Sandritter Tracy, Chevalier Rachel, Abt Rebecca, Shakhnovich Valentina
Division of Clinical Pharmacology/Medical Toxicology and Therapeutic Innovation, Children's Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USA.
Department of Pharmacy Practice, School of Pharmacy, University of Missouri-Kansas City, Kansas City, MO 64108, USA.
Pharmaceuticals (Basel). 2023 Jun 16;16(6):889. doi: 10.3390/ph16060889.
Gastroenterologists represent some of the earlier adopters of precision medicine through pharmacogenetic testing by embracing upfront genotyping for thiopurine S-methyltransferase nucleotide diphosphatase () before prescribing 6-mercaptopurine or azathioprine for the treatment of inflammatory bowel disease. Over the last two decades, pharmacogenetic testing has become more readily available for other genes relevant to drug dose individualization. Common medications prescribed by gastroenterologists for conditions other than inflammatory bowel disease now have actionable guidelines, which can improve medication efficacy and safety; however, a clear understanding of how to interpret the results remains a challenge for many clinicians, precluding wide implementation of genotype-guided dosing for drugs other than 6-mercaptopurine and azathioprine. Our goal is to provide a practical tutorial on the currently available pharmacogenetic testing options and a results interpretation for drug-gene pairs important to medications commonly used in pediatric gastroenterology. We focus on evidence-based clinical guidelines published by the Clinical Pharmacogenetics Implementation Consortium (CPIC) to highlight relevant drug-gene pairs, including proton pump inhibitors and selective serotonin reuptake inhibitors and cytochrome P450 (CYP) 2C19, ondansetron and CYP2D6, 6-mercaptopurine and and Nudix hydrolase 15 (), and budesonide and tacrolimus and CYP3A5.
胃肠病学家是精准医学的早期采用者之一,他们通过药物遗传学检测,在为炎症性肠病患者开6-巯基嘌呤或硫唑嘌呤之前,先对硫嘌呤S-甲基转移酶核苷酸二磷酸酶()进行基因分型。在过去的二十年里,药物遗传学检测对于其他与药物剂量个体化相关的基因来说变得更容易获得。胃肠病学家为炎症性肠病以外的疾病开具的常用药物现在有了可操作的指南,这可以提高药物疗效和安全性;然而,对于许多临床医生来说,清楚地理解如何解读检测结果仍然是一个挑战,这使得除了6-巯基嘌呤和硫唑嘌呤之外的药物无法广泛实施基因型指导给药。我们的目标是提供一个关于当前可用的药物遗传学检测选项的实用教程,以及对儿科胃肠病学常用药物重要的药物-基因对的结果解读。我们重点关注临床药物遗传学实施联盟(CPIC)发布的循证临床指南,以突出相关的药物-基因对,包括质子泵抑制剂和选择性5-羟色胺再摄取抑制剂与细胞色素P450(CYP)2C19、昂丹司琼与CYP2D6、6-巯基嘌呤与和Nudix水解酶15(),以及布地奈德和他克莫司与CYP3A5。