Subsequent Event Risk in Individuals With Established Coronary Heart Disease.
coronary artery disease
genetics
myocardial infarction
prognosis
secondary prevention
Journal
Circulation. Genomic and precision medicine
ISSN: 2574-8300
Titre abrégé: Circ Genom Precis Med
Pays: United States
ID NLM: 101714113
Informations de publication
Date de publication:
04 2019
04 2019
Historique:
pubmed:
22
3
2019
medline:
5
6
2020
entrez:
22
3
2019
Statut:
ppublish
Résumé
The Genetics of Subsequent Coronary Heart Disease (GENIUS-CHD) consortium was established to facilitate discovery and validation of genetic variants and biomarkers for risk of subsequent CHD events, in individuals with established CHD. The consortium currently includes 57 studies from 18 countries, recruiting 185 614 participants with either acute coronary syndrome, stable CHD, or a mixture of both at baseline. All studies collected biological samples and followed-up study participants prospectively for subsequent events. Enrollment into the individual studies took place between 1985 to present day with a duration of follow-up ranging from 9 months to 15 years. Within each study, participants with CHD are predominantly of self-reported European descent (38%-100%), mostly male (44%-91%) with mean ages at recruitment ranging from 40 to 75 years. Initial feasibility analyses, using a federated analysis approach, yielded expected associations between age (hazard ratio, 1.15; 95% CI, 1.14-1.16) per 5-year increase, male sex (hazard ratio, 1.17; 95% CI, 1.13-1.21) and smoking (hazard ratio, 1.43; 95% CI, 1.35-1.51) with risk of subsequent CHD death or myocardial infarction and differing associations with other individual and composite cardiovascular endpoints. GENIUS-CHD is a global collaboration seeking to elucidate genetic and nongenetic determinants of subsequent event risk in individuals with established CHD, to improve residual risk prediction and identify novel drug targets for secondary prevention. Initial analyses demonstrate the feasibility and reliability of a federated analysis approach. The consortium now plans to initiate and test novel hypotheses as well as supporting replication and validation analyses for other investigators.
Sections du résumé
BACKGROUND
The Genetics of Subsequent Coronary Heart Disease (GENIUS-CHD) consortium was established to facilitate discovery and validation of genetic variants and biomarkers for risk of subsequent CHD events, in individuals with established CHD.
METHODS
The consortium currently includes 57 studies from 18 countries, recruiting 185 614 participants with either acute coronary syndrome, stable CHD, or a mixture of both at baseline. All studies collected biological samples and followed-up study participants prospectively for subsequent events.
RESULTS
Enrollment into the individual studies took place between 1985 to present day with a duration of follow-up ranging from 9 months to 15 years. Within each study, participants with CHD are predominantly of self-reported European descent (38%-100%), mostly male (44%-91%) with mean ages at recruitment ranging from 40 to 75 years. Initial feasibility analyses, using a federated analysis approach, yielded expected associations between age (hazard ratio, 1.15; 95% CI, 1.14-1.16) per 5-year increase, male sex (hazard ratio, 1.17; 95% CI, 1.13-1.21) and smoking (hazard ratio, 1.43; 95% CI, 1.35-1.51) with risk of subsequent CHD death or myocardial infarction and differing associations with other individual and composite cardiovascular endpoints.
CONCLUSIONS
GENIUS-CHD is a global collaboration seeking to elucidate genetic and nongenetic determinants of subsequent event risk in individuals with established CHD, to improve residual risk prediction and identify novel drug targets for secondary prevention. Initial analyses demonstrate the feasibility and reliability of a federated analysis approach. The consortium now plans to initiate and test novel hypotheses as well as supporting replication and validation analyses for other investigators.
Identifiants
pubmed: 30896328
doi: 10.1161/CIRCGEN.119.002470
pmc: PMC6629546
mid: EMS82310
doi:
Types de publication
Journal Article
Meta-Analysis
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e002470Subventions
Organisme : British Heart Foundation
ID : PG/18/50/33837
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/18/5033837
Pays : United Kingdom
Organisme : NIGMS NIH HHS
ID : U01 GM074492
Pays : United States
Organisme : Department of Health
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 085475/B/08/Z
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R56 HL126558
Pays : United States
Organisme : Wellcome Trust
ID : 084727/Z/08/Z
Pays : United Kingdom
Organisme : Medical Research Council
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : P50 HL077113
Pays : United States
Organisme : European Research Council
ID : 335122
Pays : International
Organisme : British Heart Foundation
ID : RG/14/5/30893
Pays : United Kingdom
Organisme : NIEHS NIH HHS
ID : R01 ES025786
Pays : United States
Organisme : Wellcome Trust
ID : 072960/Z/03/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 085475/Z/08/Z
Pays : United Kingdom
Organisme : NINR NIH HHS
ID : R01 NR013396
Pays : United States
Organisme : British Heart Foundation
ID : FS/14/76/30933
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 084726/Z/08/Z
Pays : United Kingdom
Organisme : NIEHS NIH HHS
ID : P01 ES022845
Pays : United States
Organisme : British Heart Foundation
ID : FS/18/23/33512
Pays : United Kingdom
Organisme : Chief Scientist Office
ID : PCL 17/07
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : P01 HL101398
Pays : United States
Organisme : NHLBI NIH HHS
ID : P01 HL076491
Pays : United States
Organisme : Chief Scientist Office
ID : PCL/17/07
Pays : United Kingdom
Organisme : NHLBI NIH HHS
ID : R01 HL074730
Pays : United States
Organisme : CIHR
Pays : Canada
Organisme : NHLBI NIH HHS
ID : R01 HL133169
Pays : United States
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