An open trial of mirtazapine in menopausal women with depression unresponsive to estrogen replacement therapy.

H. Joffe, Heather Groninger, C. Soares, R. Nonacs, L. Cohen
{"title":"An open trial of mirtazapine in menopausal women with depression unresponsive to estrogen replacement therapy.","authors":"H. Joffe, Heather Groninger, C. Soares, R. Nonacs, L. Cohen","doi":"10.1089/152460901317193576","DOIUrl":null,"url":null,"abstract":"Treatment of major depression in menopausal women is controversial. Estrogen replacement therapy (ERT) treats mild depression but may not treat more severe depression in this population. Antidepressants are recommended as treatment for major depression in menopausal women, but the specific efficacy of antidepressants has not been examined in menopause-associated depression. Twenty-two perimenopausal and postmenopausal women aged 40-61 taking stable doses of ERT who met Structured Clinical Interview for DSM-IV (SCID-IV) criteria for major depression were accessioned into an open-label clinical trial of mirtazapine. Subjects were treated with 30-45 mg/day mirtazapine for 8 weeks and were assessed every 2 weeks with the Hamilton Depression Rating Scale-17 (HDRS-17), Beck Depression Inventory (BDI), and Clinical Global Impression (CGI) Scale. Remission of depression was defined as an HDRS-17 score < or =7 at the week 8 study visit. Sixteen (73%) of the enrolled subjects completed the 8-week study. The median HDRS-17 score declined from 20.5 (range 12-37) at baseline to 2 (range 0-9) at week 8 (Wilcoxon signed-rank test, p < 0.001). Remission of depression was achieved by 14 of 16 (87.5%) study completers. Subjects responded well to mirtazapine regardless of whether their depression preceded ERT use or developed after ERT was initiated. Therapeutic response also appeared independent of menopausal status (perimenopausal vs. postmenopausal), ERT preparation, and concomitant use of medroxyprogesterone. Mirtazapine is an effective treatment for major depression in perimenopausal and postmenopausal women whose depression precedes ERT use and does not respond to ERT or whose depression develops after ERT is initiated.","PeriodicalId":80044,"journal":{"name":"Journal of women's health & gender-based medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2001-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"57","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of women's health & gender-based medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1089/152460901317193576","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 57

Abstract

Treatment of major depression in menopausal women is controversial. Estrogen replacement therapy (ERT) treats mild depression but may not treat more severe depression in this population. Antidepressants are recommended as treatment for major depression in menopausal women, but the specific efficacy of antidepressants has not been examined in menopause-associated depression. Twenty-two perimenopausal and postmenopausal women aged 40-61 taking stable doses of ERT who met Structured Clinical Interview for DSM-IV (SCID-IV) criteria for major depression were accessioned into an open-label clinical trial of mirtazapine. Subjects were treated with 30-45 mg/day mirtazapine for 8 weeks and were assessed every 2 weeks with the Hamilton Depression Rating Scale-17 (HDRS-17), Beck Depression Inventory (BDI), and Clinical Global Impression (CGI) Scale. Remission of depression was defined as an HDRS-17 score < or =7 at the week 8 study visit. Sixteen (73%) of the enrolled subjects completed the 8-week study. The median HDRS-17 score declined from 20.5 (range 12-37) at baseline to 2 (range 0-9) at week 8 (Wilcoxon signed-rank test, p < 0.001). Remission of depression was achieved by 14 of 16 (87.5%) study completers. Subjects responded well to mirtazapine regardless of whether their depression preceded ERT use or developed after ERT was initiated. Therapeutic response also appeared independent of menopausal status (perimenopausal vs. postmenopausal), ERT preparation, and concomitant use of medroxyprogesterone. Mirtazapine is an effective treatment for major depression in perimenopausal and postmenopausal women whose depression precedes ERT use and does not respond to ERT or whose depression develops after ERT is initiated.
米氮平对雌激素替代疗法无反应的绝经期抑郁症妇女的公开试验。
更年期妇女重度抑郁症的治疗是有争议的。雌激素替代疗法(ERT)治疗轻度抑郁症,但可能不能治疗更严重的抑郁症。抗抑郁药被推荐用于治疗更年期妇女的重度抑郁症,但抗抑郁药在更年期相关抑郁症中的具体疗效尚未得到检验。22名年龄在40-61岁的围绝经期和绝经后妇女服用稳定剂量的ERT,符合DSM-IV (SCID-IV)重度抑郁症的结构化临床访谈标准,加入米氮平的开放标签临床试验。受试者服用30- 45mg /天的米氮平治疗8周,每2周用汉密尔顿抑郁评定量表-17 (HDRS-17)、贝克抑郁量表(BDI)和临床总体印象量表(CGI)进行评估。在第8周的研究访问中,HDRS-17评分<或=7,抑郁缓解被定义为。16名(73%)入组受试者完成了为期8周的研究。HDRS-17评分中位数从基线时的20.5(范围12-37)下降到第8周时的2(范围0-9)(Wilcoxon sign -rank检验,p < 0.001)。16名研究完成者中有14名(87.5%)达到抑郁缓解。受试者对米氮平反应良好,无论他们的抑郁是在ERT使用之前还是在ERT开始后发展。治疗效果也与绝经状态(围绝经期和绝经后)、ERT制剂和同时使用甲羟孕酮无关。米氮平是围绝经期和绝经后妇女重度抑郁症的有效治疗方法,这些妇女在使用ERT之前出现抑郁症,对ERT没有反应,或者在ERT开始后出现抑郁症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信