rolland, P. H., Garçon, D., Charpiot, P., Augier, T., Chareyre, C., Rolland, P. H., Garçon, D., Chango, A., Hodez, F., Tronel, H., Nuel, G., Michel, F., Frémont, S., Méjean, L., Nicolas, J. P., Candito, M., Chambon, P., Gibelin, P., Amsellem, J., Baudouy, M., Morand, P., Candito, M., Chambon, P., Pringuey, D., Aubin-Brunet, V., Beaulieu, F., Darcourt, G., Bedoucha, P., Alchaar, H., Chatel, M., Candito, M., de Valk, H. W., van der Griend, R., Eeden, M. K. G. van, de Groot, E., Duran, M., Smeitink, J. A. M., de Klerk, J. B. C., Wittebol-Post, D., Rolland, M. -O., Haas, F. J. L. M., Meuwissen, O. J. A. Th., Banga, J. D., Poll-The, B. T., de Vries, J. I. P., Dekker, G. A., van Geijn, H. P., Huigens, P. C., Jakobs, C., von Blomberg, B. M. E., Deulofeu, R., Giralt, M., Aibar, C., Bauchet, C., Ballesta, A. M., Varela, G., Vila, N., Chamorro, A., Casals, F. J., Cremades, J. Diaz, Daly, L., Meleady, R., Graham, I., den Heijer, M., Brouwer, I. A., Gerrits, W. B. J., Bos, G. M. J., Blom, H. J., den Heijer, M., Bos, G. M. J., Koster, T., Vandenbroucke, J. P., Blom, H. J., Briët, E., Rosendaal, F. R., Fischer, G., Behrend, C., Bartholmes, P., Fermo, I., Paroni, R., Vigano, S., D’Angelo, A., Fermo, I., Paroni, R., Vigano, S., D’Angelo, A., Franken, D. G., Boers, G. H. J., Blom, H. J., Hamel, B. C. J., Franken, D. G., Boers, G. H. J., Blom, H. J., Ruijs, J. H. J., Franken, D. G., Blom, H. J., Boers, G. H. J., Tangerman, A., Guttormsen, A. B., Ueland, P. M., Refsum, H., Svarstad, E., Gao, W., Goldman, E., Jakubowski, H., Sebastio, G., Sperandeo, M. P., de Franchis, R., Andria, G., Garrow, T. A., Hladovec, J., Sommerova, Z., Písariková, A., Halsted, C. H., Villanueva, J., Chandler, C. J., Stabler, S. P., Allen, R. H., Muskhelishvili, L., James, S. J., Poirer, L., Jacobsen, D. W., Savon, S. R., DiCorleto, P. E., Jourdheuil-Rahmani, D., Rolland, P. H., Garçon, D., Joosten, E., Riezler, R., Allen, R., Joosten, E., Riezler, R., Allen, R., Marquardt, T., Ullrich, K., Harms, E., Koch, H. G., Koch, H. G., Evers, S., Grotemeyer, K. H., Vogelpohl, L., von Eckardstein, A., Ullrich, K., Deufel, T., Kraus, J., Harms, E., Kozich, V., Janosik, M., Sokolová, J., Bukovská, G., Kraus, J. P., Kluitmans, L. A. J., van den Heuvel, L. P., Stevens, E., Trubels, J. M. F., Blom, H. J., Boers, G. H. J., van Oost, B. A., Kraus, J. P., Kittner, S., Macko, R., Hebel, J. R., Rohr, J., Malinow, M. R., Upson, B., Buchholz, D., Earley, C., Johnson, C., Price, T. R., Rosario, J., Sloan, M., Stern, B., Wityk, R., Wozniak, M., Sherwin, R., Stolley, P., Kluijtmans, L., Heuvel, L. van den, Stevens, E., Trijbels, F., Blom, H., Boers, G., van Oost, B., den Heijer, M., Rozen, R., Löhrer, F., Angst, C., Fowler, B., Zaugg, M., Brunner, F., Haefeli, W. E., Nedrebø, B., Ericsson, U. -B., Ueland, P. M., Refsum, H., Lien, E. A., London, J., Paly, E., Paul, V., Paris, D., Kamoun, P., Chassé, J. F., Møller, J., Rasmussen, K., Meleady, R., Graham, I., Daly, L., Verhoef, P., Meleady, R., Graham, I., Daly, L., McMartin, K. E., Phifer, T. J., Alexander, J. S., Middlebrooks, M., Childress, L. E., Nicolas, J. P., Tronel, H., Chango, A., Fremont, S., Felden, F., Guerci, B., Creton, C., Drouin, P., Oakley, G. P., Elias, P. R. P., Hann, A. C., Curtis, C. G., Rose, F. A., Tudball, N., Parrot-Roulaud, F., Cochet, C., Catargi, B., Leprat, F., Latapie, J. -L., Perna, A. F., De Santo, N. G., Ingrosso, D., Galletti, P., Zappia, V., Parrot-Roulaud, F., Sassoust, G., Boissieras, P., Blom, H. J., Majors, A. K., Ehrhart, L. A., Pezacka, E. H., Perry, I. J., Morris, R. W., Ebrahim, S. B., Shaper, A. G., Refsum, H., Ueland, P. M., Pietrzik, K., Dierkes, J., Kroesen, M., Bung, P., Rasmussen, K., Moller, J., Rasmussen, K., Remacha, A., Garcia-Die, F., Cadafalch, J., Barceló, H. J., Parellada, H., Regland, B., Gottfries, C. -G., Andersson, M., Bagby, J., Dyrehag, L. -E., Abrahamsson, L., Ronge, E., Kjellman, B., Frosst, P., Christensen, B., Goyette, P., Rosenblatt, D. S., Genest, J., Rozen, R., Riedel, B., Ueland, P. M., Svardal, A. M., Silberberg, J., Crooks, R., Fryer, J., Ray, C., Guo, X. W., Xie, L., Dudman, N., Silberberg, J., Crooks, R., Fryer, J., Ray, C., Guo, X. W., Xie, L., Dudman, N., Silberberg, J., Crooks, R., Fryer, J., Ray, C., Guo, X., Xie, L., Dudman, N., Smith, B., Kohlman-Trigoboff, D., Simsir, S., Stabler, S. P., Allen, R. H., Strydom, A. J. C., Schlüssel, E., Preibisch, G., Elstner, E. F. E., Pütter, S., Spuijbroek, M. D. E. H., Goddijn-Wessel, T. A. W., Wouters, M. G. A. J., Molen, E. F. v. d., Blom, H. J., Boers, G. H. J., Steegers-Theunissen, R. P. M., Trijbels, J. M. F., Thomas, C. M. G., Eskes, T. K. A. B., Tsai, M. Y., Hanson, N., Key, N., Schwichtenberg, K., Garg, U., Todesco, L., Fowler, B., Pollaert, N., Haefeli, W. E., Thorand, B., Hages, M., Pietrzik, K., Bung, P., Holzgreve, W., Vila, N., Chamorro, A., Deulofeu, R., Aibar, C., Giralt, M., Ballesta, A. M., van der Mooren, M. J., Wouters, M. G. A. J., Schellekens, L. A., Eskes, T. K. A. B., Rolland, R., Blom, H. J., Put, N. v. d., Trijbels, F., Heuvel, L. v. d., Blom, H., Eskes, T., Steegers-Theunissen, R., Mariman, E., Heyer, M. d., Rozen, R., Daher, R., Van Lente, F., Vilkovsky, A. B., Maev, I. V., Richter, E. L., Kirnus, M. D., Varela-Moreiras, G., Alonso-Aperte, E., Rubio, M., Gassó, M., Deulofeu, R., Alvarez, L., Caballeria, J., Rodés, J., Mato, J. M., van Aerts, L. A. G. J. M., Peereboom-Stegeman, J. H. J. Copius, Noordhoek, J., Eskes, T. K. A. B., Molen, E. F. v. d., Spuijbroek, M. D. E. H., Eskes, T. K. A. B., Heuvel, L. P. v. d., Monnens, L. A. H., Blom, H. J., van Guidener, C., Janssen, M. J. F. M., Surachno, J., Stehouwer, C. D. A., van den