| Literature DB >> 28269793 |
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.Entities:
Keywords: Duchenne muscular dystrophy; brain; magnetic resonance spectroscopy; metabolites
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Year: 2017 PMID: 28269793 DOI: 10.3233/JND-160201
Source DB: PubMed Journal: J Neuromuscul Dis