Tremor and ataxia in fragile X premutation carriers: Blinded videotape study

被引:73
作者
Berry-Kravis, E
Lewin, F
Wuu, J
Leehey, M
Hagerman, R
Hagerman, P
Goetz, CG
机构
[1] Rush Presbyterian St Lukes Med Ctr, Dept Pediat, Chicago, IL 60612 USA
[2] Rush Presbyterian St Lukes Med Ctr, Dept Neurol Sci, Chicago, IL 60612 USA
[3] Rush Presbyterian St Lukes Med Ctr, Dept Biochem, Chicago, IL 60612 USA
[4] Univ Colorado, Hlth Sci Ctr, Dept Neurol, Denver, CO 80262 USA
[5] Univ Calif Davis, Med Ctr, MIND Inst, Sacramento, CA 95817 USA
关键词
D O I
10.1002/ana.10522
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Fragile X premutation carriers do not have typical fragile X syndrome (FXS) although late-onset progressive action tremor and gait disorder with CNS atrophy was recently reported in male carriers. We compared tremor, gait disorder and parkinsonian signs in FXS premutation subjects (age 50 or more) and a similar control population, using a standardized videotaping protocol. Videotapes were rated using standard scales for tremor (CRST), ataxia (ICARS), and parkinsonian signs (UPDRS) by an investigator blinded to premutation status. Compared to all other groups pooled (n = 30), the male premutation carrier group (n = 7) had significantly higher scores on the CRST (p = 0.0008), ICARS (p = 0.001), and UPDRS (p = 0.0094). On the CRST, rest, postural and kinetic tremor scores were all higher in the male carriers. The elevated total UPDRS and ICARS scores mainly resulted from markedly higher scores for tremor and limb ataxia, respectively. The female carrier (n = 14) and control groups (n = 8) did not differ on any measure. The FMR1 premutation is associated with increased levels of CGG repeat-containing FMR1 mRNA, which may predispose to these symptoms by interfering with nuclear mechanisms. Given the relatively high population frequency of the FMR1 premutation, this mutation may be a significant cause of late-onset "idiopathic" progressive tremor.
引用
收藏
页码:616 / 623
页数:8
相关论文
共 35 条
[31]  
2-V
[32]   Elevated levels of FMR1 mRNA in carrier males:: A new mechanism of involvement in the fragile-X syndrome [J].
Tassone, F ;
Hagerman, RJ ;
Taylor, AK ;
Gane, LW ;
Godfrey, TE ;
Hagerman, PJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :6-15
[33]   Parkinsonism in multiple system atrophy: Natural history, severity (UPDRS-III), and disability assessment compared with Parkinson's disease [J].
Tison, F ;
Yekhlef, F ;
Chrysostome, V ;
Balestre, E ;
Quinn, NP ;
Poewe, W ;
Wenning, GK .
MOVEMENT DISORDERS, 2002, 17 (04) :701-709
[34]   International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome [J].
Trouillas, P ;
Takayanagi, T ;
Hallett, M ;
Currier, RD ;
Subramony, SH ;
Wessel, K ;
Bryer, A ;
Diener, HC ;
Massaquoi, S ;
Gomez, CM ;
Coutinho, P ;
BenHamida, M ;
Campanella, G ;
Filla, A ;
Schut, L ;
Timann, D ;
Honnorat, J ;
Nighoghossian, N ;
Manyam, B .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 145 (02) :205-211
[35]   IDENTIFICATION OF A GENE (FMR-1) CONTAINING A CGG REPEAT COINCIDENT WITH A BREAKPOINT CLUSTER REGION EXHIBITING LENGTH VARIATION IN FRAGILE-X SYNDROME [J].
VERKERK, AJMH ;
PIERETTI, M ;
SUTCLIFFE, JS ;
FU, YH ;
KUHL, DPA ;
PIZZUTI, A ;
REINER, O ;
RICHARDS, S ;
VICTORIA, MF ;
ZHANG, FP ;
EUSSEN, BE ;
VANOMMEN, GJB ;
BLONDEN, LAJ ;
RIGGINS, GJ ;
CHASTAIN, JL ;
KUNST, CB ;
GALJAARD, H ;
CASKEY, CT ;
NELSON, DL ;
OOSTRA, BA ;
WARREN, ST .
CELL, 1991, 65 (05) :905-914