Evidence map›Paper›PMID 40098980›Full record

ArticleFrontiers in genetics2025

Causal effects of metabolites on malignant neoplasm of bone and articular cartilage: a mendelian randomization study.

Yongwei Du, Xiqiu Xiao, Fuping Liu, Wenqing Zhu, Jianwen Mo, Zhen Liu

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In one paragraph

Article in Frontiers in genetics, 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

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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.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yongwei DuDepartment of Orthopedics, First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
Xiqiu XiaoDepartment of Orthopedics, 8th People Hospital of Nankang, Ganzhou, China.
Fuping LiuDepartment of Emergency, Shangyou Hospital of Traditional Chinese Medicine, Ganzhou, China.
Wenqing ZhuDepartment of Orthopedics, First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
Jianwen MoDepartment of Orthopedics, First Affiliated Hospital of Gannan Medical University, Ganzhou, China.
Zhen LiuDepartment of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Previous research has demonstrated that metabolites play a significant role in modulating disease phenotypes; nevertheless, the causal association between metabolites and malignant malignancies of bones and joint cartilage (MNBAC)has not been fully elucidated. Methods: This study used two-sample Mendelian randomization (MR) to explore the causal correlation between 1,400 metabolites and MNBAC. Data from recent genome-wide association studies (GWAS) involving 8,299 individuals were summarized. The GWAS summary data for metabolites were acquired from the IEU Open GWAS database, while those for MNBAC were contributed by the Finnish Consortium. We employed eight distinct MR methodologies: simple mode, maximum likelihood estimator, MR robust adjusted profile score, MR-Egger, weighted mode, weighted median, MR-PRESSO and inverse variance weighted to scrutinize the causal association between metabolites engendered by each gene and MNBAC. Consequently, we evaluated outliers, horizontal pleiotropy, heterogeneity, the impact of single nucleotide polymorphisms (SNPs), and adherence to the normal distribution assumption in the MR analysis. Results: Our findings suggested a plausible causative relationship between N-Formylmethionine (FMet) levels, lignoceroylcarnitine (C24) levels, and MNBAC. We observed a nearly significant causal association between FMet levels and MNBAC within the cohort of 1,400 metabolites ( Conclusion: The occurrence of MNBAC may be causally related to metabolites. This might unveil new possibilities for investigating early detection and treatment of MNBAC.

Indexed as

articularbonecartilagecausalitymendelian randomizationmetabolitesneoplasm

Identifiers

PMID40098980
PMCPMC11911353

What Socratic holds

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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 Socratic graph.