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Clin Gastroenterol Hepatol. 2022;20(3):682-691.e8.

A PNPLA3 Polymorphism Confers Lower Susceptibility to Incident Diabetes Mellitus in Subjects With Nonalcoholic Fatty Liver Disease.

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제1저자 문서일, 정고은 · 교신저자 구보경, 김원

소속 (6)
  1. Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea; On behalf of the Innovative Target Exploration of NAFLD (ITEN) consortium.
  2. Department of Internal Medicine, Healthcare System Gangnam Center, Seoul National University Hospital, Seoul, Korea; On behalf of the Innovative Target Exploration of NAFLD (ITEN) consortium.
  3. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, Korea; On behalf of the Innovative Target Exploration of NAFLD (ITEN) consortium.
  4. Department of Pathology, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, Korea; On behalf of the Innovative Target Exploration of NAFLD (ITEN) consortium.
  5. Division of Endocrinology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, Korea; On behalf of the Innovative Target Exploration of NAFLD (ITEN) consortium. Electronic address: bokyungkoomd@gmail.com.
  6. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, Korea; On behalf of the Innovative Target Exploration of NAFLD (ITEN) consortium. Electronic address: drwon1@snu.ac.kr.

Abstract

BACKGROUND AND AIMS We investigated the association between the patatin-like phospholipase domain-containing-3 (PNPLA3) rs738409 genotype and the risk of diabetes mellitus (DM) using a biopsy-confirmed nonalcoholic fatty liver disease (NAFLD) cohort and a longitudinal observational cohort.

METHODS Associations between genotypes and the prevalence of DM were evaluated with stratification according to the histological severity of NAFLD in the Boramae cohort (n = 706). A longitudinal cohort consisting of nondiabetic individuals with ≥2 health checkups was then selected to investigate the risk of incident DM according to the genotype (the GENIE cohort; n = 4998).

RESULTS Among subjects with NAFLD in the Boramae cohort, the G allele was independently associated with a lower prevalence of DM in both NAFL (odds ratio [OR] per 1 allele, 0.66; 95% confidence interval [CI], 0.46-0.97) and nonalcoholic steatohepatitis (OR per 1 allele, 0.59; 95% CI, 0.38-0.92). This result was replicated in the longitudinal GENIE cohort. The G allele was associated with a lower risk of incident DM during the median follow-up of 60 months in subjects with NAFLD (hazard ratio, 0.65; 95% CI, 0.45-0.93). In contrast, G allele carriers without NAFLD showed higher odds for DM in the context of the Boramae cohort (OR, 2.44; 95% CI, 1.00-5.95).

CONCLUSIONS These findings clarify conflicting results regarding the association between the PNPLA3 rs738409 genotype and the risk of DM, demonstrating a clear difference between subjects with and without NAFLD; this difference might be explained by the low metabolic risk in genetic NAFLD.

Copyright © 2022 AGA Institute. Published by Elsevier Inc. All rights reserved.

Keywords

Diabetes MellitusNonalcoholic Fatty Liver DiseaseNonalcoholic SteatohepatitisPNPLA3

그 밖의 정보
출판 형태
Journal Article, Research Support, Non-U.S. Gov't
저널
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association · eISSN 1542-7714
전자 출판
2021-04-24
MeSH
Acyltransferases* / genetics · Diabetes Mellitus* / epidemiology / genetics · Genetic Predisposition to Disease · Genotype · Humans · Lipase / genetics / metabolism · Liver / pathology · Membrane Proteins / genetics / metabolism · Non-alcoholic Fatty Liver Disease* / complications / epidemiology / genetics · Phospholipases A2, Calcium-Independent* / genetics · Polymorphism, Single Nucleotide
Substances
Acyltransferases · Lipase · Membrane Proteins · Phospholipases A2, Calcium-Independent · PNPLA3 protein, human