The SOD2 C47T polymorphism influences NAFLD fibrosis severity: Evidence from case-control and intra-familial allele association studies

Ahmad Al-Serri, Quentin M. Anstee, Luca Valenti, Valerio Nobili, Julian B S Leathart, Paola Dongiovanni, Julia Patch, Anna Fracanzani, Silvia Fargion, Christopher P. Day, Ann K. Daly

Research output: Contribution to journalArticle

Abstract

Background & Aims: Non-alcoholic fatty liver disease (NAFLD) is a complex disease trait where genetic variations and environment interact to determine disease progression. The association of PNPLA3 with advanced disease has been consistently demonstrated but many other modifier genes remain unidentified. In NAFLD, increased fatty acid oxidation produces high levels of reactive oxygen species. Manganese-dependent superoxide dismutase (MnSOD), encoded by the SOD2 gene, plays an important role in protecting cells from oxidative stress. A common non-synonymous polymorphism in SOD2 (C47T; rs4880) is associated with decreased MnSOD mitochondrial targeting and activity making it a good candidate modifier of NAFLD severity. Methods: The relevance of the SOD2 C47T polymorphism to fibrotic NAFLD was assessed by two complementary approaches: we sought preferential transmission of alleles from parents to affected children in 71 family trios and adopted a case-control approach to compare genotype frequencies in a cohort of 502 European NAFLD patients. Results: In the family study, 55 families were informative. The T allele was transmitted on 47/76 (62%) possible occasions whereas the C allele was transmitted on only 29/76 (38%) occasions, p = 0.038. In the case control study, the presence of advanced fibrosis (stage >1) increased with the number of T alleles, p = 0.008 for trend. Multivariate analysis showed susceptibility to advanced fibrotic disease was determined by SOD2 genotype (OR 1.56 (95% CI 1.09-2.25), p = 0.014), PNPLA3 genotype (p = 0.041), type 2 diabetes mellitus (p = 0.009) and histological severity of NASH (p = 2.0 × 10 -16). Conclusions: Carriage of the SOD2 C47T polymorphism is associated with more advanced fibrosis in NASH.

Original languageEnglish
Pages (from-to)448-454
Number of pages7
JournalJournal of Hepatology
Volume56
Issue number2
DOIs
Publication statusPublished - Feb 2012

Keywords

  • Gene
  • NAFLD
  • NASH
  • Oxidative stress
  • Polymorphism
  • Steatohepatitis

ASJC Scopus subject areas

  • Hepatology

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