Association of ITPA polymorphism with outcomes of peginterferon-α plus ribavirin combination therapy

AIM:To analyzed the association between inosine triphosphatase(ITPA)(rs1127354) genotypes and sustained virological response(SVR) rates in peginterferon(Peg-IFN)α + ribavirin(RBV) treatment.METHODS:Patients who underwent Peg-IFNα + RBV combination therapy were enrolled(n = 120) and they had no histo...

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Veröffentlicht in:World journal of gastrointestinal pharmacology and therapeutics 2013-08, Vol.4 (3), p.54-60
Hauptverfasser: Fujino, Tatsuya, Aoyagi, Yoko, Takahashi, Mariko, Yada, Ryoko, Yamamoto, Naoko, Ohishi, Yuki, Nishiura, Akihiko, Kohjima, Motoyuki, Yoshimoto, Tsuyoshi, Fukuizumi, Kunitaka, Nakashima, Manabu, Kato, Masaki, Kotoh, Kazuhiro, Nakamuta, Makoto, Enjoji, Munechika
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container_end_page 60
container_issue 3
container_start_page 54
container_title World journal of gastrointestinal pharmacology and therapeutics
container_volume 4
creator Fujino, Tatsuya
Aoyagi, Yoko
Takahashi, Mariko
Yada, Ryoko
Yamamoto, Naoko
Ohishi, Yuki
Nishiura, Akihiko
Kohjima, Motoyuki
Yoshimoto, Tsuyoshi
Fukuizumi, Kunitaka
Nakashima, Manabu
Kato, Masaki
Kotoh, Kazuhiro
Nakamuta, Makoto
Enjoji, Munechika
description AIM:To analyzed the association between inosine triphosphatase(ITPA)(rs1127354) genotypes and sustained virological response(SVR) rates in peginterferon(Peg-IFN)α + ribavirin(RBV) treatment.METHODS:Patients who underwent Peg-IFNα + RBV combination therapy were enrolled(n = 120) and they had no history of other IFN-based treatments.Variation in hemoglobin levels during therapy,cumulative reduction of RBV dose,frequency of treatment withdrawal,and SVR rates were investigated in each ITPA genotype.RESULTS:In patients with ITPA CC genotype,hemoglobin decline was significantly greater and the percentage of patients in whom total RBV dose was < 60% of standard and/or treatment was withdrawn was significantly higher compared with CA/AA genotype.However,SVR rates were equivalent between CC and CA/AA genotypes,and within a subset of patients with Interleukin 28B(IL28B)(rs8099917) TT genotype,SVR rates tended to be higher in patients with ITPA CC genotype,although the difference was not significant.CONCLUSION:ITPA CC genotype was a disadvantageous factor for Peg-IFNα + RBV treatment in relation to completion rates and RBV dose.However,CC genotype was not inferior to CA/AA genotype for SVR rates.When full-length treatment is accomplished,it is plausible that more SVR is achieved in patients with ITPA CC variant,especially in a background of IL28B TT genotype.
