Trunko Mary Ellen, Schwartz Terry A, Berner Laura A, Cusack Anne, Nakamura Tiffany, Bailer Ursula F, Chen Joanna Y, Kaye Walter H
Department of Psychiatry, University of California, San Diego, La Jolla, California, USA.
Department of Psychiatry and Psychotherapy, Division of Biological Psychiatry, Medical University of Vienna, Vienna, Austria.
Borderline Personal Disord Emot Dysregul. 2017 Oct 8;4:21. doi: 10.1186/s40479-017-0072-6. eCollection 2017.
There is little effective psychopharmacological treatment for individuals with eating disorders who struggle with pervasive, severe affective and behavioral dysregulation.
This pilot open series evaluated lamotrigine, a mood stabilizer, in the treatment of patients with eating disorders who did not respond adequately to antidepressant medications. Nine women with anorexia nervosa- or bulimia nervosa-spectrum eating disorders in partial hospital or intensive outpatient dialectical behavior therapy (DBT)-based eating disorder treatment took lamotrigine for 147 ± 79 days (mean final dose = 161.1 ± 48.6 mg/day). Participants completed standardized self-report measures of emotion dysregulation and impulsivity after lamotrigine initiation and approximately biweekly thereafter. Mood and eating disorder symptomatology were measured at lamotrigine initiation and at time of final assessment.
Lamotrigine and concurrent DBT were associated with large reductions in self-reported affective and behavioral dysregulation (s < 0.01). Eating disorder and mood symptoms decreased moderately.
Although our findings are limited by the confounds inherent in an open series, lamotrigine showed initial promise in reducing emotional instability and behavioral impulsivity in severely dysregulated eating-disordered patients. These preliminary results support further investigation of lamotrigine for eating disorders in rigorous controlled trials.
对于患有饮食失调症且存在普遍、严重情感和行为失调问题的个体,几乎没有有效的心理药物治疗方法。
本试点开放性系列研究评估了情绪稳定剂拉莫三嗪对对抗抑郁药物反应不佳的饮食失调症患者的治疗效果。9名患有神经性厌食症或神经性贪食症谱系饮食失调症的女性,在基于辩证行为疗法(DBT)的部分住院或强化门诊饮食失调治疗中服用拉莫三嗪147±79天(平均最终剂量 = 161.1±48.6毫克/天)。参与者在开始服用拉莫三嗪后以及此后大约每两周完成一次情绪失调和冲动性的标准化自我报告测量。在开始服用拉莫三嗪时和最终评估时测量情绪和饮食失调症状。
拉莫三嗪与同时进行的DBT与自我报告的情感和行为失调大幅减少相关(s<0.01)。饮食失调和情绪症状适度减轻。
尽管我们的研究结果受到开放性系列固有的混杂因素限制,但拉莫三嗪在降低严重失调的饮食失调患者的情绪不稳定和行为冲动方面显示出初步前景。这些初步结果支持在严格的对照试验中进一步研究拉莫三嗪用于治疗饮食失调症。