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糖尿病前期及进展为2型糖尿病的遗传风险和多基因风险评分评估

Genetic risk and polygenic risk score assessment of prediabetes and progression to type 2 diabetes.

作者信息

Aliyu Usama, Umlai Umm-Kulthum Ismail, Al-Thani Nayra M, Toor Salman M, Abou-Samra Abdul Badi, Albagha Omar M E

机构信息

College of Health and Life Sciences (CHLS), Hamad Bin Khalifa University (HBKU), Qatar Foundation (QF), Doha, Qatar.

Bioinformatics Core, Weill Cornell Medicine-Qatar, Doha, Qatar.

出版信息

Diabetes Obes Metab. 2025 Aug;27(8):4469-4479. doi: 10.1111/dom.16490. Epub 2025 Jun 5.

Abstract

AIMS

To identify susceptibility loci to prediabetes and evaluate the performance of existing polygenic risk scores (PGS) for type 2 diabetes (T2D) in predicting prevalent prediabetes and progression to diabetes.

MATERIALS AND METHODS

We conducted a case-control Genome-Wide Association Study (GWAS) on Qatar Biobank (QBB) participants with prediabetes (n = 2267) and normoglycaemia (n = 8665). We further evaluated the performance of 140 existing PGS for T2D in predicting prediabetes using logistic regression in the baseline QBB cohort (n = 10 932) and progression to T2D using Cox regression in the follow-up cohort (n = 2143).

RESULTS

GWAS identified two loci associated with prediabetes (p < 5 × 10), mapped near GCK and HK1 genes. Among 140 PGS, PGS004838 showed the strongest association with prediabetes (OR/SD: 1.37, 95% CI: 1.29-1.45, p-value: 4.45 × 10). Among 2143 individuals without diabetes at baseline, 9.3% progressed to T2D over 6.0 years of median follow-up. PGS004838 outperformed the other 139 PGS in predicting progression to T2D (HR/SD: 1.79, 95% CI: 1.53-2.10, p-value: 2.08 × 10). Individuals in the very high genetic risk quintile were younger and had a 2.4-fold increased risk of progressing to T2D compared to the intermediate genetic risk quintile.

CONCLUSIONS

This study identified two genetic loci associated with prediabetes. PGS004838 showed the highest performance in predicting prediabetes and progression to T2D, with the strongest effect reported to date. Our findings have clinical translation potential in risk stratification and early intervention.

摘要

目的

确定糖尿病前期的易感基因座,并评估现有的2型糖尿病(T2D)多基因风险评分(PGS)在预测糖尿病前期患病率和进展为糖尿病方面的性能。

材料与方法

我们对卡塔尔生物银行(QBB)中患有糖尿病前期(n = 2267)和血糖正常(n = 8665)的参与者进行了病例对照全基因组关联研究(GWAS)。我们进一步在基线QBB队列(n = 10932)中使用逻辑回归评估了140个现有的T2D PGS在预测糖尿病前期方面的性能,并在随访队列(n = 2143)中使用Cox回归评估了其在进展为T2D方面的性能。

结果

GWAS确定了两个与糖尿病前期相关的基因座(p < 5×10),位于GCK和HK1基因附近。在140个PGS中,PGS004838与糖尿病前期的关联最强(OR/SD:1.37,95%CI:1.29 - 1.45,p值:4.45×10)。在基线时无糖尿病的2143名个体中,9.3%在中位随访6.0年期间进展为T2D。PGS004838在预测进展为T2D方面优于其他139个PGS(HR/SD:1.79,95%CI:1.53 - 2.10,p值:2.08×10)。与中等遗传风险五分位数相比,遗传风险非常高的五分位数个体更年轻,进展为T2D的风险增加2.4倍。

结论

本研究确定了两个与糖尿病前期相关的基因座。PGS004838在预测糖尿病前期和进展为T2D方面表现最佳,是迄今为止报道的最强效应。我们的研究结果在风险分层和早期干预方面具有临床转化潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/24b2/12232356/15ece132523e/DOM-27-4469-g002.jpg

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