Serum levels of interleukin‐22 and hepatitis B core‐related antigen are associated with treatment response to entecavir therapy in chronic hepatitis B. Issue 10 (26th January 2014)
- Record Type:
- Journal Article
- Title:
- Serum levels of interleukin‐22 and hepatitis B core‐related antigen are associated with treatment response to entecavir therapy in chronic hepatitis B. Issue 10 (26th January 2014)
- Main Title:
- Serum levels of interleukin‐22 and hepatitis B core‐related antigen are associated with treatment response to entecavir therapy in chronic hepatitis B
- Authors:
- Okuhara, Sadahisa
Umemura, Takeji
Joshita, Satoru
Shibata, Soichiro
Kimura, Takefumi
Morita, Susumu
Komatsu, Michiharu
Matsumoto, Akihiro
Yoshizawa, Kaname
Katsuyama, Yoshihiko
Ota, Masao
Tanaka, Eiji - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12287-sec-0001" sec-type="section"> <title>Aim</title> <p>We sought to clarify the associations between serum cytokines and chemokines, hepatitis B surface antigen (HBsAg), hepatitis B core‐related antigen (HBcrAg), and hepatitis B virus (HBV) DNA and response to entecavir therapy in chronic hepatitis B.</p> </sec> <sec id="hepr12287-sec-0002" sec-type="section"> <title>Methods</title> <p>We analyzed six cytokines (interleukin [IL]‐2, IL‐6, IL‐10, IL‐12p70, IL‐21 and IL‐22) and five chemokines (CCL2, CCL3, CXCL9, CXCL10 and CXCL11) before and at 6, 12 and 24 months during entecavir therapy in 48 chronic hepatitis B patients. Quantitative measurement of HBsAg, HBcrAg and HBV DNA was performed. A virological response (VR) was defined as serum HBV DNA of less than 2.1 log copies/mL by treatment month 24.</p> </sec> <sec id="hepr12287-sec-0003" sec-type="section"> <title>Results</title> <p>Thirty‐nine patients (81%) achieved a VR. Serum IL‐6 (<italic>P</italic> = 0.031), CXCL‐9 (<italic>P</italic> = 0.002), and CXCL‐10 (<italic>P</italic> = 0.001) were high in chronic HBV and correlated positively with transaminases and bilirubin. Before treatment, elevated IL‐22 (<italic>P</italic> = 0.031) and lower HBsAg (<italic>P</italic> = 0.001) and HBcrAg (<italic>P</italic> &lt; 0.001), but not HBV DNA, were associated with a favorable treatment outcome. In multivariate analysis, high<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12287-sec-0001" sec-type="section"> <title>Aim</title> <p>We sought to clarify the associations between serum cytokines and chemokines, hepatitis B surface antigen (HBsAg), hepatitis B core‐related antigen (HBcrAg), and hepatitis B virus (HBV) DNA and response to entecavir therapy in chronic hepatitis B.</p> </sec> <sec id="hepr12287-sec-0002" sec-type="section"> <title>Methods</title> <p>We analyzed six cytokines (interleukin [IL]‐2, IL‐6, IL‐10, IL‐12p70, IL‐21 and IL‐22) and five chemokines (CCL2, CCL3, CXCL9, CXCL10 and CXCL11) before and at 6, 12 and 24 months during entecavir therapy in 48 chronic hepatitis B patients. Quantitative measurement of HBsAg, HBcrAg and HBV DNA was performed. A virological response (VR) was defined as serum HBV DNA of less than 2.1 log copies/mL by treatment month 24.</p> </sec> <sec id="hepr12287-sec-0003" sec-type="section"> <title>Results</title> <p>Thirty‐nine patients (81%) achieved a VR. Serum IL‐6 (<italic>P</italic> = 0.031), CXCL‐9 (<italic>P</italic> = 0.002), and CXCL‐10 (<italic>P</italic> = 0.001) were high in chronic HBV and correlated positively with transaminases and bilirubin. Before treatment, elevated IL‐22 (<italic>P</italic> = 0.031) and lower HBsAg (<italic>P</italic> = 0.001) and HBcrAg (<italic>P</italic> &lt; 0.001), but not HBV DNA, were associated with a favorable treatment outcome. In multivariate analysis, high IL‐22 (hazard ratio = 13.67, <italic>P</italic> = 0.046) and low HBcrAg (hazard ratio = 10.88, <italic>P</italic> = 0.048) were independently associated with a VR. The levels of IL‐22 (<italic>P</italic> &lt; 0.001), HBsAg (<italic>P</italic> &lt; 0.001), and HBcrAg (<italic>P</italic> &lt; 0.001) all decreased from baseline to 24 months of treatment in virological responders.</p> </sec> <sec id="hepr12287-sec-0004" sec-type="section"> <title>Conclusion</title> <p>Serum IL‐22 and HBcrAg are predictive markers of a VR to entecavir therapy in patients with chronic hepatitis B.</p> </sec> </abstract> … (more)
- Is Part Of:
- Hepatology research. Volume 44:Issue 10(2014:Oct.)
- Journal:
- Hepatology research
- Issue:
- Volume 44:Issue 10(2014:Oct.)
- Issue Display:
- Volume 44, Issue 10 (2014)
- Year:
- 2014
- Volume:
- 44
- Issue:
- 10
- Issue Sort Value:
- 2014-0044-0010-0000
- Page Start:
- E172
- Page End:
- E180
- Publication Date:
- 2014-01-26
- Subjects:
- Liver -- Diseases -- Periodicals
Liver Diseases -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09284346 ↗
http://firstsearch.oclc.org/journal=1386-6346;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1872-034X ↗
http://www.sciencedirect.com/science/journal/13866346 ↗
http://www3.interscience.wiley.com/journal/118507311/home ↗
http://www.blackwell-synergy.com/rd.asp?goto=journal&code=hep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hepr.12287 ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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