Krab Lianne C, de Goede-Bolder Arja, Aarsen Femke K, Pluijm Saskia M F, Bouman Marlies J, van der Geest Jos N, Lequin Maarten, Catsman Coriene E, Arts Willem Frans M, Kushner Steven A, Silva Alcino J, de Zeeuw Chris I, Moll Henriëtte A, Elgersma Ype
Department of General Pediatrics, Erasmus MC University Medical Center, Sophia Children's Hospital, Rotterdam, The Netherlands.
JAMA. 2008 Jul 16;300(3):287-94. doi: 10.1001/jama.300.3.287.
Neurofibromatosis type 1 (NF1) is among the most common genetic disorders that cause learning disabilities. Recently, it was shown that statin-mediated inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase restores the cognitive deficits in an NF1 mouse model.
To determine the effect of simvastatin on neuropsychological, neurophysiological, and neuroradiological outcome measures in children with NF1.
DESIGN, SETTING, AND PARTICIPANTS: Sixty-two of 114 eligible children (54%) with NF1 participated in a randomized, double-blind, placebo-controlled trial conducted between January 20, 2006, and February 8, 2007, at an NF1 referral center at a Dutch university hospital.
Simvastatin or placebo treatment once daily for 12 weeks.
Primary outcomes were scores on a Rey complex figure test (delayed recall), cancellation test (speed), prism adaptation, and the mean brain apparent diffusion coefficient based on magnetic resonance imaging. Secondary outcome measures were scores on the cancellation test (standard deviation), Stroop color word test, block design, object assembly, Rey complex figure test (copy), Beery developmental test of visual-motor integration, and judgment of line orientation. Scores were corrected for baseline performance, age, and sex.
No significant differences were observed between the simvastatin and placebo groups on any primary outcome measure: Rey complex figure test (beta = 0.10; 95% confidence interval [CI], -0.36 to 0.56); cancellation test (beta = -0.19; 95% CI, -0.67 to 0.29); prism adaptation (odds ratio = 2.0; 95% CI, 0.55 to 7.37); and mean brain apparent diffusion coefficient (beta = 0.06; 95% CI, -0.07 to 0.20). In the secondary outcome measures, we found a significant improvement in the simvastatin group in object assembly scores (beta = 0.54; 95% CI, 0.08 to 1.01), which was specifically observed in children with poor baseline performance (beta = 0.80; 95% CI, 0.29 to 1.30). Other secondary outcome measures revealed no significant effect of simvastatin treatment.
In this 12-week trial, simvastatin did not improve cognitive function in children with NF1. Trial Registration isrctn.org Identifier: ISRCTN14965707.
1型神经纤维瘤病(NF1)是导致学习障碍的最常见遗传疾病之一。最近的研究表明,他汀类药物介导的3-羟基-3-甲基戊二酰辅酶A还原酶抑制作用可恢复NF1小鼠模型中的认知缺陷。
确定辛伐他汀对NF1患儿神经心理学、神经生理学和神经放射学结局指标的影响。
设计、地点和参与者:在荷兰大学医院的NF1转诊中心,114名符合条件的NF1患儿中有62名(54%)参加了一项于2006年1月20日至2007年2月8日进行的随机、双盲、安慰剂对照试验。
辛伐他汀或安慰剂每日服用一次,持续12周。
主要结局指标为雷伊复杂图形测试(延迟回忆)、划消测验(速度)、棱镜适应以及基于磁共振成像的平均脑表观扩散系数得分。次要结局指标为划消测验(标准差)、斯特鲁普色词测验、积木图案、物体拼凑、雷伊复杂图形测试(临摹)、贝利视觉运动整合发育测验以及直线定向判断得分。得分根据基线表现、年龄和性别进行校正。
在任何主要结局指标方面,辛伐他汀组和安慰剂组之间均未观察到显著差异:雷伊复杂图形测试(β=0.10;95%置信区间[CI],-0.36至0.56);划消测验(β=-0.19;95%CI,-0.67至0.29);棱镜适应(优势比=2.0;95%CI,0.55至7.37);以及平均脑表观扩散系数(β=0.06;95%CI,-0.07至0.20)。在次要结局指标中,我们发现辛伐他汀组在物体拼凑得分方面有显著改善(β=0.54;95%CI,0.08至1.01),这在基线表现较差的儿童中尤为明显(β=0.80;95%CI,0.29至1.30)。其他次要结局指标显示辛伐他汀治疗无显著效果。
在这项为期12周的试验中,辛伐他汀并未改善NF1患儿的认知功能。试验注册isrctn.org标识符:ISRCTN14965707。