Fatima Syeda Sadia, Jamil Zehra, Alam Faiza, Malik Hajira Zafar, Madhani Sarosh Irfan, Ahmad Muhammad Saad, Shabbir Tayyab, Rehmani Muhammed Noman, Rabbani Amna
Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Medical College, Aga Khan University, Karachi, Pakistan.
Endocrine. 2017 Jan;55(1):124-129. doi: 10.1007/s12020-016-1058-7. Epub 2016 Aug 9.
Renalase is considered as a novel candidate gene for type 2 diabetes. In this study, we aimed to investigate the relationship of serum renalase and two single nucleotide polymorphisms with gestational diabetes mellitus. One hundred and ninety-eight normotensive pregnant females (n = 99 gestational diabetes mellitus; n = 99 euglycemic pregnant controls) were classified according to the International Association of the Diabetes and Pregnancy Study criteria. Fasting and 2-h post glucose load blood levels and anthropometric assessment was performed. Serum renalase was measured using enzyme-linked immunosorbent assay, whereas DNA samples were genotyped for renalase single nucleotide polymorphisms rs2576178 and rs10887800 using Polymerase chain reaction-Restriction fragment length polymorphism method. In an age-matched case control study, no difference was observed in the serum levels of renalase (p > 0.05). The variant rs10887800 showed an association with gestational diabetes mellitus and remained significant after multiple adjustments (p < 0.05), whereas rs2576178 showed weak association (p = 0.030) that was lost after multiple adjustments (p = 0.09). We inferred a modest association of the rs10887800 polymorphism with gestational diabetes. Although gestational diabetes mellitus is self-reversible, yet presence of this minor G allele might predispose to metabolic syndrome phenotypes in near the future.
肾酶被认为是2型糖尿病的一个新的候选基因。在本研究中,我们旨在探讨血清肾酶及两个单核苷酸多态性与妊娠期糖尿病的关系。根据国际糖尿病与妊娠研究协会标准,对198名血压正常的孕妇(n = 99例妊娠期糖尿病;n = 99例血糖正常的孕妇对照)进行分类。进行空腹及葡萄糖负荷后2小时的血糖水平测定和人体测量评估。采用酶联免疫吸附测定法检测血清肾酶,而使用聚合酶链反应-限制性片段长度多态性方法对肾酶单核苷酸多态性rs2576178和rs10887800的DNA样本进行基因分型。在一项年龄匹配的病例对照研究中,未观察到血清肾酶水平存在差异(p > 0.05)。rs10887800变异与妊娠期糖尿病相关,且在多次校正后仍具有显著性(p < 0.05),而rs2576178显示出弱相关性(p = 0.030),在多次校正后消失(p = 0.09)。我们推断rs10887800多态性与妊娠期糖尿病存在适度关联。尽管妊娠期糖尿病可自行逆转,但这种次要的G等位基因的存在可能在不久的将来易患代谢综合征表型。