Type 2 diabetes and late-onset Alzheimer's disease and related dementia: A longitudinal cohort study integrating polygenic risk score.

IF 3.4 3区 医学 Q2 NEUROSCIENCES
Sohyun Jeong, Lisha Lin, Alvaro-Pascual Leone, Yi-Hsiang Hsu
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引用次数: 0

Abstract

BackgroundThe inherent genetic effects were not established between type 2 diabetes (T2DM) and Alzheimer's disease and related dementia (ADRD).ObjectiveWe aimed to investigate the association between T2DM and ADRD by integrating T2DM polygenic risk score (PRS) and applying matching in every subgroup.MethodsWe utilized UK Biobank First-occurrences datasets. T2DM were 1:1 matched to non-T2DM using propensity scores generated by 8 covariates; age at diagnosis, sex, cerebrovascular disease, ischemic heart disease, hypertensive disorders, lipid disorders, obesity, and mood disorders. T2DM PRS was additionally matched in T2DM PRS matched analysis. Subgroup analyses by age at diagnosis, sex, and APOE4 genotype were performed with the same matching criteria within each subgroup. Cox proportional hazard and Fine & Gray competing risk model were utilized.ResultsIn T2DM PRS unmatched cohort, 24,583 T2DM were 1:1 matched to non-T2DM. The mean age at diagnosis was around 62 years old, with females constituting around 40%. Up to 25-year follow-up, ADRD rate/1000 person-years was 0.88 versus 1.52 (Non-T2DM versus T2DM); PRS unmatched (cHR: 1.72, 95% CI: 1.46-2.03) and matched (cHR:1.75, 95% CI: 1.47-2.09). Except for older age onset (≥75 years), the other subgroups demonstrated significantly increased ADRD risks in T2DM. T2DM PRS was higher in non-ADRD group across all subgroups. Contrarily, T2DM PRS was higher in ADRD in younger onset group (<55 years).ConclusionsT2DM is one of the strong risk factors of ADRD but genetic T2DM effect does not contribute to ADRD risk. However, a genetic link might be present in younger age onset group.

2型糖尿病和晚发性阿尔茨海默病及相关痴呆:一项整合多基因风险评分的纵向队列研究
背景:2型糖尿病(T2DM)与阿尔茨海默病及相关痴呆(ADRD)之间的内在遗传效应尚未确定。目的通过整合T2DM多基因风险评分(PRS)并对各亚组进行匹配,探讨T2DM与ADRD之间的关系。方法利用英国生物银行首次发病数据集。使用8个协变量生成的倾向得分,T2DM与非T2DM 1:1匹配;诊断年龄、性别、脑血管疾病、缺血性心脏病、高血压疾病、脂质疾病、肥胖、情绪障碍。在T2DM PRS匹配分析中,另外进行T2DM PRS匹配。按诊断年龄、性别和APOE4基因型进行亚组分析,每个亚组内采用相同的匹配标准。采用Cox比例风险模型和Fine & Gray竞争风险模型。结果T2DM PRS未匹配队列中,24583例T2DM患者与非T2DM患者1:1匹配。确诊时的平均年龄约为62岁,其中女性约占40%。在长达25年的随访中,ADRD率/1000人年分别为0.88和1.52(非T2DM和T2DM);PRS不匹配(cHR: 1.72, 95% CI: 1.46-2.03)和匹配(cHR:1.75, 95% CI: 1.47-2.09)。除发病年龄较大(≥75岁)外,其他亚组均表现出显著增加的2型糖尿病ADRD风险。非adrd组T2DM PRS在所有亚组中均较高。相反,年轻起病组T2DM PRS在ADRD中较高(
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来源期刊
Journal of Alzheimer's Disease
Journal of Alzheimer's Disease 医学-神经科学
CiteScore
6.40
自引率
7.50%
发文量
1327
审稿时长
2 months
期刊介绍: The Journal of Alzheimer''s Disease (JAD) is an international multidisciplinary journal to facilitate progress in understanding the etiology, pathogenesis, epidemiology, genetics, behavior, treatment and psychology of Alzheimer''s disease. The journal publishes research reports, reviews, short communications, hypotheses, ethics reviews, book reviews, and letters-to-the-editor. The journal is dedicated to providing an open forum for original research that will expedite our fundamental understanding of Alzheimer''s disease.
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