7 results on '"Pavord, I."'
Search Results
2. BASELINE CHARACTERISTICS FROM A PHASE 3, RANDOMIZED CONTROLLED TRIAL (COUGH-2) OF GEFAPIXANT, A P2X3 RECEPTOR ANTAGONIST, IN REFRACTORY OR UNEXPLAINED CHRONIC COUGH
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Muccino, D., primary, Morice, A., additional, Birring, A., additional, Mcgarvey, L., additional, Dicpinigaitis, P., additional, Pavord, I., additional, La Rosa, C., additional, Urdaneta, E., additional, Assaid, C., additional, and Smith, J., additional
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- 2020
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3. Association Between Pathogens Detected Using Quantitative Polymerase Chain Reaction With Airway Inflammation in COPD at Stable State and Exacerbations
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Barker, B, Haldar, K, Patel, H, Pavord, I, Barer, MR, Brightling, C, and Bafadhel, M
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Pulmonary and Respiratory Medicine ,Critical Care and Intensive Care Medicine ,Cardiology and Cardiovascular Medicine ,respiratory tract diseases - Abstract
BACKGROUND: Relationships between airway inflammation and respiratory potentially pathogenic microorganisms (PPMs) quantified using quantitative polymerase chain reaction (qPCR) in subjects with COPD are unclear. Our aim was to evaluate mediators of airway inflammation and their association with PPMs in subjects with COPD at stable state and during exacerbations. METHODS: Sputum from 120 stable subjects with COPD was analyzed for bacteriology (colony-forming units; total 16S; and qPCR targeting Haemophilus influenzae, Moraxella catarrhalis, and Streptococcus pneumoniae), differential cell counts, and inflammatory mediators using the Meso-Scale Discovery Platform. Subjects were classified as colonized if any PPM was identified above the threshold of detection by qPCR. Symptoms were quantified using the visual analog scale. RESULTS: At stable state, 60% of subjects were qPCR positive for H influenzae, 48% for M catarrhalis, and 28% for S pneumoniae. Elevated sputum concentrations of IL-1β, IL-10, and tumor necrosis factor (TNF)-α were detected in samples qPCR positive for either H influenzae or M catarrhalis. Bacterial loads of H influenzae positively correlated with IL-1β, IL-8, IL-10, TNF-α, and symptoms; and M catarrhalis correlated with IL-10 and TNF-α. H influenzae qPCR bacterial load was an independent predictor of sputum TNF-α and IL-1β. In 55 subjects with paired exacerbation data, qPCR bacterial load fold change at exacerbation in M catarrhalis but not H influenzae correlated to changes in sputum TNF-α and IL-1β concentrations. CONCLUSIONS: At stable state, H influenzae is associated with increased airway inflammation in COPD. The relationship between bacterial load changes of specific pathogens and airway inflammation at exacerbation and recovery warrants further investigation.
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- 2015
4. Exhaled nitric oxide in pulmonary diseases: a comprehensive review
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Barnes, P, Dweik, R, Gelb, A, Gibson, P, George, S, Grasemann, H, Pavord, I, Ratjen, F, Silkoff, P, Taylor, DR, and Zamel, N
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respiratory system ,respiratory tract diseases - Abstract
The upregulation of nitric oxide (NO) by inflammatory cytokines and mediators in central and peripheral airway sites can be monitored easily in exhaled air. It is now possible to estimate the predominant site of increased fraction of exhaled NO (FeNO) and its potential pathologic and physiologic role in various pulmonary diseases. In asthma, increased FeNO reflects eosinophilic-mediated inflammatory pathways moderately well in central and/or peripheral airway sites and implies increased inhaled and systemic corticosteroid responsiveness. Recently, five randomized controlled algorithm asthma trials reported only equivocal benefits of adding measurements of FeNO to usual clinical guideline management including spirometry; however, significant design issues may exist. Overall, FeNO measurement at a single expiratory flow rate of 50 mL/s may be an important adjunct for diagnosis and management in selected cases of asthma. This may supplement standard clinical asthma care guidelines, including spirometry, providing a noninvasive window into predominantly large-airway-presumed eosinophilic inflammation. In COPD, large/central airway maximal NO flux and peripheral/small airway/alveolar NO concentration may be normal and the role of FeNO monitoring is less clear and therefore less established than in asthma. Furthermore, concurrent smoking reduces FeNO. Monitoring FeNO in pulmonary hypertension and cystic fibrosis has opened up a window to the role NO may play in their pathogenesis and possible clinical benefits in the management of these diseases.
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- 2010
5. COPD and Hepatitis C [4] (multiple letters)
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Pavord, I, Birring, S, and Kanazawa, H
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- 2003
6. The relation between peripheral blood leukocyte counts and respiratory symptoms, atopy, lung function, and airway responsiveness in adults.
