21 results on '"Huang, Megan"'
Search Results
2. An RNA-targeting CRISPR–Cas13d system alleviates disease-related phenotypes in Huntington’s disease models
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Morelli, Kathryn H., Wu, Qian, Gosztyla, Maya L., Liu, Hongshuai, Yao, Minmin, Zhang, Chuangchuang, Chen, Jiaxu, Marina, Ryan J., Lee, Kari, Jones, Krysten L., Huang, Megan Y., Li, Allison, Smith-Geater, Charlene, Thompson, Leslie M., Duan, Wenzhen, and Yeo, Gene W.
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- 2023
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3. Quality of Life in the Phase 2/3 Trial of N-803 Plus Bacillus Calmette-Guérin in Bacillus Calmette-Guérin-Unresponsive Nonmuscle-Invasive Bladder Cancer.
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Chamie, Karim, Chang, Sam S., Kramolowsky, Eugene V., Gonzalgo, Mark L., Huang, Megan, Bhar, Paul, Spilman, Patricia, Sender, Lennie, Reddy, Sandeep K., and Soon-Shiong, Patrick
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- 2024
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4. Metabolic reprogramming through fatty acid transport protein 1 (FATP1) regulates macrophage inflammatory potential and adipose inflammation
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Johnson, Amy R., Qin, Yuanyuan, Cozzo, Alyssa J., Freemerman, Alex J., Huang, Megan J., Zhao, Liyang, Sampey, Brante P., Milner, J. Justin, Beck, Melinda A., Damania, Blossom, Rashid, Naim, Galanko, Joseph A., Lee, Douglas P., Edin, Matthew L., Zeldin, Darryl C., Fueger, Patrick T., Dietz, Brittney, Stahl, Andreas, Wu, Ying, Mohlke, Karen L., and Makowski, Liza
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- 2016
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5. Outcomes of Anatomical versus Functional Testing for Coronary Artery Disease
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Douglas, Pamela S., Hoffmann, Udo, Patel, Manesh R., Mark, Daniel B., Al-Khalidi, Hussein R., Cavanaugh, Brendan, Cole, Jason, Dolor, Rowena J., Fordyce, Christopher B., Huang, Megan, Khan, Muhammad Akram, Kosinski, Andrzej S., Krucoff, Mitchell W., Malhotra, Vinay, Picard, Michael H., Udelson, James E., Velazquez, Eric J., Yow, Eric, Cooper, Lawton S., and Lee, Kerry L.
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- 2015
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6. Differential expression of a brain aging biomarker across discrete chronic pain disorders.
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Hung, Peter Shih-Ping, Zhang, Jia Y., Noorani, Alborz, Walker, Matthew R., Huang, Megan, Zhang, Jason W., Laperriere, Normand, Rudzicz, Frank, and Hodaie, Mojgan
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- 2022
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7. Deep learning approach to determining the type of long reads
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Vrček, Lovro, Huang, Megan Hong Hui, Vaser, Robert, and Šikić, Mile
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De novo assembly ,Deep learning ,Graph simplification ,Read classification - Abstract
Single and metagenome de novo assembly of long reads is still one of the most difficult problems in bioinformatics. Often used paradigm, called Overlap-Layout-Consensus, aims at finding a Hamiltonian path through an assembly graph obtained from overlapping reads in a sample. However, these graphs can be extremely complex due to repetitive regions in genomes and sequencing artifacts such as chimeric reads, which lead to higher fragmentation of the assembly genomes. A popular approach for tackling this problem is based on dividing reads into three categories and processing them appropriately. These three categories of reads are regular, repetitive, and chimeric. A drawback of read classification with heuristic algorithms in existing assemblers is a manual selection of parameters based on just several genomes. In this work, we propose a deep learning approach for classification of reads based on their pile-o-grams, plots of coverage versus base index. The model was trained on a hand-labeled dataset consisting of pile-o-gram images from multiple bacteria, and tested on a different bacteria species not included in the training set. With such a setup, and with classes being balanced, an accuracy of 93% was achieved which opens the possibility of creating more accurate and less contiguous assemblies.
