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Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study

BACKGROUND: Pulmonary and cardiac functions decline with age, but the associations of pulmonary dysfunction with cardiac function and heart failure (HF) risk in late life is not known. We aimed to determine the associations of percent predicted forced vital capacity (ppFVC) and the ratio of forced e...

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Autores principales: Ramalho, Sergio H. R., Claggett, Brian L., Washko, George R., Jose Estepar, Raul San, Chang, Patricia P., Kitzman, Dalane W., Cipriano Junior, Gerson, Solomon, Scott D., Skali, Hicham, Shah, Amil M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707834/
https://www.ncbi.nlm.nih.gov/pubmed/35861819
http://dx.doi.org/10.1161/JAHA.121.023990
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author Ramalho, Sergio H. R.
Claggett, Brian L.
Washko, George R.
Jose Estepar, Raul San
Chang, Patricia P.
Kitzman, Dalane W.
Cipriano Junior, Gerson
Solomon, Scott D.
Skali, Hicham
Shah, Amil M.
author_facet Ramalho, Sergio H. R.
Claggett, Brian L.
Washko, George R.
Jose Estepar, Raul San
Chang, Patricia P.
Kitzman, Dalane W.
Cipriano Junior, Gerson
Solomon, Scott D.
Skali, Hicham
Shah, Amil M.
author_sort Ramalho, Sergio H. R.
collection PubMed
description BACKGROUND: Pulmonary and cardiac functions decline with age, but the associations of pulmonary dysfunction with cardiac function and heart failure (HF) risk in late life is not known. We aimed to determine the associations of percent predicted forced vital capacity (ppFVC) and the ratio of forced expired volume in 1 second (FEV(1)) to forced vital capacity (FVC; FEV(1)/FVC) with cardiac function and incident HF with preserved or reduced ejection fraction in late life. METHODS AND RESULTS: Among 3854 HF‐free participants in the ARIC (Atherosclerosis Risk in Communities) cohort study who underwent echocardiography and spirometry at the fifth study visit (2011–2013), associations of FEV(1)/FVC and ppFVC with echocardiographic measures, cardiac biomarkers, and risk of HF, HF with preserved ejection fraction, and HF with reduced ejection fraction were assessed. Multivariable linear and Cox regression models adjusted for demographics, body mass index, coronary disease, atrial fibrillation, hypertension, and diabetes. Mean age was 75±5 years, 40% were men, 19% were Black, and 61% were ever smokers. Mean FEV(1)/FVC was 72±8%, and ppFVC was 98±17%. In adjusted analyses, lower FEV(1)/FVC and ppFVC were associated with higher NT‐proBNP (N‐terminal pro‐B‐type natriuretic peptide; both P<0.001) and pulmonary artery pressure (P<0.004). Lower ppFVC was also associated with higher left ventricular mass, left ventricular filling pressure, and high‐sensitivity C‐reactive protein (all P<0.01). Lower FEV(1)/FVC was associated with a trend toward higher risk of incident HF with preserved ejection fraction (hazard ratio [HR] per 10‐point decrease, 1.31; 95% CI, 0.98–1.74; P=0.07) and HF with reduced ejection fraction (HR per 10‐point decrease, 1.24; 95% CI, 0.91–1.70; P=0.18), but these associations did not reach statistical significance. Lower ppFVC was associated with incident HF with preserved ejection fraction (HR per 10‐unit decrease, 1.21; 95% CI, 1.04–1.41; P=0.013) but not with HF with reduced ejection fraction (HR per 10‐unit decrease, 0.90; 95% CI, 0.76–1.07; P=0.24). CONCLUSIONS: Subclinical reductions in FEV(1)/FVC and ppFVC differentially associate with cardiac function and HF risk in late life.
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spelling pubmed-97078342022-11-30 Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study Ramalho, Sergio H. R. Claggett, Brian L. Washko, George R. Jose Estepar, Raul San Chang, Patricia P. Kitzman, Dalane W. Cipriano Junior, Gerson Solomon, Scott D. Skali, Hicham Shah, Amil M. J Am Heart Assoc Original Research BACKGROUND: Pulmonary and cardiac functions decline with age, but the associations of pulmonary dysfunction with cardiac function and heart failure (HF) risk in late life is not known. We aimed to determine the associations of percent predicted forced vital capacity (ppFVC) and the ratio of forced expired volume in 1 second (FEV(1)) to forced vital capacity (FVC; FEV(1)/FVC) with cardiac function and incident HF with preserved or reduced ejection fraction in late life. METHODS AND RESULTS: Among 3854 HF‐free participants in the ARIC (Atherosclerosis Risk in Communities) cohort study who underwent echocardiography and spirometry at the fifth study visit (2011–2013), associations of FEV(1)/FVC and ppFVC with echocardiographic measures, cardiac biomarkers, and risk of HF, HF with preserved ejection fraction, and HF with reduced ejection fraction were assessed. Multivariable linear and Cox regression models adjusted for demographics, body mass index, coronary disease, atrial fibrillation, hypertension, and diabetes. Mean age was 75±5 years, 40% were men, 19% were Black, and 61% were ever smokers. Mean FEV(1)/FVC was 72±8%, and ppFVC was 98±17%. In adjusted analyses, lower FEV(1)/FVC and ppFVC were associated with higher NT‐proBNP (N‐terminal pro‐B‐type natriuretic peptide; both P<0.001) and pulmonary artery pressure (P<0.004). Lower ppFVC was also associated with higher left ventricular mass, left ventricular filling pressure, and high‐sensitivity C‐reactive protein (all P<0.01). Lower FEV(1)/FVC was associated with a trend toward higher risk of incident HF with preserved ejection fraction (hazard ratio [HR] per 10‐point decrease, 1.31; 95% CI, 0.98–1.74; P=0.07) and HF with reduced ejection fraction (HR per 10‐point decrease, 1.24; 95% CI, 0.91–1.70; P=0.18), but these associations did not reach statistical significance. Lower ppFVC was associated with incident HF with preserved ejection fraction (HR per 10‐unit decrease, 1.21; 95% CI, 1.04–1.41; P=0.013) but not with HF with reduced ejection fraction (HR per 10‐unit decrease, 0.90; 95% CI, 0.76–1.07; P=0.24). CONCLUSIONS: Subclinical reductions in FEV(1)/FVC and ppFVC differentially associate with cardiac function and HF risk in late life. John Wiley and Sons Inc. 2022-07-05 /pmc/articles/PMC9707834/ /pubmed/35861819 http://dx.doi.org/10.1161/JAHA.121.023990 Text en © 2022 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Ramalho, Sergio H. R.
Claggett, Brian L.
Washko, George R.
Jose Estepar, Raul San
Chang, Patricia P.
Kitzman, Dalane W.
Cipriano Junior, Gerson
Solomon, Scott D.
Skali, Hicham
Shah, Amil M.
Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study
title Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study
title_full Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study
title_fullStr Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study
title_full_unstemmed Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study
title_short Association of Pulmonary Function With Late‐Life Cardiac Function and Heart Failure Risk: The ARIC Study
title_sort association of pulmonary function with late‐life cardiac function and heart failure risk: the aric study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9707834/
https://www.ncbi.nlm.nih.gov/pubmed/35861819
http://dx.doi.org/10.1161/JAHA.121.023990
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