Carregant...
Miniatura

Tipus de document

Article

Versió

Versió publicada

Data de publicació

Llicència de publicació

cc-by (c) Orme, Tatiana et al., 2020
Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/172897

Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies

Títol de la revista

Director/Tutor

ISSN de la revista

Títol del volum

Resum

Dementia with Lewy bodies (DLB) is a clinically heterogeneous disorder with a substantial burden on healthcare. Despite this, the genetic basis of the disorder is not well defined and its boundaries with other neurodegenerative diseases are unclear. Here, we performed whole exome sequencing of a cohort of 1118 Caucasian DLB patients, and focused on genes causative of monogenic neurodegenerative diseases. We analyzed variants in 60 genes implicated in DLB, Alzheimer's disease, Parkinson's disease, frontotemporal dementia, and atypical parkinsonian or dementia disorders, in order to determine their frequency in DLB. We focused on variants that have previously been reported as pathogenic, and also describe variants reported as pathogenic which remain of unknown clinical significance, as well as variants associated with strong risk. Rare missense variants of unknown significance were found in APP, CHCHD2, DCTN1, GRN, MAPT, NOTCH3, SQSTM1, TBK1 and TIA1. Additionally, we identified a pathogenic GRN p.Arg493* mutation, potentially adding to the diversity of phenotypes associated with this mutation. The rarity of previously reported pathogenic mutations in this cohort suggests that the genetic overlap of other neurodegenerative diseases with DLB is not substantial. Since it is now clear that genetics plays a role in DLB, these data suggest that other genetic loci play a role in this disease.

Citació

Citació

ORME, Tatiana, HERNANDEZ, Dena, ROSS, Owen a., KUN-RODRIGUES, Celia, DARWENT, Lee, SHEPHERD, Claire e., PARKKINEN, Laura, ANSORGE, Olaf, CLARK, Lorraine n., HONIG, Lawrence s., MARDER, Karen, LEMSTRA, Afina w., ROGAEVA, Ekaterina, ST GEORGE-HYSLOP, Peter, LONDOS, Elisabet, ZETTERBERG, Henrik, MORGAN, Kevin, TROAKES, Claire, AL-SARRAJ, Safa, LASHLEY, Tammaryn, HOLTON, Janice, COMPTA, Yaroslau, DEERLIN, Vivianna van, TROJANOWSKI, John q., SERRANO, Geidy e., BEACH, Thomas g., LESAGE, Suzanne, GALASKO, Douglas, MASLIAH, Eliezer, SANTANA, Isabel, PASTOR, Pau, TIENARI, Pentti j., MYLLYKANGAS, Liisa, OINAS, Minna, REVESZ, Tamas, LEES, Andrew, BOEVE, Bradley f., PETERSEN, Ronald c., FERMAN, Tanis j., ESCOTT-PRICE, Valentina. Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies. _Acta Neuropathologica Communications_. 2020. Vol. 8, núm. 5. [consulta: 21 de gener de 2026]. ISSN: 2051-5960. [Disponible a: https://hdl.handle.net/2445/172897]

Exportar metadades

JSON - METS

Compartir registre