Berg, M., Bierdrager, E., Rauwerda, J. A., Wilcken, B., Hammond, J., Wouters, M. G. A. J., Hamilton, C. J. C. M., Blom, H. J., Boers, G. H. J., Thomas, C. M. G., Borm, G. F., Eskes, T. K. A. B., Wang, H., Tsai, J. -C., Perrella, M. A., Yoshizumi, M., Sibinga, N. E. S., Haber, E., Chang, T. H. -T., Schlegel, R., Lee, M. -E., Woodside, J., McMaster, D., Yarnell, J., Young, I., Mercer, C., Byrne, K., Evans, A., Gey, F., Gao, X. M., Dougan, G., Wordsworth, P., McMichael, A., Young, P. B., Kennedy, D. G., Molloy, A. M., Scott, J. M., Ward, P., Naughten, E., Cahalane, S., Murphy, D., Mayne, P., Chauveau, P., Chadefaux-Vekemans, B., Coudé, M., Aupetit, J., Kamoun, P., Jungers, P., van Asselt, D. Z. B., Blom, H. J., de Wild, G. M., van Staveren, W. A., Hoefnagels, W. H. L., Naruszewicz, M., Staniewicz, A., Dziewanowski, K., Evrovski, J., Cole, D. E. C., Callaghan, Michael, Lindgren, A., Brattström, L., Hultberg, B., Verhoef, P., Hennekens, C. H., Allen, R. H., Stabler, S. P., Willett, W. C., Stampfer, M. J., Frantzen, F., Sundrehagen, E., Verhoef, P., Kok, F. J., Stampfer, M. J., Willett, W. C., Gaziano, J. M., Hennekens, C. H., Allen, R. H., Stabler, S. P., Reynolds, R. D., Hsu, R. -J., Shane, B., Robinson, K., Kottke-Marchant, K., Green, R., Gupta, A., Jacobsen, D., Robinson, K., Mayer, E., Gupta, A., Miller, D., Marchant, K., Green, R., Jacobsen, D., Greene, R., Chong, Y. -Y., Jacobsen, D., Robinson, K., Gupta, M., Sheppard, C. A., Matthews, R. G., Goyette, P., Frosst, P., Rozen, R., Verhoef, P., Kok, F. J., Kruyssen, H. A. C. M., Witteman, J. C. M., Ueland, P. M., Boushey, C., Beresford, S., Omenn, G., Motulsky, A. G., Nygard, O., Vollset, S. E., Kvale, G., Stensvold, I., Ueland, P. M., Refsum, H., Fiskerstrand, T., Ueland, P. M., Refsum, H., Bugge, K. H., Oshaug, A., Bjønnes, C. H., Refsum, H., Wu, J. T., Wu, L. L., and Wilson, L. W.
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- 1995
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26. Outcome measurement instrument selection for lung physiology in systemic sclerosis associated interstitial lung disease: A systematic review using the OMERACT filter 2.1 process.
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Roofeh, David, Barratt, Shaney L., Wells, Athol U, Kawano-Dourado, Leticia, Tashkin, Donald, Strand, Vibeke, Seibold, James, Proudman, Susanna, Brown, Kevin K, Dellaripa, Paul F, Doyle, Tracy, Leonard, Thomas, Matteson, Eric L, Oddis, Chester V, Solomon, Joshua J, Sparks, Jeffrey A, Vassallo, Robert, Maxwell, Lara, Beaton, Dorcas, and Christensen, Robin
- Abstract
The Outcome Measures in Rheumatology (OMERACT) is a research organization focused on improving health care outcomes for patients with autoimmune and musculoskeletal diseases. The Connective Tissue Disease-Interstitial Lung Disease (CTD-ILD) Working Group on Lung Physiology is a group within OMERACT charged with identifying outcome measures that should be implemented in studies of patients with CTD-ILD. The OMERACT Filter 2.1 is an evidence-based algorithm used to identify outcome measures that are truthful, feasible, and able to discriminate between groups of interest. Our objective was to summate evidence (published literature, key opinion leader input, patient perspectives) that would influence the CTD-ILD Working Group's vote to accept or reject the use of two measures of lung physiology, the forced vital capacity (FVC) and the diffusion capacity of carbon monoxide (DLco) for use in randomized controlled trials (RTCs) and longitudinal observational studies (LOSs) involving patients with systemic sclerosis associated ILD (SSc-ILD). Patient Research Partners (those afflicted with SSc-ILD) and the CTD-ILD Working Group on Lung Physiology were polled to assess their opinion on the FVC and DLco in terms of feasibility; the CTD-ILD Working Group was also queried on these instruments' face and content validity. We then conducted a systematic literature review to identify articles in the SSc-ILD population that assessed the following measurement properties of FVC and DLco: (1) construct validity, (2) test-retest reliability, (3) longitudinal construct validity, (4) clinical trial discrimination/sensitivity to detect change in clinical trials, and (5) thresholds of meaning. Results were summarized in a Summary of Measurement Properties (SOMP) table for each instrument. OMERACT CTD-ILD Working Group members discussed and voted on the strength of evidence supporting these two instruments and voted to endorse, provisionally endorse, or not endorse either instrument. Forty Patient Research Partners reported these two measures are feasible (are not an unnecessary burden or represent an infeasible longitudinal assessment of their disease). A majority of the 18 CTD-ILD Working Group members voted that both the FVC and DLco are feasible and have face and content validity. The systematic literature review returned 1,447 non-duplicated articles, of which 177 met eligibility for full text review. Forty-eight studies (13 RCTs, 35 LOSs) were included in the qualitative analysis. The FVC SOMP table revealed high quality, consistent data with evidence of good performance for all five measurement properties, suggesting requisite published evidence to proceed with endorsement. The DLco SOMP table showed a lack of data to support test-retest reliability and inadequate evidence to support clinical trial discrimination. There was unanimous agreement (15 [100%]) among voting CTD-ILD Working Group members to endorse the FVC as an instrument for lung physiology in RCTs and LOSs in SSc-ILD. Based on currently available evidence, DLco did not meet the OMERACT criteria and is not recommended for use in RCTs to represent lung physiology of SSc-ILD. The OMERACT Technical Advisory Group agreed with these decisions. The OMERACT Filter 2.1 was successfully applied to the domain of lung physiology in patients with SSc-ILD. The FVC was endorsed for use in RCTs and LOSs based on the Working Group's vote; DLco was not endorsed. [ABSTRACT FROM AUTHOR]
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- 2021
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27. Lifestyle and Clinical Risk Factors for Incident Rheumatoid Arthritis-associated Interstitial Lung Disease.
