Valproic acid blood genomic expression patterns in children with epilepsy - a pilot study

被引:48
作者
Tang, Y
Glauser, TA
Gilbert, DL
Hershey, AD
Privitera, MD
Ficker, DM
Szaflarski, JP
Sharp, FR
机构
[1] Univ Cincinnati, Dept Neurol, Cincinnati, OH USA
[2] Univ Cincinnati, Childrens Hosp, Med Ctr, Div Pediat Neurol, Cincinnati, OH USA
来源
ACTA NEUROLOGICA SCANDINAVICA | 2004年 / 109卷 / 03期
关键词
epilepsy; seizure; anticonvulsant; Valproic Acid; carbamazepine; gene expression; microarray; blood marker;
D O I
10.1046/j.1600-0404.2003.00253.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective - Valproic acid (VPA) is a commonly used anticonvulsant with multiple systemic effects. The purpose of this pilot study is to examine the blood genomic expression pattern associated with VPA therapy in general and secondly VPA efficacy in children with epilepsy. Materials and methods - Using oligonucleotide microarrays, gene expression in whole blood was assessed in pediatric epilepsy patients following treatment with VPA compared with children with epilepsy prior to initiation of anticonvulsant therapy (drug free patients). Results - The expression of 461 genes was altered in VPA patients (n = 11) compared with drug free patients (n = 7), among which a significant number of serine threonine kinases were down-regulated. Expression patterns in children seizure free on VPA therapy (n = 8) demonstrated 434 up-regulated genes, many in mitochondria, compared with VPA children with continuing seizures (n = 3) and drug free seizure patients (n = 7). Conclusion - VPA therapy is associated with two significant and unique blood gene expression patterns: chronic VPA monotherapy in general and a separate blood genomic profile correlated with seizure freedom. These expression patterns provide new insight into previously undetected mechanisms of VPA anticonvulsant activity.
引用
收藏
页码:159 / 168
页数:10
相关论文
共 44 条
[1]   Impaired methionine synthesis and hypomethylation in rats exposed to valproate during gestation [J].
Alonso-Aperte, E ;
Ubeda, N ;
Achón, M ;
Pérez-Miguelsanz, J ;
Varela-Moreiras, G .
NEUROLOGY, 1999, 52 (04) :750-756
[2]  
BJORGE SM, 1991, DRUG METAB DISPOS, V19, P823
[3]  
BOWDEN CL, 1995, J CLIN PSYCHIAT, V56, P3
[4]   Epileptic phenotypes associated with mitochondrial disorders [J].
Canafoglia, L ;
Franceschetti, S ;
Antozzi, C ;
Carrara, F ;
Farina, L ;
Granata, T ;
Lamantea, E ;
Savoiardo, M ;
Uziel, G ;
Villani, F ;
Zeviani, M ;
Avanzini, G .
NEUROLOGY, 2001, 56 (10) :1340-1346
[5]   Chronic valproate treatment decreases the in vivo turnover of arachidonic acid in brain phospholipids:: a possible common effect of mood stabilizers [J].
Chang, MCJ ;
Contreras, MA ;
Rosenberger, TA ;
Rintala, JJO ;
Bell, JM ;
Rapoport, SI .
JOURNAL OF NEUROCHEMISTRY, 2001, 77 (03) :796-803
[6]  
COVINGTON EC, 1998, CLEVE CLIN J MED S1, V65, pS145
[7]  
Dan S, 2002, CANCER RES, V62, P1139
[8]   Global functional profiling of gene expression [J].
Draghici, S ;
Khatri, P ;
Martins, RP ;
Ostermeier, GC ;
Krawetz, SA .
GENOMICS, 2003, 81 (02) :98-104
[9]   Altered levels of S-adenosylmethionine and S-adenosylhomocysteine in the brains of L-isoaspartyl (D-aspartyl) O-methyltransferase-deficient mice [J].
Farrar, C ;
Clarke, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (31) :27856-27863
[10]   Neuroprotective effects of creatine in a transgenic mouse model of Huntington's disease [J].
Ferrante, RJ ;
Andreassen, OA ;
Jenkins, BG ;
Dedeoglu, A ;
Kuemmerle, S ;
Kubilus, JK ;
Kaddurah-Daouk, R ;
Hersch, SM ;
Beal, MF .
JOURNAL OF NEUROSCIENCE, 2000, 20 (12) :4389-4397