Stanley Medical Research Institute, Kensington, Maryland.
Department of Psychiatry, Sheba Medical Center, Tel Hashomer, Israel.
JAMA Psychiatry. 2019 Oct 1;76(10):1009-1017. doi: 10.1001/jamapsychiatry.2019.1842.
Several lines of evidence suggest that estradiol influences the course of schizophrenia, and a previous randomized controlled trial demonstrated that transdermal estradiol improved symptoms in female patients of childbearing age. However, many initial positive findings in schizophrenia research are not later replicated.
To independently replicate the results of the effect of estradiol on schizophrenia in women of childbearing age.
DESIGN, SETTING, AND PARTICIPANTS: An 8-week randomized, placebo-controlled trial performed in the Republic of Moldova between December 4, 2015, and July 29, 2016, among 200 premenopausal women aged 19 to 46 years with schizophrenia or schizoaffective disorder as defined by the DSM-5.
Patients were randomized to receive a 200-μg estradiol patch or placebo patch changed twice a week added to their antipsychotic treatment.
The primary outcome was the positive subscale of the Positive and Negative Syndrome Scale (PANSS; lower scores indicated fewer symptoms and higher scores indicated more symptoms), analyzed with mixed models for repeated measures on an intention-to-treat basis.
A total of 100 women (median age, 38 years; interquartile range, 34-42 years) were randomized to receive an estradiol patch and 100 women (median age, 38 years; interquartile range, 31-41 years) were randomized to receive a placebo patch; the median age at baseline for the entire group of 200 women was 38.0 years (range, 19.5-46.0 years). At baseline, the mean positive PANSS score was 19.6 for both groups combined; at week 8, the mean positive PANSS score was 14.4 in the placebo group and 13.4 in the estradiol group. Compared with placebo, participants receiving add-on estradiol patches had statistically significant improvements in the primary outcome measure, PANSS positive subscale points (-0.94; 95% CI, -1.64 to -0.24; P = .008; effect size = 0.38). Post hoc heterogeneity analyses found that this effect occurred almost entirely in 100 participants older than 38.0 years (46 in placebo group vs 54 in estradiol group; difference, -1.98 points on the PANSS positive subscale; 95% CI, -2.94 to -1.02; P < .001). Younger participants did not benefit from estradiol (difference, 0.08 points on the PANSS positive subscale; 95% CI, -0.91 to 1.07; P = .87). Breast tenderness was more common in the estradiol group (n = 15) than in the placebo group (n = 1) as was weight gain (14 in estradiol group vs 1 in placebo group).
The results independently replicate the finding that transdermal estradiol is an effective add-on treatment for women of childbearing age with schizophrenia and extend it, finding improvements in negative symptoms and finding that the effect could be specific to those older than 38 years. The results should be viewed in the context of the differences in the natural course of schizophrenia between females and males.
ClinicalTrials.gov identifier: NCT03848234.
有几条证据表明雌二醇会影响精神分裂症的病程,并且之前的一项随机对照试验表明,经皮雌二醇可改善育龄期女性患者的症状。然而,精神分裂症研究中的许多最初的阳性发现后来并没有得到复制。
独立复制雌二醇对育龄期女性精神分裂症影响的结果。
设计、地点和参与者:这是一项于 2015 年 12 月 4 日至 2016 年 7 月 29 日在摩尔多瓦共和国进行的为期 8 周的随机、安慰剂对照试验,共纳入 200 名年龄在 19 至 46 岁之间、符合 DSM-5 标准的患有精神分裂症或分裂情感障碍的绝经前女性。
患者被随机分配接受每周更换两次的 200μg 雌二醇贴片或安慰剂贴片,并添加到他们的抗精神病治疗中。
主要结果是阳性和阴性症状量表(PANSS)的阳性子量表,采用混合模型对基于意向治疗的重复测量进行分析。
共有 100 名女性(中位数年龄 38 岁;四分位距 34-42 岁)被随机分配接受雌二醇贴片,100 名女性(中位数年龄 38 岁;四分位距 31-41 岁)被随机分配接受安慰剂贴片;整个 200 名女性的基线中位年龄为 38.0 岁(范围 19.5-46.0 岁)。在基线时,两组的平均阳性 PANSS 评分均为 19.6;在第 8 周时,安慰剂组的平均阳性 PANSS 评分为 14.4,雌二醇组为 13.4。与安慰剂相比,接受附加雌二醇贴片的参与者在主要结局测量,即 PANSS 阳性子量表分数上有统计学显著改善(-0.94;95%置信区间,-1.64 至 -0.24;P=0.008;效应大小 0.38)。事后异质性分析发现,这种效果几乎完全发生在 100 名年龄大于 38 岁的参与者中(安慰剂组 46 名,雌二醇组 54 名;差异,PANSS 阳性子量表上减少 1.98 分;95%置信区间,-2.94 至 -1.02;P<0.001)。年龄较小的参与者没有从雌二醇中受益(差异,PANSS 阳性子量表上增加 0.08 分;95%置信区间,-0.91 至 1.07;P=0.87)。雌二醇组(n=15)比安慰剂组(n=1)更常见乳房触痛,体重增加(雌二醇组 14 例,安慰剂组 1 例)。
结果独立复制了经皮雌二醇是育龄期精神分裂症女性有效附加治疗的发现,并将其扩展,发现对阴性症状有改善,并发现这种效果可能特定于年龄大于 38 岁的患者。结果应结合男女精神分裂症自然病程的差异来考虑。
ClinicalTrials.gov 标识符:NCT03848234。