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Kronzer, Vanessa L., Weixing Huang, Dellaripa, Paul F., Sicong Huang, Feathers, Vivi, Bing Lu, Iannaccone, Christine K., Gill, Ritu R., Hiroto Hatabu, Mizuki Nishino, Crowson, Cynthia S., Davis III, John M., Weinblatt, Michael E., Shadick, Nancy A., Doyle, Tracy J., Sparks, Jeffrey A., Huang, Weixing, Huang, Sicong, Lu, Bing, and Hatabu, Hiroto
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- 2021
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28. Serum proteomic profiling of rheumatoid arthritis–interstitial lung disease with a comparison to idiopathic pulmonary fibrosis
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Wu, Xiaoping, Jeong, Yunju, Poli de Frías, Sergio, Easthausen, Imaani, Hoffman, Katherine, Oromendia, Clara, Taheri, Shahrad, Esposito, Anthony J, Quesada Arias, Luisa, Ayaub, Ehab A, Maurer, Rie, Gill, Ritu R, Hatabu, Hiroto, Nishino, Mizuki, Frits, Michelle L, Iannaccone, Christine K, Weinblatt, Michael E, Shadick, Nancy A, Dellaripa, Paul F, Choi, Augustine M K, Kim, Edy Y, Rosas, Ivan O, Martinez, Fernando J, and Doyle, Tracy J
- Abstract
Although interstitial lung disease (ILD) causes significant morbidity and mortality in rheumatoid arthritis (RA), it is difficult to predict the development or progression of ILD, emphasising the need for improved discovery through minimally invasive diagnostic tests. Aptamer-based proteomic profiling was used to assess 1321 proteins from 159 patients with rheumatoid arthritis with interstitial lung disease (RA-ILD), RA without ILD, idiopathic pulmonary fibrosis and healthy controls. Differential expression and gene set enrichment analyses revealed molecular signatures that are strongly associated with the presence and severity of RA-ILD and provided insight into unexplored pathways of disease. These warrant further study as non-invasive diagnostic tools and future therapeutic targets.
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- 2022
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29. Rheumatoid arthritis-related lung disease detected on clinical chest computed tomography imaging: Prevalence, risk factors, and impact on mortality.
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Huang, Sicong, Doyle, Tracy J., Hammer, Mark M., Byrne, Suzanne C., Huang, Weixing, Marshall, Allison A., Iannaccone, Christine K., Huang, Jie, Feathers, Vivi, Weinblatt, Michael E., Dellaripa, Paul F., Shadick, Nancy A., and Sparks, Jeffrey A.
- Abstract
We aimed to determine the real-world prevalence and investigate risk factors for rheumatoid arthritis (RA)-related lung disease on chest computed tomography (CT) imaging. We also investigated the impact of RA-related lung disease on mortality. We studied chest CT imaging abnormalities among RA patients. We determined the presence and type of abnormalities using the chest CT imaging radiologic report. RA-related lung disease was defined as interstitial lung disease (ILD), bronchiectasis, or pleural disease. We examined whether demographics and RA characteristics were associated with RA-related lung disease using logistic regression. RA-related lung disease and mortality was described using survival curves and Cox regression. We analyzed 190 patients who had chest CT imaging performed for clinical indications. Mean age was 64.2 years (SD 11.8), 80.0% were female, and 75.3% were seropositive. RA-related lung disease was detected in 54 patients (28.4%); 30 (15.8%) had ILD, 27 (14.2%) had bronchiectasis, and 18 (9.5%) had pleural disease. RA-related lung disease was reported in both seropositive and seronegative RA (28.7% vs. 27.7%, p = 1.00). Male sex (OR 2.62, 95%CI 1.17–5.88) and current methotrexate use (OR 2.73, 95%CI 1.27–5.61 vs. not current) were associated with RA-related lung disease. Twenty-four (44.4%) patients with RA-related lung disease died during mean 7.0 years of follow-up. RA-related lung disease had HR of 5.35 (95%CI 0.72–39.9) for mortality compared to normal chest CT. In this real-world study, RA-related lung disease was commonly detected on chest CT imaging regardless of RA serostatus. RA-related lung disease had high mortality, emphasizing the importance in close monitoring of these patients. [ABSTRACT FROM AUTHOR]
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- 2020
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30. Effectiveness and tolerability of antifibrotics in rheumatoid arthritis-associated interstitial lung disease.
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Juge, Pierre-Antoine, Hayashi, Keigo, McDermott, Gregory C., Vanni, Kathleen M.M., Kowalski, Emily, Qian, Grace, Bade, Katarina, Saavedra, Alene, Dieudé, Philippe, Dellaripa, Paul F., Doyle, Tracy J., and Sparks, Jeffrey A.
- Abstract
Our aim was to investigate the effectiveness and tolerability of antifibrotics in a real-world cohort of patients with rheumatoid arthritis-associated interstitial lung diseases (RA-ILD). In this retrospective cohort study, we identified RA-ILD patients initiating antifibrotics at Mass General Brigham Integrated Health Care System, a large multi-hospital healthcare system in Boston, MA, USA. We used electronic query to identify all patients with at least 2 RA diagnosis codes and a prescription for either nintedanib or pirfenidone (2014–2023). All analyzed patients met 2010 American College of Rheumatology/European Alliance of Associations for Rheumatology classification criteria for RA and had definite RA-ILD according to Bongartz criteria. Data regarding pulmonary function test (PFT) results, adverse events (AEs), tolerability, and clinical data were collected. A linear mixed model with random intercept was used to compare the within-patient trajectory of the percent predicted forced vital capacity (FVCpp) within 18-months before to 18-months after antifibrotic initiation among those with these PFT data. Lung transplant-free survival and drug retention was estimated in a Kaplan-Meier analysis and a Cox regression analysis was performed to identify independent baseline factors associated with lung transplant or mortality. We analyzed 74 patients with RA-ILD that initiated antifibrotics (mean age 67.8 years, 53 % male); 40 patients initiated nintedanib and 34 initiated pirfenidone. Median follow-up was 89 weeks (min 4, max 387). There was a significant improvement in the estimated slope of FVCpp after antifibrotic initiation (−0.3 % per year after initiation compared to −6.2 % per year before antifibrotic initiation, p = 0.03). Nintedanib and pirfenidone had similar FVCpp trajectory. Twenty-six patients (35 %) died and 4 (5 %) had undergone lung transplantation during follow-up. Male sex and heavy smoking were each associated with the composite outcome of lung transplant or mortality. AEs were reported in 41 (55 %) patients, with gastrointestinal (GI) AEs being most common (n = 30). The initial antifibrotic was discontinued in 34 (46 %) patients mostly due to GI AEs (n = 19). The median drug retention time was 142 weeks (95 %CI 56, 262) with no difference between nintedanib and pirfenidone (p = 0.68). In this first real-world study of antifibrotic use dedicated to RA-ILD, antifibrotic initiation was associated with a modestly improved trajectory of FVCpp. AEs were frequently reported, particularly GI, and discontinuation was common. However, lung transplant and mortality rates were still high, emphasizing the need for further therapeutic strategies in patients with severe RA-ILD. These real-world data complement previous trial data that investigated efficacy and safety. [ABSTRACT FROM AUTHOR]
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- 2024
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31. A National Survey of Burnout and Depression Among Fellows Training in Pulmonary and Critical Care Medicine
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Sharp, Michelle, Burkart, Kristin M., Adelman, Mark H., Ashton, Rendell W., Daugherty Biddison, Lee, Bosslet, Gabriel T., Doyle, Stephen T., Eckmann, Thomas, Khurram S. Khan, Malik M., Lenz, Peter H., McCallister, Jennifer W., O’Toole, Jacqueline, Rand, Cynthia S., Riekert, Kristin A., Soffler, Morgan I., Winter, Gretchen R., Zaeh, Sandra, Eakin, Michelle N., Arabelovic, Senada, Baer, Alan, Greene, Jerome L., Baker, Matthew C., Bloch, Donald, Cohen, Philip, Danielides, Stamatina J., Danila, Maria, Dellaripa, Paul F., Lawrence Ford, Theresa, Fox, Robert I., Grader-Beck, Thomas, Johr, Chadwick R., Kassan, Stuart, Katsumoto, Tamiko, Kontzias, Apostolos, Koons, Kirsten, Kyttaris, Vasileios C., Lewis, Janet, Lieberman, Scott M., McCoy, Sara S., Niewold, Timothy, Noaiseh, Ghaith, Osborn, Thomas G., Culpepper Pace, Schartess, Peredo-Wende, Ruben, Pillemer, Stanley, Neal Roberts, W., Rosenstein, Elliot, Sachdev, Amit, Sandorfi, Nora, Segal, Barbara, Siva, Chokkalingam, Small, Daniel, Spiera, Robert F., Topilow, James, Treadwell, Edward L., Vivino, Frederick B., Volkmann, Elizabeth, Wallace, Daniel J., Zashin, Scott, Gupta Argula, Rahul, Barney, Joseph, Burger, Charles D., Downey, Gregory P., Gagermeier, James, Helmers, Richard A., Hewlett, Justin C., Keith, Rebecca C., Koslow, Matthew, Kotloff, Robert, Krishna, Rachana, Luckhardt, Tracy R., Robinson, Keith, Ryu, Jay H., Shifren, Adrian, Staton, Gerald, Swigris, Jeff, Vassallo, Robert, Veraldi, Kristen L., Ward, Robert W., Bromet, Evelyn J., Dale, Jeanne, Furlong, Judith A., Neall, Kerry L., Petruzzi, Lynn M., Schafer, Sarah, and Kukla, Heidi
- Abstract
The prevalence of burnout and depressive symptoms is high among physician trainees.
