Evidence map›Paper›PMID 40342965›Full record

ArticleTherapeutic advances in endocrinology and metabolism2025

Multi-omics investigation of prospective therapeutic targets for type 1 diabetes.

Yue-Yang Zhang, Qing-Tian Qiao, Bing-Xue Chen, Qin Wan

Abstract read
In one paragraph

Article in Therapeutic advances in endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Yue-Yang ZhangDepartment of Endocrinology and Metabolism, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Qing-Tian QiaoDepartment of Endocrinology and Metabolism, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Bing-Xue ChenDepartment of Ultrasound Medicine, Affiliated Hospital of Southwest Medical University, Luzhou, China.
Qin WanDepartment of Endocrinology and Metabolism, Affiliated Hospital of Southwest Medical University, No. 23 Taiping Street, Jiangyang District, Luzhou, Sichuan 646000, China.ORCID https://orcid.org/0000-0001-7765-1416

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In recent years, the incidence of type 1 diabetes has been rising steadily, positioning its prevention and treatment as a central focus of global public health initiatives. Previous Mendelian randomization (MR) studies have investigated the relationship between proteomics and type 1 diabetes. Consequently, this study aims to identify prospective therapeutic targets for type 1 diabetes through a comprehensive multi-omics analysis. Methods: This study primarily utilized the MR method, drawing on genetic data from several large-scale, publicly accessible genome-wide association studies. Within this framework, we applied two-sample MR to evaluate the relationship between five omics components and type 1 diabetes. Finally, we conducted various sensitivity analyses and bidirectional MR to ensure the robustness and reliability of our findings. Results: The inverse variance weighted method revealed that, following false discovery rate correction, 39 plasma proteins and 3 plasma protein ratios exhibited significant associations with type 1 diabetes. The genetically predicted risk of type 1 diabetes ranged from 0.05 for RBP2 to 394.51 for FMNL1. Furthermore, 4-chlorobenzoic acid levels demonstrated a potential association with type 1 diabetes. Conclusion: Our research identified numerous omics components associated with type 1 diabetes. These findings offer novel insights into the disease's etiology, diagnosis, and treatment.

Indexed as

immunophenotypeMendelian randomizationmulti-omicsplasma proteintype 1 diabetes

Identifiers

PMID40342965
PMCPMC12059444

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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.