Evidence map›Paper›PMID 26346943›Full record

ArticleGastroenterology research and practice2015

The Frequent Adiponutrin (PNPLA3) Variant p.Ile148Met Is Associated with Early Liver Injury: Analysis of a German Pediatric Cohort.

Marcin Krawczyk, Roman Liebe, Ina B Maier, Anna Janina Engstler, Frank Lammert, Ina Bergheim

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Article in Gastroenterology research and practice, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 11 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors at 3 institutions in 2 countries.

Marcin KrawczykDepartment of Medicine II, Saarland University Medical Center, Saarland University, 66421 Homburg, Germany ; Laboratory of Metabolic Liver Diseases, Department of General, Transplant and Liver Surgery, Medical University of Warsaw, 02-091 Warsaw, Poland.
Roman LiebeDepartment of Medicine II, Saarland University Medical Center, Saarland University, 66421 Homburg, Germany ; Klinik für Innere Medizin II, Klinikum Mannheim, Universität Heidelberg, 68135 Mannheim, Germany.
Ina B MaierDepartment of Nutritional Medicine, Universität Hohenheim, 70599 Stuttgart, Germany.
Anna Janina EngstlerDepartment of Nutritional Sciences, SD Model Systems of Molecular Nutrition, Friedrich-Schiller-Universität, 07743 Jena, Germany.
Frank LammertDepartment of Medicine II, Saarland University Medical Center, Saarland University, 66421 Homburg, Germany.
Ina BergheimDepartment of Nutritional Sciences, SD Model Systems of Molecular Nutrition, Friedrich-Schiller-Universität, 07743 Jena, Germany.
Saarland University · DEFriedrich Schiller University Jena · DEUniversity of Hohenheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction. The common adiponutrin (PNPLA3) variant p.Ile148Met is associated with liver injury. Here, we investigate the association of this polymorphism with hepatic and metabolic traits in a pediatric cohort. Patients and Methods. The study cohort comprised 142 German children (age 5-9 years, 98 overweight, 19 children with NAFLD). Results. Overweight children presented with increased serum ALT (P = 0.001) and GGT (P < 0.001) activities. ALT activities differed significantly (P = 0.02) between carriers of different PNPLA3 genotypes in the entire study cohort, in normal weight children (P = 0.02) and in children younger than 7 years (P = 0.02). Carriers of the prosteatotic PNPLA3 genotype p.148Met/Met displayed higher ALT activities as compared to children with the frequent genotype p.148Ile/Ile (P = 0.01). The BMI was however a stronger predictor of ALT activities compared to the PNPLA3 genotype (P < 0.001 and P = 0.06, resp.). The variant was associated with increased serum glucose levels (P = 0.01) and HOMA index (P = 0.02) in carriers of the p.148Ile/Met genotype but did not affect other metabolic traits or the presence of NAFLD. Discussion. The frequent PNPLA3 variant p.Ile148Met is associated with serum ALT activities already at a young age.

Identifiers

PMID26346943
PMCPMC4539481
OpenAlexW1637827316

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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.