Literature DB >> 18329833

MR spectroscopy of the brain in Leigh syndrome.

P E Sijens1, G P A Smit, L A Rödiger, F J van Spronsen, M Oudkerk, R J Rodenburg, R J Lunsing.   

Abstract

Brain magnetic resonance spectroscopy in two patients with Leigh syndrome revealed the presence of lactate in gray and white matter brain tissue and relatively high choline levels in the white matter. The latter observation, most probably related to an ongoing demyelination process, underlines specific involvement of white matter metabolism in Leigh syndrome even in cases without involvement of the white matter as visualized on MRI. Magnetic resonance spectroscopy might thus be of help in differentiating Leigh syndrome from a range of other mitochondrial diseases, such as ophthalmoplegia and Kearns-Sayre syndrome, showing lack of lactate in brain tissues appearing normal on MRI.

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Year:  2008        PMID: 18329833     DOI: 10.1016/j.braindev.2008.01.011

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  10 in total

Review 1.  Cerebral imaging in paediatric mitochondrial disorders.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Neuroradiol J       Date:  2018-07-06

Review 2.  MR spectroscopy in children: protocols and pitfalls in non-tumorous brain pathology.

Authors:  Jacques F Schneider
Journal:  Pediatr Radiol       Date:  2016-05-27

3.  Improving 1H MRSI measurement of cerebral lactate for clinical applications.

Authors:  Neva M Corrigan; Todd L Richards; Seth D Friedman; Helen Petropoulos; Stephen R Dager
Journal:  Psychiatry Res       Date:  2010-03-16       Impact factor: 3.222

Review 4.  The many faces of paediatric mitochondrial disease on neuroimaging.

Authors:  Fabian Baertling; Dirk Klee; Tobias B Haack; Holger Prokisch; Thomas Meitinger; Ertan Mayatepek; Jörg Schaper; Felix Distelmaier
Journal:  Childs Nerv Syst       Date:  2016-07-23       Impact factor: 1.475

5.  Lesional perfusion abnormalities in Leigh disease demonstrated by arterial spin labeling correlate with disease activity.

Authors:  Matthew T Whitehead; Bonmyong Lee; Andrea Gropman
Journal:  Pediatr Radiol       Date:  2016-04-04

6.  Metabolite measurements in the caudate nucleus, anterior cingulate cortex and hippocampus among patients with mitochondrial disorders: a case-control study using proton magnetic resonance spectroscopy.

Authors:  Rebecca E Anglin; Patricia I Rosebush; Michael D Noseworthy; Mark Tarnopolsky; Alexander M Weber; Noam Soreni; Michael F Mazurek
Journal:  CMAJ Open       Date:  2013-04-26

7.  Functional and molecular imaging with MRI: potential applications in paediatric radiology.

Authors:  Owen J Arthurs; Ferdia A Gallagher
Journal:  Pediatr Radiol       Date:  2010-10-23

8.  Clinical, Neuroimaging, and Pathological Analyses of 13 Chinese Leigh Syndrome Patients with Mitochondrial DNA Mutations.

Authors:  Xiao-Lin Yu; Chuan-Zhu Yan; Kun-Qian Ji; Peng-Fei Lin; Xue-Bi Xu; Ting-Jun Dai; Wei Li; Yu-Ying Zhao
Journal:  Chin Med J (Engl)       Date:  2018-11-20       Impact factor: 2.628

Review 9.  Molecular basis of Leigh syndrome: a current look.

Authors:  Manuela Schubert Baldo; Laura Vilarinho
Journal:  Orphanet J Rare Dis       Date:  2020-01-29       Impact factor: 4.123

10.  Posterior Cingulate Lactate as a Metabolic Biomarker in Amnestic Mild Cognitive Impairment.

Authors:  Kurt E Weaver; Todd L Richards; Rebecca G Logsdon; Ellen L McGough; Satoshi Minoshima; Elizabeth H Aylward; Natalia M Kleinhans; Thomas J Grabowski; Susan M McCurry; Linda Teri
Journal:  Biomed Res Int       Date:  2015-08-31       Impact factor: 3.411

  10 in total

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