H63D CG genotype of HFE is associated with increased risk of sporadic amyotrophic lateral sclerosis in a single population

• Main Author: Qing-Qing Zhang, Hong Jiang, Chun-Yan Li, Ya-Ling Liu, Xin-Ying Tian
• Format: Article
• Language: English
• Published: IMR (Innovative Medical Research) Press Limited 2020-09-01
• Series: Journal of Integrative Neuroscience
• Subjects: |neurogenetics|amyotrophic lateral sclerosis|motor neuron disease|hfe gene|polymorphism
• Online Access: https://jin.imrpress.com/fileup/1757-448X/PDF/1601431118347-1376775326.pdf

This paper describes the genetic etiology of sporadic amyotrophic lateral sclerosis in a single population. Polymerase chain reaction-restriction fragment length polymorphism and DNA sample sequencing of 3 common HFE gene variants (C282Y and H63D and S65C) were performed on 10 randomly selected samples of H63D gene variant (124 patients with sporadic amyotrophic lateral sclerosis) and 10 wild types of H63D samples (210 controls). The C282Y and S65C gene variant were absent. There were 24 cases (7.18%) with H63D heterozygous variants, including 16 cases (13%) in the sporadic amyotrophic lateral sclerosis group and 8 cases (4%) in the healthy control group. The polymorphism frequency of the H63D gene variant in the sporadic amyotrophic lateral sclerosis group was significantly different than that in the control group (p < 0.05), and the difference at allele level, which is still more significant (p < 0.05). H63D gene variant could be a risk factor for sporadic amyotrophic lateral sclerosis in a single population. The results showed HFE gene variants play a role in the occurrence of sporadic amyotrophic lateral sclerosis, but its effect should be carefully estimated.