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                                       Details for article 4 of 7 found articles
 
 
  LRRK2 p.G2019S mutation is not common among Alzheimer's disease patients in Brazil
 
 
Title: LRRK2 p.G2019S mutation is not common among Alzheimer's disease patients in Brazil
Author: Santos-Rebouças, Cíntia Barros
Abdalla, Cláudia Bueno
Martins, Paloma Águia
Baldi, Fábio José Rodrigues
Santos, Jussara Mendonça
Motta, Luciana Branco
de Borges, Margarete Borges
Souza, Dorotéia Rossi Silva
de Souza Pinhel, Marcela Augusta
Laks, Jerson
Pimentel, Márcia Mattos Gonçalves
Appeared in: Disease markers
Paging: Volume 27 (2009) nr. 1 pages 13-16
Year: 2009-10-12
Contents: Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene have emerged as a potential common cause for both sporadic and familial Parkinson's Disease (PD) in different populations. The pleomorphic features exhibited by LRRK2 mutation carriers and the central role of Lrrk2 protein in the proper functioning of central nervous system suggest that mutations in this protein might be involved in multiple cellular processes leading to other neurodegenerative disorders than PD. The location of LRRK2 gene on chromosome 12, close to a linkage peak for familial late-onset Alzheimer's Disease (AD), highlights that LRRK2 mutations might be involved in AD pathogenesis. We screened the most common LRRK2 mutation (p.G2019S) in a series of 180 consecutive patients clinically diagnosed with Alzheimer Disease (AD). We identified the p.G2019S in one AD patient with no PD signs, indicating that this mutation is not a common etiological factor for AD in our population (0.5%), corroborating recent data found in Norwegian, North American, Chinese and Italian populations. Nevertheless, these observations together with new information about the Lrrk2 critical multifunctionality do not rule out the possible influence of other variants within LRRK2 in AD, so that other screenings focusing in the whole extension of the LRRK2 using larger sized confirmed AD sample are urgently needed.
Publisher: IOS Press
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 4 of 7 found articles
 
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