摘要
Background: Early onset familial Alzheimer disease is caused by mutations in the amyloid precursor protein (APP), prese nilin 1 (PSEN1), or presenilin 2 ( PSEN2) genes. Phenotypic diversity has been reported to be associated with vario us mutations in PSEN1. Various mutations of PSEN1 have been reported in cases of early onset Alzheimer disease with spastic paraparesis. Objective: To describe a novel mutation in the PSEN1 gene associated with early onset Alzheimer disea se with spastic paraparesis. Patient and Methods: The patient was a 27 year ol d man who developed early onset dementia with spastic paraparesis. We examined sequences of the PSEN1, PSEN2, and APP genes from the patient and his family. To detect a possible mutation effect on the production of amyloid β.peptide (Aβ ), transfected HEK293 cells were examined for Aβ42 and Aβ40 production. Result s: We found a novel mutation (Leu85Pro) in PSEN1. This mutation influenced the p roduction of Aβ, resulting in a 2 fold elevation of Aβ42 production and of th e Aβ42/40 ratio. Conclusion: To our knowledge, this is the first report of very early onset Alzheimer disease with spastic paraparesis and with the visual var iant form of the disease, which is associated with visuospatial cognitive disord er. The Leu85Pro mutation in PSEN1 was pathogenic.
Background: Early onset familial Alzheimer disease is caused by mutations in the amyloid precursor protein (APP), prese nilin 1 (PSEN1), or presenilin 2 ( PSEN2) genes. Phenotypic diversity has been reported to be associated with vario us mutations in PSEN1. Various mutations of PSEN1 have been reported in cases of early onset Alzheimer disease with spastic paraparesis. Objective: To describe a novel mutation in the PSEN1 gene associated with early onset Alzheimer disea se with spastic paraparesis. Patient and Methods: The patient was a 27 year ol d man who developed early onset dementia with spastic paraparesis. We examined sequences of the PSEN1, PSEN2, and APP genes from the patient and his family. To detect a possible mutation effect on the production of amyloid β.peptide (Aβ ), transfected HEK293 cells were examined for Aβ42 and Aβ40 production. Result s: We found a novel mutation (Leu85Pro) in PSEN1. This mutation influenced the p roduction of Aβ, resulting in a 2 fold elevation of Aβ42 production and of th e Aβ42/40 ratio. Conclusion: To our knowledge, this is the first report of very early onset Alzheimer disease with spastic paraparesis and with the visual var iant form of the disease, which is associated with visuospatial cognitive disord er. The Leu85Pro mutation in PSEN1 was pathogenic.
出处
《世界核心医学期刊文摘（神经病学分册）》
2005年第3期25-26,共2页
Digest of the World Core Medical Journals:Clinical Neurology
