Evidence map›Paper›PMID 32638417›Full record

ReviewAlimentary pharmacology & therapeutics2020

Review article: the impact of liver-directed therapies on the atherogenic risk profile in non-alcoholic steatohepatitis.

Margery A Connelly, Jonathan Velez Rivera, John R Guyton, Mohammad Shadab Siddiqui, Arun J Sanyal

Open access · hybridAbstract readReview
In one paragraph

Review in Alimentary pharmacology & therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Observational
  4. Statins in Non-alcoholic Steatohepatitis.Frontiers in cardiovascular medicine · 2021
    Review
  5. Article
  6. Review
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 1 country.

Margery A ConnellyLaboratory Corporation of America Holdings (LabCorp), Morrisville, NC, USA.ORCID https://orcid.org/0000-0002-3917-592X
Jonathan Velez RiveraDivision of Endocrinology, Metabolism, and Nutrition, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
John R GuytonDivision of Endocrinology, Metabolism, and Nutrition, Department of Medicine, Duke University Medical Center, Durham, NC, USA.
Mohammad Shadab SiddiquiDivision of Gastroenterology and Hepatology, Virginia Commonwealth University, Richmond, VA, USA.
Arun J SanyalDivision of Gastroenterology and Hepatology, Virginia Commonwealth University, Richmond, VA, USA.ORCID https://orcid.org/0000-0001-8682-5748
Duke University · USVirginia Commonwealth University · USLabCorp (United States) · US

Funding

LIPIDOMICS BASED DIAGNOSTICS FOR NONALCOHOLIC STEATOHEPATITISR01DK105961 · NIDDK · VIRGINIA COMMONWEALTH UNIVERSITY · PI DENNIS, EDWARD A, SANYAL, ARUN J · 2015 to 2018
$2.8M
NIDDK NIH HHS R01 DK105961NIH HHS R01 DK 105961
6 · The paper itself

Abstract

backgroundPatients with non-alcoholic fatty liver disease (NAFLD), the most common cause of chronic liver disease, are at higher risk of cardiovascular disease (CVD) and associated mortality. Therefore, it is important to understand how new therapies for non-alcoholic steatohepatitis (NASH) may impact CVD risk factors in these patients.

aimsTo summarise the effects of drug therapies on lipid and lipoprotein levels in patients with NASH and provide insight into the potential mechanisms for the observed changes.

methodsPubMed searches of the literature were performed and results were compiled.

resultsRecent clinical trials have highlighted the safety and efficacy of drug candidates for the treatment of NASH. Several agents have shown improvements in the histological features of NASH and liver function. Pioglitazone, a drug that is currently available for type 2 diabetes and may be useful for NASH, exhibits beneficial effects on lipids. However, agents such as farnesoid X receptor agonists, which are in development for NASH, may adversely affect circulating lipids and lipoproteins.

conclusionsNASH is a multi-system disease with a disproportionate CVD burden. Current and future drugs for NASH have had variable impact on the atherogenic risk profile. Potential co-administration of a statin may help mitigate the negative impact of some of these therapies on lipid and lipoprotein levels.

Indexed as

AtherosclerosisCardiovascular DiseasesDrug DevelopmentHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHypolipidemic AgentsLipid MetabolismLiverLiver Function TestsNon-alcoholic Fatty Liver DiseasePioglitazoneRisk FactorsHydroxymethylglutaryl-CoA Reductase InhibitorsHypolipidemic AgentsPioglitazone

Identifiers

PMID32638417
PMCPMC7497003
OpenAlexW3041448284

What Socratic holds

Texttitle and abstract
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 Socratic graph.