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- 2021
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32. ASSOCIATIONS AND MORTALITY IMPACT OF MACHINE LEARNING-DERIVED QUANTITATIVE PARENCHYMAL LUNG COMPUTED TOMOGRAPHY FEATURES IN RHEUMATOID ARTHRITIS AND NON-RA COMPARATORS IN A MULTICENTER PROSPECTIVE COHORT OF SMOKERS.
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Mcdermott, G., Hayashi, K., Yoshida, K., Moll, M., Cho, M., Doyle, T., Dellaripa, P., Kinney, G., Wallace, Z., Regan, E., Hunninghake, G., Silverman, E., Jose Estepar, R. San, Ash, S., Washko, G., and Sparks, J.
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- 2023
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33. Pulmonary Vascular and Right Ventricular Burden During Exercise in Interstitial Lung Disease
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Oliveira, Rudolf K.F., Waxman, Aaron B., Hoover, Paul J., Dellaripa, Paul F., and Systrom, David M.
- Abstract
Pulmonary hypertension (PH) adversely affects patient’s exercise capacity in interstitial lung disease (ILD). The impact of pulmonary vascular and right ventricular (RV) dysfunction, however, has traditionally been believed to be mild and clinically relevant principally in advanced lung disease states.
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- 2020
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34. IgA Antibodies Directed Against Citrullinated Protein Antigens Are Elevated in Patients With Idiopathic Pulmonary Fibrosis
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Solomon, Joshua J., Matson, Scott, Kelmenson, Lindsay B., Chung, Jonathan H., Hobbs, Stephen B., Rosas, Ivan O., Dellaripa, Paul F., Doyle, Tracy J., Poli, Sergio, Esposito, Anthony J., Visser, Ashley, Marin, A. Itzam, Amigues, Isabelle, Fernández Pérez, Evans R., Brown, Kevin K., Mahler, Michael, Heinz, David, Cool, Carlyne, Deane, Kevin D., Swigris, Jeffrey J., and Demoruelle, M. Kristen
- Abstract
The etiology of idiopathic pulmonary fibrosis (IPF) is unknown. Because it shares genetic, histopathologic, and radiographic features with the fibrosing interstitial lung disease seen in rheumatoid arthritis (RA), the goal of this study was to investigate RA-related autoantibodies in IPF.
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- 2020
- Full Text
- View/download PDF
35. Reconciling Healthcare Professional and Patient Perspectives in the Development of Disease Activity and Response Criteria in Connective Tissue Disease Related Interstitial Lung Diseases
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Saketkoo, La, Mittoo, S, Frankel, S, Lesage, D, Sarver, C, Phillips, K, Strand, V, Matteson, El, OMERACT Baughman RP, Brown, Kk, Christmann, Rb, Dellaripa, P, Denton, Cp, Distler, O, Fischer, A, Flaherty, K, Huscher, D, Khanna, D, Kowal Bielecka, O, Merkel, Pa, Oddis, Cv, Pittrow, D, Sandorfi, N, Seibold, Jr, Swigris, J, Wells, A, Antoniou, K, Castelino, Fv, Christopher Stine, L, Collard, Hr, Cottin, V, Danoff, S, Hedlund, R, Highland, Kb, Hummers, L, Lynch, Da, Kim, Ds, Ryu, Jh, Miller, Fw, Nichols, K, Proudman, Sm, Richeldi, L, Shah, Aa, van den Assum, P, Aggarwal, R, Ainslie, G, Alkassab, F, Allanore, Y, Anderson, Me, Andonopoulos, Ap, Antin Ozerkis, D, Arrobas, A, Ascherman, Dp, Assassi, S, Baron, M, Bathon, Jm, Baughman, Rp, Behr, J, Beretta, L, Bingham, Co, Binnie, M, Birring, Ss, Boin, F, Bongartz, T, Bourdin, A, Bouros, D, Brasington, R, Bresser, P, Buch, Mh, Burge, Ps, Carmona, L, Carreira, Pe, Carvalho, Cr, Catoggio, Lj, Chan, Km, Chapman, J, Chatterjee, S, Chua, F, Chung, L, Conron, M, Corte, T, Cosgrove, G, Costabel, U, Cox, G, Crestani, B, Crofford, Lj, Csuka, Me, Curbelo, P, Czirják, L, Daniil, Z, D'Arsigny, Cl, Davis, Gs, de Andrade JA, Dellaripa, Pf, De Vuyst, P, Dempsey, Oj, Derk, Ct, Distler, J, Dixon, Wg, Downey, G, Doyle, Mk, Drent, M, Durairaj, L, Emery, P, Espinoza, Lr, Farge, D, Fathi, M, Fell, Cd, Fessler, Bj, Fitzgerald, Je, Flaherty, Kr, Foeldvari, I, Fox, Ga, Frech, Tm, Freitas, S, Furst, De, Gabrielli, A, García Vicuña, R, Georgiev, Ob, Gerbino, A, Gillisen, A, Gladman, Dd, Glassberg, M, Gochuico, Br, Gogali, A, Goh, Ns, Goldberg, A, Goldberg, Hj, Gourley, Mf, Griffing, L, Grutters, Jc, Gunnarsson, R, Hachulla, E, Hall, Fc, Harari, S, Herrick, Al, Herzog, El, Hesselstrand, R, Highland, K, Hirani, N, Hodgson, U, Hollingsworth, Hm, Homer, Rj, Hoyles, Rk, Hsu, Vm, Hubbard, Rb, Hunzelmann, N, Isasi, Me, Isasi, Es, Jacobsen, S, Jimenez, Sa, Johnson, Sr, Jones, Ch, Kahaleh, B, Kairalla, Ra, Kalluri, M, Kalra, S, Kaner, Rj, Kinder, Bw, Kiter, G, Klingsberg, Rc, Kokosi, M, Kolb, Mr, Kowal Bielecka OM, Kur Zalewska, J, Kuwana, M, Lake, Fr, Lally, Ev, Lasky, Ja, Laurindo, Im, Able, L, Lee, P, Leonard, Ct, Lien, Dc, Limper, Ah, Liossis, Sn, Lohr, Km, Loyd, Je, Lundberg, Ie, Mageto, Yn, Maher, Tm, Mahmud, Th, Manganas, H, Marie, I, Marras, Tk, Martinez, Ja, Martinez, Fj, Mathieu, A, Matucci Cerinic, M, Mayes, Md, Mckown, Km, Medsger, Ta, Meehan, Rt, Mendes, Ac, Meyer, Kc, Millar, Ab, Moğulkoc, N, Molitor, Ja, Morais, A, Mouthon, L, Müller, V, Müller Quernheim, J, Nadashkevich, O, Nador, R, Nash, P, Nathan, Sd, Navarro, C, Neves, S, Noth, I, Nunes, H, Olson, Al, Opitz, Cf, Padilla, M, Pappas, D, Parfrey, H, Pego Reigosa JM, Pereira, Ca, Perez, R, Pope, Je, Porter, Jc, Renzoni, Ea, Riemekasten, G, Riley, Dj, Rischmueller, M, Rodriguez Reyna TS, Rojas Serrano, J, Roman, J, Rosen, Gd, Rossman, M, Rothfield, N, Sahn, Sa, Sanduzzi, A, Scholand, Mb, Selman, M, Senécal, Jl, Seo, P, Shah, A, Silver, Rm, Solomon, Jj, Steen, V, Stevens, W, Strange, C, Sussman, R, Sutton, Ed, Sweiss, Nj, Tornling, G, Tzelepis, Ge, Undurraga, A, Vacca, A, Vancheri, Carlo, Varga, J, Veale, Dj, Volkov, S, Walker, Ua, Wells, Au, Wencel, M, Wesselius, Lj, Wickremasinghe, M, Wilcox, P, Wilsher, Ml, Wollheim, Fa, Wuyts, Wa, Yung, G, Zanon, P, Zappala, Cj, Groshong, Sd, Leslie, Ko, Myers, Jl, Padera, Rf, Desai, Sr, Goldin, J, Kazerooni, Ea, Klein, Js, and Keen, Kj
