Impact of the trans-ancestry polygenic risk score on type 2 diabetes risk, onset age and progression among population in Taiwan.

IF 4.2 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Shi-Heng Wang, Yu-Chuen Huang, Chun-Wen Cheng, Ya-Wen Chang, Wen-Ling Liao
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Abstract

Type 2 diabetes (T2D) prevalence in adults at a younger age has increased but the disease status may go unnoticed. This study aimed to determine whether the onset age and subsequent diabetic complications can be attributed to the polygenic architecture of T2D in the Taiwan Han population. A total of 9,627 cases with T2D and 85,606 controls from the Taiwan Biobank were enrolled. Three diabetic polygenic risk scores (PRSs), PRS_EAS and PRS_EUR, and a trans-ancestry PRS (PRS_META), calculated using summary statistic from East Asian and European populations. The onset age was identified by linking to the National Taiwan Insurance Research Database, and the incidence of different diabetic complications during follow-up was recorded. PRS_META (7.4%) explained a higher variation for T2D status. And the higher percentile of PRS is also correlated with higher percentage of T2D family history and prediabetes status. More, the PRS was negatively associated with onset age (β = -0.91 yr), and this was more evident among males (β = -1.11 vs. -0.76 for males and females, respectively). The hazard ratio of diabetic retinopathy (DR) and diabetic foot were significantly associated with PRS_EAS and PRS_META, respectively. However, the PRS was not associated with other diabetic complications, including diabetic nephropathy, cardiovascular disease, and hypertension. Our findings indicated that diabetic PRS which combined susceptibility variants from cross-population could be used as a tool for early screening of T2D, especially for high-risk populations, such as individuals with high genetic risk, and may be associated with the risk of complications in subjects with T2D. NEW & NOTEWORTHY Our findings indicated that diabetic polygenic risk score (PRS) which combined susceptibility variants from Asian and European population affect the onset age of type 2 diabetes (T2D) and could be used as a tool for early screening of T2D, especially for individuals with high genetic risk, and may be associated with the risk of diabetic complications among people in Taiwan.

跨世系多基因风险评分对台湾人口 2 型糖尿病风险、发病年龄和进展的影响。
T2D在成年人中的发病率呈年轻化趋势,但其发病状况可能不为人们所注意。本研究旨在确定台湾汉族人群的发病年龄及其后的糖尿病并发症是否与 T2D 的多基因结构有关。本研究从台湾生物库中纳入了 9,627 例 T2D 患者和 85,606 例对照。利用东亚和欧洲人群的汇总统计计算出三个糖尿病多基因风险评分(PRS)--PRS_EAS 和 PRS_EUR,以及一个跨宗族风险评分(PRS_META)。通过与国立台湾保险研究数据库的链接,确定了发病年龄,并记录了随访期间各种糖尿病并发症的发生率。PRS_META(7.4%)能解释更多的 T2D 状态变化。PRS百分位数越高,T2D家族史和糖尿病前期状态的比例也越高。此外,PRS 与发病年龄呈负相关(β=-0.91 岁),这在男性中更为明显(男性和女性的β=-1.11 对-0.76)。然而,PRS 与其他糖尿病并发症(包括糖尿病肾病、心血管疾病和高血压)无关。我们的研究结果表明,糖尿病 PRS 结合了跨人群的易感性变异,可作为早期筛查 T2D 的工具,尤其适用于高风险人群,如遗传风险较高的个体,而且可能与 T2D 受试者的并发症风险有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.80
自引率
0.00%
发文量
98
审稿时长
1 months
期刊介绍: The American Journal of Physiology-Endocrinology and Metabolism publishes original, mechanistic studies on the physiology of endocrine and metabolic systems. Physiological, cellular, and molecular studies in whole animals or humans will be considered. Specific themes include, but are not limited to, mechanisms of hormone and growth factor action; hormonal and nutritional regulation of metabolism, inflammation, microbiome and energy balance; integrative organ cross talk; paracrine and autocrine control of endocrine cells; function and activation of hormone receptors; endocrine or metabolic control of channels, transporters, and membrane function; temporal analysis of hormone secretion and metabolism; and mathematical/kinetic modeling of metabolism. Novel molecular, immunological, or biophysical studies of hormone action are also welcome.
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