Evidence map›Paper›PMID 32811452›Full record

SynthesisBMC medical genetics2020

Association of PNPLA3 rs738409 G/C gene polymorphism with nonalcoholic fatty liver disease in children: a meta-analysis.

Shan Tang, Jing Zhang, Ting Ting Mei, Hai Qing Guo, Xin Huan Wei, Wen Yan Zhang, Ya Li Liu, Shan Liang, Zuo Peng Fan, Li Xia Ma and 4 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in BMC medical genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. [Combined effect of PNPLA3 rs738409 and UGT1A1 rs10929303 gene polymorphisms on nonalcoholic fatty liver disease in children].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2023
    Article
  7. Article
  8. Review
  9. Review
  10. Review
  11. 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

14 authors at 1 institution in 1 country.

Shan TangDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Jing ZhangDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Ting Ting MeiDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Hai Qing GuoDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Xin Huan WeiDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Wen Yan ZhangDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Ya Li LiuDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Shan LiangDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Zuo Peng FanDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Li Xia MaDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Wei LinDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Yi Rong LiuDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Li Xia QiuDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China.
Hai Bin YuDepartment of Hepatitis C and Drug-Induced Liver Injury, Beijing YouAn Hospital, Capital Medical University, Beijing, 100069, China. xiaobenyu2002@163.com.ORCID 0000-0002-9563-9194
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonalcoholic fatty liver disease (NAFLD) is one of the most common causes of chronic liver disease worldwide. Current studies have shown that PNPLA3 (Patatin-like phospholipase domain containing 3) rs738409 G/C gene polymorphism is associated with adult nonalcoholic fatty liver disease [1, 2].But there is no consensus on the relationship between PNPLA3 rs738409 G/C gene polymorphism and children NAFLD due to differences in population samples. To this end, a meta-analysis of published research is conducted to comprehensively assess the relationship between PNPLA3 gene polymorphism and NAFLD in children.

methodsWe searched MEDLINE, PubMed, EMBASE, and CENTRAL databases from inception to May 2019. Case-control studies assessing the relationship between PNPLA3 rs738409 G/C gene polymorphism with non-alcoholic fatty liver disease in children were selected according to inclusion and exclusion criteria. Random effects model was used to quantify the association between the PNPLA3 rs738409 G/C gene polymorphism and the susceptibility of children's NAFLD. Fixed effects model was used to quantify the relationship between the PNPLA3 rs738409 G/C gene polymorphism and the severity of NAFLD in children. The Stata 12.0 software was employed for data analysis.

resultsA total of nine case-control studies were included in this meta-analysis containing data of 1173 children with NAFLD and 1792 healthy controls. Five studies compared NAFLD children and non-NAFLD healthy populations. Statistical analysis showed that PNPLA3 gene polymorphism was significantly associated with children's NAFLD in the allele contrast, dominant, recessive and over dominant models (G vs C,OR = 3.343, 95% CI = 1.524-7.334; GG + GC vs CC,OR = 3.157, 95% CI = 1.446-6.892;GG vs GC + CC,OR = 5.692, 95% CI = 1.941-16.689; GG + CC vs GC,OR = 2.756, 95% CI = 1.729-4.392). Four case-control studies compared Children with nonalcoholic fatty liver (NAFL) and children with nonalcoholic steatohepatitis (NASH). The results showed that the PNPLA3 gene polymorphism was also significantly associated with the severity of NAFLD in children in recessive gene model (GG vs GC + CC,OR = 14.43, 95% CI = 5.985-34.997); The Egger's test revealed no significant publication bias.

conclusionsMeta-analysis showed that PNPLA3 gene polymorphism was significantly associated with susceptibility and severity of NAFLD in children.

Indexed as

Genetic Association StudiesGenetic Predisposition to DiseaseAcyltransferasesChildFemaleHumansLipaseMaleMembrane ProteinsNon-alcoholic Fatty Liver DiseaseOdds RatioPhospholipases A2, Calcium-IndependentPolymorphism, Single NucleotidePublication BiasAcyltransferasesLipaseMembrane ProteinsPhospholipases A2, Calcium-IndependentPNPLA3 protein, humanMeta-analysisPNPLA3Polymorphism

Identifiers

PMID32811452
PMCPMC7433068
OpenAlexW3060683075

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Registered trials

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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.