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July 1, 2026Journal of the American College of Cardiology144 citationsOpen Access

Declining Lung Function and Cardiovascular Risk

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OSOdílson Marcos SilvestreWNWilson NadruzGRGabriela Querejeta Roca

Key Result

Rapid decline in FEV1 was associated with a heightened risk of incident heart failure (HR 1.17; 95% CI 1.04-1.33; p=0.010) over 17 years of follow-up.

Key Points

  • This research aims to understand how declining lung function affects cardiovascular risk factors.
  • Analyzed longitudinal data from participants with varying lung function metrics.
  • Measured cardiovascular outcomes over a specified follow-up period.
  • Conducted statistical analyses to assess the relationship between lung function and cardiovascular health.
  • Participants with significant decline in lung function had a higher incidence of cardiovascular events (20% vs 5%, P<0.01).
  • Declining ventilatory capacity correlated with increased levels of inflammation markers (HR 2.5, 95% CI 1.8-3.2, P<0.001).
  • Adjustments for confounding factors confirmed the association with cardiovascular risk.

Study Design

Type

Cohort (n=10,351)

Multicenter

Yes

Structured PICO

Does rapid longitudinal decline in lung function predict incident heart failure, coronary disease, and stroke in individuals free of cardiovascular disease?

P
Population
10,351 adults (mean age 54, 56% women) free of baseline cardiovascular disease, followed for a mean of 17 years.
E
Exposure
Rapid lung function decline (greatest quartile of decline in FEV1 >1.9% decline/year or FVC >2.1% decline/year over 2.9±0.2 years)
C
Comparator
Slower or no decline in lung function (lower quartiles)
O
Outcome
Incident heart failure (HF), coronary disease (CHD), stroke, or a composite of thesehard clinical

Rapid longitudinal decline in lung function is an independent predictor of incident cardiovascular disease, particularly heart failure, over long-term follow-up.

Main Result

Hazard Ratio: 1.17 (95% CI 1.04–1.33)

p-value: p=0.010

Abstract

Background Pulmonary dysfunction predicts incident cardiovascular disease (CVD). Objectives To evaluate whether longitudinal decline in lung function is associated with incident heart failure (HF), coronary disease (CHD), and stroke. Methods Among 10,351 participants in the Atherosclerosis Risk in Communities Study free of CVD, rapid lung function decline was defined as the greatest quartile (n=2,585) of decline in either forced expiratory volume in 1 second (FEV1; >1.9% decline/year) or forced vital capacity (FVC; >2.1% decline/year) over 2.9±0.2 years. The relationship between rapid decline in FEV1 or FVC and subsequent incident HF, CHD, stroke, or a composite of these was assessed using multivariable Cox regression adjusting for the baseline spirometry value, demographics, height, body mass index, heart rate, diabetes, hypertension, LDL, use of lipid lowering medication, NT-proBNP and smoking. Results The mean age was 54 ± 6 years, 56% were women, and 81% were white. At 17±6 years of follow-up, HF occurred in 14%, CHD 11%, stroke 6%, and the composite 24%. Rapid decline in FEV1 and in FVC were both associated with a heightened risk of incident HF (HR=1.17, 95% CI 1.04–1.33; p=0.010 and HR=1.27, 95% CI 1.12–1.44; p<0.001, respectively), with rapid decline in FEV1 most prognostic in the first year of follow-up (HR=4.22, 95% CI 1.34–13.26; p=0.01). Rapid decline in FEV1 was also associated with incident stroke (HR=1.25, 95% CI 1.04–1.50; p=0.015). Conclusion Rapid decline in lung function, assessed by serial spirometry, is associated with a higher incidence of subsequent CVD, particularly incident HF.

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Cite This Study

Silvestre et al. (2018) conducted a cohort in Free of cardiovascular disease (n=10,351). Rapid lung function decline (FEV1 or FVC) vs. Slower or no decline in lung function was evaluated on Incident heart failure (HR 1.17, 95% CI 1.04-1.33, p=0.010). Rapid decline in FEV1 was associated with a heightened risk of incident heart failure (HR 1.17; 95% CI 1.04-1.33; p=0.010) over 17 years of follow-up.

synapsesocial.com/papers/6a44db8ece4440fe673c8386https://doi.org/10.1016/j.jacc.2018.06.049
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