- Subjects
Male ,medicine.medical_specialty ,Delphi Technique ,Consensus Development Conferences as Topic ,Health Personnel ,Immunology ,Context (language use) ,Disease ,Severity of Illness Index ,Article ,Idiopathic pulmonary fibrosis ,Rheumatology ,medicine ,Immunology and Allergy ,Humans ,Disease management (health) ,Intensive care medicine ,Connective Tissue Diseases ,Randomized Controlled Trials as Topic ,business.industry ,Interstitial lung disease ,Disease Management ,respiratory system ,Focus Groups ,medicine.disease ,Comorbidity ,Connective tissue disease ,respiratory tract diseases ,Clinical trial ,Treatment Outcome ,Patient Satisfaction ,Physical therapy ,Quality of Life ,ÍNDICE DE GRAVIDADE DA DOENÇA ,Interdisciplinary Communication ,business ,Lung Diseases, Interstitial - Abstract
Interstitial lung diseases (ILD), including those related to connective tissue disease (CTD), and idiopathic pulmonary fibrosis (IPF) carry high morbidity and mortality. Great efforts are under way to develop and investigate meaningful treatments in the context of clinical trials. However, efforts have been challenged by a lack of validated outcome measures and by inconsistent use of measures in clinical trials. Lack of consensus has fragmented effective use of strategies in CTD-ILD and IPF, with a history of resultant difficulties in obtaining agency approval of treatment interventions. Until recently, the patient perspective to determine domains and outcome measures in CTD-ILD and IPF had never been applied. Efforts described here demonstrate unequivocally the value and influence of patient involvement on core set development. Regarding CTD-ILD, this is the first OMERACT working group to directly address a manifestation/comorbidity of a rheumatic disease (ILD) as well as a disease not considered rheumatic (IPF). The OMERACT 11 proceedings of the CTD-ILD Working Group describe the forward and lateral process to include both the medical and patient perspectives in the urgently needed identification of a core set of preliminary domains and outcome measures in CTD-ILD and IPF.
- Published
- 2014
36. Enthalpies of ionization for 2,3-diphosphoglyceric acid
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Dellaripa, Laura, Vickers, Leland P., and Hopkins, Jr., Harry P.
- Published
- 1983
- Full Text
- View/download PDF
37. The effect of cigarette smoking on the clinical and serological phenotypes of polymyositis and dermatomyositis.
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Schiffenbauer, Adam, Faghihi-Kashani, Sara, O'Hanlon, Terrence P., Flegel, Willy A., Adams, Sharon D., Targoff, Ira N., Oddis, Chester V., Ytterberg, Steven R., Aggarwal, Rohit, Christopher-Stine, Lisa, Shamim, Ejaz A., Dellaripa, Paul F., Danoff, Sonye K., Mammen, Andrew L., and Miller, Frederick W.
- Abstract
Abstract Objective Cigarette smoking is associated with immune-mediated disorders. We explored the contribution of smoking to polymyositis (PM) and dermatomyositis (DM) phenotypes and attempted to determine whether cigarette smoking effects differ by race and genotype. Methods Associations of tobacco smoking with disease features, autoantibodies, HLA types, and race were evaluated using multiple logistic regressions in 465 patients. Results Caucasian ever-smokers (n = 140) were more likely to have PM (adjusted OR = 2.24, 95% CI: 1.41\x963.57), anti-synthetase (adjusted OR = 1.93, 95% CI: 1.12\x963.34) and anti-Jo-1 autoantibodies (adjusted OR = 1.94, 95% CI: 1.08\x963.46) and less likely to have anti-p155/140 autoantibodies (adjusted OR = 0.36, 95% CI: 0.14\x960.92). In Caucasians, ever-smokers had a greater interstitial lung disease (ILD) frequency than never-smokers, while in African-Americans this relationship was inverted, but neither trend reached statistical significance. Pack-years of cigarette smoking showed significant positive associations with PM (adjusted OR = 1.02, 95% CI: 1.002\x961.04) and ILD (adjusted OR = 1.02, 95% CI: 1.001\x961.03) and was inversely associated with anti-p155/140 autoantibodies (adjusted OR = 0.93, 95% CI: 0.87\x960.99) in Caucasians. Caucasian heavy smokers (=20 pack-years) were more likely to have PM (adjusted OR = 2.52, 95% CI: 1.25\x965.09), ILD (adjusted OR = 2.48, 95% CI: 1.23\x965.00) and anti-Jo-1 autoantibodies (adjusted OR = 2.65, 95% CI: 1.16\x966.08) than never-smokers. In Caucasians, compared to never-smokers without HLA-DRB1*03:01 allele, ever-smokers with HLA-DRB1*03:01 allele had the highest odds of PM, ILD, ASA, and anti-Jo-1 autoantibodies. Risks for those with only one of these two factors were intermediate. An inverse pattern was observed regarding anti-p155/140 autoantibodies. Conclusion Tobacco smoking was associated with clinical and autoantibody phenotypes in Caucasians. Our findings also suggest possible interactions among HLA-DRB1*03:01 and smoking on the risk of PM and ILD, as well as, anti-synthetase, anti-Jo-1, and anti-p155/140 autoantibodies in Caucasians. [ABSTRACT FROM AUTHOR]
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- 2018
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38. Rituximab in the Treatment of Interstitial Lung Disease Associated with Antisynthetase Syndrome: A Multicenter Retrospective Case Review.
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Doyle, Tracy J., Dhillon, Namrata, Madan, Rachna, Cabral, Fernanda, Fletcher, Elaine A., Koontz, Diane C., Aggarwal, Rohit, Osorio, Juan C., Rosas, Ivan O., Oddis, Chester V., and Dellaripa, Paul F.
