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dc.contributor.author김영주*
dc.contributor.author곽혜선*
dc.date.accessioned2020-08-20T16:30:25Z-
dc.date.available2020-08-20T16:30:25Z-
dc.date.issued2020*
dc.identifier.issn1744-6872*
dc.identifier.issn1744-6880*
dc.identifier.otherOAK-27349*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/255084-
dc.description.abstractObjective The present prospective follow-up study aimed to evaluate the effects ofKCNMB2gene polymorphisms on ritodrine efficacy and adverse drug events (ADEs) in patients with preterm labor. Methods A total of 163 preterm labor patients were included in this single-center study. Nine single nucleotide polymorphisms (SNPs) in theKCNMB2gene (rs10936979, rs7624046, rs7429015, rs7625907, rs6443559, rs9839376, rs9637454, rs11918114, and rs1382045) were assessed. The primary endpoint was time to delivery, and the secondary endpoint was ritodrine-induced ADEs. Results Patients with variant homozygotes of two SNPs (rs7624046 and rs9839376), which were in linkage disequilibrium, showed 2.06 [95% confidence interval (CI), 1.14-3.73] and 2.68 (95% CI, 1.16-6.20) times the hazard of time to delivery compared to wild-type allele carriers, respectively. Among demographic characteristics, gestational age at start of drug therapy and modified Bishop score were significant factors for time to delivery. Regarding safety outcomes, patients with variant homozygotes of rs7625907 had fewer ADEs compared to those with other genotypes (odds ratio, 0.32; 95% CI, 0.13-0.83). Conclusion This pharmacogenomic study suggests that ritodrine efficacy and ADEs are associated withKCNMB2gene polymorphisms in patients with preterm labor.*
dc.languageEnglish*
dc.publisherLIPPINCOTT WILLIAMS &amp*
dc.publisherWILKINS*
dc.subjectadverse drug event*
dc.subjectKCNMB2*
dc.subjectpreterm labor*
dc.subjectritodrine*
dc.subjectsingle nucleotide polymorphism*
dc.subjecttime to delivery*
dc.titleEffects ofKCNMB2gene polymorphisms on ritodrine therapy outcomes in women with preterm labor*
dc.typeArticle*
dc.relation.issue6*
dc.relation.volume30*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage124*
dc.relation.lastpage130*
dc.relation.journaltitlePHARMACOGENETICS AND GENOMICS*
dc.identifier.doi10.1097/FPC.0000000000000404*
dc.identifier.wosidWOS:000550687800002*
dc.author.googleYoon, Ha Young*
dc.author.googlePark, Jin Young*
dc.author.googleYee, Jeong*
dc.author.googleHwang, Han Sung*
dc.author.googleChung, Jee Eun*
dc.author.googleLee, Kyung Eun*
dc.author.googleKim, Young Ju*
dc.author.googleGwak, Hye Sun*
dc.contributor.scopusid김영주(55801681000)*
dc.date.modifydate20240123100124*
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의과대학 > 의학과 > Journal papers
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