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药物遗传学指导:个性化医疗促进更好的疼痛治疗效果。

Pharmacogenetic guidance: individualized medicine promotes enhanced pain outcomes.

作者信息

Dragic Lisa Lynn, Wegrzyn Erica L, Schatman Michael E, Fudin Jeffrey

机构信息

Central Arkansas Veterans Healthcare System, Little Rock, AR, USA.

Department of Pharmacy, Albany Stratton VA Medical Center, Albany, NY, USA.

出版信息

J Pain Res. 2017 Dec 22;11:37-40. doi: 10.2147/JPR.S144560. eCollection 2018.

DOI:10.2147/JPR.S144560
PMID:29317847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5743122/
Abstract

The use of pharmacogenomics has become more prevalent over the past several years in treating many disease states. Several cytochrome P450 enzymes play a role in the metabolism of many pain medications including opioids and antidepressants. Noncytochrome P450 enzymes such as methylenetetrahydrofolate reductase (MTHFR) and catechol--methyl transferase (COMT) also play a role in the explanation of opioid dosage requirements as well as in response to certain antidepressants. We present the case of a patient with reduced and expression treated with leucovorin 10 mg daily for the management of chronic pain. The use of leucovorin in this patient decreased pain scores, which were clinically significant and increased functionality. This case demonstrates the importance of pharmacogenetics testing in patients, as this can help direct providers to better therapeutic options for their patients.

摘要

在过去几年中,药物基因组学在治疗多种疾病状态方面的应用变得更加普遍。几种细胞色素P450酶在许多止痛药物(包括阿片类药物和抗抑郁药)的代谢中发挥作用。非细胞色素P450酶,如亚甲基四氢叶酸还原酶(MTHFR)和儿茶酚 - 甲基转移酶(COMT),在解释阿片类药物剂量需求以及对某些抗抑郁药的反应方面也发挥作用。我们报告一例患者,其[此处原文可能缺失具体基因名称]表达降低,每天使用10 mg亚叶酸钙治疗慢性疼痛。该患者使用亚叶酸钙后疼痛评分降低,具有临床意义且功能得到改善。该病例证明了对患者进行药物遗传学检测的重要性,因为这有助于指导医疗服务提供者为患者选择更好的治疗方案。

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本文引用的文献

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Prog Neuropsychopharmacol Biol Psychiatry. 2018 Dec 20;87(Pt B):159-167. doi: 10.1016/j.pnpbp.2017.05.012. Epub 2017 May 15.
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A precision medicine approach to a patient with unresolved pain following orthopedic surgery: a case report.一种针对骨科手术后疼痛未缓解患者的精准医疗方法:病例报告
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The COMT Val158 allele is associated with impaired delayed-match-to-sample performance in ADHD.COMT Val158 等位基因与 ADHD 患者的延迟匹配样本任务表现受损有关。
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