全基因组多基因风险评分预测有妊娠糖尿病史女性的 2 型糖尿病发病率。

Diabetes care Pub Date : 2024-09-01 DOI:10.2337/dc24-0022
Jaewon Choi, Hyunsuk Lee, Alan Kuang, Alicia Huerta-Chagoya, Denise M Scholtens, Daeho Choi, Minseok Han, William L Lowe, Alisa K Manning, Hak Chul Jang, Kyong Soo Park, Soo Heon Kwak
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引用次数: 0

摘要

目的:有妊娠糖尿病(GDM)病史的妇女患 2 型糖尿病(T2D)的风险增加。研究设计和方法:我们利用代表四个不同血统的五个独立队列(n = 1,895),研究了全基因组 T2D 多基因风险评分(PRS)是否与 T2D 发病风险增加有关。我们还计算了将 T2D 多基因风险评分纳入临床风险模型后的接收者操作特征曲线下面积(AUROC)和连续净重分类改进(NRI),以评估其诊断效用:在 1,895 名既往有 GDM 病史的女性中,363 人(19.2%)在 2 至 30 年间患上了 T2D。患 T2D 的妇女的 T2D PRS 较高(-0.08 vs. 0.31,P = 2.3 × 10-11),并且与发生 T2D 的风险增加有关(每增加 1-SD 的几率比 1.52,95% CI 1.05-2.21,P = 0.03)。在一个包括年龄、糖尿病家族史、收缩压和体重指数的模型中,纳入 PRS 后,T2D 的 AUROC 从 0.71 增加到 0.74,NRI 也有中等程度的改善(0.32,95% CI 0.15-0.49,P = 3.0 × 10-4)。尽管存在差异,但在不同的研究队列中观察到了类似的趋势:结论:在不同血统的 GDM 女性队列中,T2D PRS 与未来 T2D 的发展有显著相关性。将 T2D PRS 纳入临床风险模型以预测 T2D 的发生时,AUROC 有明显但微小的改善。
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Genome-Wide Polygenic Risk Score Predicts Incident Type 2 Diabetes in Women With History of Gestational Diabetes.

Objective: Women with a history of gestational diabetes mellitus (GDM) are at increased risk of developing type 2 diabetes (T2D). It remains unclear whether genetic information improves prediction of incident T2D in these women.

Research design and methods: Using five independent cohorts representing four different ancestries (n = 1,895), we investigated whether a genome-wide T2D polygenic risk score (PRS) is associated with increased risk of incident T2D. We also calculated the area under the receiver operating characteristics curve (AUROC) and continuous net reclassification improvement (NRI) following the incorporation of T2D PRS into clinical risk models to assess the diagnostic utility.

Results: Among 1,895 women with previous history of GDM, 363 (19.2%) developed T2D in a range of 2 to 30 years. T2D PRS was higher in those who developed T2D (-0.08 vs. 0.31, P = 2.3 × 10-11) and was associated with an increased risk of incident T2D (odds ratio 1.52 per 1-SD increase, 95% CI 1.05-2.21, P = 0.03). In a model that includes age, family history of diabetes, systolic blood pressure, and BMI, the incorporation of PRS led to an increase in AUROC for T2D from 0.71 to 0.74 and an intermediate improvement of NRI (0.32, 95% CI 0.15-0.49, P = 3.0 × 10-4). Although there was variation, a similar trend was observed across study cohorts.

Conclusions: In cohorts of GDM women with diverse ancestry, T2D PRS was significantly associated with future development of T2D. A significant but small improvement was observed in AUROC when T2D PRS was integrated into clinical risk models to predict incident T2D.

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