Magnetic Resonance Imaging Evidence of Cytotoxic Cerebral Edema in Acute Mountain Sickness

  • Kai Kallenberg
    Department of Neuroradiology, Georg August University Medical Centre, University of Göttingen, Göttingen, Germany
  • Damian M Bailey
    Department of Physiology, Hypoxia Research Unit, University of Glamorgan, Mid-Glamorgan, South Wales, UK
  • Stefan Christ
    Department of Neuroradiology, Georg August University Medical Centre, University of Göttingen, Göttingen, Germany
  • Alexander Mohr
    Department of Neuroradiology, Georg August University Medical Centre, University of Göttingen, Göttingen, Germany
  • Robin Roukens
    Department of Internal Medicine, Division of Sports Medicine, Ruprecht-Karls-University, Heidelberg, Germany and
  • Elmar Menold
    Department of Internal Medicine, Division of Sports Medicine, Ruprecht-Karls-University, Heidelberg, Germany and
  • Thorsten Steiner
    Department of Neurology, Ruprecht-Karls-University, Heidelberg, Germany
  • Peter Bärtsch
    Department of Internal Medicine, Division of Sports Medicine, Ruprecht-Karls-University, Heidelberg, Germany and
  • Michael Knauth
    Department of Neuroradiology, Georg August University Medical Centre, University of Göttingen, Göttingen, Germany

抄録

<jats:p> The present study applied T<jats:sub>2</jats:sub>- and diffusion-weighted magnetic resonance imaging to examine if mild cerebral edema and subsequent brain swelling are implicated in the pathophysiology of acute mountain sickness (AMS). Twenty-two subjects were examined in normoxia (21% O<jats:sub>2</jats:sub>), after 16 hours passive exposure to normobaric hypoxia (12% O<jats:sub>2</jats:sub>) corresponding to a simulated altitude of 4,500 m and after 6 hours recovery in normoxia. Clinical AMS was diagnosed in 50% of subjects during hypoxia and corresponding headache scores were markedly elevated ( P < 0.05 versus non-AMS). Hypoxia was associated with a mild increase in brain volume (+ 7.0 ± 4.8 ml, P < 0.05 versus preexposure baseline) that resolved during normoxic recovery. Hypoxia was also associated with an increased T<jats:sub>2</jats:sub> relaxation time (T<jats:sub>2</jats:sub>rt) and a general trend toward an increased apparent diffusion coefficient (ADC). During the normoxic recovery, brain volume and T<jats:sub>2</jats:sub>rt recovered to pre-exposure baseline values, whereas a more marked reduction in ADC in the splenium of the corpus callosum (SCC) was observed ( P < 0.05). While changes in brain volume and T<jats:sub>2</jats:sub>rt were not selectively different in AMS, ADC values were consistently lower ( P < 0.05 versus non-AMS) and associated with the severity of neurologic symptoms. Acute mountain sickness was also characterized by an increased brain to intracranial volume ratio ( P < 0.05 versus non-AMS). These findings indicate that mild extracellular vasogenic edema contributes to the generalized brain swelling observed at high altitude, independent of AMS. In contrast, intracellular cytotoxic edema combined with an anatomic predisposition to a ‘tight-fit’ brain may prove of pathophysiologic significance, although the increase in brain volume in hypoxia was only about 0.5% of total brain volume. </jats:p>

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