Evidence map›Paper›PMID 40847308›Full record

ArticleNutrition journal2025

Development and validation of a multimodal model integrating gut microbiota and metabolite for identifying sarcopenia in patients with MASLD: a study from two centers in China.

Sizhe Wan, Mingkai Li, Wanjun Li, Yuexiang Ren, Yuankai Wu, Qingtian Luo, Wei Gong

Abstract readValidation StudyMulticenter Study
In one paragraph

Article in Nutrition journal, 2025. 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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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Sizhe Wan *Department of Gastroenterology, Shenzhen Hospital, Southern Medical University, Shenzhen, 518000, People's Republic of China.
Mingkai Li *Department of Gastroenterology, Shenzhen Hospital, Southern Medical University, Shenzhen, 518000, People's Republic of China.
Wanjun LiDepartment of Gastroenterology, Shenzhen Hospital, Southern Medical University, Shenzhen, 518000, People's Republic of China.
Yuexiang RenDepartment of Pathology, The Third Affiliated Hospital of Sun Yat-Sen University, Guangzhou, 510630, People's Republic of China.
Yuankai WuDepartment of Infection disease, The Third Affiliated Hospital of Sun Yat- Sen University, Guangzhou, 510630, People's Republic of China.
Qingtian Luo *Department of Gastroenterology and Endoscopy Center, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, 518052, People's Republic of China. qingtian881215@qq.com.
Wei Gong *Department of Gastroenterology, Shenzhen Hospital, Southern Medical University, Shenzhen, 518000, People's Republic of China. gongweismu@163.com.

Funding

Basic and Applied Basic Research Foundation of Guangdong Province 2021A1515110799National Natural Science Foundation of China 82401448Shenzhen Nanshan District Science and Technology Plan Funding Program NSZD2024015Shenzhen Science and Technology Program JCYJ20240813145414019
6 · The paper itself

Abstract

BACKGROUND AND

aimsMetabolic dysfunction-associated steatotic liver disease (MASLD) is a common chronic liver disease worldwide, and identifying sarcopenia is critical since it is correlated with poor prognosis. Little is known about mechanistic alterations in the pathogenesis of this condition. This study aimed to explore the alterations in the gut microbiome and metabolome in patients with sarcopenia and develop a predictive model.

methodsWe performed shotgun metagenomic sequencing and untargeted liquid chromatography-mass spectrometry (LC-MS) metabolomic profiling of fecal samples from the discovery cohort (70 patients without sarcopenia, 30 with sarcopenia). A microbiota-metabolite score (MM score) was developed using LASSO regression to identify key microbiome and metabolite features associated with sarcopenia. A multimodal prediction model incorporating the MM score and clinical parameters was then developed and validated in an independent cohort of 50 patients.

resultsPatients with sarcopenia exhibited altered gut microbiota and metabolomic profiles, with significantly elevated Enterococcus faecium and Bacteroides vulgatus species, and elevated bile acids. Integration of the MM score with clinical variables (age, BMI, AST, presence of diabetes) resulted in a multimodal model with an AUC of 0.911, outperforming existing models including FIB-4 (AUC 0.765), NFS (AUC 0.724), and using only MM score alone (AUC 0.818). In a prospective validation cohort, the multimodal model demonstrated superior diagnostic performance (AUC 0.897), with significant improvements in clinical utility as evidenced by calibration curves and decision curve analysis.

conclusionsThis study developed a novel multimodal model combining gut microbiome, metabolomics, and clinical data for accurate prediction of sarcopenia, offering a promising approach for early identification of high-risk MASLD patients with sarcopenia.

Indexed as

Gastrointestinal MicrobiomeMetabolomeNon-alcoholic Fatty Liver DiseaseSarcopeniaAgedChinaFecesFemaleHumansMaleMetabolomicsMiddle AgedGut microbiotaMetabolic dysfunction-associated steatotic liver diseaseMetaboliteSarcopeniaShotgun metagenomic sequencingUntargeted liquid chromatography-mass spectrometry (LC-MS) metabolomics

Identifiers

PMID40847308
PMCPMC12372311

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