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Cathepsin D polymorphism in Italian sporadic and familial Alzheimer's disease
被引:26
|作者:
Bagnoli, S
Nacmias, B
Tedde, A
Guarnieri, BM
Cellini, E
Ciantelli, M
Petruzzi, C
Bartoli, A
Ortenzi, L
Serio, A
Sorbi, S
机构:
[1] Univ Florence, Dept Neurol & Psychiat Sci, I-50134 Florence, Italy
[2] Assoc L Petruzzi, Casa Cura Villa Serena, Pescara, Italy
关键词:
Alzheimer's disease;
cathepsin D;
genetics;
apolipoprotein E;
polymorphism;
D O I:
10.1016/S0304-3940(02)00547-5
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
A recent study has shown that a genetic variation in the Cathepsin D (catD) gene is a major risk factor for the development of Alzheimer's disease (AD). CatD is an intracellular aspartyl protease involved in neurodegeneration. A C --> T (Ala --> Val) transition at position 224 has been associated with altered intracellular maturation. Recently, a significant overrepresentation of the T allele of the catD gene in AD patients compared with controls was reported. However, this finding has not yet been confirmed. We analyzed the distribution of catD and apolipoprotein E polymorphisms in Italian patients with sporadic and familial AD (FAD). Our studies revealed that the distribution of catD polymorphism did not differ in AD and FAD patients and controls. Thus, our data do not support a role for the catD gene as a genetic risk factor in the development of AD. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
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页码:273 / 276
页数:4
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