Evidence map›Paper›PMID 41140969›Full record

ArticleJournal of diabetes and metabolic disorders2025

Mendelian randomization analysis: investigating the causal association between apoptotic proteins and diabetes.

Enhui Zhou, Chong Zheng, Ye Lin, Yibing Zhou, Renhua Zhang

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Article in Journal of diabetes and metabolic disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Enhui Zhou *School of Public Health, the Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang, 550025 China.
Chong Zheng *Guizhou center for Disease Control and Prevention, Guiyang, 550004 China.
Ye LinGuizhou center for Disease Control and Prevention, Guiyang, 550004 China.
Yibing ZhouGuizhou center for Disease Control and Prevention, Guiyang, 550004 China.
Renhua ZhangGuizhou center for Disease Control and Prevention, Guiyang, 550004 China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Diabetes, commonly coexisting with hypertension, notably elevates the risk of damage to target organs. Apoptosis, a critical cellular process, maintains physiological balance but its role in the etiology of diabetes remains elusive. Study design: Mendelian randomization analysis. Methods: Utilizing summary data from genome-wide association studies (GWAS) of apoptotic proteins and diabetes, a two-sample Mendelian randomization (MR) design was employed. Our analysis included the Inverse Variance Weighted (IVW), weighted median, weighted mode, and MR-Egger regression. Sensitivity analyses included MR-Egger, MR-PRESSO, Cochran's Q test, and leave-one-out analyses, aimed at assessing and confirming the robustness and reliability of the research findings. Results: Our analysis revealed a suggestive positive correlation between increased Caspase-10 levels and heightened risk of type 1 diabetes (T1D) (OR 1.15, 95% CI 1.02-1.29, Conclusions: Our study illuminates the genetic causal ties between apoptotic proteins and the susceptibility to essential hypertension and diabetes. These insights are foundational for advancing our comprehension of disease mechanisms, facilitating preventive measures, and opening new horizons for precision medicine targeting these pathways. Supplementary Information: The online version contains supplementary material available at 10.1007/s40200-025-01771-w.

Indexed as

Apoptotic proteinsDiabetesGenome-wide association studyMendelian randomization

Identifiers

PMID41140969
PMCPMC12549466

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.