Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

Lohmann E., Guerreiro R. J., Erginel-Unaltuna N., Gurunlian N., Bilgic B., Gurvit H., ...Daha Fazla

NEUROBIOLOGY OF AGING, cilt.33, sa.8, 2012 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 33 Sayı: 8
  • Basım Tarihi: 2012
  • Doi Numarası: 10.1016/j.neurobiolaging.2012.02.020
  • Dergi Adı: NEUROBIOLOGY OF AGING
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Anahtar Kelimeler: Alzheimer disease, Presenilin, Mutation, Turkey, FAMILIAL ALZHEIMERS-DISEASE, PRECURSOR PROTEIN GENES, PRESENILIN-1 GENE, MISSENSE MUTATIONS, COMMON VARIANTS, POPULATION, JAPANESE, ASSOCIATION, PREVALENCE, EXPRESSION
  • İstanbul Üniversitesi Adresli: Evet

Özet

In order to assess the frequency of mutations in the known Alzheimer's disease causative genes in Turkish dementia patients we screened amyloid precursor protein (APP), PSEN1 and PSEN2 for mutations in a cohort of 98 Turkish dementia families. Six families were found to carry PSEN1 mutations (p.H163R, p.P264L, and p.H214Y) or variants suggested to cause the disease (p.L134R, p.L262V, and p.A396T). In 4 other families, previously reported PSEN2 variants were identified (p.R62H, p.R71W, p.M174V (n = 2), and p.S130L). The phenotype of the carriers varied from rapid progressing Alzheimer's disease to frontotemporal dementia, with spasticity and seizures also observed. Here we report a frequency of 11.2% of mutations and variants in the known Alzheimer disease genes in the dementia cohort studied and 24% in the early onset subgroup of patients, suggesting that mutations in these genes are not uncommon in Turkey and are associated with various phenotypes. We thus believe that genetic analysis should become a standardized diagnostic implement, not only for the identification of the genetic disease, but also for appropriate genetic counseling. (C) 2012 Elsevier Inc. All rights reserved.