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

被引:3
|
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 50 条
  • [31] Association between the sarcopenia-related traits and Parkinson's disease: A bidirectional two-sample Mendelian randomization study
    She, Yingqi
    He, Yaming
    Wu, Jianwei
    Liu, Ning
    ARCHIVES OF GERONTOLOGY AND GERIATRICS, 2024, 122
  • [32] Causal effects of genetically predicted testosterone on Alzheimer’s disease: a two-sample mendelian randomization study
    Qian Xu
    Hong Shen
    Yifan Zhu
    Junlei Zhang
    Zhongmei Shen
    Jianming Jiang
    Jie Zhou
    Acta Neurologica Belgica, 2024, 124 : 591 - 601
  • [33] Causal Effects of Plasma Haptoglobin Levels on Alzheimer's Disease: A Two-Sample Mendelian Randomization Study
    Lin, Yijia
    Hu, Tingjun
    Cheng, Lizhen
    Chen, Yixin
    Guo, Qihao
    Miao, Ya
    JOURNAL OF ALZHEIMERS DISEASE, 2023, 95 (01) : 339 - 348
  • [34] Exploring Causal Relationships Between Gut Microbiota and Alzheimer's Disease: A Bidirectional Mendelian Randomization Study
    Chen, Anqi
    Wang, Yuquan
    Hu, Yue-Qing
    JOURNAL OF ALZHEIMERS DISEASE REPORTS, 2024, 8 (01) : 1031 - 1040
  • [35] Causal association between celiac disease and inflammatory bowel disease: A two-sample bidirectional Mendelian randomization study
    Yuan, Shuai
    Kim, Ji Hun
    Xu, Pai
    Wang, Zhao
    FRONTIERS IN IMMUNOLOGY, 2023, 13
  • [36] Periodontal disease and risk of Alzheimer's disease: A two-sample Mendelian randomization
    Hu, Conglei
    Li, Hui
    Huang, Liping
    Wang, Rui
    Wang, Zeyu
    Ma, Rui
    Chang, Bei
    Li, Shiting
    Li, Hongcai
    Li, Guangwen
    BRAIN AND BEHAVIOR, 2024, 14 (04):
  • [37] Association between 23 drugs and Parkinson's disease: A two-sample Mendelian randomization study
    Xie, Zhixin
    Zhou, Haobin
    Qiu, Ziyu
    Fan, Zhongxi
    Yang, Weisheng
    Zhang, Jingbai
    Wang, Yezhong
    Ye, Yongyi
    BRAIN AND BEHAVIOR, 2023,
  • [38] Evaluating the causal effects between Grave's disease and diabetes mellitus: a bidirectional Mendelian randomization study
    Zhang, Yuhan
    Fu, Liuxiang
    FRONTIERS IN ENDOCRINOLOGY, 2024, 15
  • [39] Association between 23 drugs and Parkinson's disease: A two-sample Mendelian randomization study
    Xie, Zhixin
    Zhou, Haobin
    Qiu, Ziyu
    Fan, Zhongxi
    Yang, Weisheng
    Zhang, Jingbai
    Wang, Yezhong
    Ye, Yongyi
    BRAIN AND BEHAVIOR, 2023, 13 (11):
  • [40] Type 2 diabetes and inflammatory bowel disease: a bidirectional two-sample Mendelian randomization study
    Xu, Guangyi
    Xu, Yanhong
    Zheng, Taohua
    Liu, Ting
    SCIENTIFIC REPORTS, 2024, 14 (01)