Skip to main content
Journal of Psychiatry & Neuroscience : JPN logoLink to Journal of Psychiatry & Neuroscience : JPN
. 1993 Jan;18(1):33–37.

Thalamic radiodensity and cognitive performance in mild and moderate dementia of the Alzheimer type.

H Förstl 1, B Sahakian 1
PMCID: PMC1188473  PMID: 8461278

Abstract

Eighteen patients with mild to moderate dementia of the Alzheimer type underwent cranial computed tomography (CT) and tests of visual attention, recognition and learning. Two subgroups emerged. Subgroup 1 was made up of ten patients who showed impaired visual recognition learning and memory, but intact attention in marked contrast to subgroup 2, which was made up of eight patients, in whom all of these functions were impaired. Planimetric and densitometric CT measurements yielded one significant difference between the two subgroups: a decreased radiodensity in the dorsomedial thalamus of the patients from subgroup 2. Lower radiodensity in the right dorsomedial thalamic area was significantly correlated with impaired performance on the test of attentional set shifting, more specifically, with deficits at the reversal learning stage. These results are interpreted in the context of recent evidence linking reversal learning to a neural network comprising the cholinergic basal forebrain, the amygdala and the orbitofrontal cortex, as well as the mediodorsal nucleus, and recent evidence of cholinergic deficits in this structure in patients with Alzheimer's disease.

Full text

PDF
35

Selected References

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

  1. Beats B., Levy R., Förstl H. Ventricular enlargement and caudate hyperdensity in elderly depressives. Biol Psychiatry. 1991 Sep 1;30(5):452–458. doi: 10.1016/0006-3223(91)90306-7. [DOI] [PubMed] [Google Scholar]
  2. Braak H., Braak E. Alzheimer's disease affects limbic nuclei of the thalamus. Acta Neuropathol. 1991;81(3):261–268. doi: 10.1007/BF00305867. [DOI] [PubMed] [Google Scholar]
  3. Brandel J. P., Hirsch E. C., Malessa S., Duyckaerts C., Cervera P., Agid Y. Differential vulnerability of cholinergic projections to the mediodorsal nucleus of the thalamus in senile dementia of Alzheimer type and progressive supranuclear palsy. Neuroscience. 1991;41(1):25–31. doi: 10.1016/0306-4522(91)90197-v. [DOI] [PubMed] [Google Scholar]
  4. Folstein M. F., Folstein S. E., McHugh P. R. "Mini-mental state". A practical method for grading the cognitive state of patients for the clinician. J Psychiatr Res. 1975 Nov;12(3):189–198. doi: 10.1016/0022-3956(75)90026-6. [DOI] [PubMed] [Google Scholar]
  5. Gado M., Danziger W. L., Chi D., Hughes C. P., Coben L. A. Brain parenchymal density measurements by CT in demented subjects and normal controls. Radiology. 1983 Jun;147(3):703–710. doi: 10.1148/radiology.147.3.6844607. [DOI] [PubMed] [Google Scholar]
  6. Hughes C. P., Berg L., Danziger W. L., Coben L. A., Martin R. L. A new clinical scale for the staging of dementia. Br J Psychiatry. 1982 Jun;140:566–572. doi: 10.1192/bjp.140.6.566. [DOI] [PubMed] [Google Scholar]
  7. Jacobson R. R., Turner S. W., Baldy R. E., Lishman W. A. Densitometric analysis of scans: important sources of artefact. Psychol Med. 1985 Nov;15(4):879–889. doi: 10.1017/s0033291700005122. [DOI] [PubMed] [Google Scholar]
  8. Jernigan T. L., Salmon D. P., Butters N., Hesselink J. R. Cerebral structure on MRI, Part II: Specific changes in Alzheimer's and Huntington's diseases. Biol Psychiatry. 1991 Jan 1;29(1):68–81. doi: 10.1016/0006-3223(91)90211-4. [DOI] [PubMed] [Google Scholar]
  9. Jones B., Mishkin M. Limbic lesions and the problem of stimulus--reinforcement associations. Exp Neurol. 1972 Aug;36(2):362–377. doi: 10.1016/0014-4886(72)90030-1. [DOI] [PubMed] [Google Scholar]
  10. Mann U. M., Mohr E., Chase T. N. Rapidly progressive Alzheimer's disease. Lancet. 1989 Sep 30;2(8666):799–799. doi: 10.1016/s0140-6736(89)90857-x. [DOI] [PubMed] [Google Scholar]
  11. McKhann G., Drachman D., Folstein M., Katzman R., Price D., Stadlan E. M. Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease. Neurology. 1984 Jul;34(7):939–944. doi: 10.1212/wnl.34.7.939. [DOI] [PubMed] [Google Scholar]
  12. Owen A. M., Roberts A. C., Polkey C. E., Sahakian B. J., Robbins T. W. Extra-dimensional versus intra-dimensional set shifting performance following frontal lobe excisions, temporal lobe excisions or amygdalo-hippocampectomy in man. Neuropsychologia. 1991;29(10):993–1006. doi: 10.1016/0028-3932(91)90063-e. [DOI] [PubMed] [Google Scholar]
  13. Roberts A. C., Robbins T. W., Everitt B. J., Jones G. H., Sirkia T. E., Wilkinson J., Page K. The effects of excitotoxic lesions of the basal forebrain on the acquisition, retention and serial reversal of visual discriminations in marmosets. Neuroscience. 1990;34(2):311–329. doi: 10.1016/0306-4522(90)90142-q. [DOI] [PubMed] [Google Scholar]
  14. Roberts A. C., Robbins T. W., Everitt B. J., Muir J. L. A specific form of cognitive rigidity following excitotoxic lesions of the basal forebrain in marmosets. Neuroscience. 1992;47(2):251–264. doi: 10.1016/0306-4522(92)90241-s. [DOI] [PubMed] [Google Scholar]
  15. Sahakian B. J., Downes J. J., Eagger S., Evenden J. L., Levy R., Philpot M. P., Roberts A. C., Robbins T. W. Sparing of attentional relative to mnemonic function in a subgroup of patients with dementia of the Alzheimer type. Neuropsychologia. 1990;28(11):1197–1213. doi: 10.1016/0028-3932(90)90055-s. [DOI] [PubMed] [Google Scholar]
  16. Sahakian B. J., Morris R. G., Evenden J. L., Heald A., Levy R., Philpot M., Robbins T. W. A comparative study of visuospatial memory and learning in Alzheimer-type dementia and Parkinson's disease. Brain. 1988 Jun;111(Pt 3):695–718. doi: 10.1093/brain/111.3.695. [DOI] [PubMed] [Google Scholar]
  17. Salmon D. P., Thal L. J., Butters N., Heindel W. C. Longitudinal evaluation of dementia of the Alzheimer type: a comparison of 3 standardized mental status examinations. Neurology. 1990 Aug;40(8):1225–1230. doi: 10.1212/wnl.40.8.1225. [DOI] [PubMed] [Google Scholar]
  18. Singer W. Control of thalamic transmission by corticofugal and ascending reticular pathways in the visual system. Physiol Rev. 1977 Jul;57(3):386–420. doi: 10.1152/physrev.1977.57.3.386. [DOI] [PubMed] [Google Scholar]
  19. Xuereb J. H., Perry R. H., Candy J. M., Perry E. K., Marshall E., Bonham J. R. Nerve cell loss in the thalamus in Alzheimer's disease and Parkinson's disease. Brain. 1991 Jun;114(Pt 3):1363–1379. [PubMed] [Google Scholar]

Articles from Journal of Psychiatry and Neuroscience are provided here courtesy of Canadian Medical Association

RESOURCES