首页> 外文期刊>Current pharmaceutical design >Nocturnal urinary cortisol excretion over a randomized controlled trial with paroxetine vs. placebo combined with relaxation training or aerobic exercise in panic disorder.
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Nocturnal urinary cortisol excretion over a randomized controlled trial with paroxetine vs. placebo combined with relaxation training or aerobic exercise in panic disorder.

机译:帕罗西汀与安慰剂联合放松训练或有氧运动治疗恐慌症的夜尿皮质醇排泄。

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INTRODUCTION: Data on basal hypothalamo-pituitary-adrenomedullary (HPA) function over controlled treatment trials with serotonergic drugs in anxiety disorders are still rare. METHODS: 29 patients with panic disorder participating in a 10 week randomized, controlled trial (paroxetine vs. placebo with exercise or relaxation; N=60) collected urine for cortisol excretion over 3 consecutive nights before start and before termination of the treatment episode. Urinary cortisol was measured by radioimmunoassay. Efficacy measures were the Clinical Global Impression Scale (CGI) and the Panic and Agoraphobia Scale (P&A). 83% were female (p<.05 vs. males). 55% received additional aerobic exercise, and 45% relaxation. 55% received paroxetine treatment, and 45% placebo. Significantly fewer males received placebo treatment (p<.05). RESULTS: All subjects improved significantly. Cortisol excretion did not differ between treatment groups or at pre-/post measurements. Females showed a significantly higher variability of cortisol excretion compared to males, at pre-(p<.005) and post (p=.015) assessments. Males displayed a trend to lower basal HPA function at end of treatment (p=.08). HPA variability after treatment showed a trend to be higher in the paroxetine (p=.052) -who clinically improved significantly better- compared to the placebo group. No relationship between HPA activity and treatment response or with exercise was detected. DISCUSSION: HPA function shows significant gender differences, with females having a higher HPA function variability. Future studies on HPA function in treatment trials should address gender and medication effects.
机译:简介:在焦虑症中使用血清素能药物进行对照治疗试验的基础下丘脑-垂体-肾上腺髓质(HPA)功能的数据仍然很少。方法:29名恐慌症患者参加了为期10周的随机对照试验(帕罗西汀与安慰剂,进行运动或放松; N = 60),在开始治疗前和治疗终止前连续3个晚上收集尿液进行皮质醇排泄。通过放射免疫测定法测定尿皮质醇。疗效指标为临床总体印象量表(CGI)和恐慌和恐惧症量表(P&A)。 83%是女性(相对于男性,p <.05)。 55%的人接受了额外的有氧运动,而45%的人放松了。 55%接受帕罗西汀治疗,45%接受安慰剂。接受安慰剂治疗的男性明显减少(p <.05)。结果:所有受试者均明显改善。在治疗组之间或测量前后,皮质醇的排泄量没有差异。在评估前(p <.005)和评估后(p = .015),女性的皮质醇排泄变异性明显高于男性。男性在治疗结束时表现出降低基础HPA功能的趋势(p = .08)。与安慰剂组相比,帕罗西汀的临床治疗后HPA变异性呈上升趋势(p = .052),临床上显着改善。没有发现HPA活性与治疗反应或运动之间的关系。讨论:HPA功能表现出明显的性别差异,女性的HPA功能变异性更高。在治疗试验中有关HPA功能的未来研究应解决性别和药物作用。

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