绝经后伊拉克2型糖尿病骨质疏松和骨质减少患者中AGER基因多态性的流行

Murooj G Jameel, Zainab M Alhakeem, M. H. Al-Osami
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引用次数: 1

摘要

骨质疏松症(Osteoporosis, OP)是最重要的代谢性疾病之一,遗传因素和环境因素的相互作用分别约占70%和30%。遗传成分被认为对骨矿物质密度、骨构建和更替有强烈影响,因此它们在确定OP和脆性骨折的风险方面起着重要作用。本研究分为患者组和对照组;A组:绝经后OP合并骨质减少妇女70例,B组:对照组20例。5毫升的血液样本被分成三管;1管(1ml)装凝胶,用于获取血清,测量葡萄糖水平,其他管装乙二胺-四乙酸(EDTA), 2管2ml,在(-40 Co)下深度冷冻保存,直到DNA基因组分析,用于PCR基因多态性的基因分型,3管2ml用于进行糖化血红蛋白% (HbA1c)测定。在绝经后OP合并2型糖尿病的妇女中检测到RAGE多态性rs1800625和rs1800624的高发率。与对照纯合1800625和杂合1800625相比,纯合1800625和杂合1800625分别为31%和5%。纯合子1800624和杂合子1800624分别比对照纯合子1800624和杂合子1800624分别为(28.5%)和(20%)。综上所述,rs1800625和rs1800624多态性可能是绝经后伊拉克2型糖尿病妇女OP的致病风险等位基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prevalence of AGER gene polymorphism in post menopause Iraqi sample with Osteoporosis and osteopenia in type 2DM
Osteoporosis (OP)is one of the most important metabolic disorder also affected by interaction of genetic and environmental factors by almost 70% and 30% respectively. Genetic components are identified to strongly effect bone mineral density, bone building and turnover, so they play an important role in determining risk of OP and fragility fractures. This study consists of patient and control group; Group A: (70) postmenopausal women with OP and osteopenia, Group B: (20) control group.  five milliliters of blood sample were divided into three tubes; one tube (1ml) contain gel for obtain serum to measure glucose level, the others tubes containing ethylene-diamine-tetra-acetic acid (EDTA), in 2 tube 2ml stored in deep freeze at (–40 Co) until genomic analysis of DNA for the performance of PCR genotyping of gene polymorphisms of RAGE, in 3 tube 2ml used to perform Glycated Hemoglobin % (HbA1c) assays. HbA1c and Serum glucose levels is significantly increased in Group A. a high prevalence of RAGE polymorphism rs1800625 and rs1800624 were detected in postmenopausal women with OP with type2DM. Homozygous 1800625 were (31%) and heterozygous 1800625(31%) compared to control homozygous 1800625 were (5%) and heterozygous 1800625 were (5%) respectively. Homozygous 1800624 were (28.5%) and heterozygous 1800624(28.5%) compared to control homozygous 1800624 were (5%) and heterozygous 1800624 were (20%) respectively. In conclusion, the rs1800625 and rs1800624 polymorphism might be a causal risk allele for OP in post menopause Iraqi women with type2 DM.
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