首页> 外文期刊>Clinical Psychopharmacology and Neuroscience >No Association between the Response to the Addition of an Atypical Antipsychotic Drug to an SSRI or SNRI and the BDNF (Val66Met) Polymorphism in Refractory Major Depressive Disorder in Japanese Patients
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No Association between the Response to the Addition of an Atypical Antipsychotic Drug to an SSRI or SNRI and the BDNF (Val66Met) Polymorphism in Refractory Major Depressive Disorder in Japanese Patients

机译:在日本患者难治性重度抑郁症患者中,将非典型抗精神病药添加到SSRI或SNRI中的反应与BDNF(Val66Met)多态性之间没有关联

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Objective This study examined the association between the brain-derived neurotrophic factor (BDNF) (Val66Met) polymorphism and the response to the addition of an atypical antipsychotic drug to a selective serotonin reuptake inhibitor (SSRI) or serotonin-norepinephrine reuptake inhibitor (SNRI) in treatment-refractory depression. Methods The study enrolled 64 patients meeting the Diagnostic and Statistical Manual of Mental Disorders-IV criteria for major depressive disorder who were treated with at least two courses of a single antidepressant, but who had Hamilton Depression Rating Scale (HAMD-17) scores ≥15 points that were reduced less than 50% over at least a 4-week treatment period. There were 24 males and 40 females (age range 27-68 years; mean±SD, 48±13 years). The patients' clinical improvement was evaluated using the HAMD-17. Patients with at least a 50% decrease in the HAMD-17 score were defined as responders. Serum BDNF levels were assayed using enzyme-linked immunosorbent assays and the presence of the BDNF (Val66Met) polymorphism was determined using the TaqMan genotyping assay. Results No correlation was found between the BDNF (Val66Met) polymorphism and a positive response to adding an atypical antipsychotic drug. No differences were observed in the changes in the serum BDNF levels and HAMD-17 scores between Val66Val and Met-carriers. In addition, in patients who experienced remission, the atypical antipsychotic drug was discontinued after at least 3 months of treatment and the patients were then followed for 1 year; 14 of 27 patients (52%) relapsed within 1 year. Conclusion These results suggest that the BDNF (Val66Met) polymorphism is not associated with the response to the augmentation of a SSRI or SNRI with an atypical antipsychotic drug, and that the combination of an atypical antipsychotic drug and a SSRI or SNRI should be continued for 3 months or more in refractory depressed patients in the Japanese population.
机译:目的这项研究探讨了脑源性神经营养因子(BDNF)(Val66Met)多态性与非典型抗精神病药加入选择性5-羟色胺再摄取抑制剂(SSRI)或5-羟色胺-去甲肾上腺素再摄取抑制剂(SNRI)的反应之间的关系。治疗难治性抑郁症。方法该研究招募了64例符合重度抑郁症的《精神疾病诊断和统计手册-IV》标准的患者,他们接受了至少两个疗程的单一抗抑郁药治疗,但汉密尔顿抑郁量表(HAMD-17)得分≥15在至少4周的治疗期内减少的点数不到50%。男24例,女40例(年龄27-68岁;平均数±SD,48±13岁)。使用HAMD-17评估患者的临床改善。 HAMD-17评分至少降低50%的患者被定义为有反应者。使用酶联免疫吸附测定法测定血清BDNF水平,并使用TaqMan基因分型测定法确定BDNF(Val66Met)多态性的存在。结果BDNF(Val66Met)多态性与添加非典型抗精神病药的阳性反应之间没有相关性。 Val66Val和Met携带者之间的血清BDNF水平和HAMD-17得分的变化未见差异。此外,对于已缓解的患者,非典型抗精神病药物在治疗至少3个月后停药,然后对其随访1年。 27例患者中有14例(52%)在1年内复发。结论这些结果表明,BDNF(Val66Met)多态性与非典型抗精神病药对SSRI或SNRI增强的反应无关,并且非典型抗精神病药与SSRI或SNRI的组合应继续使用3在日本人群中,难治性抑郁症患者需要住院数月或更长时间。

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