| Literature DB >> 22819134 |
Livia Bernardi1, Francesca Frangipane1, Nicoletta Smirne1, Rosanna Colao1, Gianfranco Puccio1, Sabrina Am Curcio1, Maria Mirabelli1, Raffaele Maletta1, Maria Anfossi1, Maura Gallo1, Silvana Geracitano1, Maria Elena Conidi1, Raffale Di Lorenzo1, Alessandra Clodomiro1, Chiara Cupidi1, Sandra Marzano2, Francesco Comito2, Vincenzo Valenti2, Maria Angela Zirilli2, Mahdi Ghani3, Zhengrui Xi3, Christine Sato3, Danielle Moreno3, Annelisa Borelli4, Rosa Anna Leone4, Peter St George-Hyslop3,5,6, Ekaterina Rogaeva3,5, Amalia C Bruni1.
Abstract
The objectives of this study were to estimate frontotemporal dementia (FTD) prevalence, identify FTD-related mutations, and correlate FTD phenotype with mutations in a southern Italian population. The study population consisted of subjects ≥ 50 years of age residing in the Community of Biv. on January 1, 2004, and a door-to-door 2-phase design was used. Genetic and biochemical analyses were done on samples collected from 32 patients. Prevalence rates were 0.6 for Alzheimer's disease, 0.4 for vascular dementia (VD), 3.5 for FTD, 0.2 for Parkinson dementia, and 1.2 for unspecified dementia. Three GRN (1 known and 2 novel) mutations with reduced plasma protein levels were found associated to 3 distinct phenotypes (behavioral, affective, and delirious type). We report an unusually high FTD prevalence in the investigated population, but a low prevalence of Alzheimer's disease. We confirm the heterogeneity of FTD phenotype associated with different GRN mutations.Entities:
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Year: 2012 PMID: 22819134 PMCID: PMC5019339 DOI: 10.1016/j.neurobiolaging.2012.06.017
Source DB: PubMed Journal: Neurobiol Aging ISSN: 0197-4580 Impact factor: 4.673