Human Y Chromosome Exerts Pleiotropic Effects on Susceptibility to Atherosclerosis.
Chromosomes, Human, Y
Coronary Artery Disease
/ genetics
Gene Expression
Genetic Pleiotropy
Genetic Predisposition to Disease
Haplotypes
High-Throughput Nucleotide Sequencing
Humans
Macrophages
/ metabolism
Male
Minor Histocompatibility Antigens
/ genetics
Nuclear Proteins
/ genetics
Phylogeny
Risk Factors
THP-1 Cells
coronary artery disease
epigenomics
gene expression
humans
risk factors
Journal
Arteriosclerosis, thrombosis, and vascular biology
ISSN: 1524-4636
Titre abrégé: Arterioscler Thromb Vasc Biol
Pays: United States
ID NLM: 9505803
Informations de publication
Date de publication:
11 2019
11 2019
Historique:
entrez:
24
10
2019
pubmed:
24
10
2019
medline:
9
4
2020
Statut:
ppublish
Résumé
The male-specific region of the Y chromosome (MSY) remains one of the most unexplored regions of the genome. We sought to examine how the genetic variants of the MSY influence male susceptibility to coronary artery disease (CAD) and atherosclerosis. Approach and Results: Analysis of 129 133 men from UK Biobank revealed that only one of 7 common MSY haplogroups (haplogroup I1) was associated with CAD-carriers of haplogroup I1 had ≈11% increase in risk of CAD when compared with all other haplogroups combined (odds ratio, 1.11; 95% CI, 1.04-1.18; Haplogroup I1 is enriched for regulatory chromatin variants in numerous cells of relevance to CAD and increases cardiovascular risk through proatherosclerotic reprogramming of the transcriptome, partly through
Identifiants
pubmed: 31644355
doi: 10.1161/ATVBAHA.119.312405
pmc: PMC6818981
doi:
Substances chimiques
Minor Histocompatibility Antigens
0
Nuclear Proteins
0
UTY protein, human
0
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2386-2401Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL125863
Pays : United States
Organisme : British Heart Foundation
ID : PG/12/9/29376
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/16/49/32176
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 087576
Pays : United Kingdom
Organisme : British Heart Foundation
ID : CH/13/2/30154
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/12/81/29897
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_QA137853
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_17228
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/13/5/30177
Pays : United Kingdom
Commentaires et corrections
Type : CommentIn
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