Yinghua Li, Yougen Wu, T. Lu, M. Yuan, Yunqing Cui, Yunjiao Zhou, Gong Yang, Yang Hong
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引用次数: 1
Abstract
Osteoporosis is an age-related disease caused by imbalanced calcium metabolism identified to be associated with genetic variations of multiple genes including osteoprotegrin (OPG). While bone mineral density (BMD) predicts the risk of osteoporotic fractures, the urinary calcium level (UCL) may reflect calcium metabolism, which thereby indicates osteoporotic trends. BMD of 1,206 local Chinese geriatrics in Shanghai was measured by dual X-ray absorptionmetry. UCL were examined in 728 fasting geriatric urine samples by photometry. Genotyping of the OPG SNPs rs1032128, rs334061 and rs3134063 in 481 subjects including healthy controls, osteopenia and osteoporosis patients was performed and the association between the OPG SNP variations and UCL was assessed among all comparative groups. Differences in age and BMD were statistically significant between males and females with either normal BMD or osteopenia, but were not between those with osteoporosis. Significant correlations were found between BMD and genotypes of rs1032128 in males, and between BMD and age in females. The genotypes of rs1032128 were significantly correlated with BMD in males, but were correlated with UCL in females. UCL was significantly correlated with BMD in males but was associated with rs1032128 genotypes in females. The AA type of rs1032128 was independently associated with risk of osteoporosis in males. The GG type of rs1032128 was negatively associated with UCL in males but was positively associated with UCL in females. Our data suggest that the genotypes of the OPG SNP rs1032128 may protect old males from osteoporosis development, and that UCL may be useful to predict osteoporosis if combined with the genotypes of the OPG SNP, at least in some local Chinese geriatrics.
骨质疏松症是一种由钙代谢失衡引起的与年龄相关的疾病,与骨蛋白素(OPG)等多种基因的遗传变异有关。骨矿物质密度(BMD)可以预测骨质疏松性骨折的风险,而尿钙水平(UCL)可以反映钙代谢,从而提示骨质疏松的趋势。采用双x线吸收仪对上海市1206例老年人的骨密度进行了测定。采用光度法对728例空腹老年人尿液样本进行了UCL检测。对481名受试者(包括健康对照、骨质疏松症和骨质疏松症患者)的OPG SNP rs1032128、rs334061和rs3134063进行基因分型,并在所有比较组中评估OPG SNP变异与UCL之间的关系。骨密度正常或骨质减少的男性和女性在年龄和骨密度方面的差异有统计学意义,但骨质疏松症患者之间的差异无统计学意义。男性骨密度与rs1032128基因型存在显著相关性,女性骨密度与年龄存在显著相关性。rs1032128基因型与男性BMD显著相关,与女性UCL显著相关。UCL与男性骨密度显著相关,但与女性rs1032128基因型相关。rs1032128 AA型与男性骨质疏松风险独立相关。rs1032128的GG型与男性的UCL呈负相关,与女性的UCL呈正相关。我们的数据表明,OPG SNP rs1032128的基因型可能保护老年男性免受骨质疏松症的发展,如果与OPG SNP的基因型相结合,UCL可能有助于预测骨质疏松症,至少在一些中国当地的老年患者中是如此。