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Erschienen in: Neuroradiology 11/2015

01.11.2015 | Paediatric Neuroradiology

Disrupted glutamate-glutamine cycle in acute encephalopathy with biphasic seizures and late reduced diffusion

verfasst von: Jun-ichi Takanashi, Masashi Mizuguchi, Masaru Terai, A. James Barkovich

Erschienen in: Neuroradiology | Ausgabe 11/2015

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Abstract

Introduction

Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is the most common subtype of infectious pediatric encephalopathy in Japan. It is sometimes difficult to make an early diagnosis of AESD; excitotoxicity is postulated to be the pathogenesis based on elevated glutamine (Gln) and glutamate (Glu) complex (Glx = Glu + Gln) observed on MR spectroscopy. It is uncertain whether Gln or Glu contributes to the elevated Glx, or whether MR spectroscopy is useful for an early diagnosis.

Methods

Five Japanese patients with AESD (three boys and two girls, 1 year of age) were enrolled in this study. MR spectroscopy was acquired from the frontal white matter (repetition time (TR) of 5000 ms, echo time (TE) of 30 ms) with a 1.5- or 3.0-T scanner. MR spectroscopy was performed four times for two patients, three times for one patient, and two times for two patients. Quantification of Glu and Gln was performed using LCModel.

Results

Glu was elevated in three of four studies on days 1–4 and became normal or low afterward. Gln was normal in three studies on days 1–2, elevated in all seven studies on days 4–12, and became normal or low afterward.

Conclusion

These findings suggest that MR spectroscopy may be useful for an early diagnosis. Acute Glu elevation changes to subacute Gln elevation, suggesting that a disrupted Glu-Gln cycle may play an important role.
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Metadaten
Titel
Disrupted glutamate-glutamine cycle in acute encephalopathy with biphasic seizures and late reduced diffusion
verfasst von
Jun-ichi Takanashi
Masashi Mizuguchi
Masaru Terai
A. James Barkovich
Publikationsdatum
01.11.2015
Verlag
Springer Berlin Heidelberg
Erschienen in
Neuroradiology / Ausgabe 11/2015
Print ISSN: 0028-3940
Elektronische ISSN: 1432-1920
DOI
https://doi.org/10.1007/s00234-015-1573-x

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