Ghaemi S Nassir, Shirzadi Arshia A, Klugman Jeffry, Berv Douglas A, Pardo Tamara B, Filkowski Megan M
Bipolar Disorder Research Program, Department of Psychiatry, Emory University, Atlanta, GA 30322, United States.
J Affect Disord. 2008 Jan;105(1-3):311-4. doi: 10.1016/j.jad.2007.05.011. Epub 2007 Jun 21.
To assess the effectiveness and safety of zonisamide in bipolar disorder.
A chart review was conducted of naturalistic treatment with zonisamide in 35 outpatients meeting DSM-IV criteria for bipolar disorder (9 males, 26 females; mean +/- SD age = 29.2 +/- 12.7; 14 with bipolar disorder type I, 6 with bipolar disorder type II, and 14 with bipolar disorder not otherwise specified). Patients received zonisamide adjunctive therapy between January 1994 and December 2004. Treatment response was defined as a Clinical Global Impressions - Improvement (CGI-I) scale score of +2 (much improved) or + 3 (very much improved).
Zonisamide was moderately to markedly effective in 9 subjects (26%). Indication for treatment included depressive (34.3%, [12/35]), manic/hypomanic (28.6%, [10/35]), or mixed (31.4%, [11/35]) symptoms. The mean zonisamide dose was 130 mg/d for a mean duration of treatment of 27.0 +/- 32.3 weeks. Sedation (25%, [4/16]) was the most common side effect; 19/35 (54.3%) reported no side effects. 17/35 (49%) patients terminated early, mostly due to adverse effects (6/35). Using a multivariable model, predictors of response, concurrent mood stabilizers, dose and bipolar subtype (bipolar type I > type II/NOS), were controlled for in this sample.
In 35 persons with bipolar disorder taking standard mood stabilizers and other psychotropic agents, adjunctive zonisamide appears to have modest benefit in global improvement when added to a pre-existing complex medication regimen in patients with bipolar spectrum disorder. These pilot data support the need for larger studies to test the potential efficacy of zonisamide for treatment in mood disorders.
评估唑尼沙胺治疗双相情感障碍的有效性和安全性。
对35例符合DSM-IV双相情感障碍标准的门诊患者使用唑尼沙胺进行自然疗法的病历进行回顾(9例男性,26例女性;平均年龄±标准差=29.2±12.7岁;14例为I型双相情感障碍,6例为II型双相情感障碍,14例为未特定的双相情感障碍)。患者在1994年1月至2004年12月期间接受唑尼沙胺辅助治疗。治疗反应定义为临床总体印象改善(CGI-I)量表评分为+2(明显改善)或+3(非常明显改善)。
9例受试者(26%)使用唑尼沙胺有中度至显著疗效。治疗指征包括抑郁症状(34.3%,[12/35])、躁狂/轻躁狂症状(28.6%,[10/35])或混合症状(31.4%,[11/35])。唑尼沙胺平均剂量为130mg/天,平均治疗持续时间为27.0±32.3周。镇静是最常见的副作用(25%,[4/16]);19/35(54.3%)报告无副作用。17/35(49%)患者提前终止治疗,主要是由于不良反应(6/35)。在本样本中,使用多变量模型控制了反应预测因素、同时使用的心境稳定剂、剂量和双相情感障碍亚型(I型双相情感障碍>II型/未特定型双相情感障碍)。
在35例服用标准心境稳定剂和其他精神药物的双相情感障碍患者中,对于双相谱系障碍患者,在已有的复杂药物治疗方案中添加唑尼沙胺辅助治疗似乎在整体改善方面有一定益处。这些初步数据支持需要进行更大规模的研究来测试唑尼沙胺治疗心境障碍的潜在疗效。