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Helicobacter pylori infection in patients with nonalcoholic fatty liver disease.

ΤίτλοςHelicobacter pylori infection in patients with nonalcoholic fatty liver disease.
Publication TypeJournal Article
Year of Publication2013
AuthorsPolyzos, S. A., Kountouras J., Papatheodorou A., Patsiaoura K., Katsiki E., Zafeiriadou E., Zavos C., Anastasiadou K., & Terpos E.
JournalMetabolism
Volume62
Issue1
Pagination121-6
Date Published2013 Jan
ISSN1532-8600
Λέξεις κλειδιάAdult, Alanine Transaminase, Aspartate Aminotransferases, C-Reactive Protein, Chi-Square Distribution, Cross-Sectional Studies, Fatty Liver, Female, gamma-Glutamyltransferase, Helicobacter Infections, Helicobacter pylori, Humans, Immunoglobulin G, Male, Non-alcoholic Fatty Liver Disease, Tumor Necrosis Factor-alpha
Abstract

OBJECTIVE: Clinical data regarding Helicobacter pylori (Hp) infection in nonalcoholic fatty liver disease (NAFLD) are limited. The aim was the evaluation of Hp infection in patients with NAFLD and its association with disease severity.
METHODS: 28 patients with biopsy-proven NAFLD (15 with simple nonalcoholic fatty liver [NAFL], 13 with nonalcoholic steatohepatitis [NASH]) and 25 matched healthy controls were recruited. Blood samples for anti-Hp Immunoglobulin G (IgG) and standard biochemical tests were obtained after overnight fasting, and (13)C urea breath test was performed before liver biopsy in NAFLD group.
RESULTS: Higher rates of anti-Hp IgG (P=.038) were observed in NAFLD compared to control group. Only two NAFLD patients neither were Hp IgG seropositive nor did they have a history of eradication treatment compared to 11 control subjects (P=.002). Both Hp infection (assessed by history of Hp eradication treatment and/or Hp IgG seropositivity) (P=.034) and log(HOMA-IR) (P=.007) could independently predict NAFLD in logistic regression analysis. There were similar rates of Hp IgG seropositivity or positivity in (13)C urea breath test or their combination between NAFL and NASH patients. There were no significant differences in steatosis grade, fibrosis stage, lobular or portal inflammation, or ballooning, when NAFLD patients were divided according to Hp IgG seropositivity or (13)C urea breath test positivity.
CONCLUSIONS: Hp infection may represent one more hit contributing to the pathogenesis of NAFL, though not to the progression from NAFL to NASH. These results warrant further validation. If confirmed, eradicating Hp infection may have certain therapeutic perspectives in NAFLD treatment.

DOI10.1016/j.metabol.2012.06.007
Alternate JournalMetab. Clin. Exp.
PubMed ID22841522

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