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- 2020
8. Prognostic Value of Noninvasive Cardiovascular Testing in Patients With Stable Chest Pain: Insights From the PROMISE Trial (Prospective Multicenter Imaging Study for Evaluation of Chest Pain)
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Hoffmann, Udo, Ferencik, Maros, Udelson, James E, Picard, Michael H, Truong, Quynh A, Patel, Manesh R, Huang, Megan, Pencina, Michael, Mark, Daniel B, Heitner, John F, Fordyce, Christopher B, Pellikka, Patricia A, Tardif, Jean-Claude, Budoff, Matthew, Nahhas, George, Chow, Benjamin, Kosinski, Andrzej S, Lee, Kerry L, Douglas, Pamela S, and PROMISE Investigators
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Male ,Chest Pain ,Clinical Trials and Supportive Activities ,Clinical Sciences ,Coronary Artery Disease ,Cardiorespiratory Medicine and Haematology ,Stress ,Cardiovascular ,Coronary Angiography ,PROMISE Investigators ,diagnostic tests ,Clinical Research ,Humans ,Prospective Studies ,Tomography ,Heart Disease - Coronary Heart Disease ,Aged ,screening and diagnosis ,Pain Research ,Middle Aged ,Atherosclerosis ,Prognosis ,X-Ray Computed ,Detection ,routine ,Heart Disease ,Cardiovascular System & Hematology ,Echocardiography ,Public Health and Health Services ,Exercise Test ,Biomedical Imaging ,Female ,Tomography, X-Ray Computed ,4.2 Evaluation of markers and technologies ,Echocardiography, Stress ,Follow-Up Studies - Abstract
BackgroundOptimal management of patients with stable chest pain relies on the prognostic information provided by noninvasive cardiovascular testing, but there are limited data from randomized trials comparing anatomic with functional testing.MethodsIn the PROMISE trial (Prospective Multicenter Imaging Study for Evaluation of Chest Pain), patients with stable chest pain and intermediate pretest probability for obstructive coronary artery disease (CAD) were randomly assigned to functional testing (exercise electrocardiography, nuclear stress, or stress echocardiography) or coronary computed tomography angiography (CTA). Site-based diagnostic test reports were classified as normal or mildly, moderately, or severely abnormal. The primary end point was death, myocardial infarction, or unstable angina hospitalizations over a median follow-up of 26.1 months.ResultsBoth the prevalence of normal test results and incidence rate of events in these patients were significantly lower among 4500 patients randomly assigned to CTA in comparison with 4602 patients randomly assigned to functional testing (33.4% versus 78.0%, and 0.9% versus 2.1%, respectively; both P10%) who had a normal functional test were reclassified as being mildly abnormal, the discriminatory capacity improved to 0.69 (95% CI, 0.64-0.74).ConclusionsCoronary CTA, by identifying patients at risk because of nonobstructive CAD, provides better prognostic information than functional testing in contemporary patients who have stable chest pain with a low burden of obstructive CAD, myocardial ischemia, and events.Clinical trial registrationURL: http://www.clinicaltrials.gov. Unique identifier: NCT01174550.
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- 2017
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9. Maternal Dietary Diversity and Growth of Children Under 24 Months of Age in Rural Dodoma, Tanzania.
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Huang, Megan, Sudfeld, Christopher, Ismail, Abbas, Vuai, Said, Ntwenya, Julius, Mwanyika-Sando, Mary, and Fawzi, Wafaie
- Abstract
Objective: To identify predictors of maternal dietary diversity in rural Dodoma, Tanzania and assess its association with child growth outcomes.Methods: A cross-sectional survey of 361 mothers with children under 24 months of age was conducted in 5 villages in rural Dodoma, Tanzania. Maternal diets were assessed using food frequency questionnaires, and dietary diversity was categorized using Minimum Dietary Diversity for Women (MDD-W) guidelines. Child anthropometric measures were taken to calculate height-for-age z-score (HAZ), weight-for-height z-score (WHZ), and weight-for-age z-score (WAZ). Linear and logistic regressions were used to examine the association between maternal dietary diversity and children's growth outcomes.Results: About 40% of mothers did not consume a diverse diet (MDD-W < 5), and 35% of children were stunted. Household production of greater number of crops was associated with greater MDD-W scores ( P < .01). Greater maternal dietary diversity was associated with significantly greater child WHZ (mean difference = 0.44; 95% confidence interval [CI]: 0.10-0.78; P = .01), WAZ (mean difference = 0.37; 95% CI: 0.08-0.65; P = .01), and reduced risk of wasting (odds ratio = 0.22; 95% CI: 0.07-0.66; P = .01).Conclusions: Greater maternal dietary diversity was associated with improved child WHZ and WAZ outcomes. Sustainable interventions to increase maternal dietary diversity may improve WHZ and WAZ in young children in similar settings. [ABSTRACT FROM AUTHOR]- Published
- 2018
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10. Rich Food Biodiversity Amid Low Consumption of Food Items in Kilosa District, Tanzania.
