Polymorphisms of the Vitamin D Receptor Gene and Sex-Differential Associations with Lipid Profiles in Chinese Han Adults.
- Author:
Yan Mei CHEN
1
;
Ping XU
1
;
Zhou Tian WANG
1
;
Yu Mei ZHU
2
;
Chun Mei GONG
2
;
Chang Hua HUANG
3
;
Xiao Li LIU
2
;
Ji Chang ZHOU
4
,
5
,
6
Author Information
- Publication Type:Journal Article
- Keywords: Dyslipidemia; Gene polymorphism; Lipid; Vitamin D; Vitamin D receptor
- MeSH: Adult; Alleles; Asians/genetics*; China/ethnology*; Dyslipidemias/genetics*; Female; Genetic Predisposition to Disease/genetics*; Genotype; Humans; Lipids/blood*; Male; Middle Aged; Polymorphism, Single Nucleotide; Receptors, Calcitriol/genetics*; Sex Factors; Vitamin D/blood*
- From: Biomedical and Environmental Sciences 2022;35(2):115-125
- CountryChina
- Language:English
-
Abstract:
OBJECTIVE:To explore the association of single nucleotide polymorphisms (SNPs) of the vitamin D receptor gene ( VDR) with circulating lipids considering gender differences.
METHODS:Of the Han Chinese adults recruited from a health examination center for inclusion in the study, the circulating lipids, 25-hydroxyvitamin D (25OHD), and other parameters were measured. The VDR SNPs of Cdx2 (rs11568820), Fok1 (rs2228570), Apa1 (rs7975232), and Taq1 (rs731236) were genotyped with a qPCR test using blood DNA samples, and their associations with lipids were analyzed using logistic regression.
RESULTS:In the female participants ( n = 236 with dyslipidemia and 888 without dyslipidemia), multiple genotype models of Fok1 indicated a positive correlation of B (not A) alleles with LDLC level ( P < 0.05). In the male participants ( n = 299 with dyslipidemia and 564 without dyslipidemia), the recessive model of Cdx2 and the additive and recessive models of Fok1 differed ( P < 0.05) between the HDLC-classified subgroups, respectively, and Fok1 BB and Cdx2 TT presented interactions with 25OHD in the negative associations with HDLC ( P < 0.05).
CONCLUSION:In the Chinese Han adults included in the study, the Fok1 B-allele of VDR was associated with higher LDLC in females, and the Fok1 B-allele and the Cdx2 T-allele of VDR were associated with lower HDLC in males. The interaction of VD and Fok1 BB or Cdx2 TT in males synergistically decreased HDLC levels.