McElroy Susan L, Frye Mark A, Altshuler Lori L, Suppes Trisha, Hellemann Gerhard, Black David, Mintz Jim, Kupka Ralph, Nolen Willem, Leverich Gabriele S, Denicoff Kirk D, Post Robert M, Keck Paul E
Psychopharmacology Research Program, Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, OH 45267-0559, USA.
Bipolar Disord. 2007 Jun;9(4):426-34. doi: 10.1111/j.1399-5618.2007.00488.x.
Patients with bipolar disorder (BD) have an increased risk of obesity as well as psychotropic-associated weight gain. The objective of this study was to compare sibutramine and topiramate as adjunctive treatments for psychotropic-associated weight gain in overweight or obese outpatients with BD.
In this 24-week, open-label, flexible-dose, comparison trial, 46 outpatients with bipolar disorders who had a body mass index (BMI) > or =30 kg/m(2), or > or =27 kg/m(2) with obesity-related comorbidities, and psychotropic-associated weight gain were randomly assigned to receive sibutramine (n = 18; 5-15 mg/day) or topiramate (n = 28; 25-600 mg/day). The primary outcome measure was weight loss. Secondary measures included changes in BMI, percent body weight loss, and mood symptoms.
Patients randomized either to sibutramine or topiramate lost comparable amounts of weight (4.1 +/- 5.7 and 2.8 +/- 3.5 kg, respectively) and displayed similar rates of weight loss (0.85 and 0.82 kg/week, respectively). However, only four (22%) patients receiving sibutramine and six (21%) patients receiving topiramate completed the 24-week trial. In addition, the attrition patterns for the two drugs were different, with patients discontinuing topiramate doing so early in treatment and patients discontinuing sibutramine doing so throughout treatment. Also, higher ratings of manic and depressive symptoms significantly increased risk for early topiramate discontinuation compared to that for sibutramine.
Adjunctive sibutramine and topiramate may have comparable weight loss effects in overweight or obese bipolar patients with psychotropic-associated weight gain, but are each associated with similarly high discontinuation rates. In addition, they may have different attrition profiles. Compared to sibutramine, discontinuation of topiramate may be more likely to occur early in treatment and may be more dependent upon manic and depressive symptoms.
双相情感障碍(BD)患者肥胖风险增加,且存在精神药物相关的体重增加。本研究的目的是比较西布曲明和托吡酯作为辅助治疗药物,用于治疗超重或肥胖的BD门诊患者因使用精神药物导致的体重增加。
在这项为期24周的开放标签、灵活剂量的对照试验中,46例双相情感障碍门诊患者,其体重指数(BMI)≥30kg/m²,或BMI≥27kg/m²且伴有肥胖相关合并症,以及存在精神药物相关的体重增加,被随机分配接受西布曲明(n = 18;5 - 15mg/天)或托吡酯(n = 28;25 - 600mg/天)治疗。主要结局指标是体重减轻。次要指标包括BMI变化、体重减轻百分比和情绪症状。
随机接受西布曲明或托吡酯治疗的患者体重减轻量相当(分别为4.1±5.7kg和2.8±3.5kg),体重减轻率相似(分别为0.85kg/周和0.82kg/周)。然而,只有4例(22%)接受西布曲明治疗的患者和6例(21%)接受托吡酯治疗的患者完成了24周试验。此外,两种药物的脱落模式不同,停用托吡酯的患者在治疗早期停药,而停用西布曲明的患者在整个治疗过程中都有停药情况。而且,与西布曲明相比,躁狂和抑郁症状评分较高显著增加了早期停用托吡酯的风险。
辅助使用西布曲明和托吡酯在超重或肥胖且有精神药物相关体重增加的双相情感障碍患者中可能具有相当的体重减轻效果,但二者的停药率都同样较高。此外,它们的脱落情况可能不同。与西布曲明相比,托吡酯更可能在治疗早期停药,且可能更依赖于躁狂和抑郁症状。