TY - JOUR
T1 - A pan-European study of the C9orf72 repeat associated with FTLD
T2 - geographic prevalence, genomic instability, and intermediate repeats
AU - European Early-Onset Dementia Consortium
AU - van der Zee, Julie
AU - Gijselinck, Ilse
AU - Dillen, Lubina
AU - Van Langenhove, Tim
AU - Theuns, Jessie
AU - Engelborghs, Sebastiaan
AU - Philtjens, Stéphanie
AU - Vandenbulcke, Mathieu
AU - Sleegers, Kristel
AU - Sieben, Anne
AU - Bäumer, Veerle
AU - Maes, Githa
AU - Corsmit, Ellen
AU - Borroni, Barbara
AU - Padovani, Alessandro
AU - Archetti, Silvana
AU - Perneczky, Robert
AU - Diehl-Schmid, Janine
AU - de Mendonça, Alexandre
AU - Miltenberger-Miltenyi, Gabriel
AU - Pereira, Sónia
AU - Pimentel, José
AU - Nacmias, Benedetta
AU - Bagnoli, Silvia
AU - Sorbi, Sandro
AU - Graff, Caroline
AU - Chiang, Huei-Hsin
AU - Westerlund, Marie
AU - Sanchez-Valle, Raquel
AU - Llado, Albert
AU - Gelpi, Ellen
AU - Santana, Isabel
AU - Almeida, Maria Rosário
AU - Santiago, Beatriz
AU - Frisoni, Giovanni
AU - Zanetti, Orazio
AU - Bonvicini, Cristian
AU - Synofzik, Matthis
AU - Maetzler, Walter
AU - Vom Hagen, Jennifer Müller
AU - Schöls, Ludger
AU - Heneka, Michael T
AU - Cras, Patrick
AU - Van Broeckhoven, Christine
AU - Van Broeckhoven, Christine
AU - Van Broeckhoven, Christine
AU - Engelborghs, Sebastiaan
AU - Cras, Patrick
AU - Engelborghs, Sebastiaan
AU - Cras, Patrick
N1 - © 2012 Wiley Periodicals, Inc.
PY - 2013/2
Y1 - 2013/2
N2 - We assessed the geographical distribution of C9orf72 G(4) C(2) expansions in a pan-European frontotemporal lobar degeneration (FTLD) cohort (n = 1,205), ascertained by the European Early-Onset Dementia (EOD) consortium. Next, we performed a meta-analysis of our data and that of other European studies, together 2,668 patients from 15 Western European countries. The frequency of the C9orf72 expansions in Western Europe was 9.98% in overall FTLD, with 18.52% in familial, and 6.26% in sporadic FTLD patients. Outliers were Finland and Sweden with overall frequencies of respectively 29.33% and 20.73%, but also Spain with 25.49%. In contrast, prevalence in Germany was limited to 4.82%. In addition, we studied the role of intermediate repeats (7-24 repeat units), which are strongly correlated with the risk haplotype, on disease and C9orf72 expression. In vitro reporter gene expression studies demonstrated significantly decreased transcriptional activity of C9orf72 with increasing number of normal repeat units, indicating that intermediate repeats might act as predisposing alleles and in favor of the loss-of-function disease mechanism. Further, we observed a significantly increased frequency of short indels in the GC-rich low complexity sequence adjacent to the G(4) C(2) repeat in C9orf72 expansion carriers (P < 0.001) with the most common indel creating one long contiguous imperfect G(4) C(2) repeat, which is likely more prone to replication slippage and pathological expansion.
AB - We assessed the geographical distribution of C9orf72 G(4) C(2) expansions in a pan-European frontotemporal lobar degeneration (FTLD) cohort (n = 1,205), ascertained by the European Early-Onset Dementia (EOD) consortium. Next, we performed a meta-analysis of our data and that of other European studies, together 2,668 patients from 15 Western European countries. The frequency of the C9orf72 expansions in Western Europe was 9.98% in overall FTLD, with 18.52% in familial, and 6.26% in sporadic FTLD patients. Outliers were Finland and Sweden with overall frequencies of respectively 29.33% and 20.73%, but also Spain with 25.49%. In contrast, prevalence in Germany was limited to 4.82%. In addition, we studied the role of intermediate repeats (7-24 repeat units), which are strongly correlated with the risk haplotype, on disease and C9orf72 expression. In vitro reporter gene expression studies demonstrated significantly decreased transcriptional activity of C9orf72 with increasing number of normal repeat units, indicating that intermediate repeats might act as predisposing alleles and in favor of the loss-of-function disease mechanism. Further, we observed a significantly increased frequency of short indels in the GC-rich low complexity sequence adjacent to the G(4) C(2) repeat in C9orf72 expansion carriers (P < 0.001) with the most common indel creating one long contiguous imperfect G(4) C(2) repeat, which is likely more prone to replication slippage and pathological expansion.
KW - Adult
KW - Age of Onset
KW - Aged
KW - Aged, 80 and over
KW - Alleles
KW - Alzheimer Disease/genetics
KW - Base Sequence
KW - C9orf72 Protein
KW - Chromosomes, Human, Pair 9/genetics
KW - Cohort Studies
KW - DNA Repeat Expansion
KW - Europe/epidemiology
KW - Finland/epidemiology
KW - Frontotemporal Lobar Degeneration/epidemiology
KW - Genome-Wide Association Study/methods
KW - Genomic Instability
KW - Germany/epidemiology
KW - Haplotypes
KW - Humans
KW - Middle Aged
KW - Molecular Sequence Data
KW - Prevalence
KW - Proteins/genetics
KW - Spain/epidemiology
KW - Sweden/epidemiology
U2 - 10.1002/humu.22244
DO - 10.1002/humu.22244
M3 - Article
C2 - 23111906
SN - 1059-7794
VL - 34
SP - 363
EP - 373
JO - Human Mutation
JF - Human Mutation
IS - 2
ER -