PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.

<h4>Background & aims</h4>Aim of this study was to evaluate whether the PNPLA3 I148M polymorphism, previously associated with hepatocellular carcinoma (HCC) risk, influences the clinical presentation of HCC and survival.<h4>Methods</h4>we considered 460 consecutive HCC pa...

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Main Authors: Luca Valenti, Benedetta Maria Motta, Giorgio Soardo, Massimo Iavarone, Benedetta Donati, Angelo Sangiovanni, Alessia Carnelutti, Paola Dongiovanni, Raffaela Rametta, Cristina Bertelli, Floriana Facchetti, Massimo Colombo, Silvia Fargion, Anna Ludovica Fracanzani
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24155878/pdf/?tool=EBI
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spelling doaj-dcbc63d1da6c40f7a2e76c9c1c7a8ecb2021-03-03T22:50:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-01810e7598210.1371/journal.pone.0075982PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.Luca ValentiBenedetta Maria MottaGiorgio SoardoMassimo IavaroneBenedetta DonatiAngelo SangiovanniAlessia CarneluttiPaola DongiovanniRaffaela RamettaCristina BertelliFloriana FacchettiMassimo ColomboSilvia FargionAnna Ludovica Fracanzani<h4>Background & aims</h4>Aim of this study was to evaluate whether the PNPLA3 I148M polymorphism, previously associated with hepatocellular carcinoma (HCC) risk, influences the clinical presentation of HCC and survival.<h4>Methods</h4>we considered 460 consecutive HCC patients referred to tertiary care centers in Northern Italy, 353 with follow-up data.<h4>Results</h4>Homozygosity for PNPLA3 148M at risk allele was enriched in HCC patients with alcoholic liver disease or nonalcoholic fatty liver disease (ALD&NAFLD: relative risk 5.9, 95% c.i. 3.5-9.9; other liver diseases: relative risk 1.9, 95% c.i. 1.1-3.4). In ALD&NAFLD patients, the PNPLA3 148M allele was associated with younger age, shorter history of cirrhosis, less advanced (Child A) cirrhosis at HCC diagnosis, and lower HCC differentiation grade (p<0.05). Homozygosity for PNPLA3 148M was associated with reduced survival in the overall series (p = 0.009), and with a higher number of HCC lesions at presentation (p = 0.007) and reduced survival in ALD&NAFLD patients (p = 0.003; median survival 30, 95% c.i. 20-39 vs. 45, 95% c.i. 38-52 months), but not in those with HCC related to other etiologies (p = 0.86; 48, 95% c.i. 32-64 vs. 55, 95% c.i. 43-67 months). At multivariate Cox regression analysis, homozygosity for PNPLA3 148M was the only negative predictor of survival in ALD&NAFLD patients (HR of death 1.57, 95% c.i. 1.12-2.78).<h4>Conclusions</h4>PNPLA3 148M is over-represented in ALD&NAFLD HCC patients, and is associated with occurrence at a less advanced stage of liver disease in ALD&NAFLD. In ALD&NAFLD, PNPLA3 148M is associated with more diffuse HCC at presentation, and with reduced survival.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24155878/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Luca Valenti
Benedetta Maria Motta
Giorgio Soardo
Massimo Iavarone
Benedetta Donati
Angelo Sangiovanni
Alessia Carnelutti
Paola Dongiovanni
Raffaela Rametta
Cristina Bertelli
Floriana Facchetti
Massimo Colombo
Silvia Fargion
Anna Ludovica Fracanzani
spellingShingle Luca Valenti
Benedetta Maria Motta
Giorgio Soardo
Massimo Iavarone
Benedetta Donati
Angelo Sangiovanni
Alessia Carnelutti
Paola Dongiovanni
Raffaela Rametta
Cristina Bertelli
Floriana Facchetti
Massimo Colombo
Silvia Fargion
Anna Ludovica Fracanzani
PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.
PLoS ONE
author_facet Luca Valenti
Benedetta Maria Motta
Giorgio Soardo
Massimo Iavarone
Benedetta Donati
Angelo Sangiovanni
Alessia Carnelutti
Paola Dongiovanni
Raffaela Rametta
Cristina Bertelli
Floriana Facchetti
Massimo Colombo
Silvia Fargion
Anna Ludovica Fracanzani
author_sort Luca Valenti
title PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.
title_short PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.
title_full PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.
title_fullStr PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.
title_full_unstemmed PNPLA3 I148M polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.
title_sort pnpla3 i148m polymorphism, clinical presentation, and survival in patients with hepatocellular carcinoma.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description <h4>Background & aims</h4>Aim of this study was to evaluate whether the PNPLA3 I148M polymorphism, previously associated with hepatocellular carcinoma (HCC) risk, influences the clinical presentation of HCC and survival.<h4>Methods</h4>we considered 460 consecutive HCC patients referred to tertiary care centers in Northern Italy, 353 with follow-up data.<h4>Results</h4>Homozygosity for PNPLA3 148M at risk allele was enriched in HCC patients with alcoholic liver disease or nonalcoholic fatty liver disease (ALD&NAFLD: relative risk 5.9, 95% c.i. 3.5-9.9; other liver diseases: relative risk 1.9, 95% c.i. 1.1-3.4). In ALD&NAFLD patients, the PNPLA3 148M allele was associated with younger age, shorter history of cirrhosis, less advanced (Child A) cirrhosis at HCC diagnosis, and lower HCC differentiation grade (p<0.05). Homozygosity for PNPLA3 148M was associated with reduced survival in the overall series (p = 0.009), and with a higher number of HCC lesions at presentation (p = 0.007) and reduced survival in ALD&NAFLD patients (p = 0.003; median survival 30, 95% c.i. 20-39 vs. 45, 95% c.i. 38-52 months), but not in those with HCC related to other etiologies (p = 0.86; 48, 95% c.i. 32-64 vs. 55, 95% c.i. 43-67 months). At multivariate Cox regression analysis, homozygosity for PNPLA3 148M was the only negative predictor of survival in ALD&NAFLD patients (HR of death 1.57, 95% c.i. 1.12-2.78).<h4>Conclusions</h4>PNPLA3 148M is over-represented in ALD&NAFLD HCC patients, and is associated with occurrence at a less advanced stage of liver disease in ALD&NAFLD. In ALD&NAFLD, PNPLA3 148M is associated with more diffuse HCC at presentation, and with reduced survival.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/24155878/pdf/?tool=EBI
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