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• W4281569234 startingPage "24" @default.
• W4281569234 abstract "Background: Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease associated with loss of upper and lower motor neurones. It leads to death by respiratory failure and has a typical prognosis of 2-3 years. The immune system has been shown to play a role in the pathophysiology of ALS. Some of the most important immune genes are within the human leukocyte antigen (HLA) region, and a recent genome-wide association study (GWAS) has identified a risk allele for ALS within the HLA region. Older studies have also suggested an HLA association with ALS, with certain HLA alleles showing differing expression between patients and controls. This systematic review and meta-analysis examines the previous studies performed in this field.Methods: We used established publication search engines. Findings were excluded if they did not meet the selection criteria. We then undertook statistical meta-analysis on the eligible papers, using a fixed effects model.Results: There were eight eligible papers. There were three statistically significant meta-analysis findings, although these would not be significant after correction for multiple comparisons. The frequencies of HLA-A9 and HLA-DR4 genotypes were lower in ALS subjects than controls, and HLA-B35 was higher in ALS subjects.Discussion: This systematic review and meta-analysis do not confirm all the previously reported associations of HLA with ALS, but shows three alleles of interest. However, there are limitations to the studies, which include the use of older serotyping methodology and the small numbers of subjects. Given the recent GWAS association with HLA, further modern HLA studies are warranted." @default.
• W4281569234 created "2022-05-27" @default.
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• W4281569234 date "2022-05-26" @default.
• W4281569234 modified "2023-09-27" @default.
• W4281569234 title "HLA and amyotrophic lateral sclerosis: a systematic review and meta-analysis" @default.
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• W4281569234 doi "https://doi.org/10.1080/21678421.2022.2078665" @default.
• W4281569234 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35616250" @default.
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