Evidence map›Paper›PMID 27837778›Full record

ReviewGastroenterology clinics of North America2016

Nonalcoholic Fatty Liver Disease: Pathophysiology and Management.

Rotonya M Carr, Amanke Oranu, Vandana Khungar

2 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in Gastroenterology clinics of North America, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 135 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
135citing papers in PubMed, 9 pooled it
11.4field-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.

NCT06491342 nacompletednot on this mapstarted 2024, after this paper: background citation

Probiotic supplement versus placebo for decrease steatosis in metabolic dysfunction-associated steatotic liver disease (masld): a multicenter, randomized, double-blind, placebo-controlled trial

TypeinterventionalSponsorPhramongkutklao College of Medicine and HospitalRan2024 to 2025Enrolled90ConditionsFatty Liver, NonalcoholicArmsProbiotic, Placebo
NCT06676813 naunknown statusnot on this mapstarted 2024, after this paper: background citation

Effect of Alternate Day Fasting Over Standard Medical Management Alone to Reverse Non-alcoholic Steatohepatitis(NASH), A Randomized Controlled Trial. FAST Trial"

TypeinterventionalSponsorInstitute of Liver and Biliary Sciences, IndiaRan2024 to 2025Enrolled72ConditionsNon Alcoholic SteatohepatitisArmsAlternate day fasting
3 · Its place in the literature

Who cites it

135 citing papers in PubMed, 9 syntheses or guidelines pooled it, 290 citations in OpenAlex.

  1. Pooled it
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  10. Trial
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  12. Review
  13. Article
  14. Burden of MASLD and liver fibrosis: evidence from Phenome India cohort.The Lancet regional health. Southeast Asia · 2026
    Article
  15. Review
  16. Review
  17. Review
  18. Article
  19. Review
  20. Article

75 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.

Rotonya M CarrDivision of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, PA, USA. Electronic address: Rotonya.Carr@uphs.upenn.edu.
Amanke OranuDivision of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, PA, USA.
Vandana KhungarDivision of Gastroenterology and Hepatology, University of Pennsylvania, Philadelphia, PA, USA.
University of Pennsylvania · US

Funding

VIRAL VECTOR COREP30DK019525 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI DOUGLAS J EPSTEIN · 1986 to 2026
$48.3M
TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
UNIVERSITY OF PENNSYLVANIA TRAINING IN GASTROENTEROLOGYT32DK007066 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI JONATHAN P KATZ · 1986 to 2026
$11.7M
The pathogenesis of insulin resistance in alcoholic liver diseaseK08AA021424 · NIAAA · UNIVERSITY OF PENNSYLVANIA · PI CARR, ROTONYA M · 2013 to 2017
$918k
NIAAA NIH HHS K08 AA021424NIDDK NIH HHS P30 DK019525NIDDK NIH HHS P30 DK050306NIDDK NIH HHS T32 DK007066
6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is an important cause of morbidity and mortality worldwide and is rapidly becoming the leading cause of end-stage liver disease and liver transplant. With a prevalence of 30% in the United States, it has reached epidemic proportions. The clinical syndrome of NAFLD spans from bland steatosis to steatohepatitis, which can progress to fibrosis and cirrhosis. The pathogenesis includes the roles of hormones, nutritional and intestinal dysbiosis, insulin resistance, lipotoxicity, hepatic inflammation, and genes. Noninvasive testing and liver biopsy indications are reviewed. Approved and investigational therapies for NAFLD and nonalcoholic steatohepatitis are outlined in this article.

Indexed as

Combined Modality TherapyGastrointestinal AgentsHumansNon-alcoholic Fatty Liver DiseaseRisk FactorsWeight Reduction ProgramsGastrointestinal AgentsHepatic steatosisLipid dropletNASHNASH therapeuticsNonalcoholic fatty liver diseaseObesityPerilipins

Identifiers

PMID27837778
PMCPMC5127277
OpenAlexW2556576707

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.