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孕激素治疗的癫痫女性患者中别孕烯醇酮水平与癫痫发作频率。

Allopregnanolone levels and seizure frequency in progesterone-treated women with epilepsy.

机构信息

From the Harvard Neuroendocrine Unit (A.G.H.), Beth Israel Deaconess Medical Center, Boston, MA; and Department of Psychology (C.A.F.), University of Albany-SUNY, NY.

出版信息

Neurology. 2014 Jul 22;83(4):345-8. doi: 10.1212/WNL.0000000000000623. Epub 2014 Jun 18.

Abstract

OBJECTIVE

To determine whether allopregnanolone (AP) may mediate seizure reduction in progesterone-treated women with epilepsy.

METHODS

The NIH Progesterone Trial compared the efficacy of adjunctive cyclic natural progesterone therapy vs placebo treatment of intractable seizures in 294 subjects, randomized 2:1 to progesterone or placebo, stratified by catamenial vs noncatamenial designation. Treatments were compared on proportions of 50% responders, and changes in seizure frequency from 3 baseline to 3 treatment cycles. Serum AP levels were measured by radioimmunoassay from 155 women with intractable focal-onset seizures who had baseline and treatment-phase midluteal serum samples drawn each cycle for hormone measurements.

RESULTS

There was no significant correlation between percentage changes in AP levels and seizure frequencies from baseline to treatment for either the catamenial or noncatamenial stratum. There was a significant correlation for the subset of subjects who showed a significantly greater responder rate in the post hoc analysis of the trial, i.e., subjects who had a 3-fold or greater increase in average daily seizure frequency perimenstrually compared with the midfollicular and midluteal phases (C1 ≥ 3: r = -0.442, p = 0.013, and specifically for C1 ≥ 3 progesterone-treated subjects [r = -0.452, p = 0.035], but not other groups [C1 ≥ 3 placebo: r = -0.367; C1 <3 progesterone: r = 0.099; C1 <3 placebo: r = 0.131; p = not significant]).

CONCLUSIONS

The findings support AP as a mediator of seizure reduction in progesterone-treated women who have a substantial level of perimenstrually exacerbated seizures.

摘要

目的

确定是否可孕烷醇酮 (AP) 可介导孕激素治疗的癫痫女性发作减少。

方法

NIH 孕激素试验比较了辅助周期性天然孕激素治疗与安慰剂治疗 294 名难治性癫痫患者的疗效,将患者按月经周期与非月经周期分为 2:1 接受孕激素或安慰剂治疗,分层比较 50%应答者的比例以及从 3 个基线到 3 个治疗周期的发作频率变化。155 名局灶性发作性癫痫患者进行血清 AP 水平检测,这些患者具有基线和治疗阶段中黄体中期血清样本,每个周期均进行激素测量。

结果

无论是月经周期还是非月经周期,AP 水平从基线到治疗的百分比变化与发作频率均无显著相关性。在试验的事后分析中,对于显示出更高应答率的亚组患者,AP 水平变化与发作频率变化之间存在显著相关性,即与卵泡期和黄体中期相比,围经期平均每日发作频率增加了 3 倍以上的患者(C1 ≥ 3:r = -0.442,p = 0.013,尤其是 C1 ≥ 3 孕激素治疗的患者 [r = -0.452,p = 0.035],但其他组无此相关性[C1 ≥ 3 安慰剂:r = -0.367;C1 <3 孕激素:r = 0.099;C1 <3 安慰剂:r = 0.131;p 无统计学意义])。

结论

这些发现支持 AP 作为孕激素治疗的女性癫痫发作减少的中介,这些患者的围经期发作明显加重。

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