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Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study

RATIONALE: Adipose tissue produces adiponectin, an anti-inflammatory protein. Adiponectin deficiency in mice is associated with abnormal post-natal alveolar development. OBJECTIVE: We hypothesized that lower serum adiponectin concentrations are associated with lower lung function in humans, independ...

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Autores principales: Thyagarajan, Bharat, Jacobs, David R, Smith, Lewis J, Kalhan, Ravi, Gross, Myron D, Sood, Akshay
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014903/
https://www.ncbi.nlm.nih.gov/pubmed/21143922
http://dx.doi.org/10.1186/1465-9921-11-176
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author Thyagarajan, Bharat
Jacobs, David R
Smith, Lewis J
Kalhan, Ravi
Gross, Myron D
Sood, Akshay
author_facet Thyagarajan, Bharat
Jacobs, David R
Smith, Lewis J
Kalhan, Ravi
Gross, Myron D
Sood, Akshay
author_sort Thyagarajan, Bharat
collection PubMed
description RATIONALE: Adipose tissue produces adiponectin, an anti-inflammatory protein. Adiponectin deficiency in mice is associated with abnormal post-natal alveolar development. OBJECTIVE: We hypothesized that lower serum adiponectin concentrations are associated with lower lung function in humans, independent of obesity. We explored mediation of this association by insulin resistance and systemic inflammation. METHODS AND MEASUREMENTS: Spirometry testing was conducted at years 10 and 20 follow-up evaluation visits in 2,056 eligible young adult participants in the Coronary Artery Risk Development in Young Adults (CARDIA) study. Body mass index, serum adiponectin, serum C-reactive protein (a marker of systemic inflammation), and insulin resistance were assessed at year 15. MAIN RESULTS: After controlling for body mass index, years 10 and 20 forced vital capacity (FVC) were 81 ml and 82 ml lower respectively (p = 0.004 and 0.01 respectively) in the lowest vs. highest adiponectin quartiles. Similarly, years 10 and 20 forced expiratory volume in one second (FEV(1)) were 50 ml and 38 ml lower (p = 0.01 and 0.09, respectively) in the lowest vs. highest adiponectin quartiles. These associations were no longer significant after adjustment for insulin resistance and C-reactive protein. Serum adiponectin was not associated with FEV(1)/FVC or peak FEV(1). CONCLUSIONS: Independent of obesity, lower serum adiponectin concentrations are associated with lower lung function. The attenuation of this association after adjustment for insulin resistance and systemic inflammation suggests that these covariates are on a causal pathway linking adiponectin and lung function.
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spelling pubmed-30149032011-01-05 Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study Thyagarajan, Bharat Jacobs, David R Smith, Lewis J Kalhan, Ravi Gross, Myron D Sood, Akshay Respir Res Research RATIONALE: Adipose tissue produces adiponectin, an anti-inflammatory protein. Adiponectin deficiency in mice is associated with abnormal post-natal alveolar development. OBJECTIVE: We hypothesized that lower serum adiponectin concentrations are associated with lower lung function in humans, independent of obesity. We explored mediation of this association by insulin resistance and systemic inflammation. METHODS AND MEASUREMENTS: Spirometry testing was conducted at years 10 and 20 follow-up evaluation visits in 2,056 eligible young adult participants in the Coronary Artery Risk Development in Young Adults (CARDIA) study. Body mass index, serum adiponectin, serum C-reactive protein (a marker of systemic inflammation), and insulin resistance were assessed at year 15. MAIN RESULTS: After controlling for body mass index, years 10 and 20 forced vital capacity (FVC) were 81 ml and 82 ml lower respectively (p = 0.004 and 0.01 respectively) in the lowest vs. highest adiponectin quartiles. Similarly, years 10 and 20 forced expiratory volume in one second (FEV(1)) were 50 ml and 38 ml lower (p = 0.01 and 0.09, respectively) in the lowest vs. highest adiponectin quartiles. These associations were no longer significant after adjustment for insulin resistance and C-reactive protein. Serum adiponectin was not associated with FEV(1)/FVC or peak FEV(1). CONCLUSIONS: Independent of obesity, lower serum adiponectin concentrations are associated with lower lung function. The attenuation of this association after adjustment for insulin resistance and systemic inflammation suggests that these covariates are on a causal pathway linking adiponectin and lung function. BioMed Central 2010 2010-12-09 /pmc/articles/PMC3014903/ /pubmed/21143922 http://dx.doi.org/10.1186/1465-9921-11-176 Text en Copyright ©2010 Thyagarajan et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Thyagarajan, Bharat
Jacobs, David R
Smith, Lewis J
Kalhan, Ravi
Gross, Myron D
Sood, Akshay
Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study
title Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study
title_full Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study
title_fullStr Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study
title_full_unstemmed Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study
title_short Serum adiponectin is positively associated with lung function in young adults, independent of obesity: The CARDIA study
title_sort serum adiponectin is positively associated with lung function in young adults, independent of obesity: the cardia study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014903/
https://www.ncbi.nlm.nih.gov/pubmed/21143922
http://dx.doi.org/10.1186/1465-9921-11-176
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