Evaluating the Causal Association Between Type 2 Diabetes and Alzheimer's Disease: A Two-Sample Mendelian Randomization Study

被引:0
作者
Han, Si [1 ]
Lelieveldt, Tom [2 ]
Sturkenboom, Miriam [1 ]
Biessels, Geert Jan [3 ]
Ahmadizar, Fariba [1 ,4 ]
机构
[1] Univ Med Ctr Utrecht, Julius Global Hlth, Dept Data Sci & Biostat, NL-3584 CX Utrecht, Netherlands
[2] Univ Utrecht, Univ Coll Utrecht, Dept Biomed Sci, NL-3508 TC Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Brain Ctr, Dept Neurol, NL-3584 CX Utrecht, Netherlands
[4] Harvard TH Chan Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
type; 2; diabetes; Alzheimer's disease; Mendelian randomization; COGNITIVE FUNCTION; OXIDATIVE STRESS; RISK-FACTORS; DEMENTIA; METAANALYSIS; NEURODEGENERATION; INFLAMMATION; MELLITUS; INSIGHTS; LOCI;
D O I
10.3390/biomedicines13051095
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background/Objectives: Type 2 diabetes mellitus (T2DM) and Alzheimer's disease (AD) are significant global health issues. Epidemiological studies suggest T2DM increases AD risk, though confounding factors and reverse causality complicate this association. This study aims to clarify the causal relationship between T2DM and AD through a systematic review and meta-analysis of Mendelian randomization (MR) studies and a new two-sample MR analysis. Methods: A literature search across major databases was conducted through May 2024 to identify MR studies linking T2DM and AD. Fixed/random-effect models provided pooled odds ratios (ORs) with 95% confidence intervals (CIs), and heterogeneity was assessed with the I2 statistic. For our MR analysis, we pooled genetic variants from selected studies and analyzed AD outcomes using IGAP, EADB, and UKB databases. Multiple MR methods, including inverse variance weighted (IVW) and pleiotropy-robust approaches, were applied for validation. Results: Of 271 articles, 8 MR studies were included (sample sizes: 68,905 to 788,989), all from European ancestry. Our meta-analysis found no significant causal link between T2DM and AD (OR = 1.02, 95% CI: 1.00-1.04) with moderate heterogeneity (I2 = 31.3%). Similarly, our MR analysis using 512 SNPs as instrumental variables showed no significant associations in IGAP, EADB, or UKB data, which is consistent across sensitivity analyses. Conclusions: This meta-MR and MR analysis revealed no significant causal association between T2DM and AD, indicating that genetic predisposition to T2DM does not appear to causally influence AD risk, though modifiable clinical or environmental aspects of T2DM may still contribute to neurodegenerative processes. Further research should explore other mechanisms linking these conditions.
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页数:16
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