Association of IL28B polymorphisms with virological response to peginterferon and ribavirin therapy in children and adolescents with chronic hepatitis C. Issue 10 (7th January 2014)
- Record Type:
- Journal Article
- Title:
- Association of IL28B polymorphisms with virological response to peginterferon and ribavirin therapy in children and adolescents with chronic hepatitis C. Issue 10 (7th January 2014)
- Main Title:
- Association of IL28B polymorphisms with virological response to peginterferon and ribavirin therapy in children and adolescents with chronic hepatitis C
- Authors:
- Tajiri, Hitoshi
Tanaka, Yasuhito
Takano, Tomoko
Suzuki, Mitsuyoshi
Abukawa, Daiki
Miyoshi, Yoko
Shimizu, Toshiaki
Brooks, Stephen - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12206-sec-0001" sec-type="section"> <title>Aim</title> <p>The objective of the current study was to find baseline predictive factors of response to therapy with pegylated interferon and ribavirin (PEG‐IFN/RBV therapy) in children and adolescents with chronic hepatitis C.</p> </sec> <sec id="hepr12206-sec-0002" sec-type="section"> <title>Methods</title> <p> <italic>IL28B</italic> genotype and mutations in the core of hepatitis C virus (HCV) were analyzed in 30 patients treated with PEG‐IFN/RBV for HCV infection. The initial rate of decrease in the viral load was assessed during the first 2 weeks of treatment.</p> </sec> <sec id="hepr12206-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>IL28B</italic> major allele was seen more frequently in patients with sustained virologic response (SVR) than in non‐SVR patients (<italic>P</italic> &lt; 0.001). There was no difference between these two groups in frequency of Core 70 mutation. Among patients with genotype‐1, SVR was achieved in more patients (<italic>P</italic> = 0.007) in the <italic>IL28B</italic> major allele group than in those in the minor allele group. The early decrements in the viral load (log/2 weeks) were 3.80 ± 0.86 in the genotype‐2 major allele group, 1.82 ± 0.84 in the genotype‐1 major allele group, and 0.41 ± 0.33 in the genotype‐1 minor allele group.</p> </sec> <sec id="hepr12206-sec-0004"<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="hepr12206-sec-0001" sec-type="section"> <title>Aim</title> <p>The objective of the current study was to find baseline predictive factors of response to therapy with pegylated interferon and ribavirin (PEG‐IFN/RBV therapy) in children and adolescents with chronic hepatitis C.</p> </sec> <sec id="hepr12206-sec-0002" sec-type="section"> <title>Methods</title> <p> <italic>IL28B</italic> genotype and mutations in the core of hepatitis C virus (HCV) were analyzed in 30 patients treated with PEG‐IFN/RBV for HCV infection. The initial rate of decrease in the viral load was assessed during the first 2 weeks of treatment.</p> </sec> <sec id="hepr12206-sec-0003" sec-type="section"> <title>Results</title> <p> <italic>IL28B</italic> major allele was seen more frequently in patients with sustained virologic response (SVR) than in non‐SVR patients (<italic>P</italic> &lt; 0.001). There was no difference between these two groups in frequency of Core 70 mutation. Among patients with genotype‐1, SVR was achieved in more patients (<italic>P</italic> = 0.007) in the <italic>IL28B</italic> major allele group than in those in the minor allele group. The early decrements in the viral load (log/2 weeks) were 3.80 ± 0.86 in the genotype‐2 major allele group, 1.82 ± 0.84 in the genotype‐1 major allele group, and 0.41 ± 0.33 in the genotype‐1 minor allele group.</p> </sec> <sec id="hepr12206-sec-0004" sec-type="section"> <title>Conclusions</title> <p>Among pediatric patients with HCV infection the effectiveness of PEG‐IFN/RBV therapy may be lower in the group with genotype‐1 <italic>IL28B</italic> minor alleles than in other groups with <italic>IL28B</italic> major allele. Treatment strategy should be carefully implemented in patients with <italic>IL28B</italic> unfavorable type.</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:
- E38
- Page End:
- E44
- Publication Date:
- 2014-01-07
- 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.12206 ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
British Library DSC - BLDSS-3PM
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