Literature DB >> 15006700

Frontotemporal dementia and mitochondrial DNA transitions.

Manuela Grazina1, Filipe Silva, Isabel Santana, Beatriz Santiago, Cândida Mendes, Marta Simões, Miguel Oliveira, Luís Cunha, Catarina Oliveira.   

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.

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Year:  2004        PMID: 15006700     DOI: 10.1016/j.nbd.2003.11.004

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  3 in total

1.  Early-onset subcortical ischemic vascular dementia in an adult with mtDNA mutation 3316G>A.

Authors:  Giuseppe Lanza; Mariagiovanna Cantone; Sabrina Musso; Eugenia Borgione; Carmela Scuderi; Raffaele Ferri
Journal:  J Neurol       Date:  2018-02-20       Impact factor: 4.849

Review 2.  Update on the Neurobiology of Vascular Cognitive Impairment: From Lab to Clinic.

Authors:  Luisa Vinciguerra; Giuseppe Lanza; Valentina Puglisi; Francesco Fisicaro; Manuela Pennisi; Rita Bella; Mariagiovanna Cantone
Journal:  Int J Mol Sci       Date:  2020-04-23       Impact factor: 5.923

3.  Association of Mitochondrial DNA Genomic Variation With Risk of Pick Disease.

Authors:  Rebecca R Valentino; Michael G Heckman; Patrick W Johnson; Matthew C Baker; Alexandra I Soto-Beasley; Ronald L Walton; Shunsuke Koga; Shanu F Roemer; EunRan Suh; Ryan J Uitti; John Q Trojanowski; Murray Grossman; Vivianna M Van Deerlin; Rosa Rademakers; Zbigniew K Wszolek; Dennis W Dickson; Owen A Ross
Journal:  Neurology       Date:  2021-02-10       Impact factor: 9.910

  3 in total

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