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摩洛哥人群中TCF7L2基因多态性与2型糖尿病高风险的显著关联。

Significant Association of Polymorphisms in the TCF7L2 Gene with a Higher Risk of Type 2 Diabetes in a Moroccan Population.

作者信息

Elhourch Sarah, Arrouchi Housna, Mekkaoui Nour, Allou Younes, Ghrifi Fatima, Allam Loubna, Elhafidi Naima, Belyamani Lahcen, Ibrahimi Azeddine, Elomri Naoual, Eljaoudi Rachid

机构信息

Medical Biotechnology Laboratory (MedBiotech), Bioinova Research Center, Rabat Medical & Pharmacy School, Mohammed Vth University, 10000 Rabat, Morocco.

Clinical Research and Epidemiology Biostatistics Laboratory, Rabat Medical & Pharmacy School, Mohammed Vth University in Rabat, 10000 Rabat, Morocco.

出版信息

J Pers Med. 2021 May 24;11(6):461. doi: 10.3390/jpm11060461.

Abstract

BACKGROUND AND AIMS

Several studies have shown that genetic polymorphisms of the transcription factor 7-like 2 (TCF7L2) are highly associated with the development of type 2 diabetes mellitus (T2DM) and its associated complications in several populations. The aim of our study was to investigate the association of the rs7903146 (C/T) and rs12255372 (G/T) polymorphism in the TCF7L2 gene with the risk of developing T2DM in the Moroccan population.

MATERIAL AND METHODS

A total of 150 T2DM patients and 100 healthy controls were recruited for various anthropometric, biochemical and genetic parameters. Genotyping was performed by using Real Time-PCR. The frequency of genotypes, alleles, anthropometric measures, glycemia, glycated hemoglobin (HbA1c) were evaluated in patients and control, while lipid profile was available only for T2DM group.

RESULTS

Glycemia, HbA1c and body mass index (BMI) were significantly higher in T2DM group than control. Analysis of the distribution of the TCF7L2 rs7903146 genotype and allele revealed that the TT genotype was more frequent in T2DM group (24.0%) than in healthy controls (5%) (OR = 4.08, 95% confidence interval (CI = 1.95-11.80, < 0.0001). The T allele was more frequent in diabetic patients (45.2%) than healthy control (34.5%) and it was associated with high risk of diabetes (OR = 2.13, 95% CI = 1.12-7.31, = 0.005). The same results were found regarding rs12255372, TT genotype frequencies were 18,7% and 6.0% in T2DM and control group, respectively (OR = 3.11, 95% CI = 1.33-7.24, = 0.004). The T allele was over-presented in diabetics compared to controls (45.3% and 38.0%, respectively) and increases the risk of T2DM (OR = 2.01, 95% CI = 1.04-3.10, = 0.01). However, there was no significant difference between the three genotypes of rs7903146 and rs12255372 regarding age, BMI, glycemia, HbA1c and lipid profile.

CONCLUSION

The present study confirmed a significant association of the TCF7L2 gene (rs7903146 (C/T) and rs12255372 (G/T) polymorphisms with a higher risk to T2DM in the Moroccan population. No significant difference in respect to anthropometric and metabolic parameters between different genotypes.

摘要

背景与目的

多项研究表明,转录因子7样2(TCF7L2)基因的多态性在多个人群中与2型糖尿病(T2DM)的发生及其相关并发症高度相关。我们研究的目的是调查摩洛哥人群中TCF7L2基因的rs7903146(C/T)和rs12255372(G/T)多态性与发生T2DM风险之间的关联。

材料与方法

共招募了150例T2DM患者和100例健康对照者,测量了各种人体测量学、生化和遗传参数。采用实时荧光定量PCR进行基因分型。评估了患者和对照者的基因型频率、等位基因频率、人体测量指标、血糖、糖化血红蛋白(HbA1c),而血脂谱仅在T2DM组中进行了检测。

结果

T2DM组的血糖、HbA1c和体重指数(BMI)显著高于对照组。对TCF7L2 rs7903146基因型和等位基因分布的分析显示,T2DM组中TT基因型的频率(24.0%)高于健康对照组(5%)(比值比(OR)=4.08,95%置信区间(CI)=1.95 - 11.80,P<0.0001)。T等位基因在糖尿病患者中的频率(45.2%)高于健康对照组(34.5%),并且与糖尿病高风险相关(OR = 2.13,95% CI = 1.12 - 7.31,P = 0.005)。关于rs12255372也得到了相同的结果,T2DM组和对照组中TT基因型频率分别为18.7%和6.0%(OR = 3.11,95% CI = 1.33 - 7.24,P = 0.004)。与对照组相比,T等位基因在糖尿病患者中更为常见(分别为45.3%和38.0%),并增加了T2DM的风险(OR = 2.01,95% CI = 1.04 - 3.10,P = 0.01)。然而,rs7903146和rs12255372的三种基因型在年龄、BMI、血糖、HbA1c和血脂谱方面没有显著差异。

结论

本研究证实了摩洛哥人群中TCF7L2基因(rs7903146(C/T)和rs12255372(G/T)多态性与T2DM高风险之间存在显著关联。不同基因型在人体测量和代谢参数方面没有显著差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3056/8225140/0388d7645373/jpm-11-00461-g001.jpg

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