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Cytomegalovirus serology in young to mid-adult life and decline of lung function
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Clinical_Respiratory_2023-Nenna.pdf
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Affiliation
Asthma and Airway Disease Research Center, University of ArizonaMel and Enid Zuckerman College of Public Health, University of Arizona
Issue Date
2023-03-16
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John Wiley and Sons IncCitation
Nenna R, Zhai J, Spangenberg A, et al. Cytomegalovirus serology in young to mid-adult life and decline of lung function. Clin Respir J. 2023; 17(5): 468-472. doi:10.1111/crj.13600Journal
Clinical Respiratory JournalRights
© 2023 The Authors. The Clinical Respiratory Journal published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License.Collection Information
This item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.Abstract
Introduction: Cytomegalovirus (CMV) seropositivity has been recently linked to severity and progression of asthma, cystic fibrosis, and chronic obstructive pulmonary disease (COPD). To date, no longitudinal study has addressed the relation of CMV serology to levels and decline of lung function in the general adult population. Methods: We evaluated 403 participants from the Tucson Epidemiological Study of Airway Obstructive Disease (TESAOD) who at enrollment were aged 28–55 years and completed lung function tests. During follow-up, the 403 participants completed on average 7.2 lung function tests per subject for a total of 2908 observations over a mean period of 14.7 years. We tested CMV serology in serum samples from enrollment and categorized participants into low, medium, and high CMV serology based on tertiles. The relation of CMV serology at enrollment to lung function levels and decline during follow-up was tested in multivariate random coefficients models. Results: After full adjustment, participants in the highest CMV serology tertile had faster declines of forced expiratory volume in 1 s (FEV1) and FEV1/forced vital capacity (FVC) compared with subjects in the lowest tertile (by −7.9 ml/year 95% confidence interval [−13.9 ml/year, −1.93 ml/year], and by −0.13%/year [−0.23%/year, −0.026%/year], respectively). These CMV effects were additive with those of cigarette smoking. No associations were found between CMV serology and FVC, indicating specific effects of CMV seropositivity on airflow limitation. Conclusion: High CMV serology in young to mid-adult life may be linked to increased COPD risk through an accelerated decline of lung function. © 2023 The Authors. The Clinical Respiratory Journal published by John Wiley & Sons Ltd.Note
Open access articleISSN
1752-6981PubMed ID
36924061Version
Final Published Versionae974a485f413a2113503eed53cd6c53
10.1111/crj.13600
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Except where otherwise noted, this item's license is described as © 2023 The Authors. The Clinical Respiratory Journal published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License.
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