Chengappa K N, Rathore D, Levine J, Atzert R, Solai L, Parepally H, Levin H, Moffa N, Delaney J, Brar J S
Western Psychiatric Institute and Clinic, University of Pittsburgh Medical Center, PA 15215-2593, USA.
Bipolar Disord. 1999 Sep;1(1):42-53. doi: 10.1034/j.1399-5618.1999.10111.x.
Anticonvulsant agents such as carbamazepine and valproate are alternatives to lithium in treating subjects with bipolar disorder. Topiramate (Topamax), a new antiepileptic agent, is a candidate drug for bipolar disorder. We evaluated topiramate as adjunctive treatment for bipolar patients.
Eighteen patients with DSM-IV bipolar I disorder [mania (n = 12), hypomania (n = 1), mixed episode (n = 5), and rapid cycling (n = 6)], and two subjects with schizoaffective disorder bipolar type, resistant to current mood-stabilizer treatment were initiated on topiramate, 25 mg/day, increasing by 25-50 mg every 3 7 days to a target dose between 100 and 300 mg/day, as other medications were held constant for 5 weeks. The Young Mania Rating Scale (Y-MRS), Hamilton Depression Rating Scale (Ham-D), and Clinical Global Impression-Bipolar Version Scale (CGI-BP) were used to rate subjects weekly.
By 5 weeks, 12 (60%) subjects were responders, i.e., 50% reduction in the Y-MRS scores and a CGI of 'much' or 'very much improved'. Three subjects were 'minimally improved', four showed no change, and one was 'minimally worse'. Six subjects had parasthesia, three experienced fatigue, and two had 'word-finding' difficulties; in all cases, side effects were transient. All patients lost weight with a mean of 9.4 lb in 5 weeks, and a significant reduction in body mass index (BMI) occurred too.
Topiramate appears to have efficacy for the manic and mixed phases of bipolar illness. Other preliminary data suggest antidepressant efficacy too. Among obese bipolar subjects, the weight loss potential of topiramate may be beneficial. If controlled trials confirm these initial results, topiramate may be a significant addition to the available treatments for bipolar disorder.
抗惊厥药物如卡马西平和丙戊酸盐是治疗双相情感障碍患者的锂盐替代药物。托吡酯(妥泰),一种新型抗癫痫药物,是双相情感障碍的候选药物。我们评估了托吡酯作为双相情感障碍患者辅助治疗的效果。
18例符合DSM-IV双相I型障碍[躁狂发作(n = 12)、轻躁狂发作(n = 1)、混合发作(n = 5)和快速循环发作(n = 6)]的患者,以及2例双相型分裂情感性障碍患者,对当前的心境稳定剂治疗耐药,开始服用托吡酯,25毫克/天,每3至7天增加25 - 50毫克,直至目标剂量为100至300毫克/天,同时其他药物保持不变5周。每周使用杨氏躁狂评定量表(Y - MRS)、汉密尔顿抑郁评定量表(Ham - D)和临床总体印象 - 双相情感障碍版量表(CGI - BP)对患者进行评分。
到5周时,12例(60%)患者有反应,即Y - MRS评分降低50%且临床总体印象为“明显改善”或“非常明显改善”。3例患者“稍有改善”,4例无变化,1例“稍有恶化”。6例患者有感觉异常,3例感到疲劳,2例有“找词困难”;所有情况下,副作用都是短暂的。所有患者体重均下降,5周内平均下降9.4磅,体重指数(BMI)也显著降低。
托吡酯似乎对双相情感障碍的躁狂和混合发作期有效。其他初步数据也提示其有抗抑郁疗效。在肥胖的双相情感障碍患者中,托吡酯的减重潜力可能有益处。如果对照试验证实这些初步结果,托吡酯可能会成为双相情感障碍现有治疗方法的重要补充。