肌萎缩侧索硬化
生物
C9orf72
线粒体DNA
甲基化
疾病
人口
粒线体疾病
遗传学
线粒体
DNA甲基化
生物信息学
内科学
三核苷酸重复扩增
基因
医学
基因表达
等位基因
环境卫生
作者
Andrea Stoccoro,Adam R. Smith,Lorena Mosca,Alessandro Marocchi,Francesca Gerardi,Christian Lunetta,Katie Lunnon,Lucia Migliore,Fabio Coppedè
出处
期刊:Epigenomics
[Future Medicine]
日期:2024-02-01
卷期号:16 (4): 203-214
被引量:2
标识
DOI:10.2217/epi-2023-0265
摘要
Aim: To correlate mitochondrial D-loop region methylation levels and mtDNA copy number with disease duration in familial amyotrophic lateral sclerosis (ALS) patients. Patients & methods: The study population included 12 ALS patients with a mutation in SOD1 and 13 ALS patients with the C9orf72 hexanucleotide repeat expansion. Methylation levels of the D-loop region and mtDNA copy number were quantified using pyrosequencing and quantitative PCR, respectively. Results: We observed that D-loop methylation levels inversely correlated while mtDNA copy number positively correlated with disease duration. Conclusion: Considering the central role played by mitochondria in ALS, this preliminary study provides new knowledge for future studies aimed at identifying biomarkers of disease progression and new targets for therapeutic interventions.
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