Evidence map›Paper›PMID 41928880›Full record

ReviewFrontiers in endocrinology2026

Lipid metabolism-MAFLD crosstalk: mechanisms and therapy.

Bojia Li, Shengai Piao, Yin Fu, Qiang Fu, Peiyao Qin, Weitai Kong, Yidi Ma, Zhe Zhang, Xue Fang, Xiaoyang Hu

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Bojia Li *Basic Medical College, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Shengai Piao *Department of Pediatrics, The Second Affiliated Hospital of Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Yin FuBasic Medical College, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Qiang FuBasic Medical College, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Peiyao QinHeilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Weitai KongHeilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Yidi MaBasic Medical College, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Zhe ZhangBasic Medical College, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Xue FangBasic Medical College, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.
Xiaoyang HuBasic Medical College, Heilongjiang University of Chinese Medicine, Harbin, Heilongjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic dysfunction-associated fatty liver disease (MAFLD) has become the most prevalent chronic liver disorder worldwide, encompassing a spectrum that ranges from simple steatosis to metabolic dysfunction-associated steatohepatitis (MASH) and hepatic fibrosis. However, its precise pathogenic mechanisms remain incompletely understood, and effective, specific pharmacological treatments are still lacking. Disruption of hepatic lipid metabolic homeostasis represents a central event in the onset and progression of MAFLD. With advances in lipidomics and metabolomics, researchers can now more accurately delineate the aberrant accumulation of specific lipid species within hepatocytes and their pivotal roles in triggering insulin resistance, oxidative stress, and inflammatory responses. This review systematically summarizes the core mechanisms by which hepatic lipid metabolic dysregulation drives MAFLD progression and highlights recent advances in therapeutic strategies targeting lipotoxic pathways, metabolic reprogramming, and related molecular targets. These insights aim to provide a theoretical basis and new perspectives for future research and clinical intervention in this field.

Indexed as

Lipid MetabolismNon-alcoholic Fatty Liver DiseaseAnimalsHumansInsulin ResistanceOxidative Stresslipid metabolismlipotoxicitymechanismsmetabolic dysfunction-associated fatty liver diseasetherapeutic perspectives

Identifiers

PMID41928880
PMCPMC13038599

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.