CAG repeat length and clinical features in three Italian families with spinocerebellar ataxia type 2 (SCA2): early impairment of Wisconsin Card Sorting Test and saccade velocity

被引:31
作者
Gambardella, A
Annesi, G
Bono, F
Spadafora, P
Valentino, P
Pasqua, AA
Mazzei, R
Montesanti, R
Conforti, FL
Oliveri, RL
Zappia, M
Aguglia, U
Quattrone, A
机构
[1] Sch Med Catanzaro, Neurol Inst, Catanzaro, Italy
[2] Natl Res Council, Inst Expt Med & Biotechnol, Cosenza, Italy
关键词
autosomal dominant diseases; cerebellar ataxia; spinocerebellar ataxia type 2 (SCA2); saccades; trinucleotide;
D O I
10.1007/s004150050261
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We report on the clinical, neuropsychological, neurophysiological, computerized eye movement, magnetic resonance imaging (MRI) and molecular findings from 17 individuals affected with spinocerebellar ataxia type 2 (SCA2) belonging to three families. The average age at onset of the symptoms was 35.6, 11.9 (mean, SD) years. The mean age at onset of the symptoms in the parents was 44.8, 8.2 years, and in the offspring it was 28.7, 7.2 years. In 12 parent-child pairs, the mean anticipation was -15.75, 9.1 years (range -8.1 to -23.3 years, t = -4.9, P = < 0.002). The mutated SCA2 alleles ranged from 38 to 42 CAG repeats, while the normal alleles ranged from 22 to 24 repeats, with 97% of the alleles having 22 repeats. Small differences in the number of CAG repeats influenced the age at onset and rate of progression of the disease considerably. Indeed, patients presenting with their first symptom at an age of 35 years or later with a slower course of the disease harboured between 38 and 39 repeats. In contrast, patients carrying greater than or equal to 40 CAG repeats manifested the disease prior to 30 years of age and had a faster disease progression toward incapacity. The presenting symptom was always gait ataxia. Slow saccades occured from the beginning of the disease despite normal delay, accuracy and smooth pursuit eye movements. The neuropsychological study showed early and selective impairment of conceptual reasoning ability, as detected by the Wisconsin Card Sorting Test (WCST). It is noteworthy that a significant mutual relationship was observed between performance on the WCST and saccade velocity. All of these findings favour the hypothesis that the disease process of SCA2 in regions other than the cerebellum and brain stem affects severely and early those cortical structures involved in the control of both visually guided saccades and WCST performance.
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页码:647 / 652
页数:6
相关论文
共 22 条
[1]   QUANTITATIVE MEASUREMENT OF SACCADE AMPLITUDE, DURATION, AND VELOCITY [J].
BALOH, RW ;
SILLS, AW ;
KUMLEY, WE ;
HONRUBIA, V .
NEUROLOGY, 1975, 25 (11) :1065-1070
[2]   CLINICAL AND GENETIC-ANALYSIS OF A TUNISIAN FAMILY WITH AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA TYPE-1 LINKED TO THE SCA2 LOCUS [J].
BELAL, S ;
CANCEL, G ;
STEVANIN, G ;
HENTATI, F ;
KHATI, C ;
HAMIDA, CB ;
AUBURGER, G ;
AGID, Y ;
HAMIDA, MB ;
BRICE, A .
NEUROLOGY, 1994, 44 (08) :1423-1426
[3]   Computerized analysis of eye movements as a function of age [J].
Bono, F ;
Oliveri, RL ;
Zappia, M ;
Aguglia, U ;
Puccio, G ;
Quattrone, A .
ARCHIVES OF GERONTOLOGY AND GERIATRICS, 1996, 22 (03) :261-269
[4]   Autosomal dominant cerebellar ataxia type I - Clinical features and MRT in families with SCA1, SCA2 and SCA3 [J].
Burk, K ;
Abele, M ;
Fetter, M ;
Dichgans, J ;
Skalej, M ;
Laccone, F ;
Didierjean, O ;
Brice, A ;
Klockgether, T .
BRAIN, 1996, 119 :1497-1505
[5]   The anatomical localization of saccades using functional imaging studies and transcranial magnetic stimulation [J].
Carter, N ;
Zee, DS .
CURRENT OPINION IN NEUROLOGY, 1997, 10 (01) :10-17
[6]   NEUROPSYCHOLOGICAL ASSESSMENT [J].
CIPOLOTTI, L ;
WARRINGTON, EK .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1995, 58 (06) :655-664
[7]   Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies) - Clinical and neuropathological analysis of 53 patients from three unrelated SCA2 families [J].
Durr, A ;
Smadja, D ;
Cancel, G ;
Lezin, A ;
Stevanin, G ;
Mikol, J ;
Bellance, R ;
Buisson, GG ;
Chneiweiss, H ;
Dellanave, J ;
Agid, Y ;
Brice, A ;
Vernant, JC .
BRAIN, 1995, 118 :1573-1581
[8]   HAS SPINOCEREBELLAR ATAXIA TYPE-2 A DISTINCT PHENOTYPE - GENETIC AND CLINICAL-STUDY OF AN ITALIAN FAMILY [J].
FILLA, A ;
DEMICHELE, G ;
BANFI, S ;
SANTORO, L ;
PERRETTI, A ;
CAVALCANTI, F ;
PIANESE, L ;
CASTALDO, I ;
BARBIERI, F ;
CAMPANELLA, G ;
COCOZZA, S .
NEUROLOGY, 1995, 45 (04) :793-796
[9]   CHROMOSOMAL ASSIGNMENT OF THE 2ND LOCUS FOR AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA (SCA2) TO CHROMOSOME 12Q23-24.1 [J].
GISPERT, S ;
TWELLS, R ;
OROZCO, G ;
BRICE, A ;
WEBER, J ;
HEREDERO, L ;
SCHEUFLER, K ;
RILEY, B ;
ALLOTEY, R ;
NOTHERS, C ;
HILLERMANN, R ;
LUNKES, A ;
KHATI, C ;
STEVANIN, G ;
HERNANDEZ, A ;
MAGARINO, C ;
KLOCKGETHER, T ;
DURR, A ;
CHNEIWEISS, H ;
ENCZMANN, J ;
FARRALL, M ;
BECKMANN, J ;
MULLAN, M ;
WERNET, P ;
AGID, Y ;
FREUND, HJ ;
WILLIAMSON, R ;
AUBURGER, G ;
CHAMBERLAIN, S .
NATURE GENETICS, 1993, 4 (03) :295-299
[10]   A RATING SCALE FOR DEPRESSION [J].
HAMILTON, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1960, 23 (01) :56-62