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Ntwenya, Julius E., Kinabo, Joyce, Msuya, John, Mamiro, Peter, Mamiro, Delphina, Njoghomi, Elifuraha, Liwei, Philip, and Huang, Megan
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Background: Indigenous foods, which contribute largely to the majority of the households' food basket in rural Tanzanian communities, have not been fully characterized or documented.Objectives: The study aimed to document foods available and consumed in Kilosa District, Tanzania, in an attempt to promote, revive use, and build evidence for sustainable utilization of the rich local biodiversity.Methods: Data were collected from 307 households in 3 agroecological zones in Kilosa District during the beginning of the rainy season (February-May) and immediately after harvest (September-October). A list of food items was generated, and 24-hour recall was performed. Descriptive statistics were calculated and a student t test statistic was used to compare the means of the Food Biodiversity Score between the agricultural seasons.Results: A total of 183 edible food items were reported by households with more reported in the rainy season (n = 82) compared to harvest season (n = 64). The mean number of food items consumed per day during the rainy season was 4.7 (95% CI: 4.5-5.0) compared to 5.9 (95% CI: 5.7-6.1) during harvest season. About 50% of the households mentioned that wild edible foods were less accepted by household members.Conclusion: Despite the rich local food biodiversity, households relied on few food items which may be due to limited awareness and knowledge about the biodiversity of foods in the community. It is important to educate communities on the rich and affordable food base available locally to improve their food diversity, income, and nutritional status. [ABSTRACT FROM AUTHOR]- Published
- 2017
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11. Changes in Medical Therapy and Lifestyle After Anatomical or Functional Testing for Coronary Artery Disease.
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Ladapo, Joseph A., Hoffmann, Udo, Lee, Kerry L., Coles, Adrian, Huang, Megan, Mark, Daniel B., Dolor, Rowena J., Pelberg, Robert A., Budoff, Matthew, Sigurdsson, Gardar, Severance, Harry W., and Douglas, Pamela S.
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- 2016
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12. A comparison study for metalized ceramic substrate technologies: For high power module applications.
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Wei, Vincent, Huang, Megan, Lai, Roger, and Persons, Ryan
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- 2014
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13. Weight loss reversed obesity-induced HGF/c-Met pathway and basal-like breast cancer progression.
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Sundaram, Sneha, Le, Trinh L., Essaid, Luma, Freemerman, Alex J., Huang, Megan J., Galanko, Joseph A., McNaughton, Kirk K., Bendt, Katharine M., Darr, David B., roester, Melissa A., and Makowski, Liza
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BREAST cancer research ,BODY mass index ,HIGH-fat diet ,DIET research ,WEIGHT loss ,OBESITY - Abstract
Epidemiologic studies demonstrate that obesity is associated with an aggressive subtype of breast cancer called basal-like breast cancer (BBC). Using the C3(1)-T
Ag murine model of BBC, we previously demonstrated that mice displayed an early onset of tumors when fed obesogenic diets in the adult window of susceptibility. Obesity was also shown to elevate mammary gland expression and activation of hepatocyte growth factor (HGF)/c-Met compared to lean controls, a pro-tumorigenic pathway associated with BBC in patients. Epidemiologic studies estimate that weight loss could prevent a large proportion of BBC. We sought to investigate whether weight loss in adulthood prior to tumor onset would protect mice from accelerated tumorigenesis observed in obese mice. Using a life-long model of obesity, C3(1)-TAg mice were weaned onto and maintained on an obesogenic high-fat diet. Obese mice displayed significant elevations in tumor progression, but not latency or burden. Tumor progression was significantly reversed when obese mice were induced to lose weight by switching to a control low-fat diet prior to tumor onset compared to mice maintained on obesogenic diet.We investigated the HGF/c-Met pathway known to regulate tumorigenesis. Importantly, HGF/c-Met expression in normal mammary glands and c-Met in tumors was elevated with obesity and was significantly reversed with weight loss. Changes in tumor growth could not be explained by measures of HGF action including phospho-AKT or phospho-S6. Other mediators associated with oncogenesis such as hyperinsulinemia and a high leptin:adiponectin ratio were elevated by obesity and reduced with weight loss. In sum, weight loss significantly blunted the obesity-responsive protumorigenic HGF/c-Met pathway and improved several metabolic risk factors associated with BBC, which together may have contributed to the dramatic reversal of obesity-driven tumor progression. Future research aims to evaluate the role of obesity and the HGF/c-Met pathway in basal-like breast cancer progression. [ABSTRACT FROM AUTHOR]- Published
- 2014
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14. Involvement of the ACE2/Ang-(1–7)/MasR Axis in Pulmonary Fibrosis: Implications for COVID-19.
