Evidence map›Paper›PMID 41465917›Full record

ArticleMedicine2025

Unraveling the causal link between immune cells and temporomandibular disorders: A Mendelian randomization analysis.

Xinjian Zhang, Yuqi Xin, Fei He, Yang Liu, Jiahui Shao, Zichen Xu, Qingkun Jiang, Tiehan Cui, Fang Wang, Jiaxuan Qiu

Abstract read
In one paragraph

Article in Medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Xinjian ZhangJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.ORCID 0000-0002-3463-1586
Yuqi XinJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Fei HeJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Yang LiuJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Jiahui ShaoJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Zichen XuJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Qingkun JiangJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Tiehan CuiJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Fang WangJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.
Jiaxuan QiuJiangxi Provincial Key Laboratory of Oral Diseases, Department of Stomatology, The First Affiliated Hospital, Nanchang, Jiangxi Province, China.ORCID 0000-0002-4496-6056

Funding

Jiangxi Provincial Key R&D Plan Grant No. 20212BBG71005Jiangxi Provincial Science and Technology Department Science and Technology Innovation Base Construction Project No.20221ZDG020068Key Projects of Jiangxi Administration of Traditional Chinese Medicine No. GZY-KJS-2023-028The present study was supported by the National Natural Science Foundation of China Grant No.82260194
6 · The paper itself

Abstract

The host's immune inflammatory response plays a crucial role in the pathogenesis of temporomandibular disorders (TMD), involving numerous innate immune effector cells to initiate the initial inflammatory response. However, the regulation of immune function and the composition of immune cells in relation to the occurrence and development of TMD remain incompletely elucidated. The genetic causality of immune cells on TMD was studied using Mendelian randomization in a two-sample study. With the help of publicly available genetic data, we examined the causal associations between 731 immune cell signatures and TMD risk. For the causal effect analysis, an inverse variance-weighted random effect model was applied. Several sensitivity analyses were conducted by using Cochran's Q tests, funnel plots, leave-one-out analyses, and Mendelian randomization-Egger intercept tests. Twenty-nine immune cell traits might be causally related to TMD. Among these traits, 11 exhibited potential positive causal effects, while the remaining 18 displayed negative causal effects on TMD. Moreover, no substantial evidence of heterogeneity or pleiotropy was observed. We have demonstrated a close genetic connection between immune cells and TMD, unraveling the underlying mechanisms linking immune dysregulation and TMD will contribute to our understanding of the pathophysiology of this debilitating condition.

Indexed as

Temporomandibular Joint DisordersGenetic Predisposition to DiseaseHumansMendelian Randomization Analysisimmune cellsMendelian randomizationsensitivity analysestemporomandibular disorders

Identifiers

PMID41465917
PMCPMC12746926

What Socratic holds

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LicenceCC BY-NC
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Registered trials

None linked

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 Socratic graph.