Assessment of dysmyelination with RAFFn MRI: application to murine MPS I
Type I mucopolysaccharidosis (MPS I) is an autosomal recessive lysosomal storage disorder with neurological features. Humans and laboratory animals with MPS I exhibit various white matter abnormalities involving the corpus callosum and other regions. In this study, we first validated a novel MRI tec...
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Veröffentlicht in: | PloS one 2015-02, Vol.10 (2), p.e0116788-e0116788 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Type I mucopolysaccharidosis (MPS I) is an autosomal recessive lysosomal storage disorder with neurological features. Humans and laboratory animals with MPS I exhibit various white matter abnormalities involving the corpus callosum and other regions. In this study, we first validated a novel MRI technique, entitled Relaxation Along a Fictitious Field in the rotating frame of rank n (RAFFn), as a measure of myelination and dysmyelination in mice. We then examined differences between MPS I mice and heterozygotes using RAFF5 and histology. RAFF5 (i.e., RAFFn with n = 5) relaxation time constants were highly correlated with histological myelin density (R2 = 0.68, P |
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ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0116788 |