Genome‐wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Issue 10 (28th August 2019)
- Record Type:
- Journal Article
- Title:
- Genome‐wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project. Issue 10 (28th August 2019)
- Main Title:
- Genome‐wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project
- Authors:
- Moreno‐Grau, Sonia
de Rojas, Itziar
Hernández, Isabel
Quintela, Inés
Montrreal, Laura
Alegret, Montserrat
Hernández‐Olasagarre, Begoña
Madrid, Laura
González‐Perez, Antonio
Maroñas, Olalla
Rosende‐Roca, Maitée
Mauleón, Ana
Vargas, Liliana
Lafuente, Asunción
Abdelnour, Carla
Rodríguez‐Gómez, Octavio
Gil, Silvia
Santos‐Santos, Miguel Ángel
Espinosa, Ana
Ortega, Gemma
Sanabria, Ángela
Pérez‐Cordón, Alba
Cañabate, Pilar
Moreno, Mariola
Preckler, Silvia
Ruiz, Susana
Aguilera, Nuria
Pineda, Juan Antonio
Macías, Juan
Alarcón‐Martín, Emilio
Sotolongo‐Grau, Oscar
Abdelnour, C.
Aguilera, N.
Alarcon, E.
Alegret, M.
Benaque, A.
Boada, M.
Buendia, M.
Cañabate, P.
Carracedo, A.
Corbatón, A.
de Rojas, I.
Diego, S.
Espinosa, A.
Gailhajenet, A.
García González, P.
Gil, S.
Guitart, M.
González Pérez, A.
Hernández, I.
Ibarria, M.
Lafuente, A.
Macias, J.
Maroñas, O.
Martín, E.
Martínez, M.T.
Marquié, M.
Mauleón, A.
Monté‐Rubio, G.
Montrreal, L.
Moreno‐Grau, S.
Moreno, M.
Orellana, A.
Ortega, G.
Pancho, A.
Pelejà, E.
Pérez‐Cordon, A.
Pineda, J.A.
Preckler, S.
Quintela, I.
Real, L.M.
Rodríguez‐Gómez, O.
Rosende‐Roca, M.
Ruiz, A.
Ruiz, S.
Sáez, M.E.
Sanabria, A.
Santos‐Santos, M.A.
Serrano‐Rios, M.
Sotolongo‐Grau, O.
Tárraga, L.
Valero, S.
Vargas, L.
Adarmes‐Gómez, A.D.
Alarcón‐Martín, E.
Álvarez, I.
Álvarez, V.
Amer‐Ferrer, Goo
Antequera, M.
Antúnez, C.
Baquero, M.
Bernal, M.
Blesa, R.
Boada, M.
Buiza‐Rueda, D.
Bullido, M.J.
Burguera, J.A.
Calero, M.
Carrillo, F.
Carrión‐Claro, M.
Casajeros, M.J.
Clarimón, J.
Cruz‐Gamero, J.M.
de Pancorbo, M.M.
de Rojas, I.
del Ser, T.
Diez‐Fairen, M.
Fortea, J.
Franco, E.
Frank‐García, A.
García‐Alberca, J.M.
Garcia Madrona, S.
Garcia‐Ribas, G.
Gómez‐Garre, P.
Hernández, I.
Hevilla, S.
Jesús, S.
Espinosa, Labrador
Lage, C.
Legaz, A.
Lleó, A.
López de Munáin, A.
López‐García, S.
Macias, D.
Manzanares, S.
Marín, M.
Marín‐Muñoz, J.
Marín, T.
Marquié, M.
Martín Montes, A.
Martínez, B.
Martínez, C.
Martínez, V.
Martínez‐Lage Álvarez, P.
Medina, M.
Mendioroz Iriarte, M.
Menéndez‐González, M.
Mir, P.
Molinuevo, J.L.
Monté‐Rubio, G.
Montrreal, L.
Moreno‐Grau, S.
Orellana, A.
Pastor, A.B.
Pastor, P.
Pérez Tur, J.
Periñán‐Tocino, T.
Piñol Ripoll, G.
Rábano, A.
Real de Asúa, D.
Rodrigo, S.
Rodríguez‐Rodríguez, E.
Royo, J.L.
A, Ruiz
Sanchez del Valle Díaz, R.
Sánchez‐Juan, P.
Sastre, I.
Sotolongo‐Grau, O.
Tárraga, L.
Valero, S.
Vicente, M.P.
Vivancos, L.