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Lewis, Sarah A., Pavord, Ian D., Stringer, John R., Knox, Alan J., Weiss, Scott T., Britton, John R., Lewis, S A, Pavord, I D, Stringer, J R, Knox, A J, Weiss, S T, and Britton, J R
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EOSINOPHILS ,NEUTROPHILS ,ASTHMA ,OBSTRUCTIVE lung diseases - Abstract
Study Objectives: Eosinophils and neutrophils play major roles, respectively, in the pathogenesis of asthma and COPD, and it is well recognized that levels of these cells in peripheral blood are increased in relation to their pulmonary involvement. However, the relation between peripheral blood cell counts of the other major leukocyte groups and these lung diseases or markers of allergy or airflow obstruction is less clear. We have therefore investigated the association between peripheral blood levels of eosinophils, neutrophils, basophils, monocytes, and lymphocytes and the occurrence of chronic respiratory symptoms, atopy, lung function, and bronchial hyperresponsiveness, and the modifying effect of age, in adults.Design: A cross-sectional general population study.Setting: Data on > 2,000 British adults, who originally participated in a study of diet and lung health, were analyzed using multiple linear and logistic regression to adjust for potential confounders, including age, sex, and smoking history.Results: We found that, like eosinophils, the peripheral basophil count was increased in relation to asthma and associated symptoms, and to airway hyperreactivity and increased total IgE, but differed from eosinophils in that basophils were unrelated to atopy. Monocytes were predominantly associated with symptoms indicative of obstructive airway disease, in similar relation to neutrophils, but both of these leukocyte counts were also increased in asthma patients in older age groups. Lymphocyte counts were unrelated to any objective or subjective marker of disease.Conclusions: If peripheral blood cell counts reflect pulmonary involvement of these leukocyte groups, basophils and monocytes may play a distinct role in the pathogenesis of allergic and nonallergic respiratory disease. [ABSTRACT FROM AUTHOR]- Published
- 2001
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7. Promoting Prevention and Targeting Remission of Asthma: A European Forum for Research and Education in Allergy and Airway Diseases Consensus Statement on Raising the Bar in Asthma Care.
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Jesenak M, Bobcakova A, Djukanovic R, Gaga M, Hanania NA, Heaney LG, Pavord I, Quirce S, Ryan D, Fokkens W, Conti D, Hellings PW, Scadding G, Van Staeyen E, Bjermer LH, and Diamant Z
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Asthma is a common multifaceted respiratory disease with a major impact on quality of life. Despite increased insights into mechanisms underlying various asthma phenotypes and endotypes and the availability of targeted biologic treatment options, the disease remains uncontrolled in a substantial proportion of patients with risk of exacerbations, requiring systemic corticosteroids, and with progressive disease. Current international guidelines advocate a personalized management approach to patients with uncontrolled severe asthma. The European Forum for Research and Education in Allergy and Airway Diseases asthma expert panel was convened to discuss strategies to optimize asthma care and to prevent systemic corticosteroid overuse and disease progression. In this meeting report, we summarize current concepts and recommendations and provide a rationale to implement personalized asthma management at earlier stages of the disease. The ultimate goal is to move away from the current one-size-fits-most concept, which focuses on a symptom-driven treatment strategy, and shift toward a phenotype- and endotype-targeted approach aimed at curbing the disease course by improving clinical outcomes and preserving health-related quality of life. Herein, we provide a consensus view on asthma care that advocates a holistic approach and highlight some unmet needs to be addressed in future clinical trials and population studies., Competing Interests: Financial/Nonfinancial Disclosures The authors have reported to CHEST the following: M. J. has received consulting fees from ALK-Abello, Stallergenes-Greer, Takeda, and Zentiva; honoraria for lectures and presentations from ALK-Abello, Stallergenes-Greer, Takeda, Zentiva, AstraZeneca, Chiesi, CSL Behring, Novartis, and Pfizer; support for attending meetings, travel, or both from ALK-Abello, Stallergenes-Greer, Takeda, and Novartis; and honoraria for participation on advisory boards from ALK-Abello, Stallergenes-Greer, Chiesi, Novartis, Pfizer, and Sanofi Genzyme/Pasteur. A. B. received speaker’s honoraria or travel grants from Takeda, Novartis, Viatris, ALK, Zentiva, MERCK, Stallergenes