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Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics.

Authors :
Iacoangeli A
Lin T
Al Khleifat A
Jones AR
Opie-Martin S
Coleman JRI
Shatunov A
Sproviero W
Williams KL
Garton F
Restuadi R
Henders AK
Mather KA
Needham M
Mathers S
Nicholson GA
Rowe DB
Henderson R
McCombe PA
Pamphlett R
Blair IP
Schultz D
Sachdev PS
Newhouse SJ
Proitsi P
Fogh I
Ngo ST
Dobson RJB
Wray NR
Steyn FJ
Al-Chalabi A
Source :
Cell reports [Cell Rep] 2020 Oct 27; Vol. 33 (4), pp. 108323.
Publication Year :
2020

Abstract

We meta-analyze amyotrophic lateral sclerosis (ALS) genome-wide association study (GWAS) data of European and Chinese populations (84,694 individuals). We find an additional significant association between rs58854276 spanning ACSL5-ZDHHC6 with ALS (p = 8.3 × 10 <superscript>-9</superscript> ), with replication in an independent Australian cohort (1,502 individuals; p = 0.037). Moreover, B4GALNT1, G2E3-SCFD1, and TRIP11-ATXN3 are identified using a gene-based analysis. ACSL5 has been associated with rapid weight loss, as has another ALS-associated gene, GPX3. Weight loss is frequent in ALS patients and is associated with shorter survival. We investigate the effect of the ACSL5 and GPX3 single-nucleotide polymorphisms (SNPs), using longitudinal body composition and weight data of 77 patients and 77 controls. In patients' fat-free mass, although not significant, we observe an effect in the expected direction (rs58854276: -2.1 ± 1.3 kg/A allele, p = 0.053; rs3828599: -1.0 ± 1.3 kg/A allele, p = 0.22). No effect was observed in controls. Our findings support the increasing interest in lipid metabolism in ALS and link the disease genetics to weight loss in patients.<br />Competing Interests: Declaration of Interests The authors declare no competing interests.<br /> (Copyright © 2020 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2211-1247
Volume :
33
Issue :
4
Database :
MEDLINE
Journal :
Cell reports
Publication Type :
Academic Journal
Accession number :
33113361
Full Text :
https://doi.org/10.1016/j.celrep.2020.108323