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一项为期12周的单盲试验,评估喹硫平对有发展为双相I型障碍高风险青少年情绪症状的治疗效果。

A 12-week single-blind trial of quetiapine for the treatment of mood symptoms in adolescents at high risk for developing bipolar I disorder.

作者信息

DelBello Melissa P, Adler Caleb M, Whitsel Rachel M, Stanford Kevin E, Strakowski Stephen M

机构信息

Division of Bipolar Disorders Research, Department of Psychiatry, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267-0559, USA.

出版信息

J Clin Psychiatry. 2007 May;68(5):789-95. doi: 10.4088/jcp.v68n0520.

Abstract

OBJECTIVE

To investigate the effectiveness and tolerability of quetiapine for the treatment of adolescents at high risk for developing bipolar I disorder.

METHOD

Twenty adolescents (aged 12-18 years) with mood symptoms that did not meet DSM-IV-TR criteria for bipolar I disorder and who had at least one first-degree relative with bipolar I disorder were recruited from August 2003 to June 2005 to participate in a single-blind, 12-week prospective study of quetiapine. Subjects were diagnosed using the Washington University in St. Louis Kiddie Schedule of Affective Disorders and Schizophrenia and were symptomatic, defined by a Young Mania Rating Scale (YMRS) score > or = 12 or a Childhood Depression Rating Scale-Revised Version (CDRS-R) score > or = 28 at baseline. The primary effectiveness measure was an endpoint Clinical Global Impressions-Improvement scale (CGI-I) score < or = 2 ("much" or "very much" improved). Secondary efficacy measures included change from baseline to endpoint in YMRS and CDRS-R scores.

RESULTS

Mood disorder diagnoses in the adolescents consisted of bipolar disorder not otherwise specified (N = 11), dysthymia (N = 3), bipolar II disorder (N = 3), cyclothymia (N = 2), and major depressive disorder (N = 1). The majority of patients (N = 12, 60%) were non-responders to previous trials of psychotropic agents. Fifteen subjects (75%) completed all study visits. Eighty-seven percent of patients were responders (CGI-I < or = 2) to quetiapine at week 12 (mean +/- SD endpoint dose = 460 +/- 88 mg/day). YMRS scores decreased from 18.1 +/- 5.5 at baseline to 8.7 +/- 7.9 at endpoint (p < .0001), and CDRS-R scores decreased from 38.2 +/- 9.8 to 27.7 +/- 9.3, (p = .0003). The most frequently reported adverse events were somnolence, headache, musculoskeletal pain, and dyspepsia. No subjects discontinued study participation due to adverse events.

CONCLUSION

Although these findings are limited by the small sample size and open-label treatment, the results suggest that quetiapine may be an effective treatment for mood symptoms in adolescents with a familial risk for developing bipolar I disorder.

摘要

目的

探讨喹硫平治疗有发展为双相I型障碍高风险青少年的有效性和耐受性。

方法

从2003年8月至2005年6月招募了20名年龄在12 - 18岁之间、情绪症状不符合双相I型障碍的DSM-IV-TR标准且至少有一名双相I型障碍一级亲属的青少年,参与一项为期12周的喹硫平单盲前瞻性研究。使用圣路易斯华盛顿大学儿童情感障碍和精神分裂症量表对受试者进行诊断,在基线时,根据青年躁狂评定量表(YMRS)评分≥12或儿童抑郁评定量表修订版(CDRS-R)评分≥28确定为有症状。主要有效性指标是终点临床总体印象改善量表(CGI-I)评分≤2(“明显”或“非常明显”改善)。次要疗效指标包括从基线到终点YMRS和CDRS-R评分的变化。

结果

青少年的情绪障碍诊断包括未特定的双相情感障碍(N = 11)、心境恶劣障碍(N = 3)、双相II型障碍(N = 3)、环性心境障碍(N = 2)和重度抑郁症(N = 1)。大多数患者(N = 12,60%)对先前的精神药物试验无反应。15名受试者(75%)完成了所有研究访视。87%的患者在第12周时对喹硫平有反应(CGI-I≤2)(平均±标准差终点剂量 = 460±88毫克/天)。YMRS评分从基线时的18.1±5.5降至终点时的8.7±7.9(p <.0001),CDRS-R评分从38.2±9.8降至27.7±9.3(p =.0003)。最常报告的不良事件是嗜睡、头痛、肌肉骨骼疼痛和消化不良。没有受试者因不良事件而停止参与研究。

结论

尽管这些发现受样本量小和开放标签治疗的限制,但结果表明喹硫平可能是治疗有发展为双相I型障碍家族风险青少年情绪症状的有效药物。

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