Evidence map›Paper›PMID 34667947›Full record

ReviewJHEP reports : innovation in hepatology2021

New targets for NAFLD.

Lucia Parlati, Marion Régnier, Hervé Guillou, Catherine Postic

Open access · goldAbstract readReview
In one paragraph

Review in JHEP reports : innovation in hepatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 1 pooled it
20.9field-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

108 citing papers in PubMed, 1 synthesis or guideline pooled it, 161 citations in OpenAlex.

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  18. Targeting Metabolism: Innovative Therapies for MASLD Unveiled.International journal of molecular sciences · 2025
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48 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

4 authors at 3 institutions in 2 countries.

Lucia ParlatiUniversité de Paris, Institut Cochin, CNRS, INSERM, F- 75014 Paris, France.
Marion RégnierUCLouvain, Université catholique de Louvain, Walloon Excellence in Life Sciences and BIOtechnology, Louvain Drug Research Institute, Metabolism and Nutrition Research Group, Brussels, Belgium.
Hervé GuillouToxalim, Université de Toulouse, INRA, ENVT, INP-Purpan, UPS, Toulouse 31027, France.
Catherine PosticUniversité de Paris, Institut Cochin, CNRS, INSERM, F- 75014 Paris, France.
Institut Cochin · FRToxalim Research Centre in Food Toxicology · FRUCLouvain · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) is a growing cause of chronic liver disease worldwide. It is characterised by steatosis, liver inflammation, hepatocellular injury and progressive fibrosis. Several preclinical models (dietary and genetic animal models) of NAFLD have deepened our understanding of its aetiology and pathophysiology. Despite the progress made, there are currently no effective treatments for NAFLD. In this review, we will provide an update on the known molecular pathways involved in the pathophysiology of NAFLD and on ongoing studies of new therapeutic targets.

Indexed as

ACC, acetyl-CoA carboxylaseanimal modelsASK1, apoptosis signal-regulating kinase 1CAP, controlled attenuation parameterChREBPChREBP, carbohydrate responsive element–binding proteinFAS, fatty acid synthaseFFA, free fatty acidFGF21, fibroblast growth factor-21FXRFXR, farnesoid X receptorGGT, gamma glutamyltransferaseglucotoxicityHCC, hepatocellular carcinomaHFD, high-fat dietHSC, hepatic stellate cellsHSL, hormone-sensitive lipaseHVPG, hepatic venous pressure gradientIL-, interleukin-JNK, c-Jun N-terminal kinaselipotoxicityLXRLXR, liver X receptorMCD, methionine- and choline-deficientMUFA, monounsaturated fatty acidsNAFLDNAFLD, non-alcoholic fatty liver diseaseNASHNASH, non-alcoholic steatohepatitisNEFANEFA, non-esterified fatty acidPhf2, histone demethylase plant homeodomain finger 2PPARαPPARα, peroxisome proliferator-activated receptor-αPUFAs, polyunsaturated fatty acidsPY, persons/yearsRCT, randomised controlled trialSCD1, stearoyl-CoA desaturase-1SFA, saturated fatty acidSREBP-1cSREBP-1c, sterol regulatory element–binding protein-1cTCA, tricarboxylic acidTLR4, Toll-like receptor 4TNF-α, tumour necrosis factor-αVLDL, very low-density lipoprotein

Identifiers

PMID34667947
PMCPMC8507191
OpenAlexW3190185780

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.