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Phosphorus magnetic resonance spectroscopy
in multiple system atrophy and Parkinson's disease.

We performed in vivo phosphorus magnetic resonance spectroscopy on the
occipital lobes of 15 patients with multiple system atrophy (MSA; 8 with
olivopontocerebellar atrophy [OPCA] and 7 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 [Mg2+], 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 [Mg2+], and unchanged [PCr] and pH.

Comparing the MSA and PD groups, [PCr] was significantly lower in MSA than
in PD, whereas cytosolic free [Mg2+] was significantly lower in PD.

Despite a certain degree of overlap of [PCr] and [Mg2+] 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.


Mov Disord 1999 May;14(3):430-5
Barbiroli B, Martinelli P, Patuelli A, Lodi R,
Iotti S, Cortelli P, Montagna P
Biochimica Clinica, Dipartimento di Medicina Clinica e Biotecnologia
Applicata D. Campanacci, Universita di Bologna, Italy.
PMID: 10348465, UI: 99276221

http://www.ncbi.nlm.nih.gov/PubMed/

janet paterson
52 now / 41 dx / 37 onset
snail-mail: PO Box 171  Almonte  Ontario  K0A 1A0  Canada
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