doi_str_mv 10.4292/wjgpt.v4.i3.54
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All rights reserved. 2013</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2634-c805594f30d0c80121253aae33221bbcd124074e0d9cac1eb853dd2199851a913</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/71415X/71415X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729868/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3729868/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,315,728,781,785,886,27929,27930,53796,53798</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23919217$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujino, Tatsuya</creatorcontrib><creatorcontrib>Aoyagi, Yoko</creatorcontrib><creatorcontrib>Takahashi, Mariko</creatorcontrib><creatorcontrib>Yada, Ryoko</creatorcontrib><creatorcontrib>Yamamoto, Naoko</creatorcontrib><creatorcontrib>Ohishi, Yuki</creatorcontrib><creatorcontrib>Nishiura, Akihiko</creatorcontrib><creatorcontrib>Kohjima, Motoyuki</creatorcontrib><creatorcontrib>Yoshimoto, Tsuyoshi</creatorcontrib><creatorcontrib>Fukuizumi, Kunitaka</creatorcontrib><creatorcontrib>Nakashima, Manabu</creatorcontrib><creatorcontrib>Kato, Masaki</creatorcontrib><creatorcontrib>Kotoh, Kazuhiro</creatorcontrib><creatorcontrib>Nakamuta, Makoto</creatorcontrib><creatorcontrib>Enjoji, Munechika</creatorcontrib><title>Association of ITPA polymorphism with outcomes of peginterferon-α plus ribavirin combination therapy</title><title>World journal of gastrointestinal pharmacology and therapeutics</title><addtitle>World Journal of Gastrointestinal Pharmacology and Therapeutics</addtitle><description>AIM:To analyzed the association between inosine triphosphatase(ITPA)(rs1127354) genotypes and sustained virological response(SVR) rates in peginterferon(Peg-IFN)α + ribavirin(RBV) treatment.METHODS:Patients who underwent Peg-IFNα + RBV combination therapy were enrolled(n = 120) and they had no history of other IFN-based treatments.Variation in hemoglobin levels during therapy,cumulative reduction of RBV dose,frequency of treatment withdrawal,and SVR rates were investigated in each ITPA genotype.RESULTS:In patients with ITPA CC genotype,hemoglobin decline was significantly greater and the percentage of patients in whom total RBV dose was &amp;lt; 60% of standard and/or treatment was withdrawn was significantly higher compared with CA/AA genotype.However,SVR rates were equivalent between CC and CA/AA genotypes,and within a subset of patients with Interleukin 28B(IL28B)(rs8099917) TT genotype,SVR rates tended to be higher in patients with ITPA CC genotype,although the difference was not significant.CONCLUSION:ITPA CC genotype was a disadvantageous factor for Peg-IFNα + RBV treatment in relation to completion rates and RBV dose.However,CC genotype was not inferior to CA/AA genotype for SVR rates.When full-length treatment is accomplished,it is plausible that more SVR is achieved in patients with ITPA CC variant,especially in a background of IL28B TT genotype.</description><subject>28B;Inosine</subject><subject>Brief</subject><subject>C;Interleukin</subject><subject>Chronic</subject><subject>hepatitis</subject><subject>triphosphatase;Peginterferon;Ribavirin</subject><issn>2150-5349</issn><issn>2150-5349</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpVkc1O3DAURq2qqCBgy7KK1E03Cb7-SeJNpRFqAQkJFrC2HMdJjBI72Mmgeay-SJ-JDDOgqTf-JB-fe6UPoQvAGSOCXL4-t-OUrVlmacbZF3RCgOOUUya-HuRjdB7jM14O43nO4Bs6JlSAIFCcILOK0WurJutd4pvk9vFhlYy-3ww-jJ2NQ_Jqpy7x86T9YOIWGU1r3WRCY4J36b-_ydjPMQm2UmsbrEsWsLJuZ5w6E9S4OUNHjeqjOd_fp-jpz-_Hq5v07v769mp1l2qSU5bqEnMuWENxjZcMBAinShlKCYGq0jUQhgtmcC200mCqktO6JiBEyUEJoKfo1847ztVgam3cFFQvx2AHFTbSKyv_f3G2k61fS1oQUeblIvi5FwT_Mps4ycFGbfpeOePnKIFBSXNaAFvQbIfq4GMMpvkcA1hu65Hv9cg1k5ZKvv3w_XC5T_yjjAX4sTd23rUv1rUHSszzgjDK6BuQRJuy</recordid><startdate>20130806</startdate><enddate>20130806</enddate><creator>Fujino, Tatsuya</creator><creator>Aoyagi, Yoko</creator><creator>Takahashi, Mariko</creator><creator>Yada, Ryoko</creator><creator>Yamamoto, Naoko</creator><creator>Ohishi, Yuki</creator><creator>Nishiura, Akihiko</creator><creator>Kohjima, Motoyuki</creator><creator>Yoshimoto, Tsuyoshi</creator><creator>Fukuizumi, Kunitaka</creator><creator>Nakashima, Manabu</creator><creator>Kato, Masaki</creator><creator>Kotoh, Kazuhiro</creator><creator>Nakamuta, Makoto</creator><creator>Enjoji, Munechika</creator><general>Baishideng