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 |
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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 60% of standard and/or treatment was withdrawn was significantly higher compared with CA/AA genotype.However,SVR rates were equivalent between CC and CA/AA genotypes,and within a subset of patients with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. |
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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 &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 &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.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Co., Limited</pub><pmid>23919217</pmid><doi>10.4292/wjgpt.v4.i3.54</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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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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