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Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection

BACKGROUND: Hepatitis C virus (HCV) infection is associated with serum lipid abnormalities, which partly normalize following direct-acting antiviral (DAA) therapy. Here, associations of serum triglycerides (TGs) with viral genotype and markers of liver disease severity were evaluated in patients wit...

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Autores principales: Peschel, Georg, Grimm, Jonathan, Müller, Martina, Höring, Marcus, Krautbauer, Sabrina, Weigand, Kilian, Liebisch, Gerhard, Buechler, Christa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590217/
https://www.ncbi.nlm.nih.gov/pubmed/36280840
http://dx.doi.org/10.1186/s12944-022-01715-w
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author Peschel, Georg
Grimm, Jonathan
Müller, Martina
Höring, Marcus
Krautbauer, Sabrina
Weigand, Kilian
Liebisch, Gerhard
Buechler, Christa
author_facet Peschel, Georg
Grimm, Jonathan
Müller, Martina
Höring, Marcus
Krautbauer, Sabrina
Weigand, Kilian
Liebisch, Gerhard
Buechler, Christa
author_sort Peschel, Georg
collection PubMed
description BACKGROUND: Hepatitis C virus (HCV) infection is associated with serum lipid abnormalities, which partly normalize following direct-acting antiviral (DAA) therapy. Here, associations of serum triglycerides (TGs) with viral genotype and markers of liver disease severity were evaluated in patients with chronic HCV.  METHODS: The study included the serum of 177 patients with chronic HCV. TGs were quantified by flow injection analysis Fourier transform mass spectrometry. Laboratory values and noninvasive scores for liver fibrosis assessment were determined. The nonparametric Kruskal‒Wallis test, one-way ANOVA, multiple linear regression and Student’s t test were used as appropriate. P values were adjusted for multiple comparisons. RESULTS: HCV-infected women had lower serum TGs than men, and thus, a sex-specific analysis was performed. None of the 46 TG species analyzed differed in the serum of female patients with and without liver cirrhosis. In contrast, in the serum of male patients with liver cirrhosis, TGs with 53, 56 and 58 carbon atoms and three to eight double bonds were diminished. These polyunsaturated TGs were also low in males with a high fibrosis-4 score. TGs with 7 or 8 double bonds negatively correlated with the model of end-stage liver disease score in males. In addition, TGs with 49, 51 and 53 carbon atoms were reduced in male patients infected with genotype 3a in comparison to genotype 1a. TGs with 56 carbon atoms were lower in genotype 3a-infected males than in genotype 1b-infected males. TGs did not differ in females by genotype. Genotype 3-related changes disappeared at the end of therapy with DAAs. Overall, the levels of serum TGs did not change during DAA therapy in either sex. Consequently, the serum TGs of males with liver cirrhosis were lower than those of males without cirrhosis at the end of therapy. Such a difference was not apparent in females. CONCLUSIONS: The decline in TGs observed only in male patients with liver cirrhosis and male patients infected with genotype 3 illustrates sex-specific changes in lipid metabolism in chronic HCV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-022-01715-w.
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spelling pubmed-95902172022-10-25 Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection Peschel, Georg Grimm, Jonathan Müller, Martina Höring, Marcus Krautbauer, Sabrina Weigand, Kilian Liebisch, Gerhard Buechler, Christa Lipids Health Dis Research BACKGROUND: Hepatitis C virus (HCV) infection is associated with serum lipid abnormalities, which partly normalize following direct-acting antiviral (DAA) therapy. Here, associations of serum triglycerides (TGs) with viral genotype and markers of liver disease severity were evaluated in patients with chronic HCV.  METHODS: The study included the serum of 177 patients with chronic HCV. TGs were quantified by flow injection analysis Fourier transform mass spectrometry. Laboratory values and noninvasive scores for liver fibrosis assessment were determined. The nonparametric Kruskal‒Wallis test, one-way ANOVA, multiple linear regression and Student’s t test were used as appropriate. P values were adjusted for multiple comparisons. RESULTS: HCV-infected women had lower serum TGs than men, and thus, a sex-specific analysis was performed. None of the 46 TG species analyzed differed in the serum of female patients with and without liver cirrhosis. In contrast, in the serum of male patients with liver cirrhosis, TGs with 53, 56 and 58 carbon atoms and three to eight double bonds were diminished. These polyunsaturated TGs were also low in males with a high fibrosis-4 score. TGs with 7 or 8 double bonds negatively correlated with the model of end-stage liver disease score in males. In addition, TGs with 49, 51 and 53 carbon atoms were reduced in male patients infected with genotype 3a in comparison to genotype 1a. TGs with 56 carbon atoms were lower in genotype 3a-infected males than in genotype 1b-infected males. TGs did not differ in females by genotype. Genotype 3-related changes disappeared at the end of therapy with DAAs. Overall, the levels of serum TGs did not change during DAA therapy in either sex. Consequently, the serum TGs of males with liver cirrhosis were lower than those of males without cirrhosis at the end of therapy. Such a difference was not apparent in females. CONCLUSIONS: The decline in TGs observed only in male patients with liver cirrhosis and male patients infected with genotype 3 illustrates sex-specific changes in lipid metabolism in chronic HCV. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12944-022-01715-w. BioMed Central 2022-10-24 /pmc/articles/PMC9590217/ /pubmed/36280840 http://dx.doi.org/10.1186/s12944-022-01715-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Peschel, Georg
Grimm, Jonathan
Müller, Martina
Höring, Marcus
Krautbauer, Sabrina
Weigand, Kilian
Liebisch, Gerhard
Buechler, Christa
Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection
title Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection
title_full Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection
title_fullStr Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection
title_full_unstemmed Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection
title_short Sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis C virus infection
title_sort sex-specific changes in triglyceride profiles in liver cirrhosis and hepatitis c virus infection
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9590217/
https://www.ncbi.nlm.nih.gov/pubmed/36280840
http://dx.doi.org/10.1186/s12944-022-01715-w
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