Evidence map›Paper›PMID 38799148›Full record

ArticleFrontiers in medicine2024

Application of two-sample Mendelian randomization method to assess the causal relationship between rheumatoid arthritis and osteoporotic fracture.

Cai Zhenyu, Chang Le, Zeng Shiyong, Lin Jinding, Liu Mingzhong, Tang Haifeng, Zeng Rongdong

Abstract read
In one paragraph

Article in Frontiers in medicine, 2024. 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

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Cai Zhenyu *Department of Orthopedics, Quanzhou First Hospital Affiliated of Fujian Medical University, Quanzhou, Fujian, China.
Chang Le *Department of Clinical Medicine, Quanzhou Medical College, Quanzhou, Fujian, China.
Zeng ShiyongMedical Research Center of Quanzhou Medical College, Quanzhou, Fujian, China.
Lin JindingDepartment of Orthopedics, Quanzhou First Hospital Affiliated of Fujian Medical University, Quanzhou, Fujian, China.
Liu MingzhongDepartment of Orthopedics, Quanzhou First Hospital Affiliated of Fujian Medical University, Quanzhou, Fujian, China.
Tang HaifengDepartment of Orthopedics, Quanzhou First Hospital Affiliated of Fujian Medical University, Quanzhou, Fujian, China.
Zeng RongdongDepartment of Orthopedics, Quanzhou First Hospital Affiliated of Fujian Medical University, Quanzhou, Fujian, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The association between rheumatoid arthritis (RA) and osteoporotic fracture has garnered considerable attention; however, the causal relationships between diseases remain uncertain. Therefore, this study employed Mendelian randomization (MR) analysis to investigate the causal effects of RA on osteoporotic fracture. Methods: The summary data for RA and osteoporotic fracture were extracted from the genome-wide association studies (GWAS) catalog and the Finn Biobank database. The database provides information about diseased and health control subjects. We searched the database for the following conditions: RA, osteoporosis (OP), and osteoporotic fractures. Entries were published by investigating centers, which had established definitions and diagnostic criteria. We downloaded and processed the data to obtain the single-nucleotide polymorphisms (SNPs) strongly associated with RA, OP, and osteoporotic fracture. RA genetic associations were obtained from the GWAS catalog, including 1961 cases and 454,387 controls. The osteoporosis of the GWAS catalog involved 991 cases and 455,357 controls, and the data of the Finn Biobank involved 8,017 cases and 391,037 controls. Genetic associations for osteoporotic fracture were taken from the Finn Biobank of 1822 cases and 311,210 controls. Independent SNPs that are significantly associated with meeting the criteria of Results: The results provided strong evidence that RA was causally and positively associated with osteoporosis from the GWAS catalog (OR = 1.16590; 95% CI: 1.04067-1.30619; Conclusion: This study showed positive causal relationships between RA and osteoporotic fracture. These results should be considered in further studies and public health measures on osteoporosis prevention strategies.

Indexed as

inflammatory diseaseMendelian randomizationosteoporosisosteoporotic fracturerheumatoid arthritis

Identifiers

PMID38799148
PMCPMC11116583

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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.