Mitochondrial D-loop methylation levels inversely correlate with disease duration in amyotrophic lateral sclerosis

Author:

Stoccoro Andrea1ORCID,Smith Adam R2ORCID,Mosca Lorena3,Marocchi Alessandro3,Gerardi Francesca4,Lunetta Christian5,Lunnon Katie2ORCID,Migliore Lucia1,Coppedè Fabio16ORCID

Affiliation:

1. Department of Translational Research & of New Surgical & Medical Technologies, Laboratory of Medical Genetics, University of Pisa, Medical School, Via Roma 55, Pisa, 56126, Italy

2. Department of Clinical & Biomedical Sciences, Faculty of Health & Life Sciences, University of Exeter, Exeter, EX2 5DW, UK

3. Medical Genetics Unit, Department of Medical Services, ASST Grande Ospedale Metropolitano Niguarda, Milan, 20162, Italy

4. NEMO Clinical Center, Fondazione Serena Onlus, Milan, 20162, Italy

5. Istituti Clinici Scientifici Maugeri IRCCS, Neurorehabilitation Unit of Milan Institute, Milan, 20138, Italy

6. Interdepartmental Research Center of Biology & Pathology of Aging, University of Pisa, Pisa, 56126, Italy

Abstract

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.

Funder

Università di Pisa

Publisher

Informa UK Limited

Subject

Cancer Research,Genetics

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