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Author Notes:

Correspondence: Javed Butler, MD MPH, Emory University Hospital, 1365 Clifton Road NE, Suite AT430, Atlanta, GA 30322; Telephone: 404-778-5273; Fax: 404-778-5285; Email: javed.butler@emory.edu

Subjects:

Keywords:

  • Serum Albumin
  • Heart Failure
  • Epidemiology
  • Elderly

Serum Albumin Concentration and Heart Failure Risk

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Journal Title:

American Heart Journal

Volume:

Volume 160, Number 2

Publisher:

, Pages 279-285

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background How serum albumin levels are associated with risk for heart failure (HF) in the elderly is unclear. Methods We evaluated 2907 participants without HF (age, 73.6±2.9 years; 48.0% male; 58.7% white) from the community-based Health ABC Study. The association between baseline albumin and incident HF was assessed with standard and competing-risks proportional hazards models controlling for HF predictors, inflammatory markers, and incident coronary events. Results During a median follow-up of 9.4 years, 342 (11.8%) participants developed HF. Albumin was a time-dependent predictor of HF, with significance retained for up to 6 years (baseline HR per -1g/L, 1.14; 95% CI, 1.06–1.22; P<0.001; annual rate of HR decline, 2.1%; 95% CI, 0.8–3.3%; P=0.001). This association persisted in models controlling for HF predictors, inflammatory markers, and incident coronary events (baseline HR per -1g/L, 1.13; 95% CI, 1.05–1.22; P=0.001; annual rate of HR decline, 1.8%; 95% CI, 0.5–3.0%; P=0.008) and when mortality was accounted for in adjusted competing risks models (baseline HR per -1g/L, 1.13; 95% CI, 1.05–1.21; P=0.001; annual rate of HR decline, 1.9%; 95% CI, 0.7–3.1%; P=0.002). The association of albumin with HF risk was similar in men (HR per -1g/L, 1.13; 95% CI, 1.05–1.23; P=0.002) and women (HR per -1g/L, 1.12; 95% CI, 1.04–1.22; P=0.005) and in whites and blacks (HR per –1g/L, 1.13; 95% CI, 1.04–1.22; P<0.01 for both races) in adjusted models. Conclusions Low serum albumin levels are associated with increased risk for HF in the elderly in a time-dependent manner independent of inflammation and incident coronary events.

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