Skip to main content
Philosophical Transactions of the Royal Society B: Biological Sciences logoLink to Philosophical Transactions of the Royal Society B: Biological Sciences
. 1998 Nov 29;353(1377):1929–1933. doi: 10.1098/rstb.1998.0345

Coordinated expression in chronically unconscious persons.

F Plum 1, N Schiff 1, U Ribary 1, R Llinás 1
PMCID: PMC1692418  PMID: 9854265

Abstract

The clinically described 'persistent vegetative state' (PVS), consists of wakefulness unaccompanied by any evidence of the subject's awareness of self or environment. Past studies from our own and other laboratories have used positron emission tomography (PET) to study brain metabolism in approximately 20 such patients during wakeful periods. All those efforts identified global cerebral glucose metabolism at or below levels encountered during deep barbiturate anaesthesia. Nevertheless, the clinical literature includes rare reports of relatively isolated cognitive functions expressed by PVS patients late in their course. The observation raises the question of whether such activity reflects awareness or unconscious automatic behaviour. We employed magnetometry (MEG), PET scanning, MR imaging and 24-hour EEG recordings to evaluate three patients clinically vegetative between six months and 20 years after onset. Neither meticulous clinical examinations nor 24-hour EEG and video monitoring provided any hint of cognitive interaction in any subject. Nevertheless, patient 1 uttered single words once every 48 hours or more; patient 2 frequently expressed coordinated, non-purposeful, non-dystonic movements in arms and/or legs; and, patient 3 expressed strong emotional negativity without motor responses to noxious stimuli with occasional quieting in response to prosodic stimuli. All patients had whole-brain averaged global metabolism levels below 50% of normal. Patient 1, however, demonstrated preserved islands of increased metabolism in the posterior frontal and posterior temporal lobes, as well as MEG activations of Heschl's gyrus all located in the left hemisphere. In patient 2, selected increased metabolism was confined to the frontal poles and related subcortical structures. MRI in patient 3 demonstrated severe, bilateral post-traumatic cerebral atrophy. PET metabolism was diffusely reduced to 40% of normal but MEG evoked potentials indicated early and late sensory processing with abnormal later evoked components. The correlation of fragmentary behaviour with preserved metabolic and physiologic activity in cortical and subcortical regions known to support specific modular functions is novel. The finding demonstrates the capacity of severely damaged brains to partially express surviving modular functions without evidence of integrative processes that would be necessary to produce consciousness. We conclude that the mere expression of isolated neuropsychologic activity by isolated modules is insufficient to generate consciousness in overwhelmingly damaged brains.

Full Text

The Full Text of this article is available as a PDF (145.6 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Blacklock J. B., Oldfield E. H., Di Chiro G., Tran D., Theodore W., Wright D. C., Larson S. M. Effect of barbiturate coma on glucose utilization in normal brain versus gliomas. Positron emission tomography studies. J Neurosurg. 1987 Jul;67(1):71–75. doi: 10.3171/jns.1987.67.1.0071. [DOI] [PubMed] [Google Scholar]
  2. DeVolder A. G., Goffinet A. M., Bol A., Michel C., de Barsy T., Laterre C. Brain glucose metabolism in postanoxic syndrome. Positron emission tomographic study. Arch Neurol. 1990 Feb;47(2):197–204. doi: 10.1001/archneur.1990.00530020103022. [DOI] [PubMed] [Google Scholar]
  3. Jennett B., Plum F. Persistent vegetative state after brain damage. A syndrome in search of a name. Lancet. 1972 Apr 1;1(7753):734–737. doi: 10.1016/s0140-6736(72)90242-5. [DOI] [PubMed] [Google Scholar]
  4. Levy D. E., Sidtis J. J., Rottenberg D. A., Jarden J. O., Strother S. C., Dhawan V., Ginos J. Z., Tramo M. J., Evans A. C., Plum F. Differences in cerebral blood flow and glucose utilization in vegetative versus locked-in patients. Ann Neurol. 1987 Dec;22(6):673–682. doi: 10.1002/ana.410220602. [DOI] [PubMed] [Google Scholar]
  5. Phelps M. E., Huang S. C., Hoffman E. J., Selin C., Sokoloff L., Kuhl D. E. Tomographic measurement of local cerebral glucose metabolic rate in humans with (F-18)2-fluoro-2-deoxy-D-glucose: validation of method. Ann Neurol. 1979 Nov;6(5):371–388. doi: 10.1002/ana.410060502. [DOI] [PubMed] [Google Scholar]
  6. Tommasino C., Grana C., Lucignani G., Torri G., Fazio F. Regional cerebral metabolism of glucose in comatose and vegetative state patients. J Neurosurg Anesthesiol. 1995 Apr;7(2):109–116. doi: 10.1097/00008506-199504000-00006. [DOI] [PubMed] [Google Scholar]

Articles from Philosophical Transactions of the Royal Society B: Biological Sciences are provided here courtesy of The Royal Society

RESOURCES