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PMID: 18631274 Published · ppublish English Journal Article Research Support, N.I.H., Extramural

Novel measures of heart rate variability predict cardiovascular mortality in older adults independent of traditional cardiovascular risk factors: the Cardiovascular Health Study (CHS).

Journal of cardiovascular electrophysiology ·Vol. 19 ·No. 11 ·2008-11-00 ·Pages 1169-74

Stein PK, Barzilay JI, Chaves PH, Mistretta SQ, Domitrovich PP, Gottdiener JS, Rich MW, Kleiger RE

Abstract

Novel HRV Predicts CV Mortality in the Elderly. 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). 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 >or=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 (<or=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). 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). 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.

MeSH Terms
Aged Aged, 80 and over Arrhythmias, Cardiac/diagnosis,mortality Death, Sudden, Cardiac/epidemiology Electrocardiography, Ambulatory/methods,statistics & numerical data Female Heart Rate Humans Male Maryland/epidemiology Reproducibility of Results Risk Assessment/methods Risk Factors Sensitivity and Specificity Survival Analysis Survival Rate
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Stein Phyllis K
Washington University School of Medicine, St Louis, Missouri 63108, USA. [email protected]
Barzilay Joshua I
Chaves Paulo H M
Mistretta Stephanie Q
Domitrovich Peter P
Gottdiener John S
Rich Michael W
Kleiger Robert E
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Article Info
Journal
Journal of cardiovascular electrophysiology
Abbr.
J Cardiovasc Electrophysiol
ISSN
1540-8167
Published
2008-11-00
Pages
1169-74
Language
English
Region
United States
NLM ID
9010756
PMCID
PMC3638897
Subset
IM
Grants
NHLBI NIH HHS · U01 HL080295 · United States
NHLBI NIH HHS · N01 HC015103 · United States
NHLBI NIH HHS · N01HC55222 · United States
NHLBI NIH HHS · N01 HC-55222 · United States
NHLBI NIH HHS · R01 HL062181 · United States
NHLBI NIH HHS · N01-HC-85079 · United States
NHLBI NIH HHS · N01HC85079 · United States
NHLBI NIH HHS · N01 HC035129 · United States
NHLBI NIH HHS · R0-1 HL62181 · United States
NHLBI NIH HHS · N01-HC-85086 · United States
NHLBI NIH HHS · N01HC85086 · United States
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