Evidence map›Paper›PMID 42028921›Full record

ReviewThe Kaohsiung journal of medical sciences2026

Metabolic Dysfunction-Associated Steatotic Liver Disease and Obesity: Pathogenesis, Diagnostics, Risk Stratification, and Therapeutic Approach.

Beom Kyung Kim

Abstract readReview
In one paragraph

Review in The Kaohsiung journal of medical sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

1 author.

Beom Kyung KimDepartment of Internal Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

Funding

Korean Association for the Study of the Liver KASL2025-01
6 · The paper itself

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) has emerged as the most prevalent chronic liver disease worldwide, closely linked to the global rising incidence of obesity and metabolic syndrome. This review synthesizes current evidence on the pathogenesis, gut-liver axis, and multidisciplinary management of MASLD within the context of obesity. The pathophysiology of MASLD is multifactorial and involves insulin resistance, adipose tissue dysfunction, chronic low-grade inflammation, and alterations in lipid metabolism, all of which contribute to hepatic steatosis and disease progression. Recent research has increasingly focused on the gut-liver axis, where dysbiosis, increased intestinal permeability, endotoxemia, and microbial metabolites significantly influence hepatic inflammation and fibrogenesis. From a therapeutic perspective, lifestyle modifications remain foundational to management; however, their long-term sustainability is often limited. Pharmacologic interventions targeting metabolic pathways, such as incretin-based therapies, demonstrate promising efficacy in enhancing both hepatic and systemic outcomes. Given the substantial clinical and socioeconomic burden posed by MASLD, a multidisciplinary approach that integrates perspectives from hepatology, endocrinology, nutrition, and public health is essential. Future research should prioritize personalized risk assessment, early intervention in high-risk populations, and policy-level strategies to mitigate the growing impact of metabolic liver disease.

Indexed as

metabolic dysfunction‐associated steatotic liver diseaseobesitypathogenesistherapy

Identifiers

PMID42028921
PMCPMC13399682

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.