Sökning: WFRF:(Kathiresan Sekar) >
Phenotypic Refineme...
Phenotypic Refinement of Heart Failure in a National Biobank Facilitates Genetic Discovery
-
- Aragam, Krishna G. (författare)
- Broad Institute,Massachusetts General Hospital
-
- Chaffin, Mark (författare)
- Broad Institute
-
- Levinson, Rebecca T. (författare)
- Vanderbilt University Medical Center
-
visa fler...
-
- McDermott, Gregory (författare)
- Massachusetts General Hospital
-
- Choi, Seung Hoan (författare)
- Broad Institute
-
- Shoemaker, M. Benjamin (författare)
- Vanderbilt University Medical Center
-
- Haas, Mary E. (författare)
- Broad Institute,Massachusetts General Hospital
-
- Weng, Lu Chen (författare)
- Broad Institute,Massachusetts General Hospital
-
- Lindsay, Mark E. (författare)
- Massachusetts General Hospital
-
- Smith, J. Gustav (författare)
- Lund University,Lunds universitet,Cardiovascular Epigenetics,Forskargrupper vid Lunds universitet,Lund University Research Groups,Broad Institute
-
- Newton-Cheh, Christopher (författare)
- Broad Institute,Massachusetts General Hospital
-
- Roden, Dan M. (författare)
- Broad Institute,Vanderbilt University Medical Center
-
- London, Barry (författare)
- University of Iowa
-
- Wells, Quinn S. (författare)
- Vanderbilt University Medical Center
-
- Ellinor, Patrick T. (författare)
- Broad Institute,Massachusetts General Hospital
-
- Kathiresan, Sekar (författare)
- Massachusetts General Hospital,Broad Institute
-
- Lubitz, Steven A. (författare)
- Broad Institute,Massachusetts General Hospital
-
visa färre...
-
(creator_code:org_t)
- 2019
- 2019
- Engelska 13 s.
-
Ingår i: Circulation. - 0009-7322. ; 139:4, s. 489-501
- Relaterad länk:
-
http://dx.doi.org/10...
-
visa fler...
-
https://lup.lub.lu.s...
-
https://doi.org/10.1...
-
visa färre...
Abstract
Ämnesord
Stäng
- Heart failure (HF) is a morbid and heritable disorder for which the biological mechanisms are incompletely understood. We therefore examined genetic associations with HF in a large national biobank, and assessed whether refined phenotypic classification would facilitate genetic discovery. Methods: We defined all-cause HF among 488 010 participants from the UK Biobank and performed a genome-wide association analysis. We refined the HF phenotype by classifying individuals with left ventricular dysfunction and without coronary artery disease as having nonischemic cardiomyopathy (NICM), and repeated a genetic association analysis. We then pursued replication of lead HF and NICM variants in independent cohorts, and performed adjusted association analyses to assess whether identified genetic associations were mediated through clinical HF risk factors. In addition, we tested rare, loss-of-function mutations in 24 known dilated cardiomyopathy genes for association with HF and NICM. Finally, we examined associations between lead variants and left ventricular structure and function among individuals without HF using cardiac magnetic resonance imaging (n=4158) and echocardiographic data (n=30 201). Results: We identified 7382 participants with all-cause HF in the UK Biobank. Genome-wide association analysis of all-cause HF identified several suggestive loci (P<1×10 -6 ), the majority linked to upstream HF risk factors, ie, coronary artery disease (CDKN2B-AS1 and MAP3K7CL) and atrial fibrillation (PITX2). Refining the HF phenotype yielded a subset of 2038 NICM cases. In contrast to all-cause HF, genetic analysis of NICM revealed suggestive loci that have been implicated in dilated cardiomyopathy (BAG3, CLCNKA-ZBTB17). Dilated cardiomyopathy signals arising from our NICM analysis replicated in independent cohorts, persisted after HF risk factor adjustment, and were associated with indices of left ventricular dysfunction in individuals without clinical HF. In addition, analyses of loss-of-function variants implicated BAG3 as a disease susceptibility gene for NICM (loss-of-function variant carrier frequency=0.01%; odds ratio,12.03; P=3.62×10 -5 ). Conclusions: We found several distinct genetic mechanisms of all-cause HF in a national biobank that reflect well-known HF risk factors. Phenotypic refinement to a NICM subtype appeared to facilitate the discovery of genetic signals that act independently of clinical HF risk facto rs and that are associated with subclinical left ventricular dysfunction.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Kardiologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
Nyckelord
- cardiomyopathies
- cardiomyopathy
- dilated
- genome-wide association study
- heart failure
Publikations- och innehållstyp
- art (ämneskategori)
- ref (ämneskategori)
Hitta via bibliotek
Till lärosätets databas
- Av författaren/redakt...
-
Aragam, Krishna ...
-
Chaffin, Mark
-
Levinson, Rebecc ...
-
McDermott, Grego ...
-
Choi, Seung Hoan
-
Shoemaker, M. Be ...
-
visa fler...
-
Haas, Mary E.
-
Weng, Lu Chen
-
Lindsay, Mark E.
-
Smith, J. Gustav
-
Newton-Cheh, Chr ...
-
Roden, Dan M.
-
London, Barry
-
Wells, Quinn S.
-
Ellinor, Patrick ...
-
Kathiresan, Seka ...
-
Lubitz, Steven A ...
-
visa färre...
- Om ämnet
-
- MEDICIN OCH HÄLSOVETENSKAP
-
MEDICIN OCH HÄLS ...
-
och Klinisk medicin
-
och Kardiologi
-
- MEDICIN OCH HÄLSOVETENSKAP
-
MEDICIN OCH HÄLS ...
-
och Medicinska och f ...
-
och Medicinsk geneti ...
- Artiklar i publikationen
-
Circulation
- Av lärosätet
-
Lunds universitet