Evidence map›Paper›PMID 35806284›Full record

ReviewInternational journal of molecular sciences2022

Mitochondrial Dysfunction Plays Central Role in Nonalcoholic Fatty Liver Disease.

Raghu Ramanathan, Ahmad Hassan Ali, Jamal A Ibdah

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 118 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
118citing papers in PubMed, 2 pooled it
21.0field-weighted citation impact, top 1% of its field
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

118 citing papers in PubMed, 2 syntheses or guidelines pooled it, 144 citations in OpenAlex.

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  4. Vanadium(IV)-chlorodipicolinate alleviates hepatic steatosis via the AMPK/PGC-1α/CPT1a axis.Biometals : an international journal on the role of metal ions in biology, biochemistry, and medicine · 2026
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  9. Polyphenol-RichMolecules (Basel, Switzerland) · 2026
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58 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Raghu RamanathanDivision of Gastroenterology and Hepatology, University of Missouri, Columbia, MO 65212, USA.ORCID 0000-0002-6688-7359
Ahmad Hassan AliDivision of Gastroenterology and Hepatology, University of Missouri, Columbia, MO 65212, USA.ORCID 0000-0001-8553-7744
Jamal A IbdahDivision of Gastroenterology and Hepatology, University of Missouri, Columbia, MO 65212, USA.ORCID 0000-0002-5646-9014
Harry S. Truman Memorial Veterans' Hospital · US

Funding

Role of non-genomic regulation of mitochondrial trifunctional protein in NAFLDI01BX004710 · VA · HARRY S. TRUMAN MEMORIAL VA HOSPITAL · PI IBDAH, JAMAL A · 2020 to 2023
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BLRD VA I01 BX004710Veterans Administration 1BX 004710
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is a global pandemic that affects one-quarter of the world's population. NAFLD includes a spectrum of progressive liver disease from steatosis to nonalcoholic steatohepatitis (NASH), fibrosis, and cirrhosis and can be complicated by hepatocellular carcinoma. It is strongly associated with metabolic syndromes, obesity, and type 2 diabetes, and it has been shown that metabolic dysregulation is central to its pathogenesis. Recently, it has been suggested that metabolic- (dysfunction) associated fatty liver disease (MAFLD) is a more appropriate term to describe the disease than NAFLD, which puts increased emphasis on the important role of metabolic dysfunction in its pathogenesis. There is strong evidence that mitochondrial dysfunction plays a significant role in the development and progression of NAFLD. Impaired mitochondrial fatty acid oxidation and, more recently, a reduction in mitochondrial quality, have been suggested to play a major role in NAFLD development and progression. In this review, we provide an overview of our current understanding of NAFLD and highlight how mitochondrial dysfunction contributes to its pathogenesis in both animal models and human subjects. Further we discuss evidence that the modification of mitochondrial function modulates NAFLD and that targeting mitochondria is a promising new avenue for drug development to treat NAFLD/NASH.

Indexed as

Carcinoma, HepatocellularDiabetes Mellitus, Type 2Liver NeoplasmsNon-alcoholic Fatty Liver DiseaseAnimalsFibrosisHumansLiverMitochondrialivermitochondrial dysfunctionmitophagynonalcoholic fatty liver diseaseβ-oxidation

Identifiers

PMID35806284
PMCPMC9267060
OpenAlexW4283738313

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.