Effect of simvastatin on cognitive functioning in children with neurofibromatosis type 1 - A randomized controlled trial

被引:138
作者
Krab, Lianne C. [1 ,2 ]
de Goede-Bolder, Arja [1 ]
Aarsen, Femke K. [3 ]
Pluijm, Saskia M. F. [4 ]
Bouman, Marlies J. [3 ]
van der Geest, Jos N. [2 ]
Lequin, Maarten [5 ]
Catsman, Coriene E. [3 ]
Arts, Willem Frans M. [3 ]
Kushner, Steven A. [6 ,7 ,8 ,9 ]
Silva, Alcino J. [7 ,8 ,9 ]
de Zeeuw, Chris I. [2 ,10 ]
Moll, Henriette A. [1 ]
Elgersma, Ype [2 ]
机构
[1] Sophia Childrens Univ Hosp, Erasmus MC Univ Med Ctr, NF1 Core Cognit Res Team, Dept Gen Pediat, Rotterdam, Netherlands
[2] Sophia Childrens Univ Hosp, Erasmus MC Univ Med Ctr, NF1 Core Cognit Res Team, Dept Neurosci, Rotterdam, Netherlands
[3] Sophia Childrens Univ Hosp, Erasmus MC Univ Med Ctr, NF1 Core Cognit Res Team, Dept Pediat Neurol, Rotterdam, Netherlands
[4] Sophia Childrens Univ Hosp, Erasmus MC Univ Med Ctr, NF1 Core Cognit Res Team, Dept Publ Hlth, Rotterdam, Netherlands
[5] Sophia Childrens Univ Hosp, Erasmus MC Univ Med Ctr, NF1 Core Cognit Res Team, Dept Pediat Radiol, Rotterdam, Netherlands
[6] Sophia Childrens Univ Hosp, Erasmus MC Univ Med Ctr, NF1 Core Cognit Res Team, Dept Psychiat, Rotterdam, Netherlands
[7] Univ Calif Los Angeles, Brain Res Inst, Dept Neurobiol, Los Angeles, CA 90024 USA
[8] Univ Calif Los Angeles, Brain Res Inst, Dept Psychiat, Los Angeles, CA 90024 USA
[9] Univ Calif Los Angeles, Brain Res Inst, Dept Psychol, Los Angeles, CA 90024 USA
[10] Royal Acad Sci KNAW, Netherlands Inst Neurosci, Amsterdam, Netherlands
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2008年 / 300卷 / 03期
关键词
D O I
10.1001/jama.300.3.287
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context 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. Objective 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. Intervention Simvastatin or placebo treatment once daily for 12 weeks. Main Outcome Measures 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 out-come 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. Results 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. Conclusion In this 12- week trial, simvastatin did not improve cognitive function in children with NF1. Trial Registration isrctn. org Identifier: ISRCTN14965707.
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收藏
页码:287 / 294
页数:8
相关论文
共 28 条
[11]   IDENTIFICATION OF THE NEUROFIBROMATOSIS TYPE-1 GENE-PRODUCT [J].
GUTMANN, DH ;
WOOD, DL ;
COLLINS, FS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (21) :9658-9662
[12]   A GENETIC-STUDY OF VONRECKLINGHAUSEN NEUROFIBROMATOSIS IN SOUTH EAST WALES .1. PREVALENCE, FITNESS, MUTATION-RATE, AND EFFECT OF PARENTAL TRANSMISSION ON SEVERITY [J].
HUSON, SM ;
COMPSTON, DAS ;
CLARK, P ;
HARPER, PS .
JOURNAL OF MEDICAL GENETICS, 1989, 26 (11) :704-711
[13]   ISOPRENOID ADDITION TO RAS PROTEIN IS THE CRITICAL MODIFICATION FOR ITS MEMBRANE ASSOCIATION AND TRANSFORMING ACTIVITY [J].
KATO, K ;
COX, AD ;
HISAKA, MM ;
GRAHAM, SM ;
BUSS, JE ;
DER, CJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (14) :6403-6407
[14]  
KRAB LC, 2008, J CHILD NEUROL, V23
[15]   NEUROFIBROMATOSIS TYPE-1 IN CHILDHOOD - CORRELATION OF MRI FINDINGS WITH INTELLIGENCE [J].
LEGIUS, E ;
DESCHEEMAEKER, MJ ;
STEYAERT, J ;
SPAEPEN, A ;
VLIETINCK, R ;
CASAER, P ;
DEMAEREL, P ;
FRYNS, JP .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1995, 59 (06) :638-640
[16]  
Levine Terry M, 2006, Semin Pediatr Neurol, V13, P8, DOI 10.1016/j.spen.2006.01.006
[17]  
LEZAK MD, 2004, NEUROPSYCHOLOGICAL A
[18]   The HMG-CoA reductase inhibitor lovastatin reverses the learning and attention deficits in a mouse model of neurofibromatosis type 1 [J].
Li, WD ;
Cui, YJ ;
Kushner, SA ;
Brown, RAM ;
Jentsch, JD ;
Frankland, PW ;
Cannon, TD ;
Silva, AJ .
CURRENT BIOLOGY, 2005, 15 (21) :1961-1967
[19]  
*MED EV BOARD, 2005, SUMM PROD CHAR ZCR T
[20]  
National Institutes of Health, 1987, NEUROFIBROMATOSIS, V1, P172