Association between an IL‐28B genetic polymorphism and the efficacy of the response‐guided pegylated interferon therapy in children with chronic hepatic C infection. Issue 4 (13th September 2012)
- Record Type:
- Journal Article
- Title:
- Association between an IL‐28B genetic polymorphism and the efficacy of the response‐guided pegylated interferon therapy in children with chronic hepatic C infection. Issue 4 (13th September 2012)
- Main Title:
- Association between an IL‐28B genetic polymorphism and the efficacy of the response‐guided pegylated interferon therapy in children with chronic hepatic C infection
- Authors:
- Komatsu, Haruki
Inui, Ayano
Tsunoda, Tomoyuki
Sogo, Tsuyoshi
Fujisawa, Tomoo - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr1087-sec-0001" sec-type="section"> <title>Aim</title> <p>The relation between interleukin‐28B (<italic>IL‐28B</italic>) genotypes and treatment‐induced hepatitis C virus (HCV) clearance in children is unknown. This was a retrospective study to evaluate the association between an IL‐28B genotype (rs8099917) and pegylated (PEG) interferon (IFN) response.</p> </sec> <sec id="hepr1087-sec-0002" sec-type="section"> <title>Methods</title> <p>Sixty‐three children (median age, 7 years; range, 3–17 years; 22 with HCV genotype 1 and 41 with genotype non‐1) with chronic HCV infection who were treated with response‐guided PEG IFN on the basis of viral load were evaluated.</p> </sec> <sec id="hepr1087-sec-0003" sec-type="section"> <title>Results</title> <p>The duration of treatment with PEG IFN was 24 weeks in one child (2%), 36 weeks in eight children (13%), 48 weeks in 36 children (57%), 60 weeks in 11 children (17%) and 72 weeks in seven children (11%). Of the total 63 children, 54 (86%) were initially treated with PEG IFN‐α‐2a monotherapy. The remaining nine (14%) received PEG IFN plus ribavirin as the initial therapy. Of the 54 children initially treated with monotherapy, 35 (65%) continued receiving monotherapy until the end of treatment. In the remaining 19 (35%), monotherapy was changed to PEG IFN plus ribavirin at 12 or 24 weeks of treatment. Of the total 63 children, 54 (86%)<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr1087-sec-0001" sec-type="section"> <title>Aim</title> <p>The relation between interleukin‐28B (<italic>IL‐28B</italic>) genotypes and treatment‐induced hepatitis C virus (HCV) clearance in children is unknown. This was a retrospective study to evaluate the association between an IL‐28B genotype (rs8099917) and pegylated (PEG) interferon (IFN) response.</p> </sec> <sec id="hepr1087-sec-0002" sec-type="section"> <title>Methods</title> <p>Sixty‐three children (median age, 7 years; range, 3–17 years; 22 with HCV genotype 1 and 41 with genotype non‐1) with chronic HCV infection who were treated with response‐guided PEG IFN on the basis of viral load were evaluated.</p> </sec> <sec id="hepr1087-sec-0003" sec-type="section"> <title>Results</title> <p>The duration of treatment with PEG IFN was 24 weeks in one child (2%), 36 weeks in eight children (13%), 48 weeks in 36 children (57%), 60 weeks in 11 children (17%) and 72 weeks in seven children (11%). Of the total 63 children, 54 (86%) were initially treated with PEG IFN‐α‐2a monotherapy. The remaining nine (14%) received PEG IFN plus ribavirin as the initial therapy. Of the 54 children initially treated with monotherapy, 35 (65%) continued receiving monotherapy until the end of treatment. In the remaining 19 (35%), monotherapy was changed to PEG IFN plus ribavirin at 12 or 24 weeks of treatment. Of the total 63 children, 54 (86%) achieved a sustained virological response (SVR). In univariate analysis, rs8099917 genotype TT (<italic>P</italic> = 0.075) showed a weak association with SVR. However, the multivariate analysis revealed no predictive factors which had a significant association with SVR.</p> </sec> <sec id="hepr1087-sec-0004" sec-type="section"> <title>Conclusion</title> <p>The <italic>IL‐28B</italic> genotype was not a strong pretreatment predictor for SVR in a mixed genotype cohort of children treated with response‐guided PEG IFN therapy.</p> </sec> </abstract> … (more)
- Is Part Of:
- Hepatology research. Volume 43:Issue 4(2013:Apr.)
- Journal:
- Hepatology research
- Issue:
- Volume 43:Issue 4(2013:Apr.)
- Issue Display:
- Volume 43, Issue 4 (2013)
- Year:
- 2013
- Volume:
- 43
- Issue:
- 4
- Issue Sort Value:
- 2013-0043-0004-0000
- Page Start:
- 327
- Page End:
- 338
- Publication Date:
- 2012-09-13
- 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/j.1872-034X.2012.01087.x ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
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