Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with a lifetime risk of one in 350 people and an unmet need for disease-modifying therapies. We conducted a cross-ancestry genome-wide association study (GWAS) including 29,612 patients with ALS and 122,656 controls, which identified 15 risk loci. When combined with 8,953 individuals with whole-genome sequencing (6,538 patients, 2,415 controls) and a large cortex-derived expression quantitative trait locus (eQTL) dataset (MetaBrain), analyses revealed locus-specific genetic architectures in which we prioritized genes either through rare variants, short tandem repeats or regulatory effects. ALS-associated risk loci were shared with multiple traits within the neurodegenerative spectrum but with distinct enrichment patterns across brain regions and cell types. Of the environmental and lifestyle risk factors obtained from the literature, Mendelian randomization analyses indicated a causal role for high cholesterol levels. The combination of all ALS-associated signals reveals a role for perturbations in vesicle-mediated transport and autophagy and provides evidence for cell-autonomous disease initiation in glutamatergic neurons.

van Rheenen, W., van der Spek, R., Bakker, M., van Vugt, J., Hop, P., Zwamborn, R., et al. (2021). Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. NATURE GENETICS, 53(12), 1636-1648 [10.1038/s41588-021-00973-1].

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Ferrarese C.
Membro del Collaboration Group
2021

Abstract

Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with a lifetime risk of one in 350 people and an unmet need for disease-modifying therapies. We conducted a cross-ancestry genome-wide association study (GWAS) including 29,612 patients with ALS and 122,656 controls, which identified 15 risk loci. When combined with 8,953 individuals with whole-genome sequencing (6,538 patients, 2,415 controls) and a large cortex-derived expression quantitative trait locus (eQTL) dataset (MetaBrain), analyses revealed locus-specific genetic architectures in which we prioritized genes either through rare variants, short tandem repeats or regulatory effects. ALS-associated risk loci were shared with multiple traits within the neurodegenerative spectrum but with distinct enrichment patterns across brain regions and cell types. Of the environmental and lifestyle risk factors obtained from the literature, Mendelian randomization analyses indicated a causal role for high cholesterol levels. The combination of all ALS-associated signals reveals a role for perturbations in vesicle-mediated transport and autophagy and provides evidence for cell-autonomous disease initiation in glutamatergic neurons.
Articolo in rivista - Articolo scientifico
amyotrophic lateral sclerosis; blood; brain; degenerative disease; disease exacerbation; female; genetics; genome-wide association study; human; male; Mendelian randomization analysis; meta analysis; metabolism; mutation; nerve cell; quantitative trait locus; risk factor;
English
1636
1648
13
Ferrarese Carlo SLALOM Consortium
van Rheenen, W., van der Spek, R., Bakker, M., van Vugt, J., Hop, P., Zwamborn, R., et al. (2021). Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology. NATURE GENETICS, 53(12), 1636-1648 [10.1038/s41588-021-00973-1].
van Rheenen, W; van der Spek, R; Bakker, M; van Vugt, J; Hop, P; Zwamborn, R; de Klein, N; Westra, H; Bakker, O; Deelen, P; Shireby, G; Hannon, E; Moisse, M; Baird, D; Restuadi, R; Dolzhenko, E; Dekker, A; Gawor, K; Westeneng, H; Tazelaar, G; van Eijk, K; Kooyman, M; Byrne, R; Doherty, M; Heverin, M; Al Khleifat, A; Iacoangeli, A; Shatunov, A; Ticozzi, N; Cooper-Knock, J; Smith, B; Gromicho, M; Chandran, S; Pal, S; Morrison, K; Shaw, P; Hardy, J; Orrell, R; Sendtner, M; Meyer, T; Basak, N; van der Kooi, A; Ratti, A; Fogh, I; Gellera, C; Lauria, G; Corti, S; Cereda, C; Sproviero, D; D'Alfonso, S; Soraru, G; Siciliano, G; Filosto, M; Padovani, A; Chio, A; Calvo, A; Moglia, C; Brunetti, M; Canosa, A; Grassano, M; Beghi, E; Pupillo, E; Logroscino, G; Nefussy, B; Osmanovic, A; Nordin, A; Lerner, Y; Zabari, M; Gotkine, M; Baloh, R; Bell, S; Vourc'H, P; Corcia, P; Couratier, P; Millecamps, S; Meininger, V; Salachas, F; Mora Pardina, J; Assialioui, A; Rojas-Garcia, R; Dion, P; Ross, J; Ludolph, A; Weishaupt, J; Brenner, D; Freischmidt, A; Bensimon, G; Brice, A; Durr, A; Payan, C; Saker-Delye, S; Wood, N; Topp, S; Rademakers, R; Tittmann, L; Lieb, W; Franke, A; Ripke, S; Braun, A; Kraft, J; Whiteman, D; Olsen, C; Uitterlinden, A; Hofman, A; Rietschel, M; Cichon, S; Nothen, M; Amouyel, P; Traynor, B; Singleton, A; Mitne Neto, M; Cauchi, R; Ophoff, R; Wiedau-Pazos, M; Lomen-Hoerth, C; van Deerlin, V; Grosskreutz, J; Roediger, A; Gaur, N; Jork, A; Barthel, T; Theele, E; Ilse, B; Stubendorff, B; Witte, O; Steinbach, R; Hubner, C; Graff, C; Brylev, L; Fominykh, V; Demeshonok, V; Ataulina, A; Rogelj, B; Koritnik, B; Zidar, J; Ravnik-Glavac, M; Glavac, D; Stevic, Z; Drory, V; Povedano, M; Blair, I; Kiernan, M; Benyamin, B; Henderson, R; Furlong, S; Mathers, S; Mccombe, P; Needham, M; Ngo, S; Nicholson, G; Pamphlett, R; Rowe, D; Steyn, F; Williams, K; Mather, K; Sachdev, P; Henders, A; Wallace, L; de Carvalho, M; Pinto, S; Petri, S; Weber, M; Rouleau, G; Silani, V; Curtis, C; Breen, G; Glass, J; Brown, R; Landers, J; Shaw, C; Andersen, P; Groen, E; van Es, M; Pasterkamp, R; Fan, D; Garton, F; Mcrae, A; Davey Smith, G; Gaunt, T; Eberle, M; Mill, J; Mclaughlin, R; Hardiman, O; Kenna, K; Wray, N; Tsai, E; Runz, H; Franke, L; Al-Chalabi, A; Van Damme, P; van den Berg, L; Veldink, J; Ferrarese, C
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/367197
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