TNF-α启动子多态性与2型糖尿病遗传易感性的关联调查:中国汉族人群横断面研究。

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY
Wenyu Tao, Xiaoling Wang, Man Yang, Xing Zhou, Mingliu Yin, Ying Yang, Yiping Li
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引用次数: 0

摘要

2 型糖尿病(T2DM)的特点是胰岛素抵抗和胰岛素分泌相对不足。肿瘤坏死因子-α(TNF-α)通过损害胰岛素信号转导,在胰岛素抵抗中发挥着重要作用。TNF-α 启动子区域的变异被认为会影响其转录,并与 TNF-α 水平相关。因此,值得检测 TNF-α 基因变异与 T2DM 发病的关联。本研究旨在调查中国汉族人群中TNF-α基因启动子区5个变异(rs1799964、rs1800630、rs1799724、rs1800629和rs361525)与T2DM的相关性。采用 TaqMan 方法对 713 名 T2DM 受试者和 751 名非糖尿病受试者进行了基因分型。评估了五个变异基因与 T2DM 发病的相关性。分析了五个变异基因型与非糖尿病受试者代谢特征的关系。我们的数据显示,rs1800629 的 A 等位基因会增加患 T2DM 的风险(p = .002,OR = 1.563;95% CI:1.18-2.08)。根据遗传模式分析,与 G/G 基因型相比,rs1800629 的 G/A+2A/A 基因型在对数加成模式下对 T2DM 有风险影响(p = .002,OR = 1.56;95% CI:1.17-2.07)。单倍型分析发现,rs1799724-rs1800629CA 与 T2DM 的高发病风险相关(p = .002,OR = 1.559,95% CI:1.173-2.072)。相反,rs1799724-rs1800629CG 是 T2DM 的保护性单倍型(p = .001,OR = 0.732,95% CI:0.607-0.884)。此外,与 rs1799964 (T/T+C/T) 基因型相比,rs1799964 C/C 基因型与非糖尿病受试者较高的糖化血红蛋白(HbA1c)水平相关(p = .017)。我们的研究结果表明,在中国汉族人群中,TNF-α基因启动子区的rs1800629与T2DM有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigations of associations between TNF-α promoter polymorphisms and genetic susceptibility to type 2 diabetes mellitus: A cross-sectional study in Chinese Han population

Type 2 diabetes (T2DM) is characterised by insulin resistance and a relative shortage of insulin secretion. Tumour necrosis factor-α (TNF-α) plays an important role in insulin resistance by impairing insulin signal transduction. The variants of the TNF-α promoter region are considered to influence its transcription and are associated with the TNF-α level. Therefore, it is worth detecting the association of the variants in the TNF-α gene with the development of T2DM. The aim of this study was to investigate the association of five variants (rs1799964, rs1800630, rs1799724, rs1800629 and rs361525) in the TNF-α gene promoter region with T2DM in a Chinese Han population. A total of 713 subjects with T2DM and 751 nondiabetic subjects were genotyped using the TaqMan method. The associations of the five variants with the development of T2DM were evaluated. The associations of the five variant genotypes with metabolic traits in nondiabetic subjects were analysed. Our data showed that the A allele of rs1800629 could increase the risk of developing T2DM (p = .002, OR = 1.563; 95% CI: 1.18–2.08). According to inheritance mode analysis, compared with the G/G genotype, the G/A+2A/A genotype of rs1800629 showed a risk effect on T2DM in the log-additive mode (p = .002, OR = 1.56; 95% CI: 1.17–2.07). The haplotypes analysis identified that the rs1799724-rs1800629CA was associated with high risk of the development of T2DM (p = .002, OR = 1.559, 95% CI: 1.173–2.072). Conversely, the rs1799724-rs1800629CG was a protective haplotype of T2DM (p = .001, OR = 0.732, 95% CI: 0.607–0.884). Moreover, compared with the rs1799964 (T/T+C/T) genotype, the rs1799964 C/C genotype was associated with higher glycosylated haemoglobin (HbA1c) levels in nondiabetic subjects (p = .017). Our results revealed that the rs1800629 in the TNF-α gene promoter region was associated with T2DM in a Chinese Han population.

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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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