Publication

Novel Measures of Heart Rate Variability Predict Cardiovascular Mortality in Older Adults Independent of Traditional Cardiovascular Risk Factors: The Cardiovascular Health Study (CHS)

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Last modified
  • 05/22/2025
Type of Material
Authors
    Phyllis K. Stein, Washington UniversityJoshua I. Barzilay, Emory UniversityPaulo H. M. Chaves, Johns Hopkins UniversityStephanie Q. Mistretta, Washington UniversityPeter P. Domitrovich, Washington UniversityJohn S. Gottdiener, University of MarylandMichael W. Rich, Washington UniversityRobert E. Kleiger, Washington University
Language
  • English
Date
  • 2008-11-01
Publisher
  • Wiley: 12 months
Publication Version
Copyright Statement
  • © 2008 Wiley Periodicals, Inc.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1045-3873
Volume
  • 19
Issue
  • 11
Start Page
  • 1169
End Page
  • 1174
Grant/Funding Information
  • The research reported in this article was supported by contracts N01-HC-85079 through N01-HC-85086, N01-HC-35129, N01 HC-15103, N01 HC-55222, and U01 HL080295; and also by R0-1 HL62181 from the National Heart, Lung, and Blood Institute; with additional contribution from the National Institute of Neurological Disorders and Stroke.
Abstract
  • Background: It is unknown whether abnormal heart rate turbulence (HRT) and abnormal fractal properties of heart rate variability identify older adults at increased risk of cardiovascular death (CVdth). Methods: Data from 1,172 community-dwelling adults, ages 72 ± 5 (65-93) years, who participated in the Cardiovascular Health Study (CHS), a study of risk factors for CV disease in people ≥65 years. HRT and the short-term fractal scaling exponent (DFA1) derived from 24-hour Holter recordings. HRT categorized as: normal (turbulence slope [TS] and turbulence onset [TO] normal) or abnormal (TS and/or TO abnormal). DFA1 categorized as low (≤1) or high (>1). Cox regression analyses stratified by Framingham Risk Score (FRS) strata (low = <10, mid = 10-20, and high >20) and adjusted for prevalent clinical cardiovascular disease (CVD), diabetes, and quartiles of ventricular premature beat counts (VPCs). Results: CVdths (N = 172) occurred over a median follow-up of 12.3 years. Within each FRS stratum, low DFA1 + abnormal HRT predicted risk of CVdth (RR = 7.7 for low FRS; 3.6, mid FRS; 2.8, high FRS). Among high FRS stratum participants, low DFA1 alone also predicted CVdth (RR = 2.0). VPCs in the highest quartile predicted CVdth, but only in the high FRS group. Clinical CV disease predicted CVdth at each FRS stratum (RR = 2.9, low; 2.6, mid; and 1.9, high). Diabetes predicted CVdth in the highest FRS group only (RR = 2.2). Conclusions: The combination of low DFA1 + abnormal HRT is a strong risk factor for CVdth among older adults even after adjustment for conventional CVD risk measures and the presence of CVD.
Author Notes
  • Phyllis K. Stein, Ph.D., Washington University School of Medicine HRV Lab, 4625 Lindell Blvd., Suite 402, St. Louis, MO 63108. Fax: 314-286-1394; pstein@im.wustl.edu.
Keywords
Research Categories
  • Health Sciences, Medicine and Surgery

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