Greer, Ewopharma, Astra Zeneca, Chiesi, S&D Pharma, Mundipharma, and Berlin Chemie. R. D. has been on advisory boards for ALK-Abello, GSK, and Sanofi-Genzyme-Regeneron and received honoraria for speaking at academic meetings sponsored by GlaxoSmithKline. He is a cofounder and consultant for Synairgen plc, where he owns shares. N. A. H. received honoraria from Sanofi, GSK, Amgen. Teva, Astra Zeneca, Genentech, and Verona Pharma and his institution received research grants from GSK, Genentech, Sanofi, and Astra Zeneca. L. G. H. has received grant funding, participated in advisory boards, and given lectures at meetings supported by Amgen, AstraZeneca, Boehringer Ingelheim, Chiesi, Circassia, Hoffmann La Roche, GlaxoSmithKline, Novartis, Theravance, Evelo Biosciences, Sanofi, and Teva; he has received grants from MedImmune, Novartis UK, Roche/Genentech, Inc., Glaxo Smith Kline, Amgen, Genentech/Hoffman La Roche, Astra Zeneca, MedImmune, Glaxo Smith Kline, Aerocrine, and Vitalograph; has received sponsorship for attending international scientific meetings from AstraZeneca, Boehringer Ingelheim, Chiesi, GSK, and Napp Pharmaceuticals; has taken part in asthma clinical trials sponsored by AstraZeneca, Boehringer Ingelheim, Hoffmann La Roche, and GlaxoSmithKline, for which his institution received remuneration; and is the academic lead for the Medical Research Council Stratified Medicine UK Consortium in Severe Asthma, which involves industrial partnerships with a number of pharmaceutical companies including Amgen, AstraZeneca, Boehringer Ingelheim, GlaxoSmithKline, Hoffmann la Roche, and Janssen. I. P. has received speaker’s honoraria for speaking at sponsored meetings in the last 5 years from Astra Zeneca, Boehringer Ingelheim, Aerocrine, Almirall, Novartis, Teva, Chiesi, Sanofi/Regeneron, Menarini, and GSK and payments for organizing educational events from AZ, GSK, Sanofi/Regeneron, and Teva; has received honoraria for attending advisory panels from Genentech, Sanofi/Regeneron, Astra Zeneca, Boehringer Ingelheim, GSK, Novartis, Teva, Merck, Circassia, Chiesi, and Knopp; has received payments to support Food and Drug Administration approval meetings from GSK; has received sponsorship to attend international scientific meetings from Boehringer Ingelheim, GSK, AstraZeneca, Teva, and Chiesi; and has received a grant from Chiesi to support a phase 2 clinical trial in Oxford. S. Q. has been on advisory boards for and has received speaker’s honoraria from ALK, Allergy Therapeutics, AstraZeneca, GlaxoSmithKline, Novartis, Chiesi, Mundipharma, and Sanofi-Regeneron in the last 3 years. D. R. has spoken on behalf of, provided consultancy to, or been sponsored to attend meetings by Viatris, Menarini, Sanofi, Thermo-Fisher, Chiesi, and Alk-Abello in the last 3 years. W. F. has received consultation or speaker fees, or both, from Dianosic, GSK, Novartis, and Sanofi-Aventis/Regeneron and the Department of Otorhinolaryngology of the Amsterdam University Medical Centre, location AMC, received grants for research in rhinology from ALK, AllergyTherapeutics, Novartis, EU, GSK, MYLAN, Sanofi-Aventis, and Zon-MW. D. C. serves as academic manager at the European Forum for Research and Education in Allergy and Airway Diseases (EUFOREA) and as review editor at Frontiers in Allergy, rhinology section. P. W. H. has received research grants, honoraria, lecture fees, or a combination thereof from Sanofi, Regeneron, Viatris, GSK, and Novartis. G. S. has received honoraria for articles, speaker, and advisory boards from ALK, AstraZeneca, Capnia, Chiesi, Church & Dwight, Circassia, Noucor, GSK, Meda/Mylan/Viatris, Merck, Sanofi- Regeneron, and Stallergenes; is the scientific chief editor of the rhinology section of Frontiers in Allergy; is a board member and lead for allergic rhinitis of EUFOREA; and is chair of the data monitoring board for pediatric AR trials of HDM SLIT. L. H. B. has received speakers fees or attended advisory board meetings for the following companies: AstraZeneca, Acucort, Birk pharma, GlaxoSmithklein, and Sanofi Genzyme in the past 3 years. Z. D. received speaker or consultant honoraria, served on advisory boards, or both at ALK, Antabio, Arcede, Biosion, Foresee Pharmaceuticals, GalenusHealth, GlaxoSmithKline, Hippo-Dx, Pleuran, QPS-Netherlands, Sanofi-Genzyme-Regeneron, all outside the submitted work; during the last 3 years of her assignment as research director for respiratory and allergy, QPS-Netherlands received a European grant from ERA4TB and funding from Foresee Pharmaceuticals for early clinical studies; she also has been associate editor for allergy and respiratory medicine and chair of the asthma expert panel at EUFOREA (2020-2023). None declared (M. G., E. V. S.)., (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Published
- 2024
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