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  1. Pubblicazioni

Glucokinase Regulatory Protein Gene Polymorphism Affects Liver Fibrosis in Non-Alcoholic Fatty Liver Disease

Articolo
Data di Pubblicazione:
2014
Citazione:
Petta, S., Miele, L., Bugianesi, E., Cammà, C., Rosso, C., Boccia, S., Cabibi, D., Di Marco, V., Grimaudo, S., Grieco, A., Pipitone, R., Marchesini, G., Craxì, A., Glucokinase Regulatory Protein Gene Polymorphism Affects Liver Fibrosis in Non-Alcoholic Fatty Liver Disease, <>, 2014; 9 (2): N/A-N/A. [doi:10.1371/journal.pone.0087523] [http://hdl.handle.net/10807/64021]
Abstract:
BACKGROUND AND AIMS: Variant in glucokinase regulatory protein (GCKR), associated with lipid and glucose traits, has been suggested to affect fatty liver infiltration. We aimed to assess whether GCKR rs780094 C→T SNP influences the expression of steatosis, lobular inflammation and fibrosis in NAFLD patients, after correction for PNPLA3 genotype. METHODS: In 366 consecutive NAFLD patients (197 from Sicily, and 169 from center/northern Italy), we assessed anthropometric, biochemical and metabolic features; liver biopsy was scored according to Kleiner. PNPLA3 rs738409 C>G and GCKR rs780094 C>T single nucleotide polymorphisms were also assessed. RESULTS: At multivariate logistic regression analysis in the entire NAFLD cohort, the presence of significant liver fibrosis (>F1) was independently linked to high HOMA (OR 1.12, 95% CI 1.01-1.23, p = 0.02), NAFLD activity score ≥ 5 (OR 4.09, 95% CI 2.45-6.81, p<0.001), and GCKR C>T SNP (OR 2.06, 95% CI 1.43-2.98, p<0.001). Similar results were observed considering separately the two different NAFLD cohorts. GCKR C>T SNP was also associated with higher serum triglycerides (ANOVA, p = 0.02) in the entire cohort. CONCLUSIONS: In patients with NAFLD, GCKR rs780094 C>T is associated with the severity of liver fibrosis and with higher serum triglyceride levels.
Tipologia CRIS:
Articolo in rivista, Nota a sentenza
Keywords:
Glucokinase regulatory protein; gene polymorphism; liver fibrosis; non-alcoholic fatty liver disease
Elenco autori:
Petta, S; Miele, Luca; Bugianesi, E; Cammà, C; Rosso, C; Boccia, Stefania; Cabibi, D; Di Marco, V; Grimaudo, S; Grieco, Antonio; Pipitone, Rm; Marchesini, G; Craxì, A.
Link alla scheda completa:
https://publicatt.unicatt.it/handle/10807/64021
Link al Full Text:
https://publicatt.unicatt.it//retrieve/handle/10807/64021/689477/unpaywall-bitstream--1317822397.pdf
Pubblicato in:
PLOS ONE
Journal
  • Aree Di Ricerca

Aree Di Ricerca

Settori (5)


LS2_9 - Genetic epidemiology - (2011)

LS4_5 - Metabolism, biological basis of metabolism related disorders - (2011)

Settore MED/09 - MEDICINA INTERNA

Settore MED/12 - GASTROENTEROLOGIA

Settore MED/42 - IGIENE GENERALE E APPLICATA
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