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Temporal Changes in Resting Heart Rate, Left Ventricular Dysfunction, Heart Failure and Cardiovascular Disease: CARDIA Study - 31/07/20

Doi : 10.1016/j.amjmed.2019.12.035 
Chike C. Nwabuo, MD, MPH a, Duke Appiah, PhD b, Henrique T. Moreira, MD, PhD a, Henrique D. Vasconcellos, MD, MSc a, Queen N. Aghaji, MD a, Bharath Ambale-Venkatesh, PhD a, Jamal S. Rana, MD, PhD c, Norrina B. Allen, PhD d, Donald M. Lloyd-Jones, MD, ScM d, Pamela J. Schreiner, PhD e, Samuel S. Gidding, MD f, João A.C. Lima, MD, MBA a,
a Johns Hopkins University, Baltimore, Md 
b Department of Public Health, Texas Tech University Health Sciences Center, Lubbock, Tex 
c Department of Cardiology, Kaiser Permanente Northern California, Oakland, Calif 
d Northwestern University Feinberg School of Medicine, Chicago, Ill 
e University of Minnesota School of Public Health, Minneapolis 
f Nemours Cardiac Center, Alfred I. duPont Hospital for Children, Wilmington, Del 

Requests for reprints should be addressed to João A. C. Lima, MD, MBA, Professor of Medicine, Epidemiology, and Radiology, Johns Hopkins University School of Medicine, Division of Cardiology, 600 N. Wolfe Street, Blalock 524, Baltimore, MD 21287-8222.Epidemiology, and RadiologyJohns Hopkins University School of MedicineDivision of Cardiology600 N. Wolfe Street, Blalock 524BaltimoreMD21287-8222

ABSTRACT

Background

The prognostic significance of temporal changes in resting heart rate in young adults for premature heart failure and cardiovascular disease is unclear. We investigated the association between temporal changes in resting heart rate in young adults and early adult risk factors, subsequent cardiac function, and the risk of heart failure and cardiovascular by middle age.

Methods

We examined 4343 Coronary Artery Risk Development in Young Adults (CARDIA) study participants (mean [SD] age was 29.9 [3.6] years at the CARDIA Year-5 examination [1990-1991], 49% of participants were men, and 45% were African-American). Adjusted linear regression models were used to assess the association between temporal changes in resting heart rate, early life cardiovascular disease risk factors, and midlife cardiac function. Cox proportional hazard regression models were used to relate temporal changes in resting heart rate to heart failure and cardiovascular disease. Outcomes were followed up until August 31, 2017.

Results

Higher alcohol consumption (β = 0.03, P <0.001), lower physical activity (β = 0.002, P = 001), smoking (β = 1.58, P <0.001), men (P <0.001), African Americans (P <0.001), impaired left ventricular relaxation (e´,β = -0.13, P = 0.002), and worse diastolic function (E/e´, β = 0.1, P = 0.01) were associated with longitudinal increases in resting heart rate. We observed 268 cardiovascular disease and 74 heart failure events over a median of 26 years. In Cox models, baseline and temporal changes in resting heart rate were associated with higher risk of heart failure (hazard ratio [HR] =1.37 95% confidence interval [CI] [1.05-1.79] and HR = 1.38 95% CI [1.02-1.86]) and a higher risk cardiovascular disease (HR = 1.23 95% CI [1.07-1.42] and HR = 1.23 95% CI [1.05-1.44]).

Conclusions

Baseline and temporal changes in resting heart rate in young adults were associated with incident heart failure and cardiovascular disease by midlife. Contributory factors were associations between temporal increases in resting heart rate and early adult risk factors and subsequent cardiac dysfunction.

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Keywords : Cardiovascular disease, Diastolic function, Heart failure, Heart rate, Left ventricular function


Plan


 Funding: The CARDIA is conducted and supported by the National Heart, Lung, and Blood Institute (NHLBI) in collaboration with the University of Alabama at Birmingham (HHSN268201800005I & HHSN268201800007I), Northwestern University (HHSN268201800003I), University of Minnesota (HHSN268201800006I), and Kaiser Foundation Research Institute (HHSN268201800004I). This manuscript has been reviewed by CARDIA for scientific content.
 Conflicts of Interest: None.
 Authorship: All authors had access to the data and a role in writing this manuscript.


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Vol 133 - N° 8

P. 946-953 - août 2020 Retour au numéro
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