Evidence map›Paper›PMID 42047863›Full record

ArticleEuropean journal of nutrition2026

The effects of micronutrients on the risk of upper gastrointestinal diseases: a two-sample Mendelian randomization study.

Xu Zhang, Yu Cheng, Ru Ding, Juanjuan Gu

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Article in European journal of nutrition, 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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5 · Who and what money

Authors and funding

4 authors.

Xu ZhangDepartment of Gastroenterology, Shulan (Hangzhou) Hospital, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, 310022, People's Republic of China. 182218459@qq.com.
Yu ChengDepartment of Oncology, Xihu University First Hospital, Hangzhou, 310000, People's Republic of China.
Ru DingDepartment of Gastroenterology, Shulan (Hangzhou) Hospital, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, 310022, People's Republic of China.
Juanjuan GuDepartment of Gastroenterology, Shulan (Hangzhou) Hospital, Shulan International Medical College, Zhejiang Shuren University, Hangzhou, 310022, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study investigates the causal relationship between 12 micronutrients and 6 upper gastrointestinal diseases using a two-sample Mendelian randomization (MR) approach.

methodsGenome-wide association studies (GWAS) summary data for upper gastrointestinal diseases were obtained from FinnGen, and micronutrient data were sourced from the IEU OpenGWAS database. The primary analysis method was inverse variance weighted (IVW) method, supplemented by MR-Egger, weighted median, and weighted mode methods. Radial MR and iterative leave-one-out analyses were performed to identify and remove outlier single nucleotide polymorphisms (SNPs), and sensitivity analyses were conducted to assess the stability and reliability of the results.

resultsThe MR analysis of IVW results revealed significant causal associations between genetically predicted selenium (OR = 1.08, 95% CI 1.01-1.15, P = 0.02) and vitamin B12 (OR = 0.60, 95% CI 0.43-0.83, P = 0.003) with chronic gastritis. After outlier removal, several previously non-significant associations became statistically significant: potassium with gastric ulcer (OR = 0.64, P = 0.030), zinc with gastric ulcer (OR = 1.12, P = 0.009), selenium with gastroesophageal reflux disease (OR = 1.05, P = 0.038), and vitamin B6 with gastric cancer (OR = 0.36, P = 0.018). All significant findings remained robust across sensitivity analyses, with no evidence of heterogeneity or horizontal pleiotropy after outlier removal.

conclusionThis MR study suggests that genetically predicted selenium levels may increase chronic gastritis risk, while vitamin B12 may be protective. Novel associations were identified for potassium, zinc, selenium, and vitamin B6 after outlier removal, providing new insights into the roles of micronutrients in upper gastrointestinal diseases.

Indexed as

Gastrointestinal DiseasesMendelian Randomization AnalysisMicronutrientsGenome-Wide Association StudyHumansPolymorphism, Single NucleotideRisk FactorsSeleniumMicronutrientsSeleniumChronic gastritisGastrointestinal oncologyGenetic predispositionNutritional epidemiologySingle nucleotide polymorphismTrace elements

Identifiers

PMID42047863
PMCPMC13124885

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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.