Determinants of onset age in Friedreich's ataxia

被引:35
作者
De Michele, G
Filla, A
Criscuolo, C
Scarano, V
Cavalcanti, F
Pianese, L
Monticelli, A
Cocozza, S
机构
[1] Univ Naples Federico II, Neurol Clin, I-80131 Naples, Italy
[2] Univ Naples Federico II, Dept Neurol Sci, I-80131 Naples, Italy
[3] Univ Naples Federico II, CEOS, I-80131 Naples, Italy
[4] Univ Naples Federico II, Dept Mol & Cellular Biol & Pathol, I-80131 Naples, Italy
关键词
Friedreich's ataxia; age at onset; GAA expansion; triplet diseases;
D O I
10.1007/s004150050198
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
We studied the factors that might influence onset age in Friedreich's ataxia in 41 cases (20 male, 21 female) homozygous for GAA expansion on the first intron of X25 gene, Patients came from 18 multiplex families (13 couples, 5 triplets). Mean age (SD) was 18.1 (8.9) years and did not differ by gender. Onset age and the sizes of the smaller (GAA1) and the larger (GAA2) allele in each pair showed high intrafamily correlation. We found an inverse correlation between age at onset and GAA1 size, but not between age at onset and GAA2 size. Stepwise multiple regression of onset age on GAA 1 size, sibling onset age, and GAA2 size showed that GAA1 accounts for 73% of onset age variance, and sibling onset age for an additional 13%. The study demonstrates that, in addition to GAA expansion size, other environmental or genetic familial factors influence disease expression.
引用
收藏
页码:166 / 168
页数:3
相关论文
共 14 条
[1]   Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion [J].
Campuzano, V ;
Montermini, L ;
Molto, MD ;
Pianese, L ;
Cossee, M ;
Cavalcanti, F ;
Monros, E ;
Rodius, F ;
Duclos, F ;
Monticelli, A ;
Zara, F ;
Canizares, J ;
Koutnikova, H ;
Bidichandani, SI ;
Gellera, C ;
Brice, A ;
Trouillas, P ;
DeMichele, G ;
Filla, A ;
DeFrutos, R ;
Palau, F ;
Patel, PI ;
DiDonato, S ;
Mandel, JL ;
Cocozza, S ;
Koenig, M ;
Pandolfo, M .
SCIENCE, 1996, 271 (5254) :1423-1427
[2]   MAPPING OF MUTATION CAUSING FRIEDREICHS ATAXIA TO HUMAN CHROMOSOME-9 [J].
CHAMBERLAIN, S ;
SHAW, J ;
ROWLAND, A ;
WALLIS, J ;
SOUTH, S ;
NAKAMURA, Y ;
VONGABAIN, A ;
FARRALL, M ;
WILLIAMSON, R .
NATURE, 1988, 334 (6179) :248-250
[3]   Age of onset, sex, and cardiomyopathy as predictors of disability and survival in Friedreich's disease: A retrospective study on 119 patients [J].
DeMichele, G ;
Perrone, F ;
Filla, A ;
Mirante, E ;
Giordano, M ;
DePlacido, S ;
Campanella, G .
NEUROLOGY, 1996, 47 (05) :1260-1264
[4]   LATE-ONSET FRIEDREICHS-DISEASE - CLINICAL-FEATURES AND MAPPING OF MUTATION TO THE FRDA LOCUS [J].
DEMICHELE, G ;
FILLA, A ;
CAVALCANTI, F ;
DIMAIO, L ;
PIANESE, L ;
CASTALDO, I ;
CALABRESE, O ;
MONTICELLI, A ;
VARRONE, S ;
CAMPANELLA, G ;
LEONE, M ;
PANDOLFO, M ;
COCOZZA, S .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1994, 57 (08) :977-979
[5]   LATE ONSET RECESSIVE ATAXIA WITH FRIEDREICHS DISEASE PHENOTYPE [J].
DEMICHELE, G ;
FILLA, A ;
BARBIERI, F ;
PERRETTI, A ;
SANTORO, L ;
TROMBETTA, L ;
SANTORELLI, F ;
CAMPANELLA, G .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1989, 52 (12) :1398-1401
[6]   Clinical and genetic abnormalities in patients with Friedreich's ataxia [J].
Durr, A ;
Cossee, M ;
Agid, Y ;
Campuzano, V ;
Mignard, C ;
Penet, C ;
Mandel, JL ;
Brice, A ;
Koenig, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1996, 335 (16) :1169-1175
[7]  
Filla A, 1996, AM J HUM GENET, V59, P554
[8]   INTRAFAMILIAL PHENOTYPE VARIATION IN FRIEDREICHS DISEASE - POSSIBLE EXCEPTIONS TO DIAGNOSTIC-CRITERIA [J].
FILLA, A ;
DEMICHELE, G ;
CAVALCANTI, F ;
SANTORELLI, F ;
SANTORO, L ;
CAMPANELLA, G .
JOURNAL OF NEUROLOGY, 1991, 238 (03) :147-150
[9]  
Filla A, 1997, NEW ENGL J MED, V336, P1021
[10]  
GEOFFROY G, 1976, Canadian Journal of Neurological Sciences, V3, P279