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Original Articles

Elevated serum mitochondrial DNA in females and lack of altered platelet mitochondrial methylation in patients with Parkinson´s disease

ORCID Icon, , , &
Pages 279-282 | Received 12 Dec 2019, Accepted 22 Feb 2020, Published online: 11 Mar 2020

References

  • Park JS, Davis RL, Sue CM. Mitochondrial dysfunction in Parkinson’s Disease: new mechanistic insights and therapeutic perspectives. Curr Neurol Neurosci Rep. . 2018; 18(5):21.
  • Bender A, Krishnan KJ, Morris CM, Taylor GA, et al. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. Nat Genet. . 2006; 38(5):515–517.
  • Devi L, Raghavendran V, Prabhu BM, et al. Mitochondrial import and accumulation of alpha-synuclein impair complex I in human dopaminergic neuronal cultures and Parkinson disease brain. J Biol Chem. . 2008; 283(14):9089–9100.
  • Pyle A, Anugrha H, Kurzawa-Akanbi M, et al. Reduced mitochondrial DNA copy number is a biomarker of Parkinson’s disease. Neurobiol Aging. 2016; 38:216 e217–216 e210.
  • Schapira AH, Cooper JM, Dexter D, et al. Mitochondrial complex I deficiency in Parkinson’s disease. Lancet. 1989; 1(8649):1269.
  • Bindoff LA, Birch-Machin M, Cartlidge NE, et al. Mitochondrial function in Parkinson’s disease. Lancet. 1989; 2(8653):49.
  • Langston JW, Ballard P, Tetrud JW, et al. Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis. Science. 1983; 219(4587):979–980.
  • Wullner U, Kaut O, deBoni L, et al. DNA methylation in Parkinson’s disease. J Neurochem. 2016; 139 (Suppl 1):108–120.
  • Sharma A, Kaut O, Pavlova A, et al. Skewed X-chromosome inactivation and XIST locus methylation levels do not contribute to the lower prevalence of Parkinson’s disease in females. Neurobiol Aging. 2017; 57:248 e241–248 e245.
  • Sharma A, Osato N, Liu H, et al. Common genetic variants associated with Parkinson’s disease display widespread signature of epigenetic plasticity. Sci Rep. 2019; 9(1):18464.
  • Kaut O, Sharma A, Schmitt I, et al. DNA methylation of imprinted loci of autosomal chromosomes and IGF2 is not affected in Parkinson’s disease patients’ peripheral blood mononuclear cells. Neurol Res. 2017; 39(3):281–284.
  • Baccarelli AA, Byun HM. Platelet mitochondrial DNA methylation: a potential new marker of cardiovascular disease. Clin Epigenet. 2015;7(1):44.
  • Mechta M, Ingerslev LR, Fabre O, et al. Evidence Suggesting Absence of Mitochondrial DNA Methylation. Front Genet. 2017; 8:166.
  • Schafer ST, Franken L, Adamzik M, et al. Mitochondrial DNA. An endogenous trigger for immune paralysis. Anesthesiology. 2016; 124(4):923–933.

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