Δημοσίευση

Activin A and follistatin in patients with nonalcoholic fatty liver disease.

ΤίτλοςActivin A and follistatin in patients with nonalcoholic fatty liver disease.
Publication TypeJournal Article
Year of Publication2016
AuthorsPolyzos, S. A., Kountouras J., Anastasilakis A. D., Triantafyllou G. Α., & Mantzoros C. S.
JournalMetabolism
Volume65
Issue10
Pagination1550-8
Date Published2016 10
ISSN1532-8600
Λέξεις κλειδιάActivins, Adiposity, Aging, Biopsy, Body Mass Index, Case-Control Studies, Fatty Liver, Female, Follistatin, Humans, Liver Function Tests, Male, Middle Aged, Non-alcoholic Fatty Liver Disease, Obesity, Sex Characteristics
Abstract

OBJECTIVE: There are limited data on the role of activin A and its binding protein, follistatin, in nonalcoholic fatty liver disease (NAFLD). The main aim was the evaluation of serum activin A and follistatin levels in patients with biopsy-proven NAFLD vs.
METHODS: This was a case-control study. Fifteen patients with nonalcoholic simple steatosis (SS), 16 with steatohepatitis (NASH), and 52 (24 lean and 28 obese) controls were recruited. Activin A and follistatin were measured using ELISA.
RESULTS: Activin A levels showed a trend towards progressive increase (p=0.010) from the controls (lean: 356±25, 95% CI 305-408; obese 360±20, 95% CI 320-401pg/ml) to SS (407±28, 95% CI 347-466pg/ml) and NASH patients (514±70 95% CI 364-664pg/ml); this association became non-significant after adjusting for adiposity. Follistatin was not different between groups (lean controls: 1.11±0.08, 95% CI 0.95-1.28; obese controls: 1.00±0.07, 95% CI 0.86-1.14; SS: 0.86±0.07, 95% CI 0.70-1.02; NASH: 1.14±0.09, 95% CI 0.90-1.37ng/ml; p=0.13). Within the NAFLD group of patients, follistatin was associated with NASH independently from activin A, gender and age, a relationship however likely reflecting the effect of adiposity.
CONCLUSIONS: Activin A is higher in patients with NASH than both lean and obese controls. Future clinical studies are needed to confirm and expand these findings, whereas mechanistic studies exploring underlying mechanisms are also warranted.

DOI10.1016/j.metabol.2016.07.009
Alternate JournalMetab. Clin. Exp.
PubMed ID27621190
PubMed Central IDPMC5022788
Grant ListK24 DK081913 / DK / NIDDK NIH HHS / United States

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