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Morganstein, Taylor, Haidar, Zahraa, Trivlidis, Joshua, Azuelos, Ilan, Huang, Megan Jiaxin, Eidelman, David H., and Baglole, Carolyn J.
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PULMONARY fibrosis ,IDIOPATHIC pulmonary fibrosis ,COVID-19 pandemic ,SMOKING ,SARS-CoV-2 ,COVID-19 - Abstract
Pulmonary fibrosis is a chronic, fibrotic lung disease affecting 3 million people worldwide. The ACE2/Ang-(1–7)/MasR axis is of interest in pulmonary fibrosis due to evidence of its anti-fibrotic action. Current scientific evidence supports that inhibition of ACE2 causes enhanced fibrosis. ACE2 is also the primary receptor that facilitates the entry of SARS-CoV-2, the virus responsible for the current COVID-19 pandemic. COVID-19 is associated with a myriad of symptoms ranging from asymptomatic to severe pneumonia and acute respiratory distress syndrome (ARDS) leading to respiratory failure, mechanical ventilation, and often death. One of the potential complications in people who recover from COVID-19 is pulmonary fibrosis. Cigarette smoking is a risk factor for fibrotic lung diseases, including the idiopathic form of this disease (idiopathic pulmonary fibrosis), which has a prevalence of 41% to 83%. Cigarette smoke increases the expression of pulmonary ACE2 and is thought to alter susceptibility to COVID-19. Cannabis is another popular combustible product that shares some similarities with cigarette smoke, however, cannabis contains cannabinoids that may reduce inflammation and/or ACE2 levels. The role of cannabis smoke in the pathogenesis of pulmonary fibrosis remains unknown. This review aimed to characterize the ACE2-Ang-(1–7)-MasR Axis in the context of pulmonary fibrosis with an emphasis on risk factors, including the SARS-CoV-2 virus and exposure to environmental toxicants. In the context of the pandemic, there is a dire need for an understanding of pulmonary fibrotic events. More research is needed to understand the interplay between ACE2, pulmonary fibrosis, and susceptibility to coronavirus infection. [ABSTRACT FROM AUTHOR]
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- 2021
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15. Effects of prolonged calorie restriction on inflammation and immune function: a randomized controlled trial in non‐obese humans (40.4).
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Meydani, Simin, Das, Sai, Piper, Carl, Lewis, Michael, Dixit, Vishwadeep, Gupta, Alok, Villareal, Dennis, Klein, Samuel, Bhapkar, Manjushri, Huang, Megan, Fuss, Paul, Roberts, Susan, Holloszy, John, and Fontana, Luigi
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- 2014
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16. Task Order 20: Supercritical Carbon Dioxide Brayton Cycle Energy Conversion Study
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Huang, Megan [AREVA Federal Services, LLC, Charlotte, NC (United States)]
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- 2015
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17. IL-15 Superagonist NAI in BCG-Unresponsive Non-Muscle-Invasive Bladder Cancer.