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- 2018
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39. Thoracic Manifestations of Rheumatoid Arthritis
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Esposito, Anthony J., Chu, Sarah G., Madan, Rachna, Doyle, Tracy J., and Dellaripa, Paul F.
- Abstract
Rheumatoid arthritis (RA) is commonly associated with pulmonary disease that can affect any anatomic compartment of the thorax. The most common intrathoracic manifestations of RA include interstitial lung disease, airway disease, pleural disease, rheumatoid nodules, and drug-induced toxicity. Patients with RA with thoracic involvement often present with nonspecific respiratory symptoms, although many are asymptomatic. Therefore, clinicians should routinely consider pulmonary disease when evaluating any patient with RA, particularly one with known risk factors. The optimal screening, diagnostic, and treatment strategies for RA-associated pulmonary disease remain uncertain and are the focus of ongoing investigation.
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- 2019
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40. EFFICACY AND SAFETY OF ABATACEPT IN MYOSITIS ASSOCIATED INTERSTITIAL LUNG DISEASE.
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Aggarwal, R., Moghadam-Kia, S., Koontz, D., Saygin, D., Bae, S., Sullivan, D., Marder, G., Venuturupalli, S., Dellaripa, P., Danoff, S., Doyle, T., Hunninghake, G., Lee, J. S., Fischer, A., Falk, J., Kang, C. R., Lin, Y., Johnson, C., Ascherman, D., and Oddis, C. V.
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- 2023
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41. Disclosure of Personalized Rheumatoid Arthritis Risk Using Genetics, Biomarkers, and Lifestyle Factors to Motivate Health Behavior Improvements: A Randomized Controlled Trial
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Sparks, Jeffrey A., Iversen, Maura D., Yu, Zhi, Triedman, Nellie A., Prado, Maria G., Miller Kroouze, Rachel, Kalia, Sarah S., Atkinson, Michael L., Mody, Elinor A., Helfgott, Simon M., Todd, Derrick J., Dellaripa, Paul F., Bermas, Bonnie L., Costenbader, Karen H., Deane, Kevin D., Lu, Bing, Green, Robert C., and Karlson, Elizabeth W.
- Abstract
To determine the effect of disclosure of rheumatoid arthritis (RA) risk personalized with genetics, biomarkers, and lifestyle factors on health behavior intentions. We performed a randomized controlled trial among first‐degree relatives without RA. Subjects assigned to the Personalized Risk Estimator for Rheumatoid Arthritis (PRE‐RA) group received the web‐based PRE‐RAtool for RArisk factor education and disclosure of personalized RArisk estimates, including genotype/autoantibody results and behaviors (n = 158). Subjects assigned to the comparison arm received standard RAeducation (n = 80). The primary outcome was readiness for change based on the trans‐theoretical model, using validated contemplation ladder scales. Increased motivation to improve RArisk–related behaviors (smoking, diet, exercise, or dental hygiene) was defined as an increase in any ladder score compared to baseline, assessed immediately, 6 weeks, and 6 months post‐intervention. Subjects reported behavior change at each visit. We performed intent‐to‐treat analyses using generalized estimating equations for the binary outcome. Subjects randomized to PRE‐RAwere more likely to increase ladder scores over post‐intervention assessments (relative risk 1.23, 95% confidence interval [95% CI] 1.01, 1.51) than those randomized to nonpersonalized education. At 6 months, 63.9% of PRE‐RAsubjects and 50.0% of comparison subjects increased motivation to improve behaviors (age‐adjusted difference 15.8%; 95% CI2.8%, 28.8%). Compared to nonpersonalized education, more PRE‐RAsubjects increased fish intake (45.0% versus 22.1%; P= 0.005), brushed more frequently (40.7% versus 22.9%; P= 0.01), flossed more frequently (55.7% versus 34.8%; P= 0.004), and quit smoking (62.5% versus 0.0% among 11 smokers; P= 0.18). Disclosure of RArisk personalized with genotype/biomarker results and behaviors increased motivation to improve RArisk–related behaviors. Personalized medicine approaches may motivate health behavior improvements for those at risk for RAand provide rationale for larger studies evaluating effects of behavior changes on clinical outcomes, such as RA‐related autoantibody production or RAdevelopment.
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- 2018
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42. OP0001 Developing a disease activity and therapeutic response index in connective tissue disease - interstitial lung disease (CTD-ILD): Results from a delphi exercise: Consensus on domains
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Saketkoo, L.A., primary, Khanna, D., additional, Huscher, D., additional, Dellaripa, P., additional, Flaherty, K., additional, Matteson, E., additional, Oddis, C., additional, Wells, A., additional, Denton, C., additional, Distler, O., additional, Kowal-Bielecka, O., additional, Sandorfi, N., additional, Christmann, R., additional, Phillips, K., additional, Pittrow, D., additional, Strand, V., additional, Brown, K., additional, and Seibold, J., additional
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- 2013
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43. Granulomatosis with polyangiitis (Wegener's) is associated with HLA-DPB1*04 and EMA6A gene variants. Evidence from a genome-wide analysis
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Xie, G., primary, Roschandel, D., additional, Sherva, R., additional, Monach, P., additional, Lu, Y., additional, Kung, T., additional, Carrington, K., additional, Carette, S., additional, Dellaripa, P., additional, Edberg, J., additional, Hoffman, G., additional, Khalidi, N., additional, Langford, C., additional, Mahr, A., additional, St. Clair, E.W., additional, Seo, P., additional, Specks, U., additional, Spiera, R., additional, Stone, J., additional, Ytterberg, S., additional, Raychaudhuri, S., additional, De Bakker, P., additional, Farrer, L., additional, Amos, C., additional, Merkel, P., additional, and Siminovitch, K., additional
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- 2013
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44. Lung Manifestations in the Rheumatic Diseases
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Doyle, Tracy J. and Dellaripa, Paul F.
- Abstract
Lung ailments in rheumatic diseases present unique challenges for diagnosis and management and are a source of significant morbidity and mortality for patients. Unlike the idiopathic interstitial pneumonias, patients with rheumatic diseases experience lung disease in the context of a systemic disease that may make it more difficult to recognize and that may present greater risks with treatment. Despite recent advances in our awareness of these diseases, there is still a significant lack of understanding of natural history to elucidate which patients will have disease that is progressive and thus warrants treatment. What we do know is that a subset of patients with rheumatic disease experience parenchymal lung disease that can prognostically resemble idiopathic pulmonary fibrosis, such as in rheumatoid arthritis, and that others can have aggressive inflammatory lung disease in the context of autoimmune myositis, systemic sclerosis, or an undifferentiated autoimmune process. As we enter into a paradigm shift where we view lung health as a cornerstone of our care of patients with rheumatic diseases, we hopefully will improve our ability to identify those patients at highest risk for pulmonary disease and progression, and offer emerging treatments which will result in better outcomes and a better quality of life.
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- 2017
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45. The impact of rheumatological evaluation in the management of patients with interstitial lung disease
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Castelino, F. V., primary, Goldberg, H., additional, and Dellaripa, P. F., additional
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- 2010
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46. Myeloperoxidase-antineutrophil Cytoplasmic Antibodies (MPO-ANCA) and Proteinase 3-ANCA without Immunofluorescent ANCA Found by Routine Clinical Testing.
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Rao, Deepak A., Wei, Kevin, Merola, Joseph F., O'Brien, William R., Takvorian, Samuel U., Dellaripa, Paul F., and Schur, Peter H.
