Menu
GWAS Study

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

Eppinga RN, Hagemeijer Y, Burgess S et al.

27798624 PubMed ID
GWAS Study Type
265046 Participants
Scroll to explore
Chapter I

Publication Details

Comprehensive information about this research publication

Authors

ER
Eppinga RN
HY
Hagemeijer Y
BS
Burgess S
HD
Hinds DA
SK
Stefansson K
GD
Gudbjartsson DF
VV
van Veldhuisen DJ
MP
Munroe PB
VN
Verweij N
VD
van der Harst P
Chapter II

Abstract

Summary of the research findings

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.

127,919 European ancestry individuals, 2,478 Asian ancestry individuals, 1,734 Black individuals, 684 Mixed ancestry individuals, 1,436 individuals

Chapter III

Study Statistics

Key metrics and study information

265046
Total Participants
GWAS
Study Type
Yes
Replicated
130,795 European ancestry individuals
Replication Participants
Other, African unspecified, European, Asian unspecified
Ancestry
U.K., U.S., Iceland, Netherlands
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

Important Disclaimer: This review has been performed semi-automatically and is provided for informational purposes only. While we strive for accuracy, this analysis may contain errors, omissions, or misinterpretations of the original research. DNA Genics disclaims all liability for any inaccuracies, errors, or consequences arising from the use of this information. Users should independently verify all information and consult original research publications before making any decisions based on this content. This analysis is not intended as a substitute for professional scientific review or medical advice.

Analysis In Progress

Our analysis of this publication is currently being prepared. Please check back soon for comprehensive insights into the health and genetic findings discussed in this research.