胰岛素抵抗
内科学
IRS2
非酒精性脂肪肝
IRS1
基因型
内分泌学
脂肪肝
医学
等位基因
胰岛素
血压
胰岛素受体
胃肠病学
生物
疾病
基因
遗传学
作者
Reza Dabiri,Touraj Mahmoudi,Mohammad Sabzikarian,Asadollah Asadi,Hamid Farahani,Hossein Nobakht,Iradj Maleki,Fariborz Mansour‐Ghanaei,F Derakshshan,Mohammad Reza Zali
出处
期刊:PubMed
[National Institutes of Health]
日期:2020-07-01
卷期号:83 (2): 271-276
被引量:11
摘要
Nonalcoholic fatty liver disease (NAFLD) is an increasing global health concern defined by excessive hepatic fat content in the absence of excessive alcohol consumption. Regarding the key role of insulin and insulin resistance in NAFLD, we investigated whether insulin receptor substrate 1 (IRS1) and insulin receptor substrate 2 (IRS2) gene variants were associated with NAFLD risk.In this case-control study, 305 subjects including 151 cases with biopsy-proven NAFLD and 154 controls were enrolled. All the subjects were genotyped for IRS1 (rs1801278) and IRS2 (rs2289046) gene variants using PCR-RFLP method.Our findings showed that the IRS2 rs2289046 "GG+AG" genotype compared with "AA" genotype to be a marker of decreased NAFLD susceptibility and the difference remained significant even after adjustment for confounding factors including age, BMI, sex, smoking status, systolic blood pressure, and diastolic blood pressure (P=0.014; OR=0.50, 95%CI= 0.29-0.87). Furthermore, the IRS2 "G" allele was significantly underrepresented in the cases with NAFLD than controls (P=0.026 ; OR=0.62, 95%CI=0.41-0.94). However, no significant difference was found for IRS1 rs1801278 gene variant.This study suggests, for the first time, that the IRS2 gene rs2289046 variant may play a role in NAFLD susceptibility. Nevertheless, this observation warrants further investigations in other populations.
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