RETINOCALCARINE FUNCTION IN ALZHEIMERS-DISEASE - A CLINICAL AND ELECTROPHYSIOLOGICAL STUDY

被引:69
作者
RIZZO, JF
CRONINGOLOMB, A
GROWDON, JH
CORKIN, S
ROSEN, TJ
SANDBERG, MA
CHIAPPA, KH
LESSELL, S
机构
[1] MIT,DEPT BRAIN & COGNIT SCI,CAMBRIDGE,MA 02139
[2] HARVARD UNIV,SCH MED,DEPT OPHTHALMOL,BOSTON,MA 02115
[3] BOSTON UNIV,DEPT PSYCHOL,BOSTON,MA 02215
[4] MASSACHUSETTS GEN HOSP,DEPT NEUROL,BOSTON,MA 02114
[5] BOSTON UNIV,SCH MED,DEPT NEUROL,BOSTON,MA 02118
[6] MIT,CLIN RES CTR,CAMBRIDGE,MA 02139
关键词
D O I
10.1001/archneur.1992.00530250097023
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Impaired visual function in Alzheimer's disease (AD) could result from either precortical or cortical lesions, or both. In a parallel psychophysical study of visual function in AD, we found that contrast sensitivity function, color vision, stereoacuity, and backward masking were impaired relative to the performance of age-matched control subjects, whereas performance on a critical flicker fusion test was normal. The intent of the present study was to determine whether abnormalities of the retinocalcarine pathway contribute to visual dysfunction. We performed neuro-ophthalmological examinations on 38 patients with AD; from this group, 25 received additional psychophysical testing and 13 underwent electrophysiological testing. Clinical neuro-ophthalmological examinations, full-field electroretinograms, focal electroretinograms, and pattern visual evoked potentials were normal in all patients tested. There was no evidence of retinocalcarine abnormality specific to AD. We conclude that the visual impairment experienced by some patients with AD primarily results from involvement of the visual association cortices rather than from precortical damage, at least before the end stage of the disease.
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页码:93 / 101
页数:9
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