Key Laboratory of Biomedical Information Engineering of Ministry of Education, and Institute of Molecular Genetics, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, People's Republic of China.
PLoS One. 2011;6(11):e27312. doi: 10.1371/journal.pone.0027312. Epub 2011 Nov 18.
Obesity and osteoporosis are closely correlated genetically. FTO gene has been consistently identified to be associated with obesity phenotypes. A recent study reported that the mice lacking Fto could result in lower bone mineral density (BMD). Thus, we hypothesize that the FTO gene might be also important for osteoporosis phenotypes. To test for such a hypothesis, we performed an association analyses to investigate the relationship between SNPs in FTO and BMD at both hip and spine. A total of 141 SNPs were tested in two independent Chinese populations (818 and 809 unrelated Han subjects, respectively) and a Caucasian population (2,286 unrelated subjects). Combining the two Chinese samples, we identified 6 SNPs in FTO to be significantly associated with hip BMD after multiple testing adjustments, with the combined P values ranged from 4.99 × 10⁻⁴-1.47 × 10⁻⁴. These 6 SNPs are all located at the intron 8 of FTO and in high linkage disequilibrium. Each copy of the minor allele of each SNP was associated with increased hip BMD values with the effect size (beta) of ∼0.025 and ∼0.015 in the Chinese sample 1 and 2, respectively. However, none of these 6 SNPs showed significant association signal in the Caucasian sample, by presenting some extent of ethnic difference. Our findings, together with the prior biological evidence, suggest that the FTO gene might be a new candidate for BMD variation and osteoporosis in Chinese populations.
肥胖症和骨质疏松症在基因上密切相关。FTO 基因一直被认为与肥胖表型有关。最近的一项研究报告称,缺乏 Fto 的小鼠会导致骨矿物质密度(BMD)降低。因此,我们假设 FTO 基因对于骨质疏松表型也很重要。为了验证这一假设,我们进行了关联分析,以研究 FTO 基因中的 SNP 与髋部和脊柱的 BMD 之间的关系。在两个独立的中国人群(分别为 818 名和 809 名无关汉族受试者)和一个高加索人群(2286 名无关受试者)中测试了总共 141 个 SNP。将这两个中国样本合并后,我们发现 FTO 中的 6 个 SNP 与髋部 BMD 显著相关,经过多次测试调整后,合并的 P 值范围从 4.99×10⁻⁴到 1.47×10⁻⁴。这 6 个 SNP 均位于 FTO 的内含子 8 中,且高度连锁不平衡。每个 SNP 的次要等位基因的每一份拷贝都与髋部 BMD 值的增加相关,在中国样本 1 和 2 中的效应大小(β)分别约为 0.025 和 0.015。然而,这些 SNP 中没有一个在高加索人群中显示出显著的关联信号,这表明存在一定程度的种族差异。我们的发现,加上先前的生物学证据,表明 FTO 基因可能是中国人群中 BMD 变异和骨质疏松的新候选基因。