Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease
ABSTRACT: The identification of novel genetic variants contributing to the widespread in the age of onset (AOO) of Alzheimer’s disease (AD) could aid in the prognosis and/or development of new therapeutic strategies focused on early interventions. We recruited 78 individuals with AD from the Paisa g...
- Autores:
-
Vélez Valbuena, Jorge Iván
Lopera Restrepo, Francisco Javier
Creagh, Penelope K.
Piñeros, Laura B.
Das, Debjani
Cervantes Henríquez, Martha Lucía
Acosta López, Johan
Isaza Ruget, Mario A.
Espinosa, Lady G.
Easteal, Simon
Quintero, Gustavo A.
Tamar Silva, Claudia
Mastronardi, Claudio A.
Arcos Burgos, Oscar Mauricio
- Tipo de recurso:
- Article of investigation
- Fecha de publicación:
- 2019
- Institución:
- Universidad de Antioquia
- Repositorio:
- Repositorio UdeA
- Idioma:
- eng
- OAI Identifier:
- oai:bibliotecadigital.udea.edu.co:10495/23054
- Acceso en línea:
- http://hdl.handle.net/10495/23054
- Palabra clave:
- Enfermedad de Alzheimer
Alzheimer Disease
Edad de Inicio
Age of Onset
ASTN2
PSEN1
SNTG1
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by/4.0/
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| dc.title.spa.fl_str_mv |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease |
| title |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease |
| spellingShingle |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease Enfermedad de Alzheimer Alzheimer Disease Edad de Inicio Age of Onset ASTN2 PSEN1 SNTG1 |
| title_short |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease |
| title_full |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease |
| title_fullStr |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease |
| title_full_unstemmed |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease |
| title_sort |
Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's Disease |
| dc.creator.fl_str_mv |
Vélez Valbuena, Jorge Iván Lopera Restrepo, Francisco Javier Creagh, Penelope K. Piñeros, Laura B. Das, Debjani Cervantes Henríquez, Martha Lucía Acosta López, Johan Isaza Ruget, Mario A. Espinosa, Lady G. Easteal, Simon Quintero, Gustavo A. Tamar Silva, Claudia Mastronardi, Claudio A. Arcos Burgos, Oscar Mauricio |
| dc.contributor.author.none.fl_str_mv |
Vélez Valbuena, Jorge Iván Lopera Restrepo, Francisco Javier Creagh, Penelope K. Piñeros, Laura B. Das, Debjani Cervantes Henríquez, Martha Lucía Acosta López, Johan Isaza Ruget, Mario A. Espinosa, Lady G. Easteal, Simon Quintero, Gustavo A. Tamar Silva, Claudia Mastronardi, Claudio A. Arcos Burgos, Oscar Mauricio |
| dc.contributor.researchgroup.spa.fl_str_mv |
Grupo de Neurociencias de Antioquia |
| dc.subject.decs.none.fl_str_mv |
Enfermedad de Alzheimer Alzheimer Disease Edad de Inicio Age of Onset |
| topic |
Enfermedad de Alzheimer Alzheimer Disease Edad de Inicio Age of Onset ASTN2 PSEN1 SNTG1 |
| dc.subject.proposal.spa.fl_str_mv |
ASTN2 PSEN1 SNTG1 |
| description |
ABSTRACT: The identification of novel genetic variants contributing to the widespread in the age of onset (AOO) of Alzheimer’s disease (AD) could aid in the prognosis and/or development of new therapeutic strategies focused on early interventions. We recruited 78 individuals with AD from the Paisa genetic isolate in Antioquia, Colombia. These individuals belong to the world largest multigenerational and extended pedigree segregating AD as a consequence of a dominant fully penetrant mutation in the PSEN1 gene and exhibit an AOO ranging from the early 1930s to the late 1970s. To shed light on the genetic underpinning that could explain the large spread of the age of onset (AOO) of AD, 64 single nucleotide polymorphisms (SNP) associated with neuroanatomical, cardiovascular, and cognitive measures in AD were genotyped. Standard quality control and filtering procedures were applied, and single- and multi-locus linear mixed-effects models were used to identify AOO-associated SNPs. A full two-locus interaction model was fitted to define how identified SNPs interact to modulate AOO. We identified two key epistatic interactions between the APOE*E2 allele and SNPs ASTN2-rs7852878 and SNTG1-rs16914781 that delay AOO by up to ~ 8 years (95% CI 3.2–12.7, P = 1.83 × 10−3) and ~ 7.6 years (95% CI 3.3–11.8, P = 8.69 × 10−4), respectively, and validated our previous finding indicating that APOE*E2 delays AOO of AD in PSEN1 E280 mutation carriers. This new evidence involving APOE*E2 as an AOO delayer could be used for developing precision medicine approaches and predictive genomics models to potentially determine AOO in individuals genetically predisposed to AD. |
| publishDate |
2019 |
| dc.date.issued.none.fl_str_mv |
2019 |
| dc.date.accessioned.none.fl_str_mv |
2021-10-09T14:26:55Z |
| dc.date.available.none.fl_str_mv |
2021-10-09T14:26:55Z |
| 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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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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| dc.identifier.citation.spa.fl_str_mv |
