Department of Pediatric Endocrinology, Diabetes and Metabolic Diseases, University Children's Hospital, University Medical Centre, Ljubljana, Slovenia.
Diabetes Care. 2009 Dec;32(12):2258-62. doi: 10.2337/dc09-0852. Epub 2009 Sep 14.
Oxidative stress plays an important role in the development of microangiopathic complications in type 1 diabetes. We investigated polymorphic markers in genes encoding enzymes regulating production of reactive oxygen species in association with diabetic retinopathy or diabetic nephropathy.
A total of 124 patients with type 1 diabetes were investigated in this case-control study. All subjects were matched for sex, age, and duration of diabetes. Genotyping was conducted using real-time PCR for p.Val16Ala polymorphism in the MnSOD gene and c.C-262T in the promoter region of the CAT gene. Multiplex PCR method was used for determination of GSTM1 and GSTT1 polymorphic deletions. Fluorescence-labeled PCR amplicons and fragment analysis was used for assessing the number of pentanucleotide (CCTTT)n repeats in inducible nitric oxide synthase.
A positive association of MnSOD genotype Val/Val (odds ratio [OR] 2.49, 95% CI 1.00-6.16, P = 0.045) and GSTM1-1 genotype (2.63, 1.07-6.47, P = 0.031) with diabetic retinopathy but not with diabetic nephropathy was demonstrated. Additionally, the combination of the two genotypes conveyed an even higher risk (4.24, 1.37-13.40, P = 0.009). No other investigated genetic polymorphisms were associated with either diabetic retinopathy or diabetic nephropathy.
Selected polymorphisms in genes encoding MnSOD and GSTM1 could be added to a panel of genetic markers for identification of individuals with type 1 diabetes at an increased risk for developing diabetic retinopathy.
氧化应激在 1 型糖尿病微血管并发症的发展中起重要作用。我们研究了编码调节活性氧产生的酶的基因中的多态性标记与糖尿病视网膜病变或糖尿病肾病的关系。
在这项病例对照研究中,共调查了 124 例 1 型糖尿病患者。所有患者在性别、年龄和糖尿病病程方面均匹配。采用实时 PCR 法对 MnSOD 基因的 p.Val16Ala 多态性和 CAT 基因启动子区的 c.C-262T 进行基因分型。采用多重 PCR 法测定 GSTM1 和 GSTT1 缺失多态性。荧光标记 PCR 扩增子和片段分析用于评估诱导型一氧化氮合酶中五核苷酸(CCTTT)n 重复的数量。
MnSOD 基因型 Val/Val(比值比 [OR] 2.49,95%CI 1.00-6.16,P = 0.045)和 GSTM1-1 基因型(2.63,1.07-6.47,P = 0.031)与糖尿病视网膜病变呈正相关,但与糖尿病肾病无关。此外,两种基因型的组合甚至具有更高的风险(4.24,1.37-13.40,P = 0.009)。未发现其他研究的遗传多态性与糖尿病视网膜病变或糖尿病肾病相关。
MnSOD 和 GSTM1 基因编码的选定多态性可添加到一组遗传标记中,用于鉴定 1 型糖尿病患者中发生糖尿病视网膜病变风险增加的个体。