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

Author:

Ramalho Sergio H. R.123ORCID,Claggett Brian L.1ORCID,Washko George R.4,Jose Estepar Raul San5ORCID,Chang Patricia P.6,Kitzman Dalane W.7,Cipriano Junior Gerson28ORCID,Solomon Scott D.1ORCID,Skali Hicham1ORCID,Shah Amil M.1ORCID

Affiliation:

1. Division of Cardiovascular Medicine Brigham and Women’s Hospital Boston MA

2. Health Sciences and Technologies Program – University of Brasilia Brasília Brazil

3. DASA Clinical Research Center ‐ Hospital Brasília Brasília Brazil

4. Division of Pulmonary and Critical Care Medicine Brigham and Women’s Hospital Boston MA

5. Department of Radiology Brigham and Women’s Hospital Boston MA

6. University of North Carolina Chapel Hill NC

7. Wake Forest School of Medicine Winston‐Salem NC

8. Rehabilitation Sciences Program – University of Brasilia Brasília Brazil

Abstract

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.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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