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- 2015
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47. Reconciling Healthcare Professional and Patient Perspectives in the Development of Disease Activity and Response Criteria in Connective Tissue Disease–related Interstitial Lung Diseases
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Saketkoo, Lesley Ann, Mittoo, Shikha, Frankel, Sid, LeSage, Daphne, Sarver, Catherine, Phillips, Kristine, Strand, Vibeke, Matteson, Eric L., Baughman, Robert P., Brown, Kevin K., Christmann, Romy B., Dellaripa, Paul, Denton, Christopher P., Distler, Oliver, Fischer, Aryeh, Flaherty, Kevin, Huscher, Dörte, Khanna, Dinesh, Kowal-Bielecka, Otylia, Merkel, Peter A., Oddis, Chester V., Pittrow, David, Sandorfi, Nora, Seibold, James R., Swigris, Jeffrey, Wells, Athol, Antoniou, Katerina, Castelino, Flavia V., Christopher-Stine, Lisa, Collard, Harold R., Cottin, Vincent, Danoff, Sonye, Hedlund, Robert, Highland, Kristin B., Hummers, Laura, Lynch, David A., Kim, Dong Soon, Ryu, Jay H., Christopher-Stine, Lisa, Miller, Frederick W., Nichols, Karen, Proudman, Susanna M., Richeldi, Luca, Shah, Ami A., van den Assum, Pieter, Aggarwal, Rohit, Ainslie, Gillian, Alkassab, Firas, Allanore, Yannick, Anderson, Marina E., Andonopoulos, Andrew P., Antin-Ozerkis, Danielle, Antoniou, Katerina, Arrobas, Ana, Ascherman, Dana P., Assassi, Shervin, Baron, Murray, Bathon, Joan M., Baughman, Robert P., Behr, Juergen, Beretta, Lorenzo, Bingham, Clifton O., Binnie, Matthew, Birring, Surinder S., Boin, Francesco, Bongartz, Tim, Bourdin, Arnaud, Bouros, Demosthenes, Brasington, Richard, Bresser, Paul, Brown, Kevin K., Buch, Maya H., Burge, P. Sherwood, Carmona, Loreto, Castelino, Flavia V., Carreira, Patricia E., Carvalho, Carlos R.R., Catoggio, Luis J., Chan, Kevin M., Chapman, Jeffrey, Chatterjee, Soumya, Christmann, Romy B., Christopher-Stine, Lisa, Chua, Felix, Chung, Lorinda, Conron, Matthew, Corte, Tamera, Cosgrove, Gregory, Costabel, Ulrich, Cottin, Vincent, Cox, Gerard, Crestani, Bruno, Crofford, Leslie J., Csuka, Mary E., Curbelo, Pablo, Czirják, László, Daniil, Zoe, Danoff, Sonye, D’Arsigny, Christine L., Davis, Gerald S., de Andrade, Joao A., Dellaripa, Paul F., De Vuyst, Paul, Dempsey, Owen J., Denton, Christopher P., Derk, Chris T., Distler, Jörg, Distler, Oliver, Dixon, William G., Downey, Gregory, Doyle, Mittie K., Drent, Marjolein, Durairaj, Lakshmi, Emery, Paul, Espinoza, Luis R., Farge, Dominique, Fathi, Maryam, Fell, Charlene D., Fessler, Barri J., Fischer, Aryeh, Fitzgerald, John E., Flaherty, Kevin R., Foeldvari, Ivan, Fox, George A., Frech, Tracy M., Freitas, Sara, Furst, Daniel E., Gabrielli, Armando, García-Vicuña, Rosario, Georgiev, Ognian B., Gerbino, Anthony, Gillisen, Adrian, Gladman, Dafna D., Glassberg, Marilyn, Gochuico, Bernadette R., Gogali, Athena, Goh, Nicole S., Goldberg, Avram, Goldberg, Hilary J., Gourley, Mark F., Griffing, Leroy, Grutters, Jan C., Gunnarsson, Ragnar, Hachulla, Eric, Hall, Frances C., Harari, Sergio, Herrick, Ariane L., Herzog, Erica L., Hesselstrand, Roger, Highland, Kristin, Hirani, Nikhil, Hodgson, Ulla, Hollingsworth, Helen M., Homer, Robert J., Hoyles, Rachel K., Hsu, Vivien M., Hubbard, Richard B., Hummers, Laura, Hunzelmann, Nicolas, Huscher, Dörte, Isasi, Maria Eloisa, Isasi, Elida Susana, Jacobsen, Soren, Jimenez, Sergio A., Johnson, Sindhu R., Jones, Christine H., Kahaleh, Bashar, Kairalla, Ronaldo A., Kalluri, Meena, Kalra, Sanjay, Kaner, Robert J., Khanna, Dinesh, Kim, Dong Soon, Kinder, Brent W., Kiter, Goksel, Klingsberg, Ross C., Kokosi, Maria, Kolb, Martin R.J., Kowal-Bielecka, Otylia M., Kur-Zalewska, Joanna, Kuwana, Masataka, Lake, Fiona R., Lally, Edward V., Lasky, Joseph A., Laurindo, Ileda M., Able, Lawrence, Lee, Peter, Leonard, Colm T., Lien, Dale C., Limper, Andrew H., Liossis, Stamatis-Nick C., Lohr, Kristine M., Loyd, James E., Lundberg, Ingrid E., Mageto, Yolanda N., Maher, Toby M., Mahmud, Tafazzul H., Manganas, Helene, Marie, Isabelle, Marras, Theodore K., Martinez, José Antônio Baddini, Martinez, Fernando J., Mathieu, Alessandro, Matucci-Cerinic, Marco, Mayes, Maureen D., McKown, Kevin M., Medsger, Thomas A., Meehan, Richard T., Mendes, Ana Cristina, Merkel, Peter A., Meyer, Keith C., Millar, Ann B., Miller, Frederick W., Moğulkoç, Nesrin, Molitor, Jerry A., Morais, António, Mouthon, Luc, Müller, Veronika, Müller-Quernheim, Joachim, Nadashkevich, Oleg, Nador, Roland, Nash, Peter, Nathan, Steven D., Navarro, Carmen, Neves, Sofia, Noth, Imre, Nunes, Hilario, Oddis, Chester V., Olson, Amy L., Opitz, Christian F., Padilla, Maria, Pappas, Dimitrios, Parfrey, Helen, Pego-Reigosa, José M., Pereira, Carlos A.C., Perez, Rafael, Phillips, Kristine, Pittrow, David, Pope, Janet E., Porter, Joanna C., Proudman, Susanna M., Renzoni, Elisabeth A., Richeldi, Luca, Riemekasten, Gabriela, Riley, David J., Rischmueller, Maureen, Rodriguez-Reyna, Tatiana S., Rojas-Serrano, J., Roman, Jesse, Rosen, Glenn D., Rossman, Milton, Rothfield, Naomi, Ryu, Jay H., Sahn, Steven A., Sandorfi, Nora, Sanduzzi, Alessandro, Scholand, Mary Beth, Seibold, James R., Selman, Moises, Senécal, Jean-Luc, Seo, Philip, Shah, Ami, Silver, Richard M., Solomon, Joshua J., Steen, Virginia, Stevens, Wendy, Strange, Charlie, Sussman, Robert, Sutton, Evelyn D., Sweiss, Nadera J., Swigris, Jeffrey, Tornling, Göran, Tzelepis, George E., Undurraga, Alvaro, Vacca, Allessandra, Vancheri, Carlo, Varga, Janos, Veale, Douglas J., Volkov, Suncica, Walker, Ulrich A., Wells, Athol U., Wencel, Mark, Wesselius, Lewis J., Wickremasinghe, Melissa, Wilcox, Pearce, Wilsher, Margaret L., Wollheim, Frank A., Wuyts, Wim A., Yung, Gordon, Zanon, Pietro, Zappala, Christopher J., Groshong, Steve D., Leslie, Kevin O., Myers, Jeffrey L., Padera, Robert F., Desai, Sujal R., Goldin, Jonathan, Kazerooni, Ella A., Klein, Jeffrey S., Lynch, David A., and Keen, Kevin J.
