Frontotemporal dementia and mitochondrial DNA transitions

Neurobiol Dis. 2004 Mar;15(2):306-11. doi: 10.1016/j.nbd.2003.11.004.

Abstract

Frontotemporal dementia (FTD) is the second most common type of primary degenerative dementia. Some patients present an overlap between Alzheimer's disease (AD) and FTD both in neuropathological and clinical aspects. This may suggest a similar overlap in physiopathology, namely an involvement of mitochondrial DNA (mtDNA) in FTD, as it has been associated to AD. To determine if mtDNA is involved in FTD, we performed a Polymerase Chain Reaction-Restriction Fragment Length Polymorphism (PCR-RFLP) analysis, specific to mtDNA NADH Dehydrogenase subunit 1 (ND1) nucleotides 3337-3340, searching for mutations previously described in Parkinson's and AD patients. We could identify one FTD patient with two mtDNA transitions: one already known (3316 G-to-A) and another unreported (3337 G-to-A). Additionally, mitochondrial respiratory chain complex I activity was reduced in leukocytes of this patient (36% of the control mean activity). To our knowledge, this is the first report of mtDNA variants in FTD patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Apolipoproteins E / genetics
  • DNA, Mitochondrial / genetics*
  • Dementia / genetics*
  • Dementia / metabolism
  • Dementia / physiopathology
  • Electron Transport Complex I / deficiency
  • Electron Transport Complex I / genetics*
  • Electron Transport Complex I / metabolism
  • Evolution, Molecular
  • Female
  • Genotype
  • Humans
  • Leukocytes / metabolism
  • Male
  • Middle Aged
  • NADH Dehydrogenase / deficiency
  • NADH Dehydrogenase / genetics
  • Nucleotides / genetics
  • Point Mutation / genetics*
  • Protein Subunits / genetics
  • Reference Values
  • Sequence Homology, Amino Acid
  • Sequence Homology, Nucleic Acid

Substances

  • Apolipoproteins E
  • DNA, Mitochondrial
  • Nucleotides
  • Protein Subunits
  • NADH Dehydrogenase
  • Electron Transport Complex I
  • MT-ND1 protein, human