Causal relationships between type 1 diabetes mellitus and Alzheimer's disease and Parkinson's disease: a bidirectional two-sample Mendelian randomization study

被引:6
作者
Geng, Chaofan [1 ,2 ]
Meng, Ke [1 ,2 ]
Zhao, Bo [3 ]
Liu, Xiaoduo [1 ,2 ]
Tang, Yi [1 ,2 ,4 ]
机构
[1] Capital Med Univ, Xuanwu Hosp, Innovat Ctr Neurol Disorders, Natl Ctr Neurol Disorders, 45 Changchun St, Beijing 100053, Peoples R China
[2] Capital Med Univ, Xuanwu Hosp, Natl Ctr Neurol Disorders, Dept Neurol, 45 Changchun St, Beijing 100053, Peoples R China
[3] Jining Med Univ, Rongcheng Peoples Hosp, Dept Neurol, Affiliated Hosp, Weihai, Peoples R China
[4] Minist Educ Peoples Republ China, Neurodegenerat Lab, Beijing, Peoples R China
关键词
Type 1 diabetes mellitus; Mendelian randomization; Alzheimer's disease; Parkinson's disease; GENETIC-VARIANTS; RISK LOCI; INSTRUMENTS; INSULIN; METAANALYSIS;
D O I
10.1186/s40001-023-01628-z
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundPrevious compelling evidence suggests an association between Type 2 diabetes (T2D) and neurodegenerative diseases. However, it remains uncertain whether Type 1 diabetes mellitus (T1DM) exerts a causal influence on the risk of Alzheimer's disease (AD) and Parkinson's disease (PD). Consequently, this study employed a bidirectional two-sample Mendelian Randomization (MR) approach to investigate the causal relationship between T1DM and the genetic susceptibility to AD and PD.MethodsWe utilized large-scale cohorts derived from publicly available genome-wide association study datasets involving European populations to perform MR analyses. The primary analytical method employed was the inverse-variance weighted (IVW) approach. Furthermore, sensitivity analyses, including assessments of heterogeneity and horizontal pleiotropy, were carried out using Cochran's Q, MR-Egger intercept, and MR-PRESSO tests to enhance the robustness of our conclusions.ResultsUsing the IVW-based method, the MR analysis indicated no significant association between genetically determined T1DM and AD (OR = 0.984, 95% CI: 0.958-1.011, p = 0.247). Conversely, T1DM appeared to be associated with a reduced risk of genetic susceptibility to PD (IVW: OR = 0.958, 95% CI: 0.928-0.989, p = 0.001). In the reverse direction, no evidence of reverse causality was observed between AD (OR = 1.010, 95% CI: 0.911-1.116, p = 0.881) or PD (OR = 1.164, 95% CI: 0.686-2.025, p = 0.5202) and T1DM. Additionally, our analysis found no indications of the results being influenced by horizontal pleiotropy.ConclusionThis MR study reveals that T1DM is associated with a reduced genetic susceptibility to PD, whereas no significant genetic susceptibility is observed between T1DM and AD. These findings suggest that T1DM may have a distinct role in the development of neurodegenerative diseases compared to T2D. Further investigations are warranted to elucidate the underlying mechanisms and provide a more comprehensive understanding of this relationship.
引用
收藏
页数:10
相关论文
共 52 条
[1]   Impact of Early Diabetic Ketoacidosis on the Developing Brain [J].
Aye, Tandy ;
Mazaika, Paul K. ;
Mauras, Nelly ;
Marzelli, Matthew J. ;
Shen, Hanyang ;
Hershey, Tamara ;
Cato, Allison ;
Weinzimer, Stuart A. ;
White, Neil H. ;
Tsalikian, Eva ;
Jo, Booil ;
Reiss, Allan L. .
DIABETES CARE, 2019, 42 (03) :443-449
[2]   CSF markers for incipient Alzheimer's disease [J].
Blennow, K ;
Hampel, H .
LANCET NEUROLOGY, 2003, 2 (10) :605-613
[4]   Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator [J].
Bowden, Jack ;
Smith, George Davey ;
Haycock, Philip C. ;
Burgess, Stephen .
GENETIC EPIDEMIOLOGY, 2016, 40 (04) :304-314
[5]   Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data [J].
Burgess, Stephen ;
Butterworth, Adam ;
Thompson, Simon G. .
GENETIC EPIDEMIOLOGY, 2013, 37 (07) :658-665
[6]   Avoiding bias from weak instruments in Mendelian randomization studies [J].
Burgess, Stephen ;
Thompson, Simon G. .
INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2011, 40 (03) :755-764
[7]   Insulin action in the brain: cell types, circuits, and diseases [J].
Chen, Wenqiang ;
Cai, Weikang ;
Hoover, Benjamin ;
Kahn, C. Ronald .
TRENDS IN NEUROSCIENCES, 2022, 45 (05) :384-400
[8]  
Crane PK, 2013, NEW ENGL J MED, V369, P540, DOI [10.1056/NEJMoa1215740, 10.1056/NEJMc1311765]
[9]  
Davidson S, 2023, J Alzheimers Dis.
[10]   Diabetes mellitus and Parkinson's disease: dangerous liaisons between insulin and dopamine [J].
De Iuliis, Angela ;
Montinaro, Ennio ;
Fatati, Giuseppe ;
Plebani, Mario ;
Colosimo, Carlo .
NEURAL REGENERATION RESEARCH, 2022, 17 (03) :523-533