Evidence mapPaperPMID 42499064Full record

ArticleMedicine2026

Causal effects of gut microbiota on physical growth and cognitive performance via plasma metabolites: A Mendelian randomization study.

Fang-Fang Yang, Kai-Peng Luo, Zhi-Jie Liang, Zhuo-Xin Ou, Sheng-Lan Li, Jia-Mei Liang, Yu-Nan Lin

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Article in Medicine, 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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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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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

7 authors.

Fang-Fang YangThe First Clinical College, Guangxi Medical University, Nanning, China.ORCID 0009-0000-8016-9225
Kai-Peng LuoThe First Clinical College, Guangxi Medical University, Nanning, China.
Zhi-Jie LiangDepartment of Anesthesiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Zhuo-Xin OuDepartment of Anesthesiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Sheng-Lan LiDepartment of Anesthesiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Jia-Mei LiangDepartment of Anesthesiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Yu-Nan LinDepartment of Anesthesiology, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Herein, we used plasma metabolites as potential mediators to determine the causal relationship between gut microbiota, cognitive performance, and physical growth. The relationship between gut microbiota and these 3 factors has not been accurately established in human experiments and studies; our study may provide some new insights. Two-sample Mendelian randomization was performed to evaluate causal associations between gut microbial composition and 3 core phenotypes (height, body weight, cognitive performance). Publicly available GWAS-identified significant SNPs were applied as instrumental variables, and mediation analyses were further conducted to quantify the proportional metabolite-mediated effects. Causal analyses confirmed 3 microbial taxa associated with height: Enterococcus B showed a positive correlation, while CAG-485 and Rhodococcus exhibited negative effects. Six microbial signatures were significantly linked to body weight, with four taxa displaying protective associations and 2 showing adverse impacts. Rhodanobacter and UBP9 were positively associated with cognitive performance. Mediation analyses verified that distinct microbial taxa regulated the 3 phenotypes through specific metabolites, with varied mediating percentages for growth and cognitive outcomes. The study findings highlight the metabolite pathways of the gut microbiota as potential targets for precise nutritional interventions, growth optimization, and cognitive health enhancement.

Indexed as

CognitionGastrointestinal MicrobiomeBody HeightBody WeightGenome-Wide Association StudyHumansMendelian Randomization AnalysisPhenotypePolymorphism, Single Nucleotidecognitive performancegut microbiotaMendelian randomizationphysical growthplasma metabolites

Identifiers

PMID42499064
PMCPMC13406128

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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.