In vivo and in vitro NMR spectroscopy reveal a putative novel inborn error involving polyol metabolism
In vivo NMR spectroscopy was performed on the brain of a patient with a leukoencephalopathy, revealing unknown resonances between 3.5 and 4.0 ppm. In addition, urine and CSF of the patient were measured using high‐resolution NMR spectroscopy. Also in these in vitro spectra, unknown resonances were o...
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Published in | NMR in biomedicine Vol. 14; no. 3; pp. 167 - 176 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
01.05.2001
Wiley |
Subjects | |
Online Access | Get full text |
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Summary: | In vivo NMR spectroscopy was performed on the brain of a patient with a leukoencephalopathy, revealing unknown resonances between 3.5 and 4.0 ppm. In addition, urine and CSF of the patient were measured using high‐resolution NMR spectroscopy. Also in these in vitro spectra, unknown resonances were observed in the 3.5–4.0 ppm region. Homonuclear 1H two‐dimensional J‐resolved spectroscopy (JRES) and 1H–1H correlation spectroscopy (COSY) were performed on the patient's urine for more accurate assignment of resonances. The NMR spectroscopic studies showed that the unknown resonances could be assigned to arabinitol and ribitol. This was confirmed using gas chromatography. The arabinitol was identified as D‐arabinitol. The patient is likely to suffer from an as yet unknown inborn error of metabolism affecting D‐arabinitol and ribitol metabolism. The primary molecular defect has not been found yet. Urine spectra of patients suffering from diabetes mellitus or galactosemia were recorded for comparison. Resonances outside the 3.2–4.0 ppm region, which are the most easy to recognize in body fluid spectra, allow easy recognition of various sugars and polyols. The paper shows that NMR spectroscopy in body fluids may help identifying unknown resonances observed in in vivo NMR spectra. Copyright © 2001 John Wiley & Sons, Ltd.
Abbreviations used:
Cho
choline‐containing compounds
COSY
1H–1H correlation spectroscopy
Cr
creatine
CSF
cerebrospinal fluid
GC
gas chromatography
Glx
glutamine and glutamate
JRES
homonuclear 1H two‐dimensional J‐resolved spectroscopy
Myo‐Ins
myo‐inositol
NAA
N‐acetylaspartate
Scyllo‐Ins
scyllo‐inositol
STEAM
stimulated echo acquisition mode
PRESS
point resolved spectroscopy. |
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Bibliography: | istex:E19E7B3E6EC2840473C09968ADED2F02CCB578CF ArticleID:NBM690 ark:/67375/WNG-F40N9J4F-2 ObjectType-Case Study-2 SourceType-Scholarly Journals-1 ObjectType-Feature-4 content type line 23 ObjectType-Report-1 ObjectType-Article-3 |
ISSN: | 0952-3480 1099-1492 |
DOI: | 10.1002/nbm.690 |