Kaye Neil S, Graham Jay, Roberts Jeremy, Thompson Thomas, Nanry Kevin
Department of Psychiatry and Human Behavior, Jefferson Medical College, Philadelphia, PA, USA.
J Clin Psychopharmacol. 2007 Aug;27(4):387-91. doi: 10.1097/jcp.0b013e3180a76dd2.
Cognitive deficits in patients with bipolar disorder are likely to impair occupational and social functioning. In a post hoc analysis of data from a prospective, open-label study of lamotrigine in 1175 patients 13 years or older with bipolar I disorder, changes in the self-rated cognitive function scores of patients receiving lamotrigine as monotherapy or as adjunctive therapy were evaluated. Lamotrigine was given for 12 weeks, with a target dosage of 200 mg/d. Cognitive function was assessed at baseline and week 12 with the self-rated Medical Outcomes Study Cognitive (MOS-Cog) Scale. Mean MOS-Cog scores improved significantly from baseline in the overall group (+8.4 +/- 22.55 points, P < 0.0001) and in subgroups of patients receiving and not receiving concomitant valproate, antidepressants, or antipsychotics. Patients receiving lamotrigine and not receiving concomitant antipsychotics, however, exhibited a small but significantly greater degree of improvement than patients who were receiving concomitant antipsychotics (adjusted mean difference = 4.05; 95% confidence interval, 1.30-6.81; P = 0.0039). Statistically significant improvement was seen in patient subgroups with a depressive (mean change from baseline, 8.8 +/- 21.97; P < 0.0001) or a manic (mean change from baseline, 7.5 +/- 22.62; P = 0.0007) index episode. Improvements in MOS-Cog scores significantly correlated with improvement in both depressive (correlation coefficient, -0.339; P < 0.0001) and manic (correlation coefficient, -0.151; P < 0.0001) symptoms. Overall, self-rated cognitive function scores improved during open-label lamotrigine therapy in patients with bipolar I disorder whether or not they were receiving concomitant valproate, antidepressants, or antipsychotics. Additional research is needed to explore the clinical relevance of these findings.
双相情感障碍患者的认知缺陷可能会损害其职业和社交功能。在一项对1175名13岁及以上的双相I型障碍患者进行的拉莫三嗪前瞻性开放标签研究数据的事后分析中,评估了接受拉莫三嗪单药治疗或辅助治疗的患者自评认知功能评分的变化。拉莫三嗪治疗12周,目标剂量为200mg/d。在基线和第12周时,使用自评医学结局研究认知(MOS-Cog)量表评估认知功能。总体组的平均MOS-Cog评分较基线有显著改善(+8.4±22.55分,P<0.0001),在接受和未接受丙戊酸盐、抗抑郁药或抗精神病药的患者亚组中也是如此。然而,接受拉莫三嗪且未接受联合抗精神病药治疗的患者,与接受联合抗精神病药治疗的患者相比,改善程度虽小但显著更大(调整后平均差异=4.05;95%置信区间,1.30-6.81;P=0.0039)。在有抑郁(基线平均变化,8.8±21.97;P<0.0001)或躁狂(基线平均变化,7.5±22.62;P=0.0007)指数发作的患者亚组中观察到统计学上的显著改善。MOS-Cog评分的改善与抑郁(相关系数,-0.339;P<0.0001)和躁狂(相关系数,-0.151;P<0.0001)症状的改善均显著相关。总体而言,无论双相I型障碍患者是否接受丙戊酸盐、抗抑郁药或抗精神病药联合治疗,在开放标签的拉莫三嗪治疗期间,自评认知功能评分均有所改善。需要进一步的研究来探索这些发现的临床相关性。