Papanas N, Papatheodorou K, Papazoglou D, Kotsiou S, Christakidis D, Maltezos E
Second Department of Internal Medicine, Democritus University of Thrace, University Hospital of Alexandroupolis, Dragana, Alexandroupolis, Greece.
Exp Clin Endocrinol Diabetes. 2007 May;115(5):327-30. doi: 10.1055/s-2007-967084.
Alpha2B adrenoceptor (alpha2B-AR) mediates a variety of functions in humans. An insertion/deletion (I/D) polymorphism of the alpha2B-AR gene located on chromosome 2 has been described. The aim of the present study was to investigate the potential association between alpha2B gene I/D polymorphism and peripheral neuropathy in Greek patients with type 2 diabetes mellitus. The study included 130 patients (70 men) with diabetic neuropathy (group A) and 60 patients (34 men) without diabetic neuropathy (group B). There was no difference in age, gender and diabetes duration between the groups. Diabetic neuropathy was diagnosed by clinical examination using the Diabetic Neuropathy Index (DNI). Genotyping of I/D polymorphism was performed by PCR. Frequency of the D allele was significantly higher (p=0.001) in group A (26.9%) as compared to group B (11.7%). DNI score differed significantly (p=0.001) between the three genotype groups (I/I, I/D, D/D). It was significantly higher (p=0.04) in patients with I/D (3.7+/-1) than in those with I/I (2.5+/-0.9) and significantly higher (p=0.001) in patients with D/D (5.6+/-1.3) than in those with I/D (3.7+/-1).
Patients with neuropathy exhibit a significantly higher frequency of the D allele in comparison to those without neuropathy. Presence of the D allele is also associated with a higher neuropathic score. These results provide evidence for an association of the D allele with both presence and severity of neuropathy in patients with type 2 diabetes mellitus.
α2B肾上腺素能受体(α2B-AR)在人体中介导多种功能。位于2号染色体上的α2B-AR基因存在插入/缺失(I/D)多态性。本研究的目的是调查希腊2型糖尿病患者中α2B基因I/D多态性与周围神经病变之间的潜在关联。该研究纳入了130例患有糖尿病神经病变的患者(70例男性)(A组)和60例无糖尿病神经病变的患者(34例男性)(B组)。两组在年龄、性别和糖尿病病程方面无差异。使用糖尿病神经病变指数(DNI)通过临床检查诊断糖尿病神经病变。通过聚合酶链反应(PCR)进行I/D多态性的基因分型。与B组(11.7%)相比,A组D等位基因的频率显著更高(p = 0.001)(26.9%)。三个基因型组(I/I、I/D、D/D)之间的DNI评分差异显著(p = 0.001)。I/D型患者(3.7±1)的评分显著高于I/I型患者(2.5±0.9)(p = 0.04),D/D型患者(5.6±1.3)的评分显著高于I/D型患者(3.7±1)(p = 0.001)。
与无神经病变的患者相比,有神经病变的患者D等位基因频率显著更高。D等位基因的存在也与更高的神经病变评分相关。这些结果为2型糖尿病患者中D等位基因与神经病变的存在及严重程度之间的关联提供了证据。