Kelly Deanna L, Powell Megan M, Wehring Heidi J, Sayer MacKenzie A, Kearns Ann Marie, Hackman Ann L, Buchanan Robert W, Nichols Rebecca B, Adams Heather A, Richardson Charles M, Vyas Gopal, McMahon Robert P, Earl Amber K, Sullivan Kelli M, Liu Fang, Luttrell Sarah E, Dickerson Faith B, Feldman Stephanie M, Narang Supriya, Koola Maju M, Buckley Peter F, RachBeisel Jill A, McEvoy Joseph P
Department of Psychiatry, University of Maryland School of Medicine, Baltimore, MD.
Department of Psychiatry, Georgia Regents University, Augusta, GA.
J Clin Psychopharmacol. 2018 Aug;38(4):317-326. doi: 10.1097/JCP.0000000000000898.
PURPOSE/BACKGROUND: Prolactin-related adverse effects contribute to nonadherence and adverse health consequences, particularly in women with severe mental illness. Treating these adverse effects may improve treatment acceptability, adherence, and long-term outcomes.
METHODS/PROCEDURES: Premenopausal women with a Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision diagnosis of schizophrenia, schizoaffective disorder, or bipolar disorder were recruited for a randomized, double-blind, placebo-controlled 16-week trial of adjunct aripiprazole (5-15 mg/d). Participants had elevated prolactin (>24 ng/mL) and were experiencing galactorrhea, amenorrhea, oligomenorrhea, or sexual dysfunction on a prolactin-elevating antipsychotic. Participants were evaluated biweekly for prolactin elevation and galactorrhea and completed a menstrual diary review. Psychiatric symptoms and adverse effects were closely monitored.
FINDINGS/RESULTS: Forty-six women were randomized (n = 25 aripiprazole, n = 21 placebo). Thirty-seven completed at least 8 weeks of the study (n = 20 [80%] aripiprazole and n = 17 [81%] placebo). Aripiprazole (mean dose, 11.7 ± 2.4 mg/d) was effective for lowering prolactin relative to placebo (P = 0.04). In addition, 45% (9/20) of the aripiprazole group had a normalized prolactin (<24 mg/mL) compared with 12% (2/17) of the placebo group (P = 0.028). Galactorrhea resolved in 77% (10/13) of the aripiprazole-treated participants compared with 33% (4/12) in the placebo group (P = 0.028). Normalization of sexual function (<16 on the Arizona Sexual Experience Scale) occurred in 50% on aripiprazole (7/14) versus 9% (1/11) on placebo (P = 0.030). No differences between groups in symptoms or adverse effects were noted. Overall, women rated a mean score of 4.6 ± 0.6 on a 5-point Likert scale for sexual function improvement, suggesting their particular satisfaction with improvement in this domain.
IMPLICATIONS/CONCLUSIONS: Building upon prior studies, this rigorous evaluation confirms the utility of adjunctive aripiprazole as a strategy for improving prolactin and managing prolactin-related adverse effects in premenopausal women with psychosis.
目的/背景:催乳素相关的不良反应会导致治疗依从性下降和不良健康后果,在患有严重精神疾病的女性中尤为如此。治疗这些不良反应可能会提高治疗的可接受性、依从性和长期疗效。
方法/步骤:招募符合《精神障碍诊断与统计手册》第四版,文本修订版中精神分裂症、分裂情感性障碍或双相情感障碍诊断标准的绝经前女性,进行一项为期16周的随机、双盲、安慰剂对照试验,试验药物为阿立哌唑辅助治疗(5 - 15毫克/天)。参与者催乳素水平升高(>24纳克/毫升),且正在服用可升高催乳素的抗精神病药物并出现溢乳、闭经、月经过少或性功能障碍。每两周对参与者进行催乳素升高和溢乳情况评估,并完成月经日记回顾。密切监测精神症状和不良反应。
46名女性被随机分组(阿立哌唑组25名,安慰剂组21名)。37名完成了至少8周的研究(阿立哌唑组20名[80%],安慰剂组17名[81%])。与安慰剂相比,阿立哌唑(平均剂量11.7±2.4毫克/天)在降低催乳素方面有效(P = 0.04)。此外,阿立哌唑组45%(9/20)的参与者催乳素恢复正常(<24毫克/毫升),而安慰剂组为12%(2/17)(P = 0.028)。阿立哌唑治疗组77%(10/13)的溢乳症状得到缓解,安慰剂组为33%(4/12)(P = 0.028)。阿立哌唑组50%(7/14)的性功能恢复正常(亚利桑那性体验量表评分<16),安慰剂组为9%(1/11)(P = 0.030)。两组在症状或不良反应方面未发现差异。总体而言,女性对性功能改善的平均评分为4.6±0.6(5分制李克特量表),表明她们对这一领域的改善特别满意。
意义/结论:基于先前的研究,这项严谨的评估证实了辅助使用阿立哌唑作为改善绝经前精神病女性催乳素水平和管理催乳素相关不良反应的策略的有效性。