Authors
Ming Qiu, Chongyuan Lan, Zhiyuan Xia, Hongtang Wu, Zizhuo Wang, Jiayi Wei, Minglin Lin
Published in
Archives of medical science : AMS. Volume 22. Issue 4. Pages 2123-2132. Epub Sep 06, 2025.
Abstract
Traditional longitudinal epidemiological investigations have demonstrated an association between appendectomy and the cumulative incidence of colorectal cancer (CRC). However, there is a paucity of evidence for a causal relationship between appendectomy and CRC from alternative methodologies.
We extracted summary statistics for CRC, appendectomy, 1,400 metabolites, and 91 inflammatory proteins from the largest European ancestry genome-wide association studies (GWAS) and the FinnGen study. Using two-sample bidirectional Mendelian randomization (MR), we explored the potential causal relationship between genetic liability to appendectomy and CRC. Moreover, we employed a two-step MR approach to identify metabolites and inflammatory proteins that may mediate the effects of genetic liability to appendectomy on CRC risk and analyzed their potential mediator variables. Furthermore, we used the significant single nucleotide polymorphisms (SNPs) associated with the risk of CRC due to appendectomy, searched for the nearest genes in the FinnGen, and explored the relationship between these genes and CRC prognosis by analyzing transcriptomic data from The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO).
Two-sample MR analysis revealed evidence supporting a potential causal effect of genetic liability to appendectomy on an increased risk of CRC. Two-step MR analysis identified carnitine and interleukin-13 (IL-13) as key mediators potentially involved in the positive causal relationship between genetic liability to appendectomy and CRC. Survival analysis showed that upregulation of HLX and OSR1 expression is positively correlated with poor prognosis in CRC patients.
This MR investigation provides evidence supporting a potential causal relationship between genetic liability to appendectomy and CRC, with carnitine and IL-13 potentially acting as partial mediators of this effect.
PMID:
42877678
Bibliographic data and abstract were imported from PubMed on 16 Oct 2026.
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