高5 -羟色胺生物利用度在强迫症临床暴露反应和反应预防中的催化作用

T. Sampaio, C. Lima, F. Corregiari, M. Bernik
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引用次数: 4

摘要

目的:暴露与反应预防(ERP)是治疗强迫症(OCD)的有效方法,但暴露技术对其厌恶性缺乏耐受性,导致其高退出率。有报道称,5-羟色胺(5-HT)在中枢神经系统(CNS)中具有一般的应激耐受力效应,这可能是由于抑制了防御性固定动作模式。先前的研究表明,在OCD药物治疗期间,较高的5-HT基线浓度和缓慢的浓度下降是5-HT再摄取抑制剂良好临床反应的预测因素。本研究的目的是探讨治疗前富血小板血浆(PRP) 5-HT浓度是否与强迫症(OCD)的治疗反应潜伏期和对ERP方案的最终反应相关。方法:30例成人无治疗强迫症患者被纳入8周16期ERP方案。在基线和治疗后测定5-羟色胺浓度。在ERP结束时,耶鲁-布朗强迫症量表(Y-BOCS)下降≥30%的患者被定义为有反应者。结果:4周后观察到基线5-羟色胺浓度与Y-BOCS症状减轻呈正相关。基线5-HT浓度与ERP 8周后的临床反应不相关,可能是由于基线5-HT浓度较低(与较高)的患者的临床反应相似,但延迟。5-羟色胺基线浓度较高的患者在治疗后抑郁症状也有较大改善。结论:本研究结果部分支持了5-HT对强迫症患者应激耐受力影响的假说。根据文献,快速反应者可能含有更多或更大的5-HT神经元,较高的内源性5-HT合成或较低的单胺氧化酶活性;所有这些假设都有待进一步研究。
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The putative catalytic role of higher serotonin bioavailability in the clinical response to exposure and response prevention in obsessive-compulsive disorder
Objective: Exposure and response prevention (ERP) is effective to treat obsessive-compulsive disorder (OCD), but the lack of tolerance to the aversion nature of exposure techniques results in a high drop-out rate. There have been reports of a generic stress endurance effect of serotonin (5-HT) in the central nervous system (CNS) which might be explained by suppression of defensive fixed action patterns. Previous studies have proposed that higher baseline 5-HT concentration and slow decrease in concentration during drug treatment of OCD were predictors of good clinical response to 5-HT reuptake inhibitors. The objective of this study was to investigate whether pre-treatment platelet rich plasma (PRP) 5-HT concentration is associated with latency of treatment response and final response to an ERP protocol for obsessive-compulsive disorder (OCD). Methods: Thirty adult and treatment-free OCD patients were included in an 8-week, 16-session ERP protocol. 5-HT concentration was determined at baseline and after treatment. Patients with a reduction ≥30% on the Yale-Brown Obsessive Compulsive Scale (Y-BOCS) at the end of ERP were defined as responders. Results: A positive correlation between baseline 5-HT concentration and reduction of symptoms on the Y-BOCS was observed after 4 weeks. Baseline 5-HT concentration was not correlated with clinical response after 8 weeks of ERP, possibly due to the similar though delayed clinical response of patients with lower (compared to those with higher) baseline 5-HT concentration. Patients with higher 5-HT baseline concentration also showed more improvement in depressive symptoms with treatment. Conclusion: The present results partially support the hypothesis of a stress endurance effect of 5-HT in OCD patients. According to the literature, fast onset responders possibly have more or larger 5-HT containing neurons, higher endogenous 5-HT synthesis or lower monoamine oxidase activity; all these hypotheses remain to be investigated.
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