Literature DB >> 28269793

Proton Magnetic Resonance Spectroscopy Indicates Preserved Cerebral Biochemical Composition in Duchenne Muscular Dystrophy Patients.

Nathalie Doorenweerd1,2,3, Melissa Hooijmans1, Stephanie A Schubert1, Andrew G Webb1, Chiara S M Straathof3, Erik W van Zwet4, Mark A van Buchem1, Jan J G M Verschuuren3, Jos G M Hendriksen5,6, Erik H Niks3, Hermien E Kan1,2.   

Abstract

BACKGROUND: Duchenne muscular dystrophy (DMD) is caused by the absence of dystrophin. DMD is associated with specific learning and behavioural disabilities. In the brain, dystrophin is associated with GABAA receptors and aquaporin-4 in neurons and astrocytes, respectively, but little is known about its function. OBJECTIVE AND METHODS: In this study we aimed to compare the biochemical composition between patients and healthy controls in brain regions that are naturally rich in dystrophin using magnetic resonance spectroscopy. Given previous conflicting results obtained at clinical field strengths, we obtained data using a 7 Tesla system with associated higher signal-to-noise ratio and spectral resolution.
RESULTS: Results indicated unchanged biochemical composition in all regions investigated, and increased variance in glutamate in the frontal cortex.

Entities:  

Keywords:  Duchenne muscular dystrophy; brain; magnetic resonance spectroscopy; metabolites

Mesh:

Substances:

Year:  2017        PMID: 28269793     DOI: 10.3233/JND-160201

Source DB:  PubMed          Journal:  J Neuromuscul Dis


  3 in total

1.  In Vivo Evaluation of White Matter Abnormalities in Children with Duchenne Muscular Dystrophy Using DTI.

Authors:  V Preethish-Kumar; A Shah; M Kumar; M Ingalhalikar; K Polavarapu; M Afsar; J Rajeswaran; S Vengalil; S Nashi; P T Thomas; A Sadasivan; M Warrier; A Nalini; J Saini
Journal:  AJNR Am J Neuroradiol       Date:  2020-07-02       Impact factor: 3.825

Review 2.  Dystrophin Dp71 and the Neuropathophysiology of Duchenne Muscular Dystrophy.

Authors:  Michael Naidoo; Karen Anthony
Journal:  Mol Neurobiol       Date:  2019-12-13       Impact factor: 5.590

3.  Decision-Making And Selection Bias in Four Observational Studies on Duchenne and Becker Muscular Dystrophy.

Authors:  Karin J Naarding; Nathalie Doorenweerd; Zaïda Koeks; Ruben G F Hendriksen; Kinita A Chotkan; Yvonne D Krom; Imelda J M de Groot; Chiara S Straathof; Erik H Niks; Hermien E Kan
Journal:  J Neuromuscul Dis       Date:  2020
  3 in total

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