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

Ruben N Eppinga, Yanick Hagemeijer, Stephen Burgess, David A Hinds, Kari Stefansson, Daniel F Gudbjartsson, Dirk J van Veldhuisen, Patricia B Munroe, Niek Verweij, Pim van der Harst

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

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 × 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 × 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.

Original languageEnglish
Pages (from-to)1557-1563
Number of pages7
JournalNature Genetics
Volume48
Issue number12
DOIs
Publication statusPublished - Dec 2016
Externally publishedYes

Keywords

  • Arrhythmias, Cardiac/diagnosis
  • Female
  • Genetic Loci/genetics
  • Genetic Variation/genetics
  • Genome-Wide Association Study
  • Genomics/methods
  • Heart Rate
  • Humans
  • Male
  • Middle Aged
  • Rest/physiology
  • Risk Factors
  • Survival Rate

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