Gautam Amar, Gupta Stuti, Mehndiratta Mohit, Sharma Mohini, Singh Kalpana, Kalra Om P, Agarwal Sunil, Gambhir Jasvinder K
Amar Gautam, Om P Kalra, Sunil Agarwal, Department of Medicine, University College of Medical Sciences (University of Delhi) and G.T.B. Hospital, Delhi 110095, India.
World J Diabetes. 2017 Feb 15;8(2):66-73. doi: 10.4239/wjd.v8.i2.66.
To investigate the association of gene -94 ATTG insertion/deletion (rs28362491) polymorphism with inflammatory markers and risk of diabetic nephropathy in Asian Indians.
A total of 300 subjects were recruited (100 each), normoglycemic, (NG); type 2 diabetes mellitus (T2DM) without any complications (DM) and T2DM with diabetic nephropathy [DM-chronic renal disease (CRD)]. Analysis was carried out by polymerase chain reaction-restriction fragment length polymorphism and ELISA. Pearson's correlation, analysis of variance and logistic regression were used for statistical analysis.
The allelic frequencies of -94 ATTG insertion/deletion were 0.655/0.345 (NG), 0.62/0.38 (DM) and 0.775/0.225 (DM-CRD). The -94 ATTG ins allele was associated with significantly increased levels of urinary monocyte chemoattractant protein-1 (uMCP-1); uMCP-1 ( = 0.026) and plasma tumor necrosis factor-alpha (TNF-α); TNF-α ( = 0.030) and almost doubled the risk of diabetic nephropathy (OR = 1.91, 95%CI: 1.080-3.386, = 0.025).
-94 ATTG ins/ins polymorphism might be associated with increased risk of developing nephropathy in Asian Indian subjects with diabetes mellitus.
研究亚洲印度人基因-94 ATTG插入/缺失(rs28362491)多态性与炎症标志物及糖尿病肾病风险的关联。
共招募300名受试者(每组100名),分别为血糖正常者(NG)、无任何并发症的2型糖尿病患者(T2DM)以及患有糖尿病肾病的T2DM患者[糖尿病-慢性肾病(CRD)]。采用聚合酶链反应-限制性片段长度多态性和酶联免疫吸附测定法进行分析。使用Pearson相关性分析、方差分析和逻辑回归进行统计分析。
-94 ATTG插入/缺失的等位基因频率分别为0.655/0.345(NG)、0.62/0.38(DM)和0.775/0.225(DM-CRD)。-94 ATTG插入等位基因与尿单核细胞趋化蛋白-1(uMCP-1)水平显著升高相关;uMCP-1(P = 0.026)以及血浆肿瘤坏死因子-α(TNF-α);TNF-α(P = 0.030),并且使糖尿病肾病风险几乎增加一倍(OR = 1.91, 95%CI: 1.080 - 3.386, P = 0.025)。
-94 ATTG插入/插入多态性可能与亚洲印度糖尿病患者发生肾病的风险增加有关。