- Abstract
Interstitial lung diseases (ILD), including those related to connective tissue disease (CTD), and idiopathic pulmonary fibrosis (IPF) carry high morbidity and mortality. Great efforts are under way to develop and investigate meaningful treatments in the context of clinical trials. However, efforts have been challenged by a lack of validated outcome measures and by inconsistent use of measures in clinical trials. Lack of consensus has fragmented effective use of strategies in CTD-ILD and IPF, with a history of resultant difficulties in obtaining agency approval of treatment interventions. Until recently, the patient perspective to determine domains and outcome measures in CTD-ILD and IPF had never been applied. Efforts described here demonstrate unequivocally the value and influence of patient involvement on core set development. Regarding CTD-ILD, this is the first OMERACT working group to directly address a manifestation/comorbidity of a rheumatic disease (ILD) as well as a disease not considered rheumatic (IPF). The OMERACT 11 proceedings of the CTD-ILD Working Group describe the forward and lateral process to include both the medical and patient perspectives in the urgently needed identification of a core set of preliminary domains and outcome measures in CTD-ILD and IPF.
- Published
- 2014
- Full Text
- View/download PDF
48. The Diurnal Cycle of East Pacific Convection, Moisture, and CYGNSS Wind Speed and Fluxes
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Riley Dellaripa, Emily M., Maloney, Eric D., and DeMott, Charlotte A.
- Abstract
The far eastern tropical Pacific is one of the rainiest locations on Earth. This region is characterized by a robust diurnal cycle with precipitation initiating over the Andes mountains in Colombia in the late afternoon and moving offshore overnight while organizing into mesoscale convective systems (MCSs). As the MCSs move westward, they can seed tropical easterly waves that develop into tropical cyclones. Novel measurements of near‐surface wind speeds and latent heat flux (LHFLX) from the Cyclone Global Navigation Satellite System (CYGNSS) mission and ERA5 reanalysis are used to evaluate changes to regional flow patterns, moisture, and LHFLX that favor a strong westward propagating diurnal cycle of precipitation in this region. Days with strongly versus weakly westward propagating diurnal precipitation are compared during the extended boreal summer of the CYGNSS era (May–October 2018–2021). Strongly propagating days have a more moist lower troposphere with stronger vertically integrated moisture flux convergence than days with weakly propagating precipitation. The enhanced low‐level moisture is supported by increased wind‐driven LHFLX from stronger regional flows including the Choco and Caribbean Low‐Level Jets and Panama and Papagayo gap winds. Increased offshore convergence and vorticity also help sustain convection during the days with strongly propagating precipitation. Background variations in the physical environment, as opposed to diurnal variations, seem more important for supporting a robust diurnal cycle of precipitation in the region. The eastern tropical Pacific Ocean off the coast of Colombia is one of the rainiest locations on Earth. Thunderstorms frequently form in the late afternoon over the foothills of the Andes mountains and then move offshore into the eastern Pacific overnight and into the early morning while growing into bigger thunderstorms. These large thunderstorms are important because they can eventually lead to tropical cyclone development as they move westward over the eastern Pacific parallel to central America. We evaluate environmental conditions that favor days when thunderstorms move far away from the Colombian coast along central America versus days when thunderstorms stay closer to the Colombian coast. We find that days when the thunderstorms move farther away from the Colombian coast have more moisture near the Earth's surface. This enhanced moisture is supported by increased winds near the surface in the east Pacific and Caribbean that help transport moisture from areas near the Pacific equator and Caribbean to offshore of Colombia and transfer moisture from the far eastern Pacific Ocean surface into the overlying atmosphere. Measurements from eight microwave‐size satellites in space were critical to determine the role of the transfer of moisture from the ocean surface to the atmosphere. An index is developed to distinguish between days with strong versus weak westward‐propagating diurnal precipitation in the far east PacificStrongly propagating days have increased low‐level moisture, regional circulations, and gap winds relative to weakly propagating daysCyclone Global Navigation Satellite System measurements show that increased moisture on the strongly propagating days is supported by increased wind‐induced latent heat fluxes An index is developed to distinguish between days with strong versus weak westward‐propagating diurnal precipitation in the far east Pacific Strongly propagating days have increased low‐level moisture, regional circulations, and gap winds relative to weakly propagating days Cyclone Global Navigation Satellite System measurements show that increased moisture on the strongly propagating days is supported by increased wind‐induced latent heat fluxes
- Published
- 2023
- Full Text
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49. Diurnal Cycle of Wind Speed and Precipitation Over the Northern Australia Coastal Region: CYGNSS Observations
- Author
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Bui, Hien X., Maloney, Eric D., Short, Ewan, and Riley Dellaripa, Emily M.
- Abstract
The diurnal cycle of precipitation and its associated land‐sea breeze circulation over coastal northern Australia are investigated using surface wind speed and enthalpy (latent and sensible heat) fluxes from the Cyclone Global Navigation Satellite System. Composite results during the austral summer of 2018–2022 show that diurnal precipitation propagates westward from the Cape York Peninsula into the Gulf of Carpentaria. The diurnal cycle of precipitation and surface wind speed are strongly coupled, with the wind speed maximum slightly leading the precipitation maximum. Additionally, analysis of the moist static energy budget shows that surface fluxes help support the westward‐propagation of diurnal precipitation. These results—based on novel satellite data and reanalysis—are consistent with previous studies that have examined the impact of the land‐sea breeze on the diurnal cycle of precipitation. The results provide a benchmark for model representation of this important atmosphere‐ocean‐land interaction. The modulation of the diurnal cycle of precipitation over coastal northern Australia by surface winds was studied using the recently launched NASA Cyclone Global Navigation Satellite System (CYGNSS). Results show a strong connection between the daily cycles of precipitation and surface wind speed, with an offshore wind speed maximum leading the precipitation maximum by a few hours. Westward propagation of diurnal precipitation and wind speed signals occurs from the Cape York Peninsula into the Gulf of Carpentaria. A thermodynamic analysis supports the importance of the wind speed signal and associated surface fluxes for fostering offshore precipitation propagation. The novelty of this paper lies in the use of the new CYGNSS retrievals, which provide better space and time coverage of surface wind speed than previous satellite‐based measurements and are not as negatively affected by precipitation contamination. Cyclone Global Navigation Satellite System wind speeds and latent heat fluxes are used to study the diurnal cycle over the northern Australia coastal regionEnhanced diurnal precipitation is associated with enhanced surface wind speed and convergenceDiurnal precipitation and surface wind speed signals propagate westward in tandem from the Cape York Peninsula Cyclone Global Navigation Satellite System wind speeds and latent heat fluxes are used to study the diurnal cycle over the northern Australia coastal region Enhanced diurnal precipitation is associated with enhanced surface wind speed and convergence Diurnal precipitation and surface wind speed signals propagate westward in tandem from the Cape York Peninsula
- Published
- 2023
- Full Text
- View/download PDF
50. Nutritional Issues in Vasculitis.
- Author
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Bendich, Adrianne, Coleman, Laura A., Dellaripa, Paul F., and Howard, Donough
- Abstract
• Gastrointestinal involvement is common in systemic vasculitis. • Chronic systemic inflammation is common in vasculitis and frequently leads to weight loss and cachexia. • Immunosuppressive medications can cause gastrointestinal toxicity. • There is little evidence of any dietary manipulations or supplementations having any impact on the course of vasculitis. [ABSTRACT FROM AUTHOR]
- Published
- 2008
- Full Text
- View/download PDF
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