TY - JOUR
T1 - ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry
AU - the ITALSGEN and SARDINALS consortia
AU - Borghero, Giuseppe
AU - Pugliatti, Maura
AU - Marrosu, Francesco
AU - Marrosu, Maria Giovanna
AU - Murru, Maria Rita
AU - Floris, Gianluca
AU - Cannas, Antonino
AU - Parish, Leslie D.
AU - Cau, Tea B.
AU - Loi, Daniela
AU - Ticca, Anna
AU - Traccis, Sebastiano
AU - Manera, Umberto
AU - Canosa, Antonio
AU - Moglia, Cristina
AU - Calvo, Andrea
AU - Barberis, Marco
AU - Brunetti, Maura
AU - Renton, Alan E.
AU - Nalls, Mike A.
AU - Traynor, Bryan J.
AU - Restagno, Gabriella
AU - Chiò, Adriano
AU - Logullo, Francesco O.
AU - Simone, Isabella
AU - Logroscino, Giancarlo
AU - Salvi, Fabrizio
AU - Bartolomei, Ilaria
AU - Capasso, Margherita
AU - Caponnetto, Claudia
AU - Mancardi, Gianluigi
AU - Mandich, Paola
AU - Origone, Paola
AU - Conforti, Francesca L.
AU - Mora, Gabriele
AU - Marinou, Kalliopi
AU - Sideri, Riccardo
AU - Lunetta, Christian
AU - Penco, Silvana
AU - Mosca, Lorena
AU - Nilo, Riva
AU - Pinter, Giuseppe Lauria
AU - Corbo, Massimo
AU - Volanti, Paolo
AU - Mandrioli, Jessica
AU - Fini, Nicola
AU - Georgoulopoulou, Eleni
AU - Tremolizzo, Lucio
AU - Maria Rosaria Monsurrò, Rosaria Monsurrò
AU - Tedeschi, Gioacchino
N1 - Funding Information:
This work was in part supported by the Italian Ministry of Health ( Ministero della Salute , Ricerca Sanitaria Finalizzata, 2010, grant RF-2010–2309489 ), the European Community's Health Seventh Framework Programme (FP7/2007–2013 under grant agreement 259867 ), the Joint Programme—Neurodegenerative Disease Research (Italian Ministry of Education and University) (Sophia and Strength Projects), the Agenzia Italiana per la Ricerca sulla SLA (ARISLA) (SARDINIALS project), the Associazione Piemontese per l’Assistenza alla SLA (APASLA), Torino, Italy, and the Fondazione Mario e Anna Magnetto , Alpignano, Torino, Italy. This work was supported by the Intramural Research Program of the National Institute on Aging (project Z01 AG000949-02), the National Institute of Neurological Disorders and Stroke , and the National Institute of Mental Health . Study concept and design was contributed by Borghero, Pugliatti, Traynor, Restagno, Chiò. Acquisition of data was done by Murru, Floris, Cannas, Parish, Occhineri, Cau, Loi, Ticca, Manera, Canosa, Miglia, Calvo, Barberis, Brunetti, Renton, Nalls. Analysis and interpretation of data was done by Borghero, Pugliatti, F. Marrosu, M.G: Marrosu, Murru, Renton, Nalls, Traynor, Restagno, Chiò. Drafting of the manuscript was done by Borghero, Pugliatti, Traynor, Chiò. Critical revision of the manuscript for important intellectual content was done by Borghero, Pugliatti, F. Marrosu, M.G Marrosu, Murru, Floris, Cannas, Parish, Occhineri, Cau, Loi, Ticca, Manera, Canosa, Moglia, Calvo, Barberis, Brunetti, Renton, Nalls, Traynor, Restagno, Chiò. Funding was obtained from Borghero, Pugliatti, Restagno, Chiò. Administrative, technical, and material support was from Murru, Floris, Cannas, Parish, Occhineri, Cau, Loi, Ticca, Manera, Canosa, Moglia, Calvo, Barberis, Brunetti, Renton, Nalls. Study supervision was done by Borghero, Pugliatti, Traynor, Restagno, Chiò. Adriano Chiò has full access to data. The corresponding author confirm that all authors have read and approved the final draft of the manuscript and given written permission to include their names in the manuscript.
Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2015/10/1
Y1 - 2015/10/1
N2 - Intermediate-length CAG expansions (encoding 27-33 glutamines, polyQ) of the Ataxin2 (ATXN2) gene represent a risk factor for amyotrophic lateral sclerosis (ALS). Recently, it has been proposed that ≥31 CAG expansions may influence ALS phenotype. We assessed whether ATXN2 intermediate-length polyQ expansions influence ALS phenotype in a series of 375 patients of Sardinian ancestry. Controls were 247 neurologically healthy subjects, resident in the study area, age- and gender-matched to cases. The frequency of ≥31 polyQ ATNX2 repeats was significantly more common in ALS cases (4 patients vs. no control, p = 0.0001). All patients with ≥31 polyQ repeats had a spinal onset versus 73.3% of patients with <31 polyQ repeats. Patients with an increased number of polyQ repeats have a shorter survival than those with <31 repeats (1.2 vs. 4.2 years, p = 0.035). In this large series of ALS patients of Sardinian ancestry, we have found that ≥31 polyQ repeats of the ATXN2 gene influenced patients' phenotype, being associated to a spinal onset and a significantly shorter survival.
AB - Intermediate-length CAG expansions (encoding 27-33 glutamines, polyQ) of the Ataxin2 (ATXN2) gene represent a risk factor for amyotrophic lateral sclerosis (ALS). Recently, it has been proposed that ≥31 CAG expansions may influence ALS phenotype. We assessed whether ATXN2 intermediate-length polyQ expansions influence ALS phenotype in a series of 375 patients of Sardinian ancestry. Controls were 247 neurologically healthy subjects, resident in the study area, age- and gender-matched to cases. The frequency of ≥31 polyQ ATNX2 repeats was significantly more common in ALS cases (4 patients vs. no control, p = 0.0001). All patients with ≥31 polyQ repeats had a spinal onset versus 73.3% of patients with <31 polyQ repeats. Patients with an increased number of polyQ repeats have a shorter survival than those with <31 repeats (1.2 vs. 4.2 years, p = 0.035). In this large series of ALS patients of Sardinian ancestry, we have found that ≥31 polyQ repeats of the ATXN2 gene influenced patients' phenotype, being associated to a spinal onset and a significantly shorter survival.
KW - Amyotrophic lateral sclerosis
KW - Ataxin 2 gene
KW - Genetic modifier
UR - http://www.scopus.com/inward/record.url?scp=84976337440&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2015.06.013
DO - 10.1016/j.neurobiolaging.2015.06.013
M3 - Article
C2 - 26208502
AN - SCOPUS:84976337440
SN - 0197-4580
VL - 36
SP - 2906.e1-2906.e5
JO - Neurobiology of Aging
JF - Neurobiology of Aging
IS - 10
ER -