Evaluating the Causal Effect of Type 2 Diabetes on Alzheimer's Disease Using Large-Scale Genetic Data

被引:0
|
作者
Liu, D. [1 ,2 ,3 ]
Baranova, A. [4 ,5 ]
Zhang, Fuquan [6 ,7 ]
机构
[1] Nanjing Univ, Nanjing Drum Tower Hosp, Affiliated Hosp,Med Sch, Dept Radiol, Nanjing 210008, Peoples R China
[2] Nanjing Univ, Inst Med Imaging & Artificial Intelligence, Nanjing 210008, Peoples R China
[3] Nanjing Univ, Affiliated Drum Tower Hosp, Med Imaging Ctr, Med Sch, Nanjing 210008, Peoples R China
[4] George Mason Univ, Sch Syst Biol, Manassas, VA 20110 USA
[5] Res Ctr Med Genet, Moscow 115478, Russia
[6] Nanjing Med Univ, Affiliated Brain Hosp, Inst Neuropsychiat, Nanjing 210029, Peoples R China
[7] Nanjing Med Univ, Dept Psychiat, Affiliated Brain Hosp, 264 Guangzhou Rd, Nanjing 210029, Peoples R China
基金
中国博士后科学基金;
关键词
Alzheimer's disease; mendelian randomization; type; 2; diabetes; INSIGHTS;
D O I
10.14283/jpad.2024.148
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundAlzheimer's disease (AD) has a high comorbidity with type 2 diabetes (T2D). However, there is still some controversy over whether T2D has a causal impact on AD at present.ObjectivesWe aimed to reveal whether T2D has a causal effect on AD using large-scale genetic data.MethodsFirstly, we performed a primary two-sample Mendelian randomization (MR) analysis to assess the potential causal effects of T2D on AD. For this analysis, we used the largest available genome-wide association studies (GWAS) T2D (T2D1, including 80,154 cases and 853,816 controls) and AD (AD1, including 111,326 cases and 677,663 controls) datasets. Additionally, we performed a validation MR analysis using two largely overlapping-sample datasets from FinnGen, including T2D (T2D2, including 57,698 cases and 308,252 controls) and AD (AD2, including 13,393 cases and 363,884 controls). In all MR analyses, the inverse variance-weighted method was used as the primary analysis method, supplemented by the weighted-median and MR-Egger techniques.ResultsIn the primary analysis, we found that T2D was not associated with the risk of AD (OR: 0.98, CI: 0.95-1.01, P=0.241). Similarly, no significant association was detected in the validation MR analysis (OR: 0.97, CI: 0.64-1.47, P=0.884).ConclusionOur findings provide robust evidence that T2D does not have a causal impact on AD. Future studies need to further explore the effect of T2D on the non-AD components of the dementia phenotype.
引用
收藏
页码:1280 / 1282
页数:3
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