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Chamie K, Chang SS, Kramolowsky E, Gonzalgo ML, Agarwal PK, Bassett JC, Bjurlin M, Cher ML, Clark W, Cowan BE, David R, Goldfischer E, Guru K, Jalkut MW, Kaffenberger SD, Kaminetsky J, Katz AE, Koo AS, Sexton WJ, Tikhonenkov SN, Trabulsi EJ, Trainer AF, Spilman P, Huang M, Bhar P, Taha SA, Sender L, Reddy S, and Soon-Shiong P
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- Humans, BCG Vaccine, Interleukin-15, Non-Muscle Invasive Bladder Neoplasms, Urinary Bladder Neoplasms therapy
- Abstract
BACKGROUND: Patients with Bacillus Calmette–Guérin (BCG)–unresponsive non–muscle-invasive bladder cancer (NMIBC) have limited treatment options. The immune cell–activating interleukin-15 (IL-15) superagonist Nogapendekin alfa inbakicept (NAI), also known as N-803, may act synergistically with BCG to elicit durable complete responses (CRs) in this patient population. METHODS: In this open-label, multicenter study, patients with BCG-unresponsive bladder carcinoma in situ (CIS) with or without Ta/T1 papillary disease were treated with intravesical NAI plus BCG (cohort A) or NAI alone (cohort C). Patients with BCG-unresponsive high-grade Ta/T1 papillary NMIBC also received NAI plus BCG (cohort B). The primary end point was the incidence of CR at the 3- or 6-month assessment visit for cohorts A and C, and the disease-free survival (DFS) rate at 12 months for cohort B. Durability, cystectomy avoidance, progression-free survival, disease-specific survival (DSS), and overall survival were secondary end points for cohort A. RESULTS: In cohort A, CR was achieved in 58 (71%) of 82 patients (95% confidence interval [CI]=59.6 to 80.3; median follow-up, 23.9 months), with a median duration of 26.6 months (95% CI=9.9 months to [upper bound not reached]). At 24 months in patients with CR, the Kaplan–Meier estimated probability of avoiding cystectomy and of DSS was 89.2% and 100%, respectively. In cohort B (n=72), the Kaplan–Meier estimated DFS rate was 55.4% (95% CI=42.0% to 66.8%) at 12 months, with median DFS of 19.3 months (95% CI=7.4 months to [upper bound not reached]). Most treatment-emergent adverse events for patients receiving BCG plus NAI were grade 1 to 2 (86%); three grade 3 immune-related treatment-emergent adverse events occurred. CONCLUSIONS: In patients with BCG-unresponsive bladder carcinoma in situ and papillary NMIBC treated with BCG and the novel agent NAI, CRs were achieved with a persistence of effect, cystectomy avoidance, and 100% bladder cancer–specific survival at 24 months. The study is ongoing, with an estimated target enrollment of 200 participants (Funded by ImmunityBio.)
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- 2023
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18. Prognostic Value of Noninvasive Cardiovascular Testing in Patients With Stable Chest Pain: Insights From the PROMISE Trial (Prospective Multicenter Imaging Study for Evaluation of Chest Pain).
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Hoffmann U, Ferencik M, Udelson JE, Picard MH, Truong QA, Patel MR, Huang M, Pencina M, Mark DB, Heitner JF, Fordyce CB, Pellikka PA, Tardif JC, Budoff M, Nahhas G, Chow B, Kosinski AS, Lee KL, and Douglas PS
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- Aged, Coronary Angiography methods, Coronary Artery Disease diagnostic imaging, Coronary Artery Disease physiopathology, Echocardiography, Stress methods, Exercise Test methods, Female, Follow-Up Studies, Humans, Male, Middle Aged, Prognosis, Prospective Studies, Tomography, X-Ray Computed methods, Chest Pain diagnostic imaging, Chest Pain physiopathology, Coronary Angiography standards, Echocardiography, Stress standards, Exercise Test standards, Tomography, X-Ray Computed standards
- Abstract
Background: Optimal management of patients with stable chest pain relies on the prognostic information provided by noninvasive cardiovascular testing, but there are limited data from randomized trials comparing anatomic with functional testing., Methods: In the PROMISE trial (Prospective Multicenter Imaging Study for Evaluation of Chest Pain), patients with stable chest pain and intermediate pretest probability for obstructive coronary artery disease (CAD) were randomly assigned to functional testing (exercise electrocardiography, nuclear stress, or stress echocardiography) or coronary computed tomography angiography (CTA). Site-based diagnostic test reports were classified as normal or mildly, moderately, or severely abnormal. The primary end point was death, myocardial infarction, or unstable angina hospitalizations over a median follow-up of 26.1 months., Results: Both the prevalence of normal test results and incidence rate of events in these patients were significantly lower among 4500 patients randomly assigned to CTA in comparison with 4602 patients randomly assigned to functional testing (33.4% versus 78.0%, and 0.9% versus 2.1%, respectively; both P <0.001). In CTA, 54.0% of events (n=74/137) occurred in patients with nonobstructive CAD (1%-69% stenosis). Prevalence of obstructive CAD and myocardial ischemia was low (11.9% versus 12.7%, respectively), with both findings having similar prognostic value (hazard ratio, 3.74; 95% confidence interval [CI], 2.60-5.39; and 3.47; 95% CI, 