Evidence map›Paper›PMID 40772123›Full record

ArticleJournal of pain research2025

Causal Effects of Inflammatory Arthritis Subtypes on Fibromyalgia: A Comprehensive Mendelian Randomization Study.

Fei Wang, Dengxu Jiang, Zhong Zhang, Zhengjun Hu, Yijian Liang

Abstract read
In one paragraph

Article in Journal of pain research, 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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2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Fei WangDepartment of Spinal Surgery, Chengdu BOE Hospital, Chengdu, People's Republic of China.
Dengxu JiangDepartment of Orthopaedics, The Third People's Hospital of Chengdu/The Affiliated Hospital of Southwest Jiaotong University, Chengdu, People's Republic of China.
Zhong ZhangDepartment of Orthopaedics, The Third People's Hospital of Chengdu/The Affiliated Hospital of Southwest Jiaotong University, Chengdu, People's Republic of China.
Zhengjun HuDepartment of Orthopaedics, The Third People's Hospital of Chengdu/The Affiliated Hospital of Southwest Jiaotong University, Chengdu, People's Republic of China.
Yijian LiangDepartment of Spinal Surgery, Chengdu BOE Hospital, Chengdu, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Fibromyalgia (FM) is a chronic pain disorder characterized by widespread musculoskeletal pain and central sensitization, often co-occurring with inflammatory arthritis (IA) in clinical presentation. While observational studies suggest a higher prevalence of FM among IA patients, the causal relationship between IA and FM remains uncertain due to potential confounding factors and the possibility of reverse causation. Patients and Methods: We employed a two-sample Mendelian randomization (TSMR) approach to evaluate the causal effect of nine IA subtypes on FM, utilizing genetic summary data from large-scale genome-wide association studies (GWAS) encompassing up to 201,581 participants (exposure: IA phenotypes) and 168,378 participants (outcome: FM). The primary analysis was conducted using the Inverse-Variance Weighted (IVW) method, with sensitivity analyses assessing robustness and pleiotropy. Results: MR analysis revealed significant causal links between several IA subtypes and FM. Rheumatoid arthritis (OR 1.105, 95% CI 1.020-1.198), enteropathic arthritis (OR 1.207, 95% CI 1.123-1.299), Juvenile Idiopathic Arthritis (OR 1.307, 95% CI 1.183-1.445), and other IA subtypes showed an increased risk of FM (all Conclusion: This study provides genetic evidence supporting a causal relationship between IA subtypes and an increased risk of FM. However, no significant causal link was found between psoriatic arthritis and FM. These findings emphasize the role of immune-mediated inflammation in FM pathogenesis and highlight the differential impact of various IA subtypes on FM risk.

Indexed as

fibromyalgiagenetic associationinflammatory arthritisMendelian randomizationpsoriatic arthritisrheumatoid arthritis

Identifiers

PMID40772123
PMCPMC12326446

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