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High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis

BACKGROUND & AIMS: Progression of alcohol-associated liver disease (ALD) is driven by genetic predisposition. The rs13702 variant in the lipoprotein lipase (LPL) gene is linked to non-alcoholic fatty liver disease. We aimed at clarifying its role in ALD. METHODS: Patients with alcohol-associated...

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Autores principales: Schmalz, Franziska, Fischer, Janett, Innes, Hamish, Buch, Stephan, Möller, Christine, Matz-Soja, Madlen, von Schönfels, Witigo, Krämer, Benjamin, Langhans, Bettina, Klüners, Alexandra, Soyka, Michael, Stickel, Felix, Nattermann, Jacob, Strassburg, Christian P., Berg, Thomas, Lutz, Philipp, Nischalke, Hans Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985032/
https://www.ncbi.nlm.nih.gov/pubmed/36879887
http://dx.doi.org/10.1016/j.jhepr.2023.100684
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author Schmalz, Franziska
Fischer, Janett
Innes, Hamish
Buch, Stephan
Möller, Christine
Matz-Soja, Madlen
von Schönfels, Witigo
Krämer, Benjamin
Langhans, Bettina
Klüners, Alexandra
Soyka, Michael
Stickel, Felix
Nattermann, Jacob
Strassburg, Christian P.
Berg, Thomas
Lutz, Philipp
Nischalke, Hans Dieter
author_facet Schmalz, Franziska
Fischer, Janett
Innes, Hamish
Buch, Stephan
Möller, Christine
Matz-Soja, Madlen
von Schönfels, Witigo
Krämer, Benjamin
Langhans, Bettina
Klüners, Alexandra
Soyka, Michael
Stickel, Felix
Nattermann, Jacob
Strassburg, Christian P.
Berg, Thomas
Lutz, Philipp
Nischalke, Hans Dieter
author_sort Schmalz, Franziska
collection PubMed
description BACKGROUND & AIMS: Progression of alcohol-associated liver disease (ALD) is driven by genetic predisposition. The rs13702 variant in the lipoprotein lipase (LPL) gene is linked to non-alcoholic fatty liver disease. We aimed at clarifying its role in ALD. METHODS: Patients with alcohol-associated cirrhosis, with (n = 385) and without hepatocellular carcinoma (HCC) (n = 656), with HCC attributable to viral hepatitis C (n = 280), controls with alcohol abuse without liver damage (n = 366), and healthy controls (n = 277) were genotyped regarding the LPL rs13702 polymorphism. Furthermore, the UK Biobank cohort was analysed. LPL expression was investigated in human liver specimens and in liver cell lines. RESULTS: Frequency of the LPL rs13702 CC genotype was lower in ALD with HCC in comparison to ALD without HCC both in the initial (3.9% vs. 9.3%) and the validation cohort (4.7% vs. 9.5%; p <0.05 each) and compared with patients with viral HCC (11.4%), alcohol misuse without cirrhosis (8.7%), or healthy controls (9.0%). This protective effect (odds ratio [OR] = 0.5) was confirmed in multivariate analysis including age (OR = 1.1/year), male sex (OR = 3.0), diabetes (OR = 1.8), and carriage of the PNPLA3 I148M risk variant (OR = 2.0). In the UK Biobank cohort, the LPL rs13702 C allele was replicated as a risk factor for HCC. Liver expression of LPL mRNA was dependent on LPL rs13702 genotype and significantly higher in patients with ALD cirrhosis compared with controls and alcohol-associated HCC. Although hepatocyte cell lines showed negligible LPL protein expression, hepatic stellate cells and liver sinusoidal endothelial cells expressed LPL. CONCLUSIONS: LPL is upregulated in the liver of patients with alcohol-associated cirrhosis. The LPL rs13702 high producer variant confers protection against HCC in ALD, which might help to stratify people for HCC risk. IMPACT AND IMPLICATIONS: Hepatocellular carcinoma is a severe complication of liver cirrhosis influenced by genetic predisposition. We found that a genetic variant in the gene encoding lipoprotein lipase reduces the risk for hepatocellular carcinoma in alcohol-associated cirrhosis. This genetic variation may directly affect the liver, because, unlike in healthy adult liver, lipoprotein lipase is produced from liver cells in alcohol-associated cirrhosis.
