Journal
SCIENTIFIC REPORTS
Volume 12, Issue 1, Pages -Publisher
NATURE PORTFOLIO
DOI: 10.1038/s41598-022-16772-5
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Funding
- Wellcome Trust [103952/Z/14/Z]
- United Kingdom, Medical Research Council [MR/L501529/1, MR/R024804/1]
- Economic and Social Research Council [ES/L008238/1]
- Motor Neurone Disease Association
- NIHR [NIHR202421]
- JPND
- My Name'5 Doddie Foundation
- Alan Davidson Foundation
- National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London
- South London and Maudsley NHS Foundation Trust
- MND Scotland
- National Institute for Health Research
- Spastic Paraplegia Foundation
- Rosetrees Trust
- Maudsley Charity [980]
- Guy's and St Thomas' Charity [TR130505]
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ALS is a devastating neurodegenerative disease with unclear association with the cerebellar role, recent findings suggest certain gene variants are significantly linked to ALS risk. Gene-based and tissue enrichment analysis show a specific relationship between cerebellar tissue and ALS, calling for a re-evaluation of cerebellar involvement in ALS pathology.
Amyotrophic lateral sclerosis (ALS) is a devastating, heterogeneous neurodegenerative neuromuscular disease that leads to a fatal outcome within 2-5 years, and yet, a precise nature of the association between its major phenotypes and the cerebellar role in ALS pathology remains unknown. Recently, repeat expansions in several genes in which variants appreciably contribute to cerebellar pathology, including C9orf72, NIPA1, ATXN2 and ATXN1, have been found to confer a significant risk for ALS. To better define this relationship, we performed MAGMA gene-based analysis and tissue enrichment analysis using genome-wide association study summary statistics based on a study of 27,205 people with ALS and 110,881 controls. Our preliminary results imply a striking cerebellar tissue specificity and further support increasing calls for re-evaluation of the cerebellar role in the ALS pathology.
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