Search:
Computing and Library Services - delivering an inspiring information environment

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus

La Morgia, Chiara, Achilli, Alessandro, Iommarini, Luisa, Barboni, Piero, Pala, Maria, Olivieri, Anna, Zanna, Claudia, Vidoni, Sara, Tonon, Caterina, Lodi, Raffaele, Vetrugno, Roberto, Mostacci, Barbara, Liguori, Rocco, Carroccia, Rosanna, Montagna, Pasquale, Rugolo, Michela, Torroni, Antonio and Carelli, Valerio (2008) Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus. Neurology, 70 (10). pp. 762-770. ISSN 0028-3878

Metadata only available from this repository.

Abstract

Objective: To investigate the mechanisms underlying myoclonus in Leber hereditary optic neuropathy (LHON).

Methods: Five patients and one unaffected carrier from two Italian families bearing the homoplasmic 11778/ND4 and 3460/ND1 mutations underwent a uniform investigation including neurophysiologic studies, muscle biopsy, serum lactic acid after exercise, and muscle (31P) and cerebral (1H) magnetic resonance spectroscopy (MRS). Biochemical investigations on fibroblasts and complete mitochondrial DNA (mtDNA) sequences of both families were also performed.

Results: All six individuals had myoclonus. In spite of a normal EEG background and the absence of giant SEPs and C reflex, EEG-EMG back-averaging showed a preceding jerk-locked EEG potential, consistent with a cortical generator of the myoclonus. Specific comorbidities in the 11778/ND4 family included muscular cramps and psychiatric disorders, whereas features common to both families were migraine and cardiologic abnormalities. Signs of mitochondrial proliferation were seen in muscle biopsies and lactic acid elevation was observed in four of six patients. 31P-MRS was abnormal in five of six patients and 1H-MRS showed ventricular accumulation of lactic acid in three of six patients. Fibroblast ATP depletion was evident at 48 hours incubation with galactose in LHON/myoclonus patients. Sequence analysis revealed haplogroup T2 (11778/ND4 family) and U4a (3460/ND1 family) mtDNAs. A functional role for the non-synonymous 4136A>G/ND1, 9139G>A/ATPase6, and 15773G>A/cyt b variants was supported by amino acid conservation analysis.

Conclusions: Myoclonus and other comorbidities characterized our Leber hereditary optic neuropathy (LHON) families. Functional investigations disclosed a bioenergetic impairment in all individuals. Our sequence analysis suggests that the LHON plus phenotype in our cases may relate to the synergic role of mtDNA variants.

Item Type: Article
Subjects: Q Science > Q Science (General)
Q Science > QH Natural history > QH426 Genetics
Schools: School of Applied Sciences
Depositing User: Cherry Edmunds
Date Deposited: 10 Oct 2012 15:14
Last Modified: 11 Oct 2012 14:54
URI: http://eprints.hud.ac.uk/id/eprint/15492

Item control for Repository Staff only:

View Item

University of Huddersfield, Queensgate, Huddersfield, HD1 3DH Copyright and Disclaimer All rights reserved ©