Psychiatric Research Centre, Örebro County Council, School of Health and Medical Sciences, Örebro University, Örebro, Sweden.
BMC Psychiatry. 2013 Dec 23;13:344. doi: 10.1186/1471-244X-13-344.
The drug treatments of choice for obsessive-compulsive disorder (OCD) are serotonin reuptake inhibitors (SRIs). However, a correlation between the neuropeptide oxytocin in cerebrospinal fluid and the severity of OCD has previously been shown, and oxytocin and serotonin are interconnected within the brain. Few studies have investigated whether SRIs have any effect on oxytocin; thus, our aim was to explore the possibility that oxytocinergic mechanisms contribute to the anti-obsessive effect of SRIs.
In a randomized, double-blind trial, comparing SRIs (clomipramine and paroxetine) with placebo in 36 adults with OCD (characterized for subtypes), plasma oxytocin was measured with radioimmunoassay after plasma extraction, at baseline, after 1 week, and after 4 weeks of treatment, and related to baseline severity and clinical response after 12 weeks, as measured by the Yale-Brown Obsessive Compulsive Scale (Y-BOCS).
Baseline oxytocin levels correlated positively with baseline Y-BOCS ratings, but only among the future SRI responders. Patients with early onset of OCD had higher baseline oxytocin. During treatment, plasma oxytocin did not differ between SRI and placebo treatment. In SRI responders, plasma oxytocin first decreased and then increased; in non-responders (to SRI as well as to placebo), the reverse was the case. After 4 weeks, treatment responders had attained higher oxytocin levels compared to non-responders. The intra-individual range (i.e., the variability) of plasma oxytocin between measurements was the measure that best differentiated responders from non-responders. This range was higher in responders than non-responders, and lower in patients with autistic traits.
SRIs have highly variable effects on plasma oxytocin between individuals. The associations between baseline oxytocin and OCD severity and between oxytocin changes and treatment response support the notions that oxytocin is involved in OCD pathophysiology, and that the anti-obsessive effects of SRIs are partly exerted through oxytocinergic mechanisms.
强迫症(OCD)的首选药物治疗是选择性 5-羟色胺再摄取抑制剂(SSRIs)。然而,此前已经表明,脑脊液中的神经肽催产素与 OCD 的严重程度之间存在相关性,并且催产素和 5-羟色胺在大脑中相互关联。很少有研究调查 SSRIs 是否对催产素有任何影响;因此,我们的目的是探讨催产素能机制是否有助于 SSRIs 的抗强迫作用。
在一项随机、双盲试验中,我们比较了 36 名强迫症患者(根据亚型进行了分类)接受 SSRIs(氯米帕明和帕罗西汀)与安慰剂治疗的效果,使用放射免疫分析法测量血浆催产素,在基线、治疗 1 周后和 4 周后进行血浆提取,并与治疗 12 周后的基线严重程度和临床反应相关,使用耶鲁-布朗强迫症量表(Y-BOCS)进行评估。
基线催产素水平与基线 Y-BOCS 评分呈正相关,但仅在未来的 SSRIs 反应者中存在这种相关性。OCD 发病早的患者基线催产素水平较高。在治疗过程中,SSRIs 治疗与安慰剂治疗之间的血浆催产素水平没有差异。在 SSRIs 反应者中,血浆催产素先下降后上升;在非反应者(对 SSRIs 和安慰剂均无反应)中则相反。治疗 4 周后,反应者的催产素水平高于非反应者。个体之间测量的血浆催产素的个体内范围(即变异性)是区分反应者和非反应者的最佳指标。反应者的个体内范围高于非反应者,且具有自闭症特征的患者的个体内范围较低。
SSRIs 对个体之间的血浆催产素有高度可变的影响。基线催产素与 OCD 严重程度之间的关联,以及催产素变化与治疗反应之间的关联,支持了催产素参与 OCD 病理生理学的观点,并且 SSRIs 的抗强迫作用部分是通过催产素能机制发挥作用的。