4.8 Article

Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality

Journal

NATURE GENETICS
Volume 48, Issue 12, Pages 1557-1563

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/ng.3708

Keywords

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Funding

  1. Netherlands organization for health research and development (ZonMw) [90.700.441]
  2. Wellcome Trust [100114]
  3. NIHR Cardiovascular Biomedical Research Unit at Barts
  4. London School of Medicine and Dentistry, Queen Mary University of London
  5. Netherlands Heart Institute
  6. Marie Sklodowska-Curie Global Fellowship [661395]
  7. Medical Research Council [MC_qA137853] Funding Source: researchfish

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Resting heart rate is a heritable trait correlated with life span. Little is known about the genetic contribution to resting heart rate and its relationship with mortality. We performed a genome-wide association discovery and replication analysis starting with 19.9 million genetic variants and studying up to 265,046 individuals to identify 64 loci associated with resting heart rate (P < 5 x 10(-8)); 46 of these were novel. We then used the genetic variants identified to study the association between resting heart rate and all-cause mortality. We observed that a genetically predicted resting heart rate increase of 5 beats per minute was associated with a 20% increase in mortality risk (hazard ratio 1.20, 95% confidence interval 1.11-1.28, P = 8.20 x 10(-7)) translating to a reduction in life expectancy of 2.9 years for males and 2.6 years for females. Our findings provide evidence for shared genetic predictors of resting heart rate and all-cause mortality.

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