Perna G, Bertani A, Caldirola D, Smeraldi E, Bellodi L
Department of Neuropsychiatric Sciences, University Vita e Salute, Istituto Scientifico Ospedale San Raffaele, Milan, Italy.
Pharmacopsychiatry. 2001 May;34(3):85-90. doi: 10.1055/s-2001-14283.
Serotonin Selective Re-uptake Inhibitors (SSRIs) are the drugs of choice for treating panic disorder (PD). In vitro studies have shown different pharmacodynamic profiles for SSRIs, but their clinical relevance is still unknown. Paroxetine, the SSRI with the strongest serotonergic effect, also shows significant cholinergic and noradrenergic activities. In this class of drugs, citalopram is the most selective for serotonin. We compared these two drugs and their effectiveness and tolerability in a sample of patients with PD in a two-month treatment course.
Fifty-eight patients with PD were randomly assigned to either the paroxetine or the citalopram treatment group in a single-blind, randomized design. Each patient was assessed at days 0, 7 and 60 by the Panic Associated Symptoms Scale (PASS), the Sheehan Disability Scale (SDS) and the Fear Questionnaire (FQ). Primary outcome measures were the percentage of patients free of panic attacks, anticipatory anxiety and phobic avoidance in the last week of the trial and the percentage of good responders, as defined by a reduction of at least 50% from baseline of both PASS and SDS global scores at day 60.
At day 60, 86% of patients receiving citalopram and 84% of those receiving paroxetine responded well to treatment. No significant differences between the two drugs were found. Both were well tolerated, although sexual side effects and weight gain were frequent. Anticipatory anxiety decreased significantly after the first week of treatment, and no initial worsening in the panic attacks was observed.
Paroxetine and citalopram show similar anti-panic properties and a good tolerability profile. Our results support evidence that the serotonergic system plays a significant role in the anti-panic properties of these two SSRIs.
5-羟色胺再摄取抑制剂(SSRIs)是治疗惊恐障碍(PD)的首选药物。体外研究显示了SSRIs不同的药效学特征,但其临床相关性仍不明确。帕罗西汀是具有最强5-羟色胺能效应的SSRI,也显示出显著的胆碱能和去甲肾上腺素能活性。在这类药物中,西酞普兰对5-羟色胺最具选择性。我们在一个为期两个月的治疗过程中,对这两种药物及其在一组PD患者中的有效性和耐受性进行了比较。
58例PD患者采用单盲随机设计,随机分配至帕罗西汀或西酞普兰治疗组。在第0、7和60天,通过惊恐相关症状量表(PASS)、希恩残疾量表(SDS)和恐惧问卷(FQ)对每位患者进行评估。主要结局指标为在试验最后一周无惊恐发作、预期焦虑和恐惧回避的患者百分比,以及根据第60天PASS和SDS总体评分较基线至少降低50%定义的良好反应者百分比。
在第60天,接受西酞普兰治疗的患者中有86%、接受帕罗西汀治疗的患者中有84%对治疗反应良好。未发现两种药物之间有显著差异。两者耐受性均良好,尽管性副作用和体重增加较为常见。治疗第一周后预期焦虑显著降低,且未观察到惊恐发作最初恶化的情况。
帕罗西汀和西酞普兰显示出相似的抗惊恐特性和良好的耐受性。我们的结果支持了5-羟色胺能系统在这两种SSRI的抗惊恐特性中起重要作用的证据。