Evidence map›Paper›PMID 31889754›Full record

ReviewJournal of clinical and experimental hepatology

Antidiabetic Drugs and Statins in Nonalcoholic Fatty Liver Disease.

Sneha Kothari, Hiteshi Dhami-Shah, Samir R Shah

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of clinical and experimental hepatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.5field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 65 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Current developments in nutrition · 2024
    Article
  8. Review
  9. Carvedilol impairs bile acid homeostasis in mice: implication for nonalcoholic steatohepatitis.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Foods (Basel, Switzerland) · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. Article
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.

Sneha KothariGlobal Hospitals Mumbai, India.
Hiteshi Dhami-ShahDepartment of Hepatology, Global Hospitals, Mumbai, India.
Samir R ShahDepartment of Hepatology, Global Hospitals, Mumbai, India.
Global Hospitals · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) has become the most prevalent liver disease worldwide. Despite its high prevalence and rising incidence, there are currently no specific targeted pharmacotherapies approved by the Food and Drug Administration (FDA) for nonalcoholic steatohepatitis (NASH). Current therapies for patients with NAFLD include lifestyle modification. Vitamin E and pioglitazone are recommended for those confirmed to have NASH. However, there are concerns about the long-term safety of both pioglitazone and vitamin E in higher doses. Metformin is essential for managing the abnormal metabolic parameters in patients with NAFLD. Glucagon-like peptide-1 analogue, sodium-dependent glucose cotransporter inhibitors, and peroxisome proliferator-activated receptor agonists have shown benefits in improving metabolic parameters and reducing hepatic lipid accumulation and inflammation. However, the role of these antidiabetic agents in specifically reversing NASH needs to be established. Indeed, statins have been underprescribed in patients with NASH owing to fear of hepatotoxicity despite coronary artery disease being a common cause of death in patients with NAFLD. Statins reduce the risk of cardiovascular morbidity and mortality in patients with NASH and dyslipidemia. However, their use specifically for treatment of NASH needs further evaluation. Optimizing the control of risk factors remains the main strategy for treatment until targeted pharmacotherapies for NASH are available.

Indexed as

5′ adenosine monophosphate-activated protein kinase, AMPKAlanine Aminotransferase, ALTAspartate transaminase, ASTbody mass index, BMIcardiovascular disease, CVDdipeptidyl peptidase-4 inhibitors, DPP-4iEASL/EASD/EASO, European Association for the Study of the Liver/European Association for the Study of Diabetes/European Association for the Study of ObesityGLP-1 receptor agonistglucagon-like peptide-1 receptor agonist, GLP-1RALFT, liver function testmetabolic syndrome, MetSnonalcoholic fatty liver diseaseNon alcoholic fatty liver disease, NAFLDNonalcoholic steatohepatitis, NASHPeroxisome proliferator-activated receptor agonist, PPAR agonistPPAR agonistSGLT2 inhibitorsSodium-dependent glucose cotransporter inhibitor, SGLT-2istatinstype 2 diabetes, T2D

Identifiers

PMID31889754
PMCPMC6926203
OpenAlexW2953477699

What Socratic holds

Textmetadata
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 Socratic graph.