Relation of Elevated Resting Heart Rate in Mid-Life to Cognitive Decline Over 20 Years (from the Atherosclerosis Risk in Communities [ARIC] Study)

Stephanie Wang, Oluwaseun E. Fashanu, Di Zhao, Eliseo Guallar, Rebecca F. Gottesman, Andrea L.C. Schneider, John W. McEvoy, Faye L. Norby, Amer I. Aladin, Alvaro Alonso, Erin D. Michos

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Resting heart rate (RHR) is independently associated with cardiovascular disease (CVD) risk. We determined whether RHR, measured in mid-life, is also associated with cognitive decline. We studied 13,720 middle-aged white and black ARIC participants without a history of stroke or atrial fibrillation. RHR was obtained from a 12-lead resting electrocardiogram at the baseline visit (1990 to 1992) and categorized into groups as <60 (reference), 60 to 69, 70 to 79 and ≥80 beats/min. Cognitive scores were obtained at baseline and at up to 2 additional visits (1996 to 1998 and 2011 to 2013). The primary outcome was a global composite cognitive score (Z-score) derived from 3 tests: delayed word recall, digit symbol substitution, and word fluency. The associations of RHR with cognitive decline and incident dementia were examined using linear mixed-effects and Cox hazard models, respectively, adjusting for sociodemographics, CVD risk factors, and AV-nodal blockade use. Multiple imputation methods were used to account for attrition over follow-up. Participants had mean ± SD age of 58 ± 6 years; 56% were women, 24% black. Average RHR was 66 ± 10 beats/min. Over a mean follow-up of 20 years, those with RHR ≥80 beats/min had greater global cognitive decline (average adjusted Z-score difference −0.12 [95% confidence interval −0.21, −0.03]) and increased risk for incident dementia (hazard ratio 1.28 (1.04, 1.57), compared with those with RHR <60 beats/min. In conclusion, elevated RHR is independently associated with greater cognitive decline and incident dementia over 20 years. Further studies are needed to determine whether the associations are causal or secondary to another underlying process, and whether modification of RHR can affect cognitive decline.

Original languageEnglish (US)
Pages (from-to)334-340
Number of pages7
JournalAmerican Journal of Cardiology
Volume123
Issue number2
DOIs
StatePublished - Jan 15 2019

Bibliographical note

Funding Information:
Sources of Funding: Drs. Michos and Zhao are supported by the Blumenthal Scholars Fund for Preventive Cardiology research. The Atherosclerosis Risk in Communities Study is carried out as a collaborative study supported by National Heart, Lung, and Blood Institute contracts ( HHSN268201100005C , HHSN268201100006C , HHSN268201100007C , HHSN268201100008C , HHSN268201100009C , HHSN268201100010C , HHSN268201100011C , and HHSN268201100012C ). The ARIC-Neurocognitive Study was funded by grants from the National Heart, Lung, and Blood Institute. ( HL096812 , HL096814 , HL096899 , HL096902 , HL096917 ), with additional support from the National Institute of Neurological Disorders and Stroke . Additionally, Dr. Schneider is supported by the National Institute of Neurological Disorders and Stroke through an administrative supplement to award R25NS065729 . Dr. Gottesman is supported by K24 AG052573 from the National Institute on Aging.

Funding Information:
Sources of Funding: Drs. Michos and Zhao are supported by the Blumenthal Scholars Fund for Preventive Cardiology research. The Atherosclerosis Risk in Communities Study is carried out as a collaborative study supported by National Heart, Lung, and Blood Institute contracts (HHSN268201100005C, HHSN268201100006C, HHSN268201100007C, HHSN268201100008C, HHSN268201100009C, HHSN268201100010C, HHSN268201100011C, and HHSN268201100012C). The ARIC-Neurocognitive Study was funded by grants from the National Heart, Lung, and Blood Institute. (HL096812, HL096814, HL096899, HL096902, HL096917), with additional support from the National Institute of Neurological Disorders and Stroke. Additionally, Dr. Schneider is supported by the National Institute of Neurological Disorders and Stroke through an administrative supplement to award R25NS065729. Dr. Gottesman is supported by K24 AG052573 from the National Institute on Aging.

Publisher Copyright:
© 2018

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