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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.

Authors :
Zhang, Ming
Zhang, Ming
Ferrari, Raffaele
Tartaglia, Maria Carmela
Keith, Julia
Surace, Ezequiel I
Wolf, Uri
Sato, Christine
Grinberg, Mark
Liang, Yan
Xi, Zhengrui
Dupont, Kyle
McGoldrick, Philip
Weichert, Anna
McKeever, Paul M
Schneider, Raphael
McCorkindale, Michael D
Manzoni, Claudia
Rademakers, Rosa
Graff-Radford, Neill R
Dickson, Dennis W
Parisi, Joseph E
Boeve, Bradley F
Petersen, Ronald C
Miller, Bruce L
Seeley, William W
van Swieten, John C
van Rooij, Jeroen
Pijnenburg, Yolande
van der Zee, Julie
Van Broeckhoven, Christine
Le Ber, Isabelle
Van Deerlin, Vivianna
Suh, EunRan
Rohrer, Jonathan D
Mead, Simon
Graff, Caroline
Öijerstedt, Linn
Pickering-Brown, Stuart
Rollinson, Sara
Rossi, Giacomina
Tagliavini, Fabrizio
Brooks, William S
Dobson-Stone, Carol
Halliday, Glenda M
Hodges, John R
Piguet, Olivier
Binetti, Giuliano
Benussi, Luisa
Ghidoni, Roberta
Nacmias, Benedetta
Sorbi, Sandro
Bruni, Amalia C
Galimberti, Daniela
Scarpini, Elio
Rainero, Innocenzo
Rubino, Elisa
Clarimon, Jordi
Lleó, Alberto
Ruiz, Agustin
Hernández, Isabel
Pastor, Pau
Diez-Fairen, Monica
Borroni, Barbara
Pasquier, Florence
Deramecourt, Vincent
Lebouvier, Thibaud
Perneczky, Robert
Diehl-Schmid, Janine
Grafman, Jordan
Huey, Edward D
Mayeux, Richard
Nalls, Michael A
Hernandez, Dena
Singleton, Andrew
Momeni, Parastoo
Zeng, Zhen
Hardy, John
Robertson, Janice
Zinman, Lorne
Rogaeva, Ekaterina
International FTD-Genomics Consortium (IFGC)
Zhang, Ming
Zhang, Ming
Ferrari, Raffaele
Tartaglia, Maria Carmela
Keith, Julia
Surace, Ezequiel I
Wolf, Uri
Sato, Christine
Grinberg, Mark
Liang, Yan
Xi, Zhengrui
Dupont, Kyle
McGoldrick, Philip
Weichert, Anna
McKeever, Paul M
Schneider, Raphael
McCorkindale, Michael D
Manzoni, Claudia
Rademakers, Rosa
Graff-Radford, Neill R
Dickson, Dennis W
Parisi, Joseph E
Boeve, Bradley F
Petersen, Ronald C
Miller, Bruce L
Seeley, William W
van Swieten, John C
van Rooij, Jeroen
Pijnenburg, Yolande
van der Zee, Julie
Van Broeckhoven, Christine
Le Ber, Isabelle
Van Deerlin, Vivianna
Suh, EunRan
Rohrer, Jonathan D
Mead, Simon
Graff, Caroline
Öijerstedt, Linn
Pickering-Brown, Stuart
Rollinson, Sara
Rossi, Giacomina
Tagliavini, Fabrizio
Brooks, William S
Dobson-Stone, Carol
Halliday, Glenda M
Hodges, John R
Piguet, Olivier
Binetti, Giuliano
Benussi, Luisa
Ghidoni, Roberta
Nacmias, Benedetta
Sorbi, Sandro
Bruni, Amalia C
Galimberti, Daniela
Scarpini, Elio
Rainero, Innocenzo
Rubino, Elisa
Clarimon, Jordi
Lleó, Alberto
Ruiz, Agustin
Hernández, Isabel
Pastor, Pau
Diez-Fairen, Monica
Borroni, Barbara
Pasquier, Florence
Deramecourt, Vincent
Lebouvier, Thibaud
Perneczky, Robert
Diehl-Schmid, Janine
Grafman, Jordan
Huey, Edward D
Mayeux, Richard
Nalls, Michael A
Hernandez, Dena
Singleton, Andrew
Momeni, Parastoo
Zeng, Zhen
Hardy, John
Robertson, Janice
Zinman, Lorne
Rogaeva, Ekaterina
International FTD-Genomics Consortium (IFGC)
Source :
Brain : a journal of neurology; vol 141, iss 10, 2895-2907; 0006-8950
Publication Year :
2018

Abstract

The G4C2-repeat expansion in C9orf72 is the most common known cause of amyotrophic lateral sclerosis and frontotemporal dementia. The high phenotypic heterogeneity of C9orf72 patients includes a wide range in age of onset, modifiers of which are largely unknown. Age of onset could be influenced by environmental and genetic factors both of which may trigger DNA methylation changes at CpG sites. We tested the hypothesis that age of onset in C9orf72 patients is associated with some common single nucleotide polymorphisms causing a gain or loss of CpG sites and thus resulting in DNA methylation alterations. Combined analyses of epigenetic and genetic data have the advantage of detecting functional variants with reduced likelihood of false negative results due to excessive correction for multiple testing in genome-wide association studies. First, we estimated the association between age of onset in C9orf72 patients (n = 46) and the DNA methylation levels at all 7603 CpG sites available on the 450 k BeadChip that are mapped to common single nucleotide polymorphisms. This was followed by a genetic association study of the discovery (n = 144) and replication (n = 187) C9orf72 cohorts. We found that age of onset was reproducibly associated with polymorphisms within a 124.7 kb linkage disequilibrium block tagged by top-significant variation, rs9357140, and containing two overlapping genes (LOC101929163 and C6orf10). A meta-analysis of all 331 C9orf72 carriers revealed that every A-allele of rs9357140 reduced hazard by 30% (P = 0.0002); and the median age of onset in AA-carriers was 6 years later than GG-carriers. In addition, we investigated a cohort of C9orf72 negative patients (n = 2634) affected by frontotemporal dementia and/or amyotrophic lateral sclerosis; and also found that the AA-genotype of rs9357140 was associated with a later age of onset (adjusted P = 0.007 for recessive model). Phenotype analyses detected significant association only in the largest subgroup of pa

Details

Database :
OAIster
Journal :
Brain : a journal of neurology; vol 141, iss 10, 2895-2907; 0006-8950
Notes :
application/pdf, Brain : a journal of neurology vol 141, iss 10, 2895-2907 0006-8950
Publication Type :
Electronic Resource
Accession number :
edsoai.on1367381837
Document Type :
Electronic Resource