Department of Osteoporosis, Metabolic Bone Disease and Genetics Research Unit, The Shanghai Sixth People's Hospital, Shanghai Jiaotong University, Shanghai, China.
Acta Pharmacol Sin. 2009 Dec;30(12):1634-42. doi: 10.1038/aps.2009.169.
The goal of this study was to determine whether polymorphisms in the vitamin D receptor (VDR) and estrogen receptor alpha (ESR1) genes are associated with variations of peak bone mineral density (BMD) and obesity phenotypes in young Chinese men.
A total of 1215 subjects from 400 Chinese nuclear families were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and allele-specific multiple PCR (ASM-PCR) analysis at the ApaI, FokI, and CDX2 sites in the VDR gene and the PvuII and XbaI sites in the ESR1 gene. BMD at the lumbar spine and hip, total fat mass, and total lean mass were measured using dual energy X-ray absorptiometry. The associations between VDR and ESR1 gene polymorphisms with peak BMD, body mass index (BMI), total fat mass, total lean mass, and percentage fat mass (PFM) were determined using quantitative transmission disequilibrium tests (QTDTs).
Using QTDTs, no significant within-family associations were obtained between genotypes or haplotypes of the VDR and ESR1 genes and peak BMD. For the obesity phenotypes, the within-family associations were significant between CDX2 genotypes and BMI (P=0.046), fat mass (P=0.004), and PFM (P=0.020). Further, PvuII was significantly associated with the variation of fat mass and PFM (P=0.002 and P=0.039, respectively). A subsequent 1000 permutations were in agreement with these within-family association results.
Our findings showed that VDR and ESR1 polymorphisms were associated with total fat mass in young Chinese men, but we failed to find a significant association between VDR and ESR1 genotypes and peak BMD. These findings suggested that the VDR and ESR1 genes are quantitative trait loci (QTL) underlying fat mass variation in young Chinese men.
本研究旨在探讨维生素 D 受体(VDR)和雌激素受体 α(ESR1)基因多态性与中国年轻男性峰值骨密度(BMD)和肥胖表型的变化是否相关。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和等位基因特异性多重 PCR(ASM-PCR)分析方法,对 400 个中国核心家庭的 1215 例个体的 VDR 基因 ApaI、FokI 和 CDX2 位点以及 ESR1 基因 PvuII 和 XbaI 位点进行基因分型。采用双能 X 线吸收法测量腰椎和髋部的 BMD、总脂肪量和总瘦体重。采用定量传递不平衡检验(QTDT)确定 VDR 和 ESR1 基因多态性与峰值 BMD、体重指数(BMI)、总脂肪量、总瘦体重和体脂百分比(PFM)之间的关系。
采用 QTDT 方法,未发现 VDR 和 ESR1 基因的基因型或单倍型与峰值 BMD 之间存在显著的家系内关联。对于肥胖表型,CDX2 基因型与 BMI(P=0.046)、脂肪量(P=0.004)和 PFM(P=0.020)之间存在显著的家系内关联。此外,PvuII 与脂肪量和 PFM 的变化显著相关(P=0.002 和 P=0.039)。随后的 1000 次随机置换结果与这些家系内关联结果一致。
本研究结果表明,VDR 和 ESR1 多态性与中国年轻男性的总脂肪量有关,但我们未能发现 VDR 和 ESR1 基因型与峰值 BMD 之间存在显著关联。这些发现提示 VDR 和 ESR1 基因是中国年轻男性脂肪量变异的数量性状基因座(QTL)。