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spelling pubmed-99850322023-03-05 High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis Schmalz, Franziska Fischer, Janett Innes, Hamish Buch, Stephan Möller, Christine Matz-Soja, Madlen von Schönfels, Witigo Krämer, Benjamin Langhans, Bettina Klüners, Alexandra Soyka, Michael Stickel, Felix Nattermann, Jacob Strassburg, Christian P. Berg, Thomas Lutz, Philipp Nischalke, Hans Dieter JHEP Rep Research Article BACKGROUND & AIMS: Progression of alcohol-associated liver disease (ALD) is driven by genetic predisposition. The rs13702 variant in the lipoprotein lipase (LPL) gene is linked to non-alcoholic fatty liver disease. We aimed at clarifying its role in ALD. METHODS: Patients with alcohol-associated cirrhosis, with (n = 385) and without hepatocellular carcinoma (HCC) (n = 656), with HCC attributable to viral hepatitis C (n = 280), controls with alcohol abuse without liver damage (n = 366), and healthy controls (n = 277) were genotyped regarding the LPL rs13702 polymorphism. Furthermore, the UK Biobank cohort was analysed. LPL expression was investigated in human liver specimens and in liver cell lines. RESULTS: Frequency of the LPL rs13702 CC genotype was lower in ALD with HCC in comparison to ALD without HCC both in the initial (3.9% vs. 9.3%) and the validation cohort (4.7% vs. 9.5%; p <0.05 each) and compared with patients with viral HCC (11.4%), alcohol misuse without cirrhosis (8.7%), or healthy controls (9.0%). This protective effect (odds ratio [OR] = 0.5) was confirmed in multivariate analysis including age (OR = 1.1/year), male sex (OR = 3.0), diabetes (OR = 1.8), and carriage of the PNPLA3 I148M risk variant (OR = 2.0). In the UK Biobank cohort, the LPL rs13702 C allele was replicated as a risk factor for HCC. Liver expression of LPL mRNA was dependent on LPL rs13702 genotype and significantly higher in patients with ALD cirrhosis compared with controls and alcohol-associated HCC. Although hepatocyte cell lines showed negligible LPL protein expression, hepatic stellate cells and liver sinusoidal endothelial cells expressed LPL. CONCLUSIONS: LPL is upregulated in the liver of patients with alcohol-associated cirrhosis. The LPL rs13702 high producer variant confers protection against HCC in ALD, which might help to stratify people for HCC risk. IMPACT AND IMPLICATIONS: Hepatocellular carcinoma is a severe complication of liver cirrhosis influenced by genetic predisposition. We found that a genetic variant in the gene encoding lipoprotein lipase reduces the risk for hepatocellular carcinoma in alcohol-associated cirrhosis. This genetic variation may directly affect the liver, because, unlike in healthy adult liver, lipoprotein lipase is produced from liver cells in alcohol-associated cirrhosis. Elsevier 2023-01-25 /pmc/articles/PMC9985032/ /pubmed/36879887 http://dx.doi.org/10.1016/j.jhepr.2023.100684 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Schmalz, Franziska
Fischer, Janett
Innes, Hamish
Buch, Stephan
Möller, Christine
Matz-Soja, Madlen
von Schönfels, Witigo
Krämer, Benjamin
Langhans, Bettina
Klüners, Alexandra
Soyka, Michael
Stickel, Felix
Nattermann, Jacob
Strassburg, Christian P.
Berg, Thomas
Lutz, Philipp
Nischalke, Hans Dieter
High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
title High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
title_full High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
title_fullStr High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
title_full_unstemmed High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
title_short High producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
title_sort high producer variant of lipoprotein lipase may protect from hepatocellular carcinoma in alcohol-associated cirrhosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985032/
https://www.ncbi.nlm.nih.gov/pubmed/36879887
http://dx.doi.org/10.1016/j.jhepr.2023.100684
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