| Literature DB >> 22475797 |
David Wallon1, Stéphane Rousseau, Anne Rovelet-Lecrux, Muriel Quillard-Muraine, Lucie Guyant-Maréchal, Olivier Martinaud, Jérémie Pariente, Michèle Puel, Adeline Rollin-Sillaire, Florence Pasquier, Isabelle Le Ber, Marie Sarazin, Bernard Croisile, Claire Boutoleau-Bretonnière, Catherine Thomas-Antérion, Claire Paquet, Olivier Moreaud, Audrey Gabelle, François Sellal, Mathilde Sauvée, Annie Laquerrière, Charles Duyckaerts, Marie-Bernadette Delisle, Nathalie Streichenberger, Béatrice Lannes, Thierry Frebourg, Didier Hannequin, Dominique Campion.
Abstract
We describe 56 novel autosomal dominant early-onset Alzheimer disease (ADEOAD) families with PSEN1, PSEN2, and AβPP mutations or duplications, raising the total of families with mutations on known genes to 111 (74 PSEN1, 8 PSEN2, 16 AβPP, and 13 AβPP duplications) in the French series. In 33 additional families (23% of the series), the genetic determinism remained uncharacterized after this screening. Cerebrospinal fluid (CSF) biomarker levels were obtained for patients of 58 families (42 with known mutations and 16 without genetic characterization). CSF biomarkers profile was consistent with an AD diagnosis in 90% of families carrying mutations on known genes. In families without mutation, CSF biomarkers were consistent with AD diagnosis in 14/16 cases. Overall, these results support further genetic heterogeneity in the determinism of ADEOAD and suggest that other major genes remain to be characterized.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22475797 DOI: 10.3233/JAD-2012-120172
Source DB: PubMed Journal: J Alzheimers Dis ISSN: 1387-2877 Impact factor: 4.472