Evidence map›Paper›PMID 26494964›Full record

ReviewWorld journal of gastroenterology2015

Genetic background in nonalcoholic fatty liver disease: A comprehensive review.

Fabio Salvatore Macaluso, Marcello Maida, Salvatore Petta

Open access · bronzeAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
6.3field-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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Journal of clinical medicine · 2026
    Article
  4. Review
  5. Article
  6. Article
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  9. Review
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  11. Polymorphisms of theLife (Basel, Switzerland) · 2023
    Article
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  17. Review
  18. Review
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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

3 authors at 1 institution in 1 country.

Fabio Salvatore MacalusoFabio Salvatore Macaluso, Marcello Maida, Salvatore Petta, Section of Gastroenterology, DIBIMIS, University of Palermo, 90127 Palermo, Italy.
Marcello MaidaFabio Salvatore Macaluso, Marcello Maida, Salvatore Petta, Section of Gastroenterology, DIBIMIS, University of Palermo, 90127 Palermo, Italy.
Salvatore PettaFabio Salvatore Macaluso, Marcello Maida, Salvatore Petta, Section of Gastroenterology, DIBIMIS, University of Palermo, 90127 Palermo, Italy.
University of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the Western world, nonalcoholic fatty liver disease (NAFLD) is considered as one of the most significant liver diseases of the twenty-first century. Its development is certainly driven by environmental factors, but it is also regulated by genetic background. The role of heritability has been widely demonstrated by several epidemiological, familial, and twin studies and case series, and likely reflects the wide inter-individual and inter-ethnic genetic variability in systemic metabolism and wound healing response processes. Consistent with this idea, genome-wide association studies have clearly identified Patatin-like phosholipase domain-containing 3 gene variant I148M as a major player in the development and progression of NAFLD. More recently, the transmembrane 6 superfamily member 2 E167K variant emerged as a relevant contributor in both NAFLD pathogenesis and cardiovascular outcomes. Furthermore, numerous case-control studies have been performed to elucidate the potential role of candidate genes in the pathogenesis and progression of fatty liver, although findings are sometimes contradictory. Accordingly, we performed a comprehensive literature search and review on the role of genetics in NAFLD. We emphasize the strengths and weaknesses of the available literature and outline the putative role of each genetic variant in influencing susceptibility and/or progression of the disease.

Indexed as

Genetic VariationGenetic MarkersGenetic Predisposition to DiseaseGenome-Wide Association StudyHeredityHumansNon-alcoholic Fatty Liver DiseasePedigreePhenotypeRisk FactorsGenetic MarkersCandidate gene studiesGeneticsGenome-wide association studiesNonalcoholic fatty liver diseaseNonalcoholic steatohepatitisPatatin-like phospholipase domain-containing 3Transmembrane 6 superfamily member 2

Identifiers

PMID26494964
PMCPMC4607907
OpenAlexW1852026737

What OpenQuestion 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 OpenQuestion graph.