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炎症和氧化应激基因的遗传变异性影响肌萎缩侧索硬化症患者的发病、疾病进展和生存。

Genetic Variability of Inflammation and Oxidative Stress Genes Affects Onset, Progression of the Disease and Survival of Patients with Amyotrophic Lateral Sclerosis.

机构信息

Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.

Institute of Clinical Neurophysiology, Division of Neurology, University Medical Centre Ljubljana, 1000 Ljubljana, Slovenia.

出版信息

Genes (Basel). 2022 Apr 25;13(5):757. doi: 10.3390/genes13050757.

DOI:10.3390/genes13050757
PMID:35627142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9140599/
Abstract

Inflammation and oxidative stress are recognized as important contributors to amyotrophic lateral sclerosis (ALS) disease pathogenesis. Our aim was to evaluate the impact of selected single-nucleotide polymorphisms in genes involved in inflammation and oxidative stress on ALS susceptibility and modification. One-hundred-and-eighty-five ALS patients and 324 healthy controls were genotyped for nine polymorphisms in seven antioxidant and inflammatory genes using competitive allele-specific PCR. Logistic regression; nonparametric tests and survival analysis were used in the statistical analysis. Investigated polymorphisms were not associated with ALS susceptibility. Carriers of at least one polymorphic rs4880 T or rs1071676 C allele more often had bulbar ALS onset ( = 0.036 and = 0.039; respectively). rs1071676 was also associated with a higher rate of disease progression ( = 0.015). After adjustment for clinical parameters; carriers of two polymorphic rs1071676 C alleles had shorter survival (HR = 5.02; 95% CI = 1.92-13.16; = 0.001); while carriers of at least one polymorphic rs1001179 T allele had longer survival (HR = 0.68; 95% CI = 0.47-0.99; = 0.046). Our data suggest that common genetic variants in the antioxidant and inflammatory pathways may modify ALS disease. Such genetic information could support the identification of patients that may be responsive to the immune or antioxidant system-based therapies.

摘要

炎症和氧化应激被认为是肌萎缩侧索硬化症 (ALS) 发病机制的重要因素。我们的目的是评估参与炎症和氧化应激的基因中的一些单核苷酸多态性对 ALS 易感性和修饰的影响。使用竞争性等位基因特异性 PCR 对 7 个抗氧化和炎症基因中的 9 个多态性,在 185 名 ALS 患者和 324 名健康对照者中进行基因分型。在统计分析中使用逻辑回归、非参数检验和生存分析。研究的多态性与 ALS 易感性无关。至少携带一个多态性 rs4880 T 或 rs1071676 C 等位基因的携带者更常发生延髓 ALS 发病(=0.036 和=0.039;分别)。rs1071676 也与疾病进展率更高相关(=0.015)。在调整临床参数后;携带两个多态性 rs1071676 C 等位基因的携带者的生存率更短(HR=5.02;95%CI=1.92-13.16;=0.001);而携带至少一个多态性 rs1001179 T 等位基因的携带者的生存率更长(HR=0.68;95%CI=0.47-0.99;=0.046)。我们的数据表明,抗氧化和炎症途径中的常见遗传变异可能修饰 ALS 疾病。这种遗传信息可以支持识别可能对基于免疫或抗氧化系统的治疗有反应的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f67c/9140599/f0df5a125a9f/genes-13-00757-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f67c/9140599/d5606d98d240/genes-13-00757-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f67c/9140599/f0df5a125a9f/genes-13-00757-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f67c/9140599/d5606d98d240/genes-13-00757-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f67c/9140599/f0df5a125a9f/genes-13-00757-g002.jpg

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