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Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis

BACKGROUND & AIMS: Dysmetabolic conditions could drive liver fibrosis in patients with non-alcoholic fatty liver disease (NAFLD), increasing susceptibility to hepatocellular carcinoma (HCC). We therefore aimed to identify novel predictive biomarkers of HCC in patients with and without liver fibr...

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Autores principales: Crudele, Lucilla, De Matteis, Carlo, Piccinin, Elena, Gadaleta, Raffaella Maria, Cariello, Marica, Di Buduo, Ersilia, Piazzolla, Giuseppina, Suppressa, Patrizia, Berardi, Elsa, Sabbà, Carlo, Moschetta, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763866/
https://www.ncbi.nlm.nih.gov/pubmed/36561127
http://dx.doi.org/10.1016/j.jhepr.2022.100627
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author Crudele, Lucilla
De Matteis, Carlo
Piccinin, Elena
Gadaleta, Raffaella Maria
Cariello, Marica
Di Buduo, Ersilia
Piazzolla, Giuseppina
Suppressa, Patrizia
Berardi, Elsa
Sabbà, Carlo
Moschetta, Antonio
author_facet Crudele, Lucilla
De Matteis, Carlo
Piccinin, Elena
Gadaleta, Raffaella Maria
Cariello, Marica
Di Buduo, Ersilia
Piazzolla, Giuseppina
Suppressa, Patrizia
Berardi, Elsa
Sabbà, Carlo
Moschetta, Antonio
author_sort Crudele, Lucilla
collection PubMed
description BACKGROUND & AIMS: Dysmetabolic conditions could drive liver fibrosis in patients with non-alcoholic fatty liver disease (NAFLD), increasing susceptibility to hepatocellular carcinoma (HCC). We therefore aimed to identify novel predictive biomarkers of HCC in patients with and without liver fibrosis. METHODS: A total of 1,234 patients with putative metabolic conditions and NAFLD were consecutively assessed in our outpatient clinic. Clinical and biochemical data were recorded, and then liver ultrasonography was performed annually for 5 years to detect HCC onset. For the analysis, the population was first divided according to HCC diagnosis; then a further subdivision of those who did not develop HCC was performed based on the presence or absence of liver fibrosis at time 0. RESULTS: Sixteen HCC cases were recorded in 5 years. None of our patients had been diagnosed with cirrhosis before HCC was detected. Compared to patients who did not develop HCC, those who did had higher liver transaminases and fibrosis scores at time 0 (p <0.001). In addition, they presented with increased glycated haemoglobin levels and lower 25-OH vitamin D levels (p <0.05). Intriguingly, patients with higher liver fibrosis scores who subsequently developed HCC had lower HDL-cholesterol (HDL-c) levels at time 0 (p <0.001). Furthermore, in the 484 patients presenting with lower HDL-c at baseline, we found that waist circumference, and then vitamin D and glycated haemoglobin levels, were significantly different in those who developed HCC, regardless of liver fibrosis (p <0.05). CONCLUSIONS: This study identifies HDL-c as a bona fide novel marker to predict HCC in patients with NAFLD. Increased waist circumference and deranged metabolic pathways represent additional predisposing factors among patients with low HDL-c, highlighting the importance of studying cholesterol metabolism and integrating clinical approaches with dietary regimens and a healthy lifestyle to prevent HCC. IMPACT AND IMPLICATIONS: Visceral adiposity and its associated conditions, such as chronic inflammation and insulin resistance, may play a pivotal role in hepatocellular carcinoma development in patients with non-alcoholic fatty liver disease. We provide new insights on the underlying mechanisms of its pathogenesis, shedding light on the involvement of low levels of “good” HDL-cholesterol. We recommend integrating dietary regimens and advice on healthy lifestyles into the clinical management of non-alcoholic fatty liver disease, with the goal of reducing the incidence of hepatocellular carcinoma.
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spelling pubmed-97638662022-12-21 Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis Crudele, Lucilla De Matteis, Carlo Piccinin, Elena Gadaleta, Raffaella Maria Cariello, Marica Di Buduo, Ersilia Piazzolla, Giuseppina Suppressa, Patrizia Berardi, Elsa Sabbà, Carlo Moschetta, Antonio JHEP Rep Research Article BACKGROUND & AIMS: Dysmetabolic conditions could drive liver fibrosis in patients with non-alcoholic fatty liver disease (NAFLD), increasing susceptibility to hepatocellular carcinoma (HCC). We therefore aimed to identify novel predictive biomarkers of HCC in patients with and without liver fibrosis. METHODS: A total of 1,234 patients with putative metabolic conditions and NAFLD were consecutively assessed in our outpatient clinic. Clinical and biochemical data were recorded, and then liver ultrasonography was performed annually for 5 years to detect HCC onset. For the analysis, the population was first divided according to HCC diagnosis; then a further subdivision of those who did not develop HCC was performed based on the presence or absence of liver fibrosis at time 0. RESULTS: Sixteen HCC cases were recorded in 5 years. None of our patients had been diagnosed with cirrhosis before HCC was detected. Compared to patients who did not develop HCC, those who did had higher liver transaminases and fibrosis scores at time 0 (p <0.001). In addition, they presented with increased glycated haemoglobin levels and lower 25-OH vitamin D levels (p <0.05). Intriguingly, patients with higher liver fibrosis scores who subsequently developed HCC had lower HDL-cholesterol (HDL-c) levels at time 0 (p <0.001). Furthermore, in the 484 patients presenting with lower HDL-c at baseline, we found that waist circumference, and then vitamin D and glycated haemoglobin levels, were significantly different in those who developed HCC, regardless of liver fibrosis (p <0.05). CONCLUSIONS: This study identifies HDL-c as a bona fide novel marker to predict HCC in patients with NAFLD. Increased waist circumference and deranged metabolic pathways represent additional predisposing factors among patients with low HDL-c, highlighting the importance of studying cholesterol metabolism and integrating clinical approaches with dietary regimens and a healthy lifestyle to prevent HCC. IMPACT AND IMPLICATIONS: Visceral adiposity and its associated conditions, such as chronic inflammation and insulin resistance, may play a pivotal role in hepatocellular carcinoma development in patients with non-alcoholic fatty liver disease. We provide new insights on the underlying mechanisms of its pathogenesis, shedding light on the involvement of low levels of “good” HDL-cholesterol. We recommend integrating dietary regimens and advice on healthy lifestyles into the clinical management of non-alcoholic fatty liver disease, with the goal of reducing the incidence of hepatocellular carcinoma. Elsevier 2022-11-15 /pmc/articles/PMC9763866/ /pubmed/36561127 http://dx.doi.org/10.1016/j.jhepr.2022.100627 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Crudele, Lucilla
De Matteis, Carlo
Piccinin, Elena
Gadaleta, Raffaella Maria
Cariello, Marica
Di Buduo, Ersilia
Piazzolla, Giuseppina
Suppressa, Patrizia
Berardi, Elsa
Sabbà, Carlo
Moschetta, Antonio
Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis
title Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis
title_full Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis
title_fullStr Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis
title_full_unstemmed Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis
title_short Low HDL-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis
title_sort low hdl-cholesterol levels predict hepatocellular carcinoma development in individuals with liver fibrosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9763866/
https://www.ncbi.nlm.nih.gov/pubmed/36561127
http://dx.doi.org/10.1016/j.jhepr.2022.100627
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