Pharmacogenetic Testing in Treatment-resistant Panic Disorder: a Preliminary Analysis.

Q2 Medicine
Marcos Fidry, Morena Mourao Zugliani, Mariana Costa do Cabo, Renan Machado Martins, Manuella Assad Gomez, Clara Gitahy Falcão Faria, Antonio Egidio Nardi, Rafael C Freire
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引用次数: 0

Abstract

Background: Many pharmacological treatments are considered effective in the treatment of panic disorder (PD), however, about 20 to 40% of the patients have treatment-resistant PD. Pharmacogenetics could explain why some patients are treatment-resistant.

Objective: Our objective was to gather preliminary data on the clinical usefulness of pharmacogenetic testing in this disorder.

Methods: Twenty patients with treatment-resistant PD were included in this observational study and submitted to commercial pharmacogenetic testing. Testing panel included gene polymorphisms related to CYP, genes EPHX1, UGT1A4, UGT2B15, ABCB1, ADRA2A, ANKK1, COMT, DRD2, FKBP5, GRIK4, GSK3B, HTR1A, HTR2A, HTR2C, MC4R, OPRM1, SCN1A, SLC6A4 and MTHFR. Participants received treatment-as-usual for PD before being enrolled in this study, including first-line and second-line medications for PD.

Results: In 30% of the patients, the tests indicated reduced chance of response to the prescribed drug, while they indicated very low serum levels of the prescribed drug in 20% of the subjects. The pharmacogenetic tests predicted reduction of MTHFR enzyme activity in 74% of the patients. ABCB1 gene alleles associated to drug resistance were found in 90% of the samples.

Conclusion: Commercial pharmacogenetic testing failed to predict negative treatment outcome in most patients with PD. The association between treatment-resistance in PD and the genes CYP2C19, MTHFR and ABCB1 deserves further study.

难治性惊恐障碍的药物遗传学检测:初步分析。
背景:许多药物治疗被认为对惊恐障碍(PD)的治疗有效,然而,大约20 - 40%的患者有治疗抵抗性PD。药物遗传学可以解释为什么有些病人对治疗有抗药性。目的:我们的目的是收集药物遗传学检测在这种疾病中的临床应用的初步数据。方法:将20例难治性帕金森病患者纳入这项观察性研究,并进行商业化药物遗传学检测。检测组包括CYP、EPHX1、UGT1A4、UGT2B15、ABCB1、ADRA2A、ANKK1、COMT、DRD2、FKBP5、GRIK4、GSK3B、HTR1A、HTR2A、HTR2C、MC4R、OPRM1、SCN1A、SLC6A4和MTHFR相关基因多态性。在参加这项研究之前,参与者接受了常规的PD治疗,包括一线和二线药物治疗。结果:在30%的患者中,测试表明对处方药反应的机会降低,而在20%的受试者中,测试表明处方药的血清水平非常低。药物遗传学试验预测74%的患者MTHFR酶活性降低。在90%的样本中发现与耐药相关的ABCB1基因等位基因。结论:商业药物遗传学检测无法预测大多数PD患者的阴性治疗结果。PD耐药与CYP2C19、MTHFR和ABCB1基因的关系值得进一步研究。
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来源期刊
Clinical Practice and Epidemiology in Mental Health
Clinical Practice and Epidemiology in Mental Health Medicine-Psychiatry and Mental Health
CiteScore
5.30
自引率
0.00%
发文量
17
期刊介绍: Clinical Practice & Epidemiology in Mental Health is an open access online journal, which publishes Research articles, Reviews, Letters in all areas of clinical practice and epidemiology in mental health covering the following topics: Clinical and epidemiological research in psychiatry and mental health; diagnosis, prognosis and treatment of mental health conditions; and frequencies and determinants of mental health conditions in the community and the populations at risk; research and economic aspects of psychiatry, with special attention given to manuscripts presenting new results and methods in the area; and clinical epidemiologic investigation of pharmaceutical agents. Clinical Practice & Epidemiology in Mental Health, a peer reviewed journal, aims to provide the most complete and reliable source of information on current developments in the field. The emphasis will be on publishing quality articles rapidly and freely available worldwide.
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