Cargando…
Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C
The clinical significance of mac-2 binding protein glycosylation isomer (M2BPGi) levels based on virological responses due to antiviral therapy has not been fully evaluated. We compared the change before and 24 weeks after the therapy with daclatasvir and asunaprevir (DCV+ASV) of M2BPGi levels with...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227298/ https://www.ncbi.nlm.nih.gov/pubmed/34201309 http://dx.doi.org/10.3390/biomedicines9060660 |
_version_ | 1783712492044681216 |
---|---|
author | Takakusagi, Satoshi Sato, Ken Marubashi, Kyoko Kizawa, Kazuko Kosone, Takashi Kakizaki, Satoru Takagi, Hitoshi Uraoka, Toshio |
author_facet | Takakusagi, Satoshi Sato, Ken Marubashi, Kyoko Kizawa, Kazuko Kosone, Takashi Kakizaki, Satoru Takagi, Hitoshi Uraoka, Toshio |
author_sort | Takakusagi, Satoshi |
collection | PubMed |
description | The clinical significance of mac-2 binding protein glycosylation isomer (M2BPGi) levels based on virological responses due to antiviral therapy has not been fully evaluated. We compared the change before and 24 weeks after the therapy with daclatasvir and asunaprevir (DCV+ASV) of M2BPGi levels with those of other fibrosis markers in 73 chronic hepatitis C cases. Moreover, we examined the association between M2BPGi levels and hepatocarcinogenesis in sustained virological response (SVR) and non-SVR cases. M2BPGi levels were significantly improved at post-treatment week 24 (PTW24) in SVR but not non-SVR cases, whereas the changes of other fibrosis markers showed the same tendency in both SVR and non-SVR cases. M2BPGi levels were well correlated with other fibrosis markers at baseline but not PTW24. The incidence of hepatocellular carcinoma (HCC) was significantly associated with M2BPGi levels at PTW24. The achievement of SVR significantly affected the improvement of M2BPGi levels that best reflected the effect of direct-acting antivirals among the fibrosis markers. Furthermore, M2BPGi levels at PTW24 were also associated with the incidence of HCC in only SVR cases. However, the rapid decrease of M2BPGi levels might reflect the amelioration of liver inflammation rather than the improvement of liver fibrosis, which should be further elucidated. |
format | Online Article Text |
id | pubmed-8227298 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-82272982021-06-26 Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C Takakusagi, Satoshi Sato, Ken Marubashi, Kyoko Kizawa, Kazuko Kosone, Takashi Kakizaki, Satoru Takagi, Hitoshi Uraoka, Toshio Biomedicines Article The clinical significance of mac-2 binding protein glycosylation isomer (M2BPGi) levels based on virological responses due to antiviral therapy has not been fully evaluated. We compared the change before and 24 weeks after the therapy with daclatasvir and asunaprevir (DCV+ASV) of M2BPGi levels with those of other fibrosis markers in 73 chronic hepatitis C cases. Moreover, we examined the association between M2BPGi levels and hepatocarcinogenesis in sustained virological response (SVR) and non-SVR cases. M2BPGi levels were significantly improved at post-treatment week 24 (PTW24) in SVR but not non-SVR cases, whereas the changes of other fibrosis markers showed the same tendency in both SVR and non-SVR cases. M2BPGi levels were well correlated with other fibrosis markers at baseline but not PTW24. The incidence of hepatocellular carcinoma (HCC) was significantly associated with M2BPGi levels at PTW24. The achievement of SVR significantly affected the improvement of M2BPGi levels that best reflected the effect of direct-acting antivirals among the fibrosis markers. Furthermore, M2BPGi levels at PTW24 were also associated with the incidence of HCC in only SVR cases. However, the rapid decrease of M2BPGi levels might reflect the amelioration of liver inflammation rather than the improvement of liver fibrosis, which should be further elucidated. MDPI 2021-06-08 /pmc/articles/PMC8227298/ /pubmed/34201309 http://dx.doi.org/10.3390/biomedicines9060660 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Takakusagi, Satoshi Sato, Ken Marubashi, Kyoko Kizawa, Kazuko Kosone, Takashi Kakizaki, Satoru Takagi, Hitoshi Uraoka, Toshio Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C |
title | Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C |
title_full | Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C |
title_fullStr | Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C |
title_full_unstemmed | Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C |
title_short | Impact of M2BPGi on the Hepatocarcinogenesis after the Combination Therapy with Daclatasvir and Asunaprevir for Hepatitis C |
title_sort | impact of m2bpgi on the hepatocarcinogenesis after the combination therapy with daclatasvir and asunaprevir for hepatitis c |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8227298/ https://www.ncbi.nlm.nih.gov/pubmed/34201309 http://dx.doi.org/10.3390/biomedicines9060660 |
work_keys_str_mv | AT takakusagisatoshi impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc AT satoken impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc AT marubashikyoko impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc AT kizawakazuko impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc AT kosonetakashi impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc AT kakizakisatoru impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc AT takagihitoshi impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc AT uraokatoshio impactofm2bpgionthehepatocarcinogenesisafterthecombinationtherapywithdaclatasvirandasunaprevirforhepatitisc |