Post Robert M, Altshuler Lori L, Frye Mark A, Suppes Trisha, McElroy Susan L, Keck Paul E, Leverich Gabriele S, Kupka Ralph, Nolen Willem A, Luckenbaugh David A, Walden Jorg, Grunze Heinz
Biological Psychiatry Branch, National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892, USA.
J Clin Psychiatry. 2005 Mar;66(3):370-4. doi: 10.4088/jcp.v66n0314.
Levetiracetam is a recently approved, well-tolerated anticonvulsant with a unique mechanism of action yielding efficacy in treatment-refractory seizure disorders and positive effects in an animal model of mania. Given the effectiveness of a range of other anticonvulsants in bipolar disorder, we sought to evaluate levetiracetam in patients with treatment-resistant illness.
Thirty-four patients received 500 to 1000 mg of levetiracetam titrated to a target dose of 2000 mg/day (maximum dose = 3000 mg/day) as open, adjunctive treatment for clinically significant symptoms of depression (N = 13), mania (N = 7), or cycling (N = 14) despite ongoing treatment with mood stabilizers. Inventory for Depressive Symptomatology-Clinician version (IDS-C), Young Mania Rating Scale (YMRS), and Clinical Global Impressions scale for use in Bipolar Illness ratings were completed at each visit for 8 weeks, and partial responders were offered continuation treatment. Data were collected from July 2001 to December 2002.
Five of 16 (31%; 13 depressed, 3 cycling) patients with initial depressive symptoms met the criterion for remission (IDS-C score of < or = 13) at last observation. All of these patients were less severely ill at baseline, whereas none of those more severely depressed at baseline responded. The majority of the 16 patients (7 manic, 9 cycling) with manic symptoms at baseline showed improvement in the YMRS in the first 2 weeks. While 7 of the 16 (44%) patients met the criterion for manic response and remission at last observation, 4 showed intervening periods of moderate to marked exacerbation. Levetiracetam was weight neutral.
Other pilot trials should explore possible areas of psychotropic action of levetiracetam prior to the conduct of more controlled clinical trials.
左乙拉西坦是一种最近获批且耐受性良好的抗惊厥药物,其作用机制独特,对难治性癫痫疾病有效,并且在躁狂动物模型中具有积极作用。鉴于其他多种抗惊厥药物在双相情感障碍中的有效性,我们试图评估左乙拉西坦对治疗抵抗性疾病患者的疗效。
34例患者接受500至1000毫克左乙拉西坦,滴定至目标剂量2000毫克/天(最大剂量=3000毫克/天),作为开放辅助治疗,用于治疗尽管正在使用心境稳定剂但仍有明显抑郁(N=13)、躁狂(N=7)或循环发作(N=14)症状的患者。在为期8周的每次就诊时,完成抑郁症状量表-临床版(IDS-C)、青年躁狂评定量表(YMRS)以及用于双相情感障碍评定的临床总体印象量表,对部分有反应的患者给予继续治疗。数据收集于2001年7月至2002年12月。
16例初始有抑郁症状的患者中(13例抑郁,3例循环发作),5例(31%)在末次观察时达到缓解标准(IDS-C评分≤13)。所有这些患者基线时病情较轻,而基线时病情较重的患者均无反应。16例基线时有躁狂症状的患者中(7例躁狂,9例循环发作),大多数在最初2周内YMRS评分有所改善。虽然16例患者中有7例(44%)在末次观察时达到躁狂反应和缓解标准,但有4例出现中度至重度病情加重的中间期。左乙拉西坦对体重无影响。
在进行更具对照性的临床试验之前,其他初步试验应探索左乙拉西坦可能的精神药物作用领域。