CYP2C9*2 is associated with indomethacin treatment failure for patent ductus arteriosus.

Sydney R Rooney, Elaine L Shelton, Ida Aka, Christian M Shaffer, Ronald I Clyman, John M Dagle, Kelli Ryckman, Tamorah R Lewis, Jeff Reese, Sara L Van Driest, Prince J Kannankeril
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Abstract

Aims: To identify clinical andgenetic factors associated with indomethacin treatment failure in preterm neonates with patent ductus arteriosus (PDA). Patients & Methods: This is a multicenter cohort study of 144 preterm infants (22-32 weeks gestational age) at three centers who received at least one treatment course of indomethacin for PDA. Indomethacin failure was defined as requiring subsequent surgical intervention. Results: In multivariate analysis, gestational age (AOR 0.76, 95% CI 0.60-0.96), surfactant use (AOR 9.77, 95% CI 1.15-83.26), and CYP2C9*2 (AOR 3.74; 95% CI 1.34-10.44) were each associated with indomethacin failure. Conclusion: Age, surfactant use, and CYP2C9*2 influence indomethacin treatment outcome in preterm infants with PDA. This combination of clinical and genetic factors may facilitate targeted indomethacin use for PDA.

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CYP2C9*2 与吲哚美辛治疗动脉导管未闭失败有关。
目的:确定与吲哚美辛治疗早产儿动脉导管未闭(PDA)失败相关的临床和遗传因素。患者和方法:这是一项多中心队列研究,在三个中心对 144 名早产儿(胎龄 22-32 周)进行了研究,这些早产儿至少接受过一个疗程的吲哚美辛治疗 PDA。吲哚美辛治疗失败的定义是随后需要手术干预。结果在多变量分析中,胎龄(AOR 0.76,95% CI 0.60-0.96)、表面活性物质的使用(AOR 9.77,95% CI 1.15-83.26)和 CYP2C9*2 (AOR 3.74;95% CI 1.34-10.44)均与吲哚美辛失败有关。结论年龄、表面活性物质的使用和 CYP2C9*2 会影响 PDA 早产儿的吲哚美辛治疗效果。临床和遗传因素的结合可能有助于有针对性地使用吲哚美辛治疗 PDA。
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