GIPR基因变异与2型糖尿病风险的关系:一项病例对照研究

Shahrzad Manavi Nameghi
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引用次数: 0

摘要

背景2型糖尿病(T2DM)是一种多因素疾病,环境和遗传因素共同影响其致病性,是一种全球性的健康挑战。胃抑制多肽受体(GIPR)是一种控制肠道激素释放和胰岛素分泌的G-pro受体。本研究旨在探讨GIPR rs1800437基因变异在T2DM易感性中的作用。材料与方法共招募确诊T2DM患者108例,正常对照100例。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法检测GIPR rs1800437基因型。结果T2DM组与对照组GIPR rs1800437基因型(CC、CG、GG)变异频率差异有统计学意义(P = 0.02)。该变异的纯合子CC基因型与杂合子GC基因型相比,显著降低了糖尿病风险的优势比(OR),约为50%。病例中C等位基因的出现频率明显低于对照组(P = 0.002, OR = 0.51, CI = 0.33 ~ 0.79)。结论本研究结果充分证明rs1800437 GIPR基因变异与T2DM发病风险存在显著相关性。
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Association of GIPR gene variant on the risk of type 2 diabetes mellitus: A case-control study

Background

Type 2 diabetes mellitus (T2DM), as a worldwide health challenge, is a multifactorial disease that environmental and genetic factors contribute to its pathogenicity. Gastric Inhibitory Polypeptide Receptor (GIPR) is a G-pro receptor that controls the gut hormones release and insulin secretion. The current study aimed to investigate the role of the GIPR rs1800437 gene variant in T2DM susceptibility.

Material and methods

A total of 108 confirmed T2DM patients and 100 normal controls were recruited in the study. The GIPR rs1800437 genotypes were determined by Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) assay.

Results

A significant difference was found in genotypes (CC, CG, and GG) frequency of the GIPR rs1800437 variant between T2DM and control groups (P = 0.02). The homozygote CC genotype of the variant significantly decreased the odds ratio (OR) of diabetes mellitus risk, approximately 50 %, in comparison with the heterozygous GC genotype. The frequency of the C allele among cases was considerably lower than controls (P = 0.002, OR = 0.51, CI = 0.33–0.79).

Conclusion

The findings of the study show enough evidence that there is a significant association between the rs1800437 GIPR genetic variant and the risk of T2DM.

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来源期刊
Endocrine and Metabolic Science
Endocrine and Metabolic Science Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.80
自引率
0.00%
发文量
4
审稿时长
84 days
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