Evidence map›Paper›PMID 41872385›Full record

ArticleDiscover oncology2026

Causal effects of drug exposure on gastric cancer risk: a Mendelian randomization study involving 23 commonly used medications in the European population.

Ganlu Zhang, Jindan Xia, Yi Zhou, Jin Qian, Dashan Yin, Wangxia Lv

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Article in Discover oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ganlu Zhang *Department of Oncology, Zhejiang Hospital, Hangzhou, 310030, China.
Jindan Xia *Department of Oncology, The First People's Hospital of Yuhang District, Hangzhou, 311100, China.
Yi ZhouThe Second School of Clinical Medical, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Jin QianThe Second School of Clinical Medical, Zhejiang Chinese Medical University, Hangzhou, 310053, China.
Dashan YinSchool of Medicine, Zhejiang University, Hangzhou, 310058, China.
Wangxia LvDepartment of Colorectal Medicine, Zhejiang Cancer Hospital, No. 1, Banshan East Road, Gongshu District, Hangzhou, 310022, Zhejiang, P.R. China. lvwx@zjcc.org.cn.

Funding

Medical Science and Technology Project of Zhejiang Province 2024KY594The independently deployed project of Chinese Academy of Sciences Hangzhou Institute of Medicine 2024ZZBS20
6 · The paper itself

Abstract

backgroundPrevious studies have indicated potential associations between some drugs and cancer risk, but the causal relationship with gastric cancer remains unclear. This study aimed to explore the causality between 23 medications and gastric cancer using Mendelian randomization (MR) analysis.

methodsA two-sample MR analysis was conducted to assess the causal effects of medications on gastric cancer risk. Primary causal estimates were derived using the inverse variance weighted method, complemented by weighted median, MR-Egger, simple mode, and weighted mode methods. Sensitivity analyses (MR-PRESSO, MR-Egger regression, Cochran's Q test, leave-one-out analysis, Steiger filtering) validated the robustness of significant findings. Furthermore, enrichment analysis was used to analyze the biological functions of medication-related genes.

resultsAfter Bonferroni correction, anti-migraine formulations (OR, 0.83 [95% CI, 0.70-0.98]; p = 0.0253), drugs acting on the renin-angiotensin system (OR, 0.83 [95% CI, 0.73-0.94]; p = 0.0035), and adrenergic drugs/inhalants (OR, 0.86 [95% CI, 0.76-0.98]; p = 0.0212) were found to be suggestively associated with a reduced risk of gastric cancer in European populations. Sensitivity analyses revealed no significant heterogeneity or horizontal pleiotropy (all p > 0.05), and the Steiger filtering excluded reverse causality-related bias, collectively supporting the robustness of the primary findings. No significant causal relationship was found between the remaining 20 medications and gastric cancer risk. The causal association between 23 medications and gastric cancer differed between East Asian and European populations, indicating that the applicability of the causalities to non-European populations remains limited.

conclusionThis study revealed negative genetically proxied associations related to drug targets of anti-migraine formulations, drugs acting on the renin-angiotensin system, and adrenergic drugs/inhalants with gastric cancer risk. These hypothesis-generating findings may help inform future mechanistic and clinical investigations.

Indexed as

23 medicationsCausal relationshipGastric cancerMendelian randomization

Identifiers

PMID41872385
PMCPMC13133289

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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.