2.42-4.99). When test findings were stratified as mildly, moderately, or severely abnormal, hazard ratios for events in comparison with normal tests increased proportionally for CTA (2.94, 7.67, 10.13; all P <0.001) but not for corresponding functional testing categories (0.94 [ P =0.87], 2.65 [ P =0.001], 3.88 [ P <0.001]). The discriminatory ability of CTA in predicting events was significantly better than functional testing (c-index, 0.72; 95% CI, 0.68-0.76 versus 0.64; 95% CI, 0.59-0.69; P =0.04). If 2714 patients with at least an intermediate Framingham Risk Score (>10%) who had a normal functional test were reclassified as being mildly abnormal, the discriminatory capacity improved to 0.69 (95% CI, 0.64-0.74)., Conclusions: Coronary CTA, by identifying patients at risk because of nonobstructive CAD, provides better prognostic information than functional testing in contemporary patients who have stable chest pain with a low burden of obstructive CAD, myocardial ischemia, and events., Clinical Trial Registration: URL: http://www.clinicaltrials.gov. Unique identifier: NCT01174550., (© 2017 American Heart Association, Inc.)
- Published
- 2017
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19. Socio-economic and spatial correlates of subclinical iodine deficiency among pregnant women age 15-49 years in Tanzania.
- Author
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Mtumwa AH, Ntwenya JE, Paul E, Huang M, and Vuai S
- Abstract
Background: Iodine deficiency is a widespread global health problem that affects about 2 billion people each year. Pregnant women are particularly vulnerable to iodine deficiency due to increased iodine requirement leading to death, miscarriage, and stillbirth. Iodine deficiency also has significant negative effects on newborns including impaired cognitive development, impaired learning capabilities, and stunting. This study looks at the association between subclinical iodine deficiency and demographic factors including age, wealth index, education, family size, geographical zone, number of children, fish consumption, pregnancy trimester and household salt in pregnant women aged 15-49 years in Tanzania., Methods: The 2010 Tanzania Demographic and Health Survey (TDHS) data was re analysed. Subclinical iodine deficiency is classified as a urinary iodine concentration (UIC) of <150 μ g/L., Results: Results showed that the prevalence of iodine deficiency (54%) was unacceptably high among pregnant women. The results of multiple logistic regression model found that number of children, wealth index, household salt, and geographical zone were significantly associated with iodine deficiency in these women., Conclusion: These results indicate a need to implement interventions to increase iodine intake that targets pregnant women with the specific demographic characteristics., Competing Interests: The authors declare that they have no competing interests., (© The Author(s). 2017.)
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- 2017
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20. Long-term moderate calorie restriction inhibits inflammation without impairing cell-mediated immunity: a randomized controlled trial in non-obese humans.
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Meydani SN, Das SK, Pieper CF, Lewis MR, Klein S, Dixit VD, Gupta AK, Villareal DT, Bhapkar M, Huang M, Fuss PJ, Roberts SB, Holloszy JO, and Fontana L
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- Adult, Biomarkers blood, C-Reactive Protein metabolism, Energy Intake, Female, Humans, Inflammation blood, Intercellular Adhesion Molecule-1 blood, Leptin blood, Lymphocyte Count, Male, Middle Aged, Treatment Outcome, Tumor Necrosis Factor-alpha blood, Body Composition physiology, Caloric Restriction, Diet, Inflammation diet therapy
- Abstract
Calorie restriction (CR) inhibits inflammation and slows aging in many animal species, but in rodents housed in pathogen-free facilities, CR impairs immunity against certain pathogens. However, little is known about the effects of long-term moderate CR on immune function in humans. In this multi-center, randomized clinical trial to determine CR's effect on inflammation and cell-mediated immunity, 218 healthy non-obese adults (20-50 y), were assigned 25% CR (n=143) or an ad-libitum (AL) diet (n=75), and outcomes tested at baseline, 12, and 24 months of CR. CR induced a 10.4% weight loss over the 2-y period. Relative to AL group, CR reduced circulating inflammatory markers, including total WBC and lymphocyte counts, ICAM-1 and leptin. Serum CRP and TNF-α concentrations were about 40% and 50% lower in CR group, respectively. CR had no effect on the delayed-type hypersensitivity skin response or antibody response to vaccines, nor did it cause difference in clinically significant infections. In conclusion, long-term moderate CR without malnutrition induces a significant and persistent inhibition of inflammation without impairing key in vivo indicators of cell-mediated immunity. Given the established role of these pro-inflammatory molecules in the pathogenesis of multiple chronic diseases, these CR-induced adaptations suggest a shift toward a healthy phenotype., Competing Interests: Conflict of Interests Statement None of the authors have conflict of interest.
