Evidence map›Paper›PMID 41193695›Full record

ReviewNature reviews. Endocrinology2026

Sarcopenia and MASLD: novel insights and the future.

Chang-Hai Liu, Qing-Min Zeng, Won Kim, Seung Up Kim, Zobair M Younossi, Giovanni Targher, Christopher D Byrne, Christos S Mantzoros, Phunchai Charatcharoenwitthaya, Isabelle Anne Leclercq and 3 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. A probioticGut microbes · 2026
    Article
  2. Review
  3. Review
  4. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Chang-Hai Liu *Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0003-3901-3039
Qing-Min Zeng *Center of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0001-5162-222X
Won KimDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-2926-1007
Seung Up KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-9658-8050
Zobair M YounossiCenter for Liver Disease, Department of Medicine, Inova Fairfax Medical Campus, Falls Church, VA, USA.ORCID http://orcid.org/0000-0001-9313-577X
Giovanni TargherDepartment of Medicine, University of Verona, Verona, Italy.ORCID http://orcid.org/0000-0002-4325-3900
Christopher D ByrneSouthampton National Institute for Health and Care Research Biomedical Research Centre, University Hospital Southampton and University of Southampton, Southampton General Hospital, Southampton, UK.ORCID http://orcid.org/0000-0001-6322-7753
Christos S MantzorosDepartment of Internal Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0003-3755-8158
Phunchai CharatcharoenwitthayaDivision of Gastroenterology, Department of Medicine, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.ORCID http://orcid.org/0000-0002-8334-0267
Isabelle Anne LeclercqLaboratory of Hepato-Gastroenterology, Institute of Experimental and Clinical Research, UCLouvain, Brussels, Belgium.ORCID http://orcid.org/0000-0001-7934-6693
Manuel Romero-GómezDigestive Diseases Unit, Virgen del Rocío University Hospital, SeLiver group at Institute of Biomedicine of Seville, University of Seville, Seville, Spain.ORCID http://orcid.org/0000-0001-8494-8947
Hong TangCenter of Infectious Diseases, West China Hospital, Sichuan University, Chengdu, China. tanghong6198@wchscu.cn.ORCID http://orcid.org/0000-0002-9790-6225
Ming-Hua ZhengMAFLD Research Center, Department of Hepatology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China. zhengmh@wmu.edu.cn.ORCID http://orcid.org/0000-0003-4984-2631

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD; previously known as non-alcoholic fatty liver disease) is the leading cause of chronic liver disease worldwide and is closely linked to the obesity epidemic. MASLD often coexists with sarcopenia, an age-related loss of muscle mass and muscle function. These conditions are closely connected, and metabolic syndrome and its associated metabolic factors have a crucial role in their relationship. Metabolic syndrome considerably affects the risk and progression of MASLD and sarcopenia and promotes their development through various mechanisms. This Review explores the epidemiological link between MASLD and sarcopenia and the effect of metabolic syndrome and its components on both conditions, summarizing current treatment strategies and emerging evidence. To effectively manage both MASLD and sarcopenia, it is crucial to incorporate the five metabolic risk factors of metabolic syndrome into risk assessment and treatment strategies. Future research should continue to investigate the mechanisms linking metabolic syndrome, MASLD and sarcopenia. Establishing standardized definitions of sarcopenia for patients with MASLD and developing personalized treatment strategies through precision medicine will improve diagnosis, interventions and overall patient outcomes.

Indexed as

Metabolic SyndromeNon-alcoholic Fatty Liver DiseaseSarcopeniaHumansObesityRisk Factors

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.