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 language | English |
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Pages (from-to) | 1557-1563 |
Number of pages | 7 |
Journal | Nature Genetics |
Volume | 48 |
Issue number | 12 |
DOIs | |
Publication status | Published - Dec 2016 |
Externally published | Yes |
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