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- 2016
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21. Effect of Two-Year Caloric Restriction on Bone Metabolism and Bone Mineral Density in Non-Obese Younger Adults: A Randomized Clinical Trial.
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Villareal DT, Fontana L, Das SK, Redman L, Smith SR, Saltzman E, Bales C, Rochon J, Pieper C, Huang M, Lewis M, and Schwartz AV
- Subjects
- Adult, Biomarkers blood, Female, Humans, Male, Middle Aged, Aging blood, Body Weight, Bone Density, Caloric Restriction adverse effects, Lumbar Vertebrae metabolism, Osteoporosis blood, Osteoporosis etiology
- Abstract
Although caloric restriction (CR) could delay biologic aging in humans, it is unclear if this would occur at the cost of significant bone loss. We evaluated the effect of prolonged CR on bone metabolism and bone mineral density (BMD) in healthy younger adults. Two-hundred eighteen non-obese (body mass index [BMI] 25.1 ± 1.7 kg/m(2) ), younger (age 37.9 ± 7.2 years) adults were randomly assigned to 25% CR (CR group, n = 143) or ad libitum (AL group, n = 75) for 2 years. Main outcomes were BMD and markers of bone turnover. Other outcomes included body composition, bone-active hormones, nutrient intake, and physical activity. Body weight (-7.5 ± 0.4 versus 0.1 ± 0.5 kg), fat mass (-5.3 ± 0.3 versus 0.4 ± 0.4 kg), and fat-free mass (-2.2 ± 0.2 versus -0.2 ± 0.2 kg) decreased in the CR group compared with AL (all between group p < 0.001). Compared with AL, the CR group had greater changes in BMD at 24 months: lumbar spine (-0.013 ± 0.003 versus 0.007 ± 0.004 g/cm(2) ; p < 0.001), total hip (-0.017 ± 0.002 versus 0.001 ± 0.003 g/cm(2) ; p < 0.001), and femoral neck (-0.015 ± 0.003 versus -0.005 ± 0.004 g/cm(2) ; p = 0.03). Changes in bone markers were greater at 12 months for C-telopeptide (0.098 ± 0.012 versus 0.025 ± 0.015 μg/L; p < 0.001), tartrate-resistant acid phosphatase (0.4 ± 0.1 versus 0.2 ± 0.1 U/L; p = 0.004), and bone-specific alkaline phosphatase (BSAP) (-1.4 ± 0.4 versus -0.3 ± 0.5 U/L; p = 0.047) but not procollagen type 1 N-propeptide; at 24 months, only BSAP differed between groups (-1.5 ± 0.4 versus 0.9 ± 0.6 U/L; p = 0.001). The CR group had larger increases in 25-hydroxyvitamin D, cortisol, and adiponectin and decreases in leptin and insulin compared with AL. However, parathyroid hormone and IGF-1 levels did not differ between groups. The CR group also had lower levels of physical activity. Multiple regression analyses revealed that body composition, hormones, nutrients, and physical activity changes explained ∼31% of the variance in BMD and bone marker changes in the CR group. Therefore, bone loss at clinically important sites of osteoporotic fractures represents a potential limitation of prolonged CR for extending life span. Further long-term studies are needed to determine if CR-induced bone loss in healthy adults contributes to fracture risk and if bone loss can be prevented with exercise., (© 2015 American Society for Bone and Mineral Research.)
- Published
- 2016
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