論文

査読有り 国際誌
2013年

PET Molecular Imaging to Investigate Higher Brain Dysfunction in Patients with Neurotrauma

Brain Edema XV
  • Tadashi Nariai
  • ,
  • Motoki Inaji
  • ,
  • Yoji Tanaka
  • ,
  • Mikio Hiura
  • ,
  • Chihiro Hosoda
  • ,
  • Kenji Ishii
  • ,
  • Kikuo Ohno

118
開始ページ
251
終了ページ
254
記述言語
英語
掲載種別
論文集(書籍)内論文
DOI
10.1007/978-3-7091-1434-6_47
出版者・発行元
Springer Vienna

INTRODUCTION: Many neurotrauma patients suffer from higher brain dysfunction even when focal brain damage is not detected with MRI. We performed functional imaging with positron emission tomography (PET) to clarify the relationship between the functional deficit and symptoms of such patients. METHODS: Patients who complain of higher brain dysfunction without apparent morphological cortical damage were recruited. Thirteen patients underwent PET study to image glucose metabolism by (18)F-FDG, and central benzodiazepine receptor (cBZD-R) by (11)C-flumazenil, together with measurement of cognition. RESULTS: Diffuse axonal injury (DAI) patients have a significant decrease in glucose metabolism and cBZD-R distribution in the cingulated cortex than normal controls. Score of cognition test was variable among patients. The degree of decreased glucose metabolism and cBZD-R in the dominant hemisphere corresponded well to the severity of cognitive disturbance. Patients with a milder type of diffuse brain injury (i.e., cerebral concussion) also showed abnormal glucose metabolism and cBZD-R distribution when they suffered from cognitive deficit. CONCLUSION: PET molecular imaging was useful for depicting the cortical dysfunction of neurotrauma patients even when morphological change was not apparent. This method may be promising in clarifying the pathophysiology of higher brain dysfunction of patients with neurotrauma, but without morphological abnormality.

リンク情報
DOI
https://doi.org/10.1007/978-3-7091-1434-6_47
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/23564142
URL
http://link.springer.com/content/pdf/10.1007/978-3-7091-1434-6_47
ID情報
  • DOI : 10.1007/978-3-7091-1434-6_47
  • PubMed ID : 23564142

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