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为期 6 周的依西酞普兰治疗对 CCK-4 挑战的影响:CCK-4 敏感的健康志愿者的安慰剂对照研究。

The effect of 6-week treatment with escitalopram on CCK-4 challenge: a placebo-controlled study in CCK-4-sensitive healthy volunteers.

机构信息

Department of Psychiatry, University of Tartu, Tartu, Estonia.

出版信息

Eur Neuropsychopharmacol. 2013 Jul;23(7):645-52. doi: 10.1016/j.euroneuro.2012.08.011. Epub 2012 Aug 29.

Abstract

Cholecystokinin-tetrapeptide (CCK-4)-induced panic attacks are reportedly attenuated by effective treatment with antipanic antidepressants in patients with panic disorder, but in healthy volunteers such effects are not well studied. The aim of this study was to assess the effect of 6-week treatment with an SSRI escitalopram on CCK-4-induced symptoms in healthy volunteers, who previously responded with a panic attack to CCK-4 challenge. A total of 18 healthy subjects (10 males and eight females, mean age 22.5 ± 5.8) received a 6-week treatment with escitalopram (10 mg/day) and placebo followed by CCK-4 challenge (50 μg) in a double-blind crossover design. The panic rate was 67% after treatment with escitalopram and 56% after treatment with placebo (p = 0.7). Thus, the results showed a significant reduction in CCK-4-induced panic rates without significant differences between escitalopram and placebo conditions. There were no significant effects of either treatment on any other variable of anxiety or cardiovascular indices. Secondary analysis showed no effect of gender or 5-HTTLPR polymorphism on response to CCK-4 challenge. This study demonstrated that in contrast to the findings in patients with panic disorder, in CCK-4-sensitive healthy volunteers the treatment with an antipanic SSRI did not cause a reduction of CCK-4-induced panic attacks beyond the effect of placebo. The mechanisms behind this discrepancy and the reasons of the decrease in sensitivity to CCK-4 challenge on repeated administration remain to be clarified in future studies.

摘要

胆囊收缩素-4 四肽(CCK-4)诱导的惊恐发作在惊恐障碍患者中经有效的抗惊恐药物治疗后据称会减轻,但在健康志愿者中,此类作用尚未得到充分研究。本研究旨在评估 6 周抗抑郁药依地普仑治疗对健康志愿者 CCK-4 诱发症状的影响,这些志愿者之前曾对 CCK-4 挑战产生过惊恐发作。共有 18 名健康受试者(10 名男性和 8 名女性,平均年龄 22.5 ± 5.8)接受了 6 周的依地普仑(10 mg/天)和安慰剂治疗,然后进行了双盲交叉设计的 CCK-4 挑战(50 μg)。依地普仑治疗后惊恐发作率为 67%,安慰剂治疗后为 56%(p = 0.7)。因此,结果表明 CCK-4 诱导的惊恐发作率显著降低,依地普仑和安慰剂之间无显著差异。两种治疗方法对焦虑或心血管指数的任何其他变量均无显著影响。二次分析显示,性别或 5-HTTLPR 多态性对 CCK-4 挑战的反应无影响。本研究表明,与惊恐障碍患者的研究结果相反,在 CCK-4 敏感的健康志愿者中,抗惊恐 SSRI 治疗并未导致 CCK-4 诱导的惊恐发作减少,超过安慰剂的效果。未来的研究仍需阐明这种差异的背后机制以及在重复给药时对 CCK-4 挑战的敏感性降低的原因。

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