硫嘌呤疗法的个性化:当前建议和未来展望。

IF 2.1 4区 医学 Q3 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Pub Date : 2024-09-14 Print Date: 2024-09-01 DOI:10.2478/acph-2024-0030
Dunja Urbančič, Flaka Pasha, Alenka Šmid, Irena Mlinarič-Raščan
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引用次数: 0

摘要

尽管生物制剂领域取得了巨大的治疗进步,但硫嘌呤等小分子合成药物(包括硫唑嘌呤、巯嘌呤和硫鸟嘌呤)仍然是治疗炎症性肠病、其他自身免疫性疾病和癌症的重要治疗支柱。本综述介绍了硫嘌呤用药的最新指南,强调了在药物基因组学指导下进行个体化治疗的重要性。文章强调了基于纽狄克水解酶 15 (NUDT15) 和硫嘌呤 S-甲基转移酶 (TPMT) 基因型的剂量调整,以及硫嘌呤 S-甲基转移酶活性和硫嘌呤代谢概况。此外,文章还对硫嘌呤药物基因组学领域的新兴研究进行了深入探讨,其中包括新型遗传标记和基因检测技术的发展。最后,文章强调了结合遗传、代谢和临床因素的综合方法在进一步个体化硫嘌呤治疗方面的潜力。
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Personalization of thiopurine therapy: Current recommendations and future perspectives.

Despite great therapeutic advances in the field of biologics, small synthetic molecules such as thiopurines, including azathioprine, mercaptopurine, and thioguanine, remain an important therapeutic pillar in the treatment of inflammatory bowel disease, other autoimmune disorders, and cancer. This review presents the latest guidelines for thiopurine administration, highlighting the importance of individualized therapy guided by pharmacogenomics. It emphasizes dose adjustment based on nudix hydrolase 15 (NUDT15) and thiopurine S-methyltransferase (TPMT) genotype, along side thiopurine S-methyltransferase activity and thiopurine metabolic profile. In addition, the article takes a critical look at emerging research in the field of thiopurine pharmaco genomics featuring novel genetic markers and technological developments in genetic testing. Finally, the potential of integrated approaches that combine genetic, meta bolic, and clinical factors to further individualize thiopurine therapy is highlighted.

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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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