Vélez, J.I., Lopera, F., Creagh, P.K. et al. Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer’s Disease. Mol Neurobiol 56, 3235–3243 (2019). https://doi.org/10.1007/s12035-018-1298-z |
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0893-7648 |
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1559-1182 |
| dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10495/23054 |
| dc.identifier.doi.none.fl_str_mv |
10.1007/s12035-018-1298-z |
| identifier_str_mv |
Vélez, J.I., Lopera, F., Creagh, P.K. et al. Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer’s Disease. Mol Neurobiol 56, 3235–3243 (2019). https://doi.org/10.1007/s12035-018-1298-z 0893-7648 1559-1182 10.1007/s12035-018-1298-z |
| url |
http://hdl.handle.net/10495/23054 |
| dc.language.iso.spa.fl_str_mv |
eng |
| language |
eng |
| dc.relation.ispartofjournalabbrev.spa.fl_str_mv |
Mol. Neurobiol. |
| dc.relation.citationendpage.spa.fl_str_mv |
3243 |
| dc.relation.citationstartpage.spa.fl_str_mv |
3235 |
| dc.relation.citationvolume.spa.fl_str_mv |
56 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Molecular Neurobiology |
| dc.rights.uri.spa.fl_str_mv |
https://creativecommons.org/licenses/by/4.0/ |
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http://creativecommons.org/licenses/by/2.5/co/ |
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info:eu-repo/semantics/openAccess |
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http://purl.org/coar/access_right/c_abf2 |
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https://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/2.5/co/ http://purl.org/coar/access_right/c_abf2 |
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openAccess |
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9 |
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application/pdf |
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Springer |
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Clifton, Estados Unidos |
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Vélez Valbuena, Jorge IvánLopera Restrepo, Francisco JavierCreagh, Penelope K.Piñeros, Laura B.Das, DebjaniCervantes Henríquez, Martha LucíaAcosta López, JohanIsaza Ruget, Mario A.Espinosa, Lady G.Easteal, SimonQuintero, Gustavo A.Tamar Silva, ClaudiaMastronardi, Claudio A.Arcos Burgos, Oscar MauricioGrupo de Neurociencias de Antioquia2021-10-09T14:26:55Z2021-10-09T14:26:55Z2019Vélez, J.I., Lopera, F., Creagh, P.K. et al. Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer’s Disease. Mol Neurobiol 56, 3235–3243 (2019). https://doi.org/10.1007/s12035-018-1298-z0893-76481559-1182http://hdl.handle.net/10495/2305410.1007/s12035-018-1298-zABSTRACT: The identification of novel genetic variants contributing to the widespread in the age of onset (AOO) of Alzheimer’s disease (AD) could aid in the prognosis and/or development of new therapeutic strategies focused on early interventions. We recruited 78 individuals with AD from the Paisa genetic isolate in Antioquia, Colombia. These individuals belong to the world largest multigenerational and extended pedigree segregating AD as a consequence of a dominant fully penetrant mutation in the PSEN1 gene and exhibit an AOO ranging from the early 1930s to the late 1970s. To shed light on the genetic underpinning that could explain the large spread of the age of onset (AOO) of AD, 64 single nucleotide polymorphisms (SNP) associated with neuroanatomical, cardiovascular, and cognitive measures in AD were genotyped. Standard quality control and filtering procedures were applied, and single- and multi-locus linear mixed-effects models were used to identify AOO-associated SNPs. A full two-locus interaction model was fitted to define how identified SNPs interact to modulate AOO. We identified two key epistatic interactions between the APOE*E2 allele and SNPs ASTN2-rs7852878 and SNTG1-rs16914781 that delay AOO by up to ~ 8 years (95% CI 3.2–12.7, P = 1.83 × 10−3) and ~ 7.6 years (95% CI 3.3–11.8, P = 8.69 × 10−4), respectively, and validated our previous finding indicating that APOE*E2 delays AOO of AD in PSEN1 E280 mutation carriers. This new evidence involving APOE*E2 as an AOO delayer could be used for developing precision medicine approaches and predictive genomics models to potentially determine AOO in individuals genetically predisposed to AD.COL00107449application/pdfengSpringerClifton, Estados Unidoshttps://creativecommons.org/licenses/by/4.0/http://creativecommons.org/licenses/by/2.5/co/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Targeting Neuroplasticity, Cardiovascular, and Cognitive-Associated Genomic Variants in Familial Alzheimer's DiseaseArtículo 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/publishedVersionEnfermedad de AlzheimerAlzheimer DiseaseEdad de InicioAge of OnsetASTN2PSEN1SNTG1Mol. 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