Evidence map›Paper›PMID 35286799›Full record

ReviewClinical and molecular hepatology2022

Old and new classes of glucose-lowering agents as treatments for non-alcoholic fatty liver disease: A narrative review.

Lei Miao, Jing Xu, Giovanni Targher, Christopher D Byrne, Ming-Hua Zheng

Open access · goldAbstract readReview
In one paragraph

Review in Clinical and molecular hepatology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
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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

5 authors at 3 institutions in 3 countries.

Lei MiaoDepartment of Gastroenterology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Jing XuDepartment of Endocrinology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Giovanni TargherSection of Endocrinology, Diabetes and Metabolism, Department of Medicine, University and Azienda Ospedaliera Universitaria Integrata of Verona, Verona, Italy.
Christopher D ByrneSouthampton National Institute for Health Research Biomedical Research Centre, University Hospital Southampton, Southampton General Hospital, Southampton, UK.
Ming-Hua ZhengNAFLD Research Center, Department of Hepatology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Wenzhou Medical University · CNAzienda Ospedaliera Universitaria Integrata Verona · ITSouthampton General Hospital · GB

Funding

High Level Creative Talents from the Department of Public Health in Zhejiang Province S2032102600032National Natural Science Foundation of China 82070588Project of New Century 551 Talent Nurturing in WenzhouSouthampton NIHR Biomedical Research Centre IS-BRC-20004University School of Medicine of Verona
6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) has become the most common chronic liver disease with a global prevalence of about 55% in people with type 2 diabetes mellitus (T2DM). T2DM, obesity and NAFLD are three closely inter-related pathological conditions. In addition, T2DM is one of the strongest clinical risk factors for the faster progression of NAFLD to non-alcoholic steatohepatitis (NASH), cirrhosis and hepatocellular carcinoma. Increasing evidence suggests that newer classes of glucose-lowering drugs, such as peroxisome proliferator-activated receptor agonists, glucagon-like peptide-1 receptor agonists, dipeptidyl peptidase-4 inhibitors or sodium-glucose cotransporter-2 inhibitors, could reduce the rates of NAFLD progression. This narrative review aims to briefly summarize the recent results from randomized controlled trials testing the efficacy and safety of old and new glucose-lowering drugs for the treatment of NAFLD or NASH in adults both with and without coexisting T2DM.

Indexed as

Diabetes Mellitus, Type 2Non-alcoholic Fatty Liver DiseaseSodium-Glucose Transporter 2 InhibitorsDipeptidyl-Peptidases and Tripeptidyl-PeptidasesGlucagon-Like Peptide-1 ReceptorGlucoseHumansPeroxisome Proliferator-Activated ReceptorsSodiumDipeptidyl-Peptidases and Tripeptidyl-PeptidasesGlucagon-Like Peptide-1 ReceptorGlucosePeroxisome Proliferator-Activated ReceptorsSodiumSodium-Glucose Transporter 2 InhibitorsGlucose-lowering drugsMetabolic dysfunctionassociated fatty liver diseaseNon-alcoholic fatty liver diseaseType 2 diabetes mellitus

Identifiers

PMID35286799
PMCPMC9597221
OpenAlexW4221005344

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.