TY - JOUR
T1 - DNA Methylation and High-Density Lipoprotein Functionality-Brief Report
T2 - The REGICOR Study (Registre Gironi del Cor)
AU - Sayols-Baixeras, Sergi
AU - Hernáez, Alvaro
AU - Subirana, Issac
AU - Lluis-Ganella, Carla
AU - Muñoz, Daniel
AU - Fitó, Montserrat
AU - Marrugat, Jaume
AU - Elosua, Roberto
N1 - Publisher Copyright:
© 2017 American Heart Association, Inc.
PY - 2017/3/1
Y1 - 2017/3/1
N2 - Objective-The function of high-density lipoproteins (HDLs) may better reflect their atheroprotective role, compared with HDL-cholesterol levels. The association between DNA methylation and HDL function has not yet been established. Approach and Results-We designed an epigenome-wide association study including 645 individuals from the REGICOR study (Registre Gironi del Cor). We determined DNA methylation from peripheral blood cells using the HumanMethylation450 array. We analyzed HDL functionality by determining HDL cholesterol efflux capacity and HDL inflammatory index. We discovered 3 methylation sites located in HOXA3, PEX5, and PER3 related to cholesterol efflux capacity and 1 located in GABRR1 related to HDL inflammatory index. Using a candidate gene approach, we also found 2 methylation sites located in CMIP related to cholesterol efflux capacity. Conclusions-We identified 6 potential loci associated with HDL functionality in HOXA3, PEX5, PER3, CMIP, and GABRR1. Additional studies are warranted to validate these findings in other populations.
AB - Objective-The function of high-density lipoproteins (HDLs) may better reflect their atheroprotective role, compared with HDL-cholesterol levels. The association between DNA methylation and HDL function has not yet been established. Approach and Results-We designed an epigenome-wide association study including 645 individuals from the REGICOR study (Registre Gironi del Cor). We determined DNA methylation from peripheral blood cells using the HumanMethylation450 array. We analyzed HDL functionality by determining HDL cholesterol efflux capacity and HDL inflammatory index. We discovered 3 methylation sites located in HOXA3, PEX5, and PER3 related to cholesterol efflux capacity and 1 located in GABRR1 related to HDL inflammatory index. Using a candidate gene approach, we also found 2 methylation sites located in CMIP related to cholesterol efflux capacity. Conclusions-We identified 6 potential loci associated with HDL functionality in HOXA3, PEX5, PER3, CMIP, and GABRR1. Additional studies are warranted to validate these findings in other populations.
KW - DNA methylation
KW - atherosclerosis
KW - blood cells
KW - lipoproteins
KW - risk factors
UR - http://www.scopus.com/inward/record.url?scp=85008350911&partnerID=8YFLogxK
U2 - 10.1161/ATVBAHA.116.308831
DO - 10.1161/ATVBAHA.116.308831
M3 - Article
C2 - 28062490
AN - SCOPUS:85008350911
SN - 1079-5642
VL - 37
SP - 567
EP - 569
JO - Arteriosclerosis, Thrombosis, and Vascular Biology
JF - Arteriosclerosis, Thrombosis, and Vascular Biology
IS - 3
ER -