Department of Endocrinology and Internal Medicine THG, Aarhus University Hospital, 8000, Århus C, Denmark.
Osteoporos Int. 2011 Oct;22(10):2655-66. doi: 10.1007/s00198-010-1491-z. Epub 2010 Nov 23.
Stimulation of PPARγ turns mesenchymal stem cells into adipocytes instead of osteoblasts. We investigated the effect of polymorphisms in the PPARγ gene on BMD and fracture risk in two Danish cohorts and found opposing effects of certain SNPs and haplotypes in the two cohorts probably owing to environmental factors.
Stimulation of PPARγ causes development of mesenchymal stem cells to adipocytes instead of osteoblasts leading to decreased osteoblast number and BMD. The aim of this study was to examine the effect of PPARG polymorphisms on BMD and fracture risk in two Danish cohorts: AROS, a case-control population comprising 809 individuals and DOPS, a population comprising 1,716 perimenopausal women allocated to hormone therapy or not at baseline and followed for 10 years. On the basis of linkage disequilibrium between SNPs throughout the gene and previous studies we chose 10 polymorphisms for investigation.
In AROS, individuals heterozygous for the polymorphisms rs12497191, rs4135263, and rs1151999 had an increased risk of vertebral fractures (OR = 1.48-1.76, p = 0.005-0.04) compared with individuals homozygous for the common allele. In DOPS, individuals heterozygous for rs1151999 had an increased BMD at the hip sites (p ≤ 0.02). An interaction between rs1151999 and diet was found on BMD in both cohorts.
For the polymorphism rs1152003 there was an interaction with body weight on BMD at all sites in both cohorts (p ≤ 0.07). Stratified analyses revealed that in the high weight group in AROS individuals homozygous for the variant allele had a decreased BMD (p ≤ 0.02), whereas the same pattern was found in the low weight group in DOPS (p ≤ 0.03). A number of haplotype associations were found as well, the direction of which was opposite in the two cohorts.
Our study suggests an association SNPs in PPARG and haplotypes thereof and BMD and fracture risk. The effect however appears to be modifiable by environmental factors.
刺激过氧化物酶体增殖物激活受体 γ(PPARγ)会将间充质干细胞转化为脂肪细胞,而非成骨细胞。我们研究了 PPARγ 基因中的多态性对两个丹麦队列的骨密度(BMD)和骨折风险的影响,发现某些单核苷酸多态性(SNPs)和单倍型在两个队列中存在相反的作用,这可能是由于环境因素所致。
刺激过氧化物酶体增殖物激活受体 γ(PPARγ)会导致间充质干细胞向脂肪细胞分化,从而减少成骨细胞数量和骨密度。本研究旨在探讨 PPARG 多态性对两个丹麦队列的 BMD 和骨折风险的影响:AROS 是一个包含 809 人的病例对照人群,而 DOPS 是一个包含 1716 名绝经前妇女的队列,她们在基线时被分配接受或不接受激素治疗,并随访 10 年。基于基因内 SNPs 之间的连锁不平衡和先前的研究,我们选择了 10 个多态性进行研究。
在 AROS 中,与常见等位基因相比,杂合子携带 rs12497191、rs4135263 和 rs1151999 多态性的个体发生椎体骨折的风险增加(比值比 [OR] = 1.48-1.76,p = 0.005-0.04)。在 DOPS 中,杂合子携带 rs1151999 多态性的个体髋部骨密度增加(p≤0.02)。在两个队列中都发现了 rs1151999 多态性与饮食之间的相互作用。
对于 rs1152003 多态性,在两个队列的所有部位都存在与体重的交互作用(p≤0.07)。分层分析显示,在 AROS 中,高体重组的变异等位基因纯合子的 BMD 降低(p≤0.02),而 DOPS 中低体重组也出现了同样的模式(p≤0.03)。还发现了一些单倍型关联,其方向在两个队列中相反。
我们的研究表明,PPARγ 基因中的 SNPs 及其单倍型与 BMD 和骨折风险有关。然而,这种影响似乎可以通过环境因素来调节。