Genotype-phenotype correlation in cystic fibrosis patients compound heterozygous for the A455E mutation

被引:34
作者
DeBraekeleer, M [1 ]
Allard, C [1 ]
Leblanc, JP [1 ]
Simard, F [1 ]
Aubin, G [1 ]
机构
[1] HOP CHICOUTIMI, CLIN FIBROSE KYST, CHICOUTIMI, PQ G7H 2B1, CANADA
关键词
D O I
10.1007/s004390050616
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Cystic fibrosis (CF) has a high incidence in the French-Canadian population of Saguenay Lac-Saint-Jean (Quebec), The A455E mutation accounts for 8.3% of the CF chromosomes. This mutation was shown to be associated with a milder lung disease in the Dutch population. Twenty two CF patients distributed in 17 families and compound heterozygotes for the A455E mutation have been followed at the Clinique de Fibrose Kystique de Chicoutimi. Fourteen patients also carried the Delta F508 mutation while the remaining eight patients had the 621+ IG-->T mutation. Each patient was matched by sex and age to a patient homozygous for the Delta F508 mutation, The pairs were analyzed for several clinical and laboratory variables. The A455E compound heterozygotes were diagnosed at a later age (P = 0.003) and had chloride concentrations at the sweat test lower than those homozygous for the Delta F508 mutation (P = 0.007), More patients were pancreatic sufficient (P = 0.004). They had a higher Shwachman score (P = 0.001) and better pulmonary function tests (P < 0.02), CF patients compound heterozygous for the A455E mutation have a milder pancreatic and lung disease than the Delta F508 homozygotes. Therefore, the A455E should be associated with a better prognosis.
引用
收藏
页码:208 / 211
页数:4
相关论文
共 19 条
[1]  
Boat T, 1989, CYSTIC FIBROSIS META, P2649
[2]  
*CYST FIBR GEN AN, 1994, HUM MUTAT, V41, P167
[3]  
DAIGNEAULT J, 1992, HUM BIOL, V64, P115
[4]  
DAIGNEAULT J, 1991, CLIN GENET, V40, P298
[5]  
DEBRAEKELEER M, 1995, CLIN GENET, V47, P110
[6]   Genealogy and geographical distribution of CFTR mutations in Saguenay Lac-Saint-Jean (Quebec, Canada) [J].
DeBraekeleer, M ;
Daigneault, J ;
Allard, C ;
Simard, F ;
Aubin, G .
ANNALS OF HUMAN BIOLOGY, 1996, 23 (05) :345-352
[7]  
DeBraekeleer M, 1997, CLIN GENET, V51, P214
[8]  
DEBRAEKELEER M, 1997, IN PRESS CLIN CHEM
[9]  
DEBRAEKELEER M, 1997, IN PRESS J MED GENET
[10]  
DEBRAEKELEER M, 1997, IN PRESS J MED GENET, V34