Biologically Informed Polygenic Scores for Brain Insulin Receptor Network Are Associated with Cardiometabolic Risk Markers and Diabetes in Women.

IF 6.8 2区 医学 Q1 ENDOCRINOLOGY & METABOLISM
Diabetes & Metabolism Journal Pub Date : 2024-09-01 Epub Date: 2024-03-25 DOI:10.4093/dmj.2023.0039
Jannica S Selenius, Patricia P Silveira, Mikaela von Bonsdorff, Jari Lahti, Hannu Koistinen, Riitta Koistinen, Markku Seppälä, Johan G Eriksson, Niko S Wasenius
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引用次数: 0

Abstract

Backgruound: To investigate associations between variations in the co-expression-based brain insulin receptor polygenic score and cardiometabolic risk factors and diabetes mellitus.

Methods: This cross-sectional study included 1,573 participants from the Helsinki Birth Cohort Study. Biologically informed expression-based polygenic risk scores for the insulin receptor gene network were calculated for the hippocampal (hePRS-IR) and the mesocorticolimbic (mePRS-IR) regions. Cardiometabolic markers included body composition, waist circumference, circulating lipids, insulin-like growth factor 1 (IGF-1), and insulin-like growth factor-binding protein 1 and 3 (IGFBP-1 and -3). Glucose and insulin levels were measured during a standardized 2-hour 75 g oral glucose tolerance test and impaired glucose regulation status was defined by the World Health Organization 2019 criteria. Analyzes were adjusted for population stratification, age, smoking, alcohol consumption, socioeconomic status, chronic diseases, birth weight, and leisure-time physical activity.

Results: Multinomial logistic regression indicated that one standard deviation increase in hePRS-IR was associated with increased risk of diabetes mellitus in all participants (adjusted relative risk ratio, 1.17; 95% confidence interval, 1.01 to 1.35). In women, higher hePRS-IR was associated with greater waist circumference and higher body fat percentage, levels of glucose, insulin, total cholesterol, low-density lipoprotein cholesterol, triglycerides, apolipoprotein B, insulin, and IGFBP-1 (all P≤0.02). The mePRS-IR was associated with decreased IGF-1 level in women (P=0.02). No associations were detected in men and studied outcomes.

Conclusion: hePRS-IR is associated with sex-specific differences in cardiometabolic risk factor profiles including impaired glucose regulation, abnormal metabolic markers, and unfavorable body composition in women.

脑胰岛素受体网络的生物学多基因评分与女性的心脏代谢风险标志物和糖尿病有关。
背景:研究基于共表达的脑胰岛素受体多基因评分变异与心脏代谢风险因素和糖尿病之间的关系:研究基于共表达的脑胰岛素受体多基因评分的变异与心脏代谢风险因素和糖尿病之间的关系:这项横断面研究包括赫尔辛基出生队列研究的 1,573 名参与者。研究人员计算了海马区(hePRS-IR)和皮质中叶区(mePRS-IR)的胰岛素受体基因网络基于生物学表达的多基因风险评分。心脏代谢指标包括身体成分、腰围、循环血脂、胰岛素样生长因子1(IGF-1)、胰岛素样生长因子结合蛋白1和3(IGFBP-1和-3)。葡萄糖和胰岛素水平是在标准化的 2 小时 75 克口服葡萄糖耐量试验中测量的,糖调节受损状态是根据世界卫生组织 2019 年标准界定的。分析对人口分层、年龄、吸烟、饮酒、社会经济地位、慢性病、出生体重和业余体力活动进行了调整:多项式逻辑回归表明,在所有参与者中,hePRS-IR每增加一个标准差,患糖尿病的风险就会增加(调整后相对风险比为 1.17;95% 置信区间为 1.01 至 1.35)。在女性中,hePRS-IR越高,腰围越大,体脂率越高,血糖、胰岛素、总胆固醇、低密度脂蛋白胆固醇、甘油三酯、脂蛋白B、胰岛素和IGFBP-1水平越高(均P≤0.02)。女性的 mePRS-IR 与 IGF-1 水平下降有关(P=0.02)。结论:hePRS-IR 与女性心血管代谢风险因素的性别差异有关,包括葡萄糖调节功能受损、代谢指标异常和不利的身体组成。
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来源期刊
Diabetes & Metabolism Journal
Diabetes & Metabolism Journal Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
10.40
自引率
6.80%
发文量
92
审稿时长
52 weeks
期刊介绍: The aims of the Diabetes & Metabolism Journal are to contribute to the cure of and education about diabetes mellitus, and the advancement of diabetology through the sharing of scientific information on the latest developments in diabetology among members of the Korean Diabetes Association and other international societies. The Journal publishes articles on basic and clinical studies, focusing on areas such as metabolism, epidemiology, pathogenesis, complications, and treatments relevant to diabetes mellitus. It also publishes articles covering obesity and cardiovascular disease. Articles on translational research and timely issues including ubiquitous care or new technology in the management of diabetes and metabolic disorders are welcome. In addition, genome research, meta-analysis, and randomized controlled studies are welcome for publication. The editorial board invites articles from international research or clinical study groups. Publication is determined by the editors and peer reviewers, who are experts in their specific fields of diabetology.
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