Marquié, Marta
Monté‐Rubio, Gemma
Valero, Sergi
Benaque, Alba
Clarimón, Jordi
Bullido, Maria Jesus
García‐Ribas, Guillermo
Pástor, Pau
Sánchez‐Juan, Pascual
Álvarez, Victoria
Piñol‐Ripoll, Gerard
García‐Alberca, Jose Maria
Royo, José Luis
Franco, Emilio
Mir, Pablo
Calero, Miguel
Medina, Miguel
Rábano, Alberto
Ávila, Jesús
Antúnez, Carmen
Real, Luis Miguel
Orellana, Adelina
Carracedo, Ángel
Sáez, María Eugenia
Tárraga, Lluís
Boada, Mercè
Ruiz, Agustín
… (more) - Abstract:
- Abstract: Introduction: Large variability among Alzheimer's disease (AD) cases might impact genetic discoveries and complicate dissection of underlying biological pathways. Methods: Genome Research at Fundacio ACE (GR@ACE) is a genome‐wide study of dementia and its clinical endophenotypes, defined based on AD's clinical certainty and vascular burden. We assessed the impact of known AD loci across endophenotypes to generate loci categories. We incorporated gene coexpression data and conducted pathway analysis per category. Finally, to evaluate the effect of heterogeneity in genetic studies, GR@ACE series were meta‐analyzed with additional genome‐wide association study data sets. Results: We classified known AD loci into three categories, which might reflect the disease clinical heterogeneity. Vascular processes were only detected as a causal mechanism in probable AD. The meta‐analysis strategy revealed the ANKRD31 ‐rs4704171 and NDUFAF6 ‐rs10098778 and confirmed SCIMP ‐rs7225151 and CD33 ‐rs3865444. Discussion: The regulation of vasculature is a prominent causal component of probable AD. GR@ACE meta‐analysis revealed novel AD genetic signals, strongly driven by the presence of clinical heterogeneity in the AD series. Highlights: We detected three gene categories operating differently in AD subgroups of patients. Vasculature regulation may be an essential part of the causative mechanism in pure AD. Two novel signals reached genome‐wide significance in ANKRD31 and NDUFAF6 loci.Abstract: Introduction: Large variability among Alzheimer's disease (AD) cases might impact genetic discoveries and complicate dissection of underlying biological pathways. Methods: Genome Research at Fundacio ACE (GR@ACE) is a genome‐wide study of dementia and its clinical endophenotypes, defined based on AD's clinical certainty and vascular burden. We assessed the impact of known AD loci across endophenotypes to generate loci categories. We incorporated gene coexpression data and conducted pathway analysis per category. Finally, to evaluate the effect of heterogeneity in genetic studies, GR@ACE series were meta‐analyzed with additional genome‐wide association study data sets. Results: We classified known AD loci into three categories, which might reflect the disease clinical heterogeneity. Vascular processes were only detected as a causal mechanism in probable AD. The meta‐analysis strategy revealed the ANKRD31 ‐rs4704171 and NDUFAF6 ‐rs10098778 and confirmed SCIMP ‐rs7225151 and CD33 ‐rs3865444. Discussion: The regulation of vasculature is a prominent causal component of probable AD. GR@ACE meta‐analysis revealed novel AD genetic signals, strongly driven by the presence of clinical heterogeneity in the AD series. Highlights: We detected three gene categories operating differently in AD subgroups of patients. Vasculature regulation may be an essential part of the causative mechanism in pure AD. Two novel signals reached genome‐wide significance in ANKRD31 and NDUFAF6 loci. We confirmed SCIMP‐rs7225151 and CD33‐rs3865444 to be genome‐wide significant. Genetic discoveries are strongly impacted by the presence of subgroups of AD. … (more)
- Is Part Of:
- Alzheimer's & dementia. Volume 15:Issue 10(2019)
- Journal:
- Alzheimer's & dementia
- Issue:
- Volume 15:Issue 10(2019)
- Issue Display:
- Volume 15, Issue 10 (2019)
- Year:
- 2019
- Volume:
- 15
- Issue:
- 10
- Issue Sort Value:
- 2019-0015-0010-0000
- Page Start:
- 1333
- Page End:
- 1347
- Publication Date:
- 2019-08-28
- Subjects:
- Alzheimer's disease -- Vascular pathology -- Cerebral amyloid angiopathy -- GWAS -- Biological pathway
Alzheimer's disease -- Periodicals
Alzheimer Disease -- Periodicals
Dementia -- Periodicals
Démence
Maladie d'Alzheimer
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
616.83 - Journal URLs:
- http://www.sciencedirect.com/science/journal/15525260 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jalz.2019.06.4950 ↗
- Languages:
- English
- ISSNs:
- 1552-5260
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0806.255333
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13186.xml