Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene
ABSTRACT: In Antioquia, Colombia, investigators have recently discovered the largest family with the E280A mutation in the presenilin 1 gene that causes one type of familial Alzheimer’s disease (FAD). The current study compares two groups within this family: those diagnosed with Alzheimer’s disease...
- Autores:
-
Arango Lasprilla, Juan Carlos
Lopera Restrepo, Francisco Javier
Iglesias Dorado, Jaime
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2003
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/34396
- Palabra clave:
- Chromosomes, Human, Pair 14
Cromosomas Humanos Par 14
Alzheimer Disease
Enfermedad de Alzheimer
Presenilin-1
Presenilina-1
Mutation
Mutación
Neuropsychological Tests
Pruebas Neuropsicológicas
- Rights
- openAccess
- License
- http://creativecommons.org/licenses/by-nc/2.5/co/
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Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene |
| title |
Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene |
| spellingShingle |
Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene Chromosomes, Human, Pair 14 Cromosomas Humanos Par 14 Alzheimer Disease Enfermedad de Alzheimer Presenilin-1 Presenilina-1 Mutation Mutación Neuropsychological Tests Pruebas Neuropsicológicas |
| title_short |
Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene |
| title_full |
Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene |
| title_fullStr |
Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene |
| title_full_unstemmed |
Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene |
| title_sort |
Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 Gene |
| dc.creator.fl_str_mv |
Arango Lasprilla, Juan Carlos Lopera Restrepo, Francisco Javier Iglesias Dorado, Jaime |
| dc.contributor.author.none.fl_str_mv |
Arango Lasprilla, Juan Carlos Lopera Restrepo, Francisco Javier Iglesias Dorado, Jaime |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo de Neurociencias de Antioquia |
| dc.subject.decs.none.fl_str_mv |
Chromosomes, Human, Pair 14 Cromosomas Humanos Par 14 Alzheimer Disease Enfermedad de Alzheimer Presenilin-1 Presenilina-1 Mutation Mutación Neuropsychological Tests Pruebas Neuropsicológicas |
| topic |
Chromosomes, Human, Pair 14 Cromosomas Humanos Par 14 Alzheimer Disease Enfermedad de Alzheimer Presenilin-1 Presenilina-1 Mutation Mutación Neuropsychological Tests Pruebas Neuropsicológicas |
| description |
ABSTRACT: In Antioquia, Colombia, investigators have recently discovered the largest family with the E280A mutation in the presenilin 1 gene that causes one type of familial Alzheimer’s disease (FAD). The current study compares two groups within this family: those diagnosed with Alzheimer’s disease (AD) in its early stage (nine subjects) and relatives (carriers) who did not show any signs of dementia (nine subjects). A battery of the following neuropsychological tests was administered to subjects in both groups: the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD), a Phonological Verbal Fluency test, the Visual “A” Cancellation Test, memory of three phrases, the Rey-Osterrieth Complex Figure, and the Trail Making Test Part A. Statistical analyses of the average test scores of each group showed that the AD group scored significantly (p< 0.01 or p < 0.05) lower on 29 of the 43 neuropsychological variables measured (67 percent). Therefore, this specific battery was useful in discriminating subjects with AD from their healthy relatives who are carriers of the disease. The AD group as a whole presented slight dementia with predominant deficits in memory, language, praxis, and attention. This profile is similar to those reported in subjects with sporadic AD in its early stage and confirms the findings found in other neuropsychological studies of subjects with FAD linked to mutations in chromosome 14. |
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2003 |
| dc.date.issued.none.fl_str_mv |
2003 |
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2023-03-31T19:57:52Z |
| dc.date.available.none.fl_str_mv |
2023-03-31T19:57:52Z |
| dc.type.spa.fl_str_mv |
Artículo de investigación |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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1533-3175 |
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https://hdl.handle.net/10495/34396 |
| dc.identifier.doi.none.fl_str_mv |
10.1177/153331750301800306 |
| dc.identifier.eissn.none.fl_str_mv |
1938-2731 |
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https://doi.org/10.1177/153331750301800306 |
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1533-3175 10.1177/153331750301800306 1938-2731 |
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https://hdl.handle.net/10495/34396 https://doi.org/10.1177/153331750301800306 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Am. J. Alzheimers Dis. Other Demen. |
| dc.relation.citationendpage.spa.fl_str_mv |
146 |
| dc.relation.citationissue.spa.fl_str_mv |
3 |
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137 |
| dc.relation.citationvolume.spa.fl_str_mv |
18 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
American Journal of Alzheimer's Disease and other Dementias |
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http://creativecommons.org/licenses/by-nc/2.5/co/ |
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SAGE Publications |
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Weston, Estados Unidos |
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sin facultad - programa |
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Universidad de Antioquia |
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Arango Lasprilla, Juan CarlosLopera Restrepo, Francisco JavierIglesias Dorado, JaimeGrupo de Neurociencias de Antioquia2023-03-31T19:57:52Z2023-03-31T19:57:52Z20031533-3175https://hdl.handle.net/10495/3439610.1177/1533317503018003061938-2731https://doi.org/10.1177/153331750301800306ABSTRACT: In Antioquia, Colombia, investigators have recently discovered the largest family with the E280A mutation in the presenilin 1 gene that causes one type of familial Alzheimer’s disease (FAD). The current study compares two groups within this family: those diagnosed with Alzheimer’s disease (AD) in its early stage (nine subjects) and relatives (carriers) who did not show any signs of dementia (nine subjects). A battery of the following neuropsychological tests was administered to subjects in both groups: the Consortium to Establish a Registry for Alzheimer’s Disease (CERAD), a Phonological Verbal Fluency test, the Visual “A” Cancellation Test, memory of three phrases, the Rey-Osterrieth Complex Figure, and the Trail Making Test Part A. Statistical analyses of the average test scores of each group showed that the AD group scored significantly (p< 0.01 or p < 0.05) lower on 29 of the 43 neuropsychological variables measured (67 percent). Therefore, this specific battery was useful in discriminating subjects with AD from their healthy relatives who are carriers of the disease. The AD group as a whole presented slight dementia with predominant deficits in memory, language, praxis, and attention. This profile is similar to those reported in subjects with sporadic AD in its early stage and confirms the findings found in other neuropsychological studies of subjects with FAD linked to mutations in chromosome 14.COL001074410application/pdfengSAGE PublicationsWeston, Estados Unidossin facultad - programahttp://creativecommons.org/licenses/by-nc/2.5/co/https://creativecommons.org/licenses/by-nc/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Neuropsychological Study of Familial Alzheimer's Disease Caused by Mutation E280A in the Presenilin 1 GeneArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionChromosomes, Human, Pair 14Cromosomas Humanos Par 14Alzheimer DiseaseEnfermedad de AlzheimerPresenilin-1Presenilina-1MutationMutaciónNeuropsychological TestsPruebas NeuropsicológicasAm. J. Alzheimers Dis. 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