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Phosphorus magnetic resonance spectroscopy in multiple system atrophy and Parkinson's disease
Author(s) -
Barbiroli Bruno,
Martinelli Paolo,
Patuelli Alberto,
Lodi Raffaele,
Iotti Stefano,
Cortelli Pietro,
Montagna Pasquale
Publication year - 1999
Publication title -
movement disorders
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.352
H-Index - 198
eISSN - 1531-8257
pISSN - 0885-3185
DOI - 10.1002/1531-8257(199905)14:3<430::aid-mds1007>3.0.co;2-s
Subject(s) - olivopontocerebellar atrophy , phosphocreatine , atrophy , chemistry , parkinson's disease , medicine , magnetic resonance imaging , nuclear magnetic resonance spectroscopy , metabolite , endocrinology , central nervous system disease , nuclear magnetic resonance , degenerative disease , pathology , disease , stereochemistry , physics , radiology , energy metabolism
We performed in vivo phosphorus magnetic resonance spectroscopy on the occipital lobes of 15 patients with multiple system atrophy (MSA; eight with olivopontocerebellar atrophy [OPCA] and seven with the striatonigral degeneration variant [SND]), 13 patients with idiopathic Parkinson's disease (PD), and 16 age‐matched healthy subjects. The MSA group showed significantly reduced phosphocreatine (PCr), increased inorganic phosphate (Pi), and unchanged cytosolic free [Mg 2+ ], and pH. We did not find any significant difference between the OPCA and SND variants. However, patients with PD showed significantly increased content of Pi, decreased cytosolic free [Mg 2+ ], and unchanged [PCr] and pH. Comparing the MSA and PD groups, [PCr] was significantly lower in MSA than in PD, whereas cytosolic free [Mg 2+ ] was significantly lower in PD. Despite a certain degree of overlap of [PCr] and [Mg 2+ ] values between the two groups, by considering both variables at the same time it was possible to classify correctly 93% of cases by discriminant analysis. We conclude that phosphorus magnetic resonance spectroscopy discloses abnormal phosphate metabolite and ion contents in both MSA and PD, respectively, and may provide noninvasive diagnostic help to differentiate MSA from PD.