Title | Genetic loci associated with heart rate variability and their effects on cardiac disease risk. |
Publication Type | Publication |
Year | 2017 |
Authors | Nolte IM, M Munoz L, Tragante V, Amare AT, Jansen R, Vaez A, von der Heyde B, Avery CL, Bis JC, Dierckx B et al. |
Journal | Nat Commun |
Volume | 8 |
Pagination | 15805 |
Date Published | 2017 Jun 14 |
ISSN | 2041-1723 |
Keywords | blood pressure, Cohort Studies, Genetic Predisposition to Disease, genome-wide association study, Heart Diseases, heart rate, Humans, Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels, Muscle Proteins, Polymorphism, Single Nucleotide, Potassium Channels, Quantitative Trait Loci, RGS Proteins, Risk Factors, White People |
Abstract | Reduced cardiac vagal control reflected in low heart rate variability (HRV) is associated with greater risks for cardiac morbidity and mortality. In two-stage meta-analyses of genome-wide association studies for three HRV traits in up to 53,174 individuals of European ancestry, we detect 17 genome-wide significant SNPs in eight loci. HRV SNPs tag non-synonymous SNPs (in NDUFA11 and KIAA1755), expression quantitative trait loci (eQTLs) (influencing GNG11, RGS6 and NEO1), or are located in genes preferentially expressed in the sinoatrial node (GNG11, RGS6 and HCN4). Genetic risk scores account for 0.9 to 2.6% of the HRV variance. Significant genetic correlation is found for HRV with heart rate (-0.74 |
DOI | 10.1038/ncomms15805 |
Alternate Journal | Nat Commun |
PubMed ID | 28613276 |
PubMed Central ID | PMC5474732 |
Grant List | R01 HL120393 / HL / NHLBI NIH HHS / United States U01 HL130114 / HL / NHLBI NIH HHS / United States P01 GM099568 / GM / NIGMS NIH HHS / United States UL1 TR000124 / TR / NCATS NIH HHS / United States R01 HL105756 / HL / NHLBI NIH HHS / United States S10 OD020069 / OD / NIH HHS / United States K23 HL114724 / HL / NHLBI NIH HHS / United States R01 HL116747 / HL / NHLBI NIH HHS / United States P30 DK063491 / DK / NIDDK NIH HHS / United States I01 BX002558 / BX / BLRD VA / United States MC_UU_12019/1 / MRC_ / Medical Research Council / United Kingdom UL1 TR001881 / TR / NCATS NIH HHS / United States P2C HD050924 / HD / NICHD NIH HHS / United States |
MS#:
0289
ECI:
Manuscript Affiliation:
HCHS/SOL Genetic Analysis Center - University of Washington, Seattle
Manuscript Status:
Published