Publishing Group Co., Limited</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20130806</creationdate><title>Association of ITPA polymorphism with outcomes of peginterferon-α plus ribavirin combination therapy</title><author>Fujino, Tatsuya ; Aoyagi, Yoko ; Takahashi, Mariko ; Yada, Ryoko ; Yamamoto, Naoko ; Ohishi, Yuki ; Nishiura, Akihiko ; Kohjima, Motoyuki ; Yoshimoto, Tsuyoshi ; Fukuizumi, Kunitaka ; Nakashima, Manabu ; Kato, Masaki ; Kotoh, Kazuhiro ; Nakamuta, Makoto ; Enjoji, Munechika</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2634-c805594f30d0c80121253aae33221bbcd124074e0d9cac1eb853dd2199851a913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>28B;Inosine</topic><topic>Brief</topic><topic>C;Interleukin</topic><topic>Chronic</topic><topic>hepatitis</topic><topic>triphosphatase;Peginterferon;Ribavirin</topic><toplevel>online_resources</toplevel><creatorcontrib>Fujino, Tatsuya</creatorcontrib><creatorcontrib>Aoyagi, Yoko</creatorcontrib><creatorcontrib>Takahashi, Mariko</creatorcontrib><creatorcontrib>Yada, Ryoko</creatorcontrib><creatorcontrib>Yamamoto, Naoko</creatorcontrib><creatorcontrib>Ohishi, Yuki</creatorcontrib><creatorcontrib>Nishiura, Akihiko</creatorcontrib><creatorcontrib>Kohjima, Motoyuki</creatorcontrib><creatorcontrib>Yoshimoto, Tsuyoshi</creatorcontrib><creatorcontrib>Fukuizumi, Kunitaka</creatorcontrib><creatorcontrib>Nakashima, Manabu</creatorcontrib><creatorcontrib>Kato, Masaki</creatorcontrib><creatorcontrib>Kotoh, Kazuhiro</creatorcontrib><creatorcontrib>Nakamuta, Makoto</creatorcontrib><creatorcontrib>Enjoji, Munechika</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastrointestinal pharmacology and therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujino, Tatsuya</au><au>Aoyagi, Yoko</au><au>Takahashi, Mariko</au><au>Yada, Ryoko</au><au>Yamamoto, Naoko</au><au>Ohishi, Yuki</au><au>Nishiura, Akihiko</au><au>Kohjima, Motoyuki</au><au>Yoshimoto, Tsuyoshi</au><au>Fukuizumi, Kunitaka</au><au>Nakashima, Manabu</au><au>Kato, Masaki</au><au>Kotoh, Kazuhiro</au><au>Nakamuta, Makoto</au><au>Enjoji, Munechika</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of ITPA polymorphism with outcomes of peginterferon-α plus ribavirin combination therapy</atitle><jtitle>World journal of gastrointestinal pharmacology and therapeutics</jtitle><addtitle>World Journal of Gastrointestinal Pharmacology and Therapeutics</addtitle><date>2013-08-06</date><risdate>2013</risdate><volume>4</volume><issue>3</issue><spage>54</spage><epage>60</epage><pages>54-60</pages><issn>2150-5349</issn><eissn>2150-5349</eissn><abstract>AIM:To analyzed the association between inosine triphosphatase(ITPA)(rs1127354) genotypes and sustained virological response(SVR) rates in peginterferon(Peg-IFN)α + ribavirin(RBV) treatment.METHODS:Patients who underwent Peg-IFNα + RBV combination therapy were enrolled(n = 120) and they had no history of other IFN-based treatments.Variation in hemoglobin levels during therapy,cumulative reduction of RBV dose,frequency of treatment withdrawal,and SVR rates were investigated in each ITPA genotype.RESULTS:In patients with ITPA CC genotype,hemoglobin decline was significantly greater and the percentage of patients in whom total RBV dose was &amp;lt; 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subjects 28B
Inosine
Brief
C
Interleukin
Chronic
hepatitis
triphosphatase
Peginterferon
Ribavirin
title Association of ITPA polymorphism with outcomes of peginterferon-α plus ribavirin combination therapy
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