Evidence map›Paper›PMID 39045929›Full record

ArticleRevista da Associacao Medica Brasileira (1992)2024

The rs1862513 promoter variant of resistin gene influences susceptibility to nonalcoholic fatty liver disease.

Shadi Nouri, Mahsa Navari, Radmehr Shafiee, Touraj Mahmoudi, Gholamreza Rezamand, Asadollah Asadi, Hossein Nobakht, Reza Dabiri, Hamid Farahani, Seidamir Pasha Tabaeian

Abstract read
In one paragraph

Article in Revista da Associacao Medica Brasileira (1992), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Shadi NouriArak University of Medical Sciences, School of Medicine, Department of Radiology - Arak, Iran.ORCID http://orcid.org/0000-0002-5818-7002
Mahsa NavariShahid Beheshti University of Medical Sciences, Research Institute for Gastroenterology and Liver Diseases, Gastroenterology and Liver Diseases Research Center - Tehran, Iran.ORCID http://orcid.org/0009-0001-9707-0827
Radmehr ShafieeTehran University, Faculty of Veterinary Medicine, Department of Clinical Pathology - Tehran, Iran.ORCID http://orcid.org/0009-0006-9067-0586
Touraj MahmoudiShahid Beheshti University of Medical Sciences, Research Institute for Gastroenterology and Liver Diseases, Gastroenterology and Liver Diseases Research Center - Tehran, Iran.ORCID http://orcid.org/0000-0002-3220-6252
Gholamreza RezamandIran University of Medical Sciences, School of Medicine, Department of Internal Medicine - Tehran, Iran.ORCID http://orcid.org/0000-0002-4305-2420
Asadollah AsadiUniversity of Mohaghegh Ardabili, Faculty of Science, Department of Biology - Ardabil, Iran.ORCID http://orcid.org/0000-0003-3314-2948
Hossein NobakhtSemnan University of Medical Sciences, Department of Internal Medicine - Semnan, Iran.ORCID http://orcid.org/0000-0001-9386-2280
Reza DabiriSemnan University of Medical Sciences, Department of Internal Medicine - Semnan, Iran.ORCID http://orcid.org/0000-0003-4506-9901
Hamid FarahaniQom University of Medical Sciences, School of Medicine, Department of Physiology and Pharmacology - Qom, Iran.ORCID http://orcid.org/0000-0002-1262-1854
Seidamir Pasha TabaeianIran University of Medical Sciences, School of Medicine, Department of Internal Medicine - Tehran, Iran.ORCID http://orcid.org/0000-0001-5260-5667

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesNonalcoholic fatty liver disease is the term used for a range of conditions in which fat builds up in the liver and exceeds 5% of hepatocytes without inordinate alcohol intake or other causes of lipid accumulation. Regarding the fact that insulin resistance and obesity play key roles in the pathogenesis of nonalcoholic fatty liver disease, as well as the connection between resistin and these metabolic diseases, the association between nonalcoholic fatty liver disease and a resistin gene (RETN) polymorphism was examined.

methodsIn this genetic case-control association study, 150 biopsy-proven nonalcoholic fatty liver disease patients and 154 controls were enrolled and genotyped for the RETN rs1862513 (-420C>G) gene polymorphism using PCR-RFLP method.

resultsThe -420C>G genotype frequency distributions in both groups were consistent with Hardy-Weinberg equilibrium (HWE; p>0.05). The carriers of the RETN -420C>G "CC" genotype compared with the "GG" genotype occurred less frequently in the cases with nonalcoholic fatty liver disease than in the controls, and the difference remained significant even after adjustment for confounding factors (p=0.030; OR=0.47, 95%CI=0.36-0.93). Interestingly, the RETN -420C>G "C" allele was also associated with a decreased risk for nonalcoholic fatty liver disease too (p=0.042; OR=0.72, 95%CI=0.53-0.95).

conclusionWe found for the first time an association between biopsy-proven nonalcoholic fatty liver disease and RETN -420C>G promoter polymorphism. The carriers of the RETN -420C>G "CC" genotype had a 53% decreased risk for nonalcoholic fatty liver disease. Our findings, however, need to be corroborated by further studies.

Indexed as

Genetic Predisposition to DiseaseGenotypeNon-alcoholic Fatty Liver DiseasePromoter Regions, GeneticResistinAdultCase-Control StudiesFemaleGene FrequencyHumansMaleMiddle AgedPolymerase Chain ReactionPolymorphism, Restriction Fragment LengthPolymorphism, Single NucleotideRisk FactorsResistinRETN protein, human

Identifiers

PMID39045929
PMCPMC11262324

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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.