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Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients

Chronic hepatitis C (CHC) is strongly associated with risks of cardiovascular diseases. The impact of direct acting antiviral (DAA) therapy on central blood pressure remains unclear. This investigation evaluates changes in central blood pressure following DAA therapy. One hundred and two DAA-treated...

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Autores principales: Cheng, Pin-Nan, Chen, Ju-Yi, Chiu, Yen-Cheng, Chiu, Hung-Chih, Tsai, Liang-Miin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363767/
https://www.ncbi.nlm.nih.gov/pubmed/30723238
http://dx.doi.org/10.1038/s41598-018-37829-4
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author Cheng, Pin-Nan
Chen, Ju-Yi
Chiu, Yen-Cheng
Chiu, Hung-Chih
Tsai, Liang-Miin
author_facet Cheng, Pin-Nan
Chen, Ju-Yi
Chiu, Yen-Cheng
Chiu, Hung-Chih
Tsai, Liang-Miin
author_sort Cheng, Pin-Nan
collection PubMed
description Chronic hepatitis C (CHC) is strongly associated with risks of cardiovascular diseases. The impact of direct acting antiviral (DAA) therapy on central blood pressure remains unclear. This investigation evaluates changes in central blood pressure following DAA therapy. One hundred and two DAA-treated patients were prospectively enrolled. Lipid profiles and pulse wave analysis of brachial artery by cuff sphygmomanometry including augmentation index (AIx), a parameter of central artery stiffness, were evaluated. All of the 102 patients achieved sustained virological response (SVR12). Cholesterol and LDL significantly increased following SVR12. Along with lipid changes, significantly higher central diastolic pressure (78.2 ± 14.2 mm Hg at baseline vs. 83.3 ± 13.9 mm Hg at SVR12, p = 0.011) and AIx (33.0 ± 12.7% at baseline vs. 36.9 ± 12.9% at SVR12, p = 0.012) were only observed in the advanced fibrosis patients. Co-morbid diseases, including hypertension (33.4 ± 13.0% vs. 39.7 ± 12.6%, p = 0.003), abnormal waist circumference (33.8 ± 12.2% vs. 38.0 ± 13.2%, p = 0.027), and metabolic syndrome (34.5 ± 12.1% vs. 39.0 ± 11.2%, p = 0.043) were associated with augmented AIx upon SVR12. The augmented central artery stiffness following viral eradication by DAA therapy may raise the concern of short-term cardiovascular risk in CHC patients.
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spelling pubmed-63637672019-02-07 Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients Cheng, Pin-Nan Chen, Ju-Yi Chiu, Yen-Cheng Chiu, Hung-Chih Tsai, Liang-Miin Sci Rep Article Chronic hepatitis C (CHC) is strongly associated with risks of cardiovascular diseases. The impact of direct acting antiviral (DAA) therapy on central blood pressure remains unclear. This investigation evaluates changes in central blood pressure following DAA therapy. One hundred and two DAA-treated patients were prospectively enrolled. Lipid profiles and pulse wave analysis of brachial artery by cuff sphygmomanometry including augmentation index (AIx), a parameter of central artery stiffness, were evaluated. All of the 102 patients achieved sustained virological response (SVR12). Cholesterol and LDL significantly increased following SVR12. Along with lipid changes, significantly higher central diastolic pressure (78.2 ± 14.2 mm Hg at baseline vs. 83.3 ± 13.9 mm Hg at SVR12, p = 0.011) and AIx (33.0 ± 12.7% at baseline vs. 36.9 ± 12.9% at SVR12, p = 0.012) were only observed in the advanced fibrosis patients. Co-morbid diseases, including hypertension (33.4 ± 13.0% vs. 39.7 ± 12.6%, p = 0.003), abnormal waist circumference (33.8 ± 12.2% vs. 38.0 ± 13.2%, p = 0.027), and metabolic syndrome (34.5 ± 12.1% vs. 39.0 ± 11.2%, p = 0.043) were associated with augmented AIx upon SVR12. The augmented central artery stiffness following viral eradication by DAA therapy may raise the concern of short-term cardiovascular risk in CHC patients. Nature Publishing Group UK 2019-02-05 /pmc/articles/PMC6363767/ /pubmed/30723238 http://dx.doi.org/10.1038/s41598-018-37829-4 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Cheng, Pin-Nan
Chen, Ju-Yi
Chiu, Yen-Cheng
Chiu, Hung-Chih
Tsai, Liang-Miin
Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients
title Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients
title_full Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients
title_fullStr Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients
title_full_unstemmed Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients
title_short Augmenting central arterial stiffness following eradication of HCV by direct acting antivirals in advanced fibrosis patients
title_sort augmenting central arterial stiffness following eradication of hcv by direct acting antivirals in advanced fibrosis patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6363767/
https://www.ncbi.nlm.nih.gov/pubmed/30723238
http://dx.doi.org/10.1038/s41598-018-37829-4
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