Suppr超能文献

血管内皮生长因子(VEGF)基因C936T多态性及p22phox基因C242T多态性与2型糖尿病及远端糖尿病性多发性神经病变的关联研究

Association study of C936T polymorphism of the VEGF gene and the C242T polymorphism of the p22phox gene with diabetes mellitus type 2 and distal diabetic polyneuropathy.

作者信息

Ghisleni Melissa Mottin, Biolchi Vanderlei, Jordon Bruna Cristina, Rempel Claudete, Genro Júlia Pasqualini, Pozzobon Adriane

机构信息

Department of Biological and Health Sciences, Postgraduate Program in Biotechnology, Univates University Center, Rio Grande do Sul, Lajeado 95900‑000, Brazil.

出版信息

Mol Med Rep. 2015 Sep;12(3):4626-1633. doi: 10.3892/mmr.2015.3988. Epub 2015 Jun 23.

Abstract

Even with long‑term glycemic control, diabetes mellitus type 2 (DM2) remains the predominant cause of diabetic neuropathy. Single nucleotide polymorphism (SNP) C936T of the vascular endothelial growth factor (VEGF) gene and the SNP C242T of the p22phox (CYBA) gene have been investigated in relation to DM2 and its complications. The aim of the present study was to investigate the association between these two SNPs and DM2, and also between the SNPs and the signs and symptoms of diabetic distal polyneuropathy. The DM2 group consisted of 98 individuals and the control group consisted of 104 individuals. The results demonstrated that there was no association between the different genotypes or alleles and increased risk of the disease (P>0.05). With SNP C242T, a significant association with body mass index between the CTxTT genotypes (P=0.043) was identified; and the greatest body mass indexes were among individuals with the TT genotype. An association between the degree of neuropathic symptoms and genotypic/allelic distribution of these polymorphisms was not observed. In conclusion, the investigated polymorphisms are not correlated with the risk of developing DM2.

摘要

即使进行长期血糖控制,2型糖尿病(DM2)仍是糖尿病性神经病变的主要原因。血管内皮生长因子(VEGF)基因的单核苷酸多态性(SNP)C936T和p22phox(CYBA)基因的SNP C242T已针对DM2及其并发症进行了研究。本研究的目的是调查这两个SNP与DM2之间的关联,以及SNP与糖尿病性远端多发性神经病变的体征和症状之间的关联。DM2组由98名个体组成,对照组由104名个体组成。结果表明,不同基因型或等位基因与疾病风险增加之间无关联(P>0.05)。对于SNP C242T,在CTxTT基因型之间发现与体重指数存在显著关联(P=0.043);体重指数最高的是TT基因型个体。未观察到神经病变症状程度与这些多态性的基因型/等位基因分布之间存在关联。总之,所研究的多态性与发生DM2的风险无关。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验