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作 者:韩燕[1] 王金堂[2] 王宇飞[2] 孙健[1,3]
机构地区:[1]西安交通大学医学院遗传学与分子生物学系,西安710049 [2]西安交通大学医学院第一附属医院骨科 [3]西安交通大学环境与疾病相关基因教育部重点实验室
出 处:《中国骨质疏松杂志》2010年第6期397-400,共4页Chinese Journal of Osteoporosis
基 金:中国科学院"西部之光"人才培养计划([2009]236);陕西省科技计划项目(2002K10-G5省卫生厅)
摘 要:目的从分子流行病学角度探讨陕西关中地区人群Ⅰ型胶原α1基因SPl位点多态性与原发性骨质疏松症、骨质疏松性骨折的相关性。方法选取陕西关中地区无血缘关系汉族绝经后骨质疏松患者83例及健康女性98例,生物化学方法检测剔除任何其他影响骨代谢因素后,骨密度仪检测腰椎、股骨BMD,及限制性片段长度多态性(RFLP)方法检测其CoLⅠA1SPl位点多态性。结果所研究181例样本CoLⅠA1基因SP1位点均为SS,所选样本未发现CoLⅠA1基因SP1位点多态性存在。结论陕西关中地区原发性骨质疏松女性患者与CoLⅠA1基因SPl位点多态性无相关性。Objective From molecular epidemiology suggest the relativities about the collagen Ⅰ A1 (CoL Ⅰ Al ) genes polymorphism between primay osteoporosis and osteoporotic fracture in Shaanxi Guanzhong area people as possibly implicated in reduced bone mineral density ( BMD). Tbrough researching osteoporosis from molecular level, to elucidate the genetic basis of osteoporosis and provide theoretical base for preventing, diagnosing and treating osteoporosis. Methods Selecting the eighty-three Han post-menopausal women patients who were not related and ninety-eight health adult women from Shaanxi Guanzhong area, measure BMD of lumbar and thighbone by Bone Sonometers, and array the polymorphism of CoL [ A1 SP[ through the method of RFLP. Results ALL the people of CoL l A1 genotype is the "SS" type, And the people of "s" type was not found in the people of CoL I A1 genotype. Coaelusion In Shaanxi Guanzhong area,original, the polymorphism of CoL I A1 SPI in original osteoporosis woman patients is not related with osteoporosis.
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