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Cytomegalovirus serology in young to mid‐adult life and decline of lung function

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 th...

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Autores principales: Nenna, Raffaella, Zhai, Jing, Spangenberg, Amber, Sherrill, Duane L., Martinez, Fernando D., Halonen, Marilyn, Guerra, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214568/
https://www.ncbi.nlm.nih.gov/pubmed/36924061
http://dx.doi.org/10.1111/crj.13600
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author Nenna, Raffaella
Zhai, Jing
Spangenberg, Amber
Sherrill, Duane L.
Martinez, Fernando D.
Halonen, Marilyn
Guerra, Stefano
author_facet Nenna, Raffaella
Zhai, Jing
Spangenberg, Amber
Sherrill, Duane L.
Martinez, Fernando D.
Halonen, Marilyn
Guerra, Stefano
author_sort Nenna, Raffaella
collection PubMed
description 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 (FEV(1)) and FEV(1)/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.
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spelling pubmed-102145682023-05-27 Cytomegalovirus serology in young to mid‐adult life and decline of lung function Nenna, Raffaella Zhai, Jing Spangenberg, Amber Sherrill, Duane L. Martinez, Fernando D. Halonen, Marilyn Guerra, Stefano Clin Respir J Brief Reports 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 (FEV(1)) and FEV(1)/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. John Wiley and Sons Inc. 2023-03-16 /pmc/articles/PMC10214568/ /pubmed/36924061 http://dx.doi.org/10.1111/crj.13600 Text en © 2023 The Authors. The Clinical Respiratory Journal published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Brief Reports
Nenna, Raffaella
Zhai, Jing
Spangenberg, Amber
Sherrill, Duane L.
Martinez, Fernando D.
Halonen, Marilyn
Guerra, Stefano
Cytomegalovirus serology in young to mid‐adult life and decline of lung function
title Cytomegalovirus serology in young to mid‐adult life and decline of lung function
title_full Cytomegalovirus serology in young to mid‐adult life and decline of lung function
title_fullStr Cytomegalovirus serology in young to mid‐adult life and decline of lung function
title_full_unstemmed Cytomegalovirus serology in young to mid‐adult life and decline of lung function
title_short Cytomegalovirus serology in young to mid‐adult life and decline of lung function
title_sort cytomegalovirus serology in young to mid‐adult life and decline of lung function
topic Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214568/
https://www.ncbi.nlm.nih.gov/pubmed/36924061
http://dx.doi.org/10.1111/crj.13600
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