Dendritic injury is a pathological substrate for human immunodeficiency virus-related cognitive disorders

被引:404
作者
Masliah, E
Heaton, RK
Marcotte, TD
Ellis, RJ
Wiley, CA
Mallory, M
Achim, CL
McCutchan, JA
Nelson, JA
Atkinson, JH
Grant, I
Chandler, JL
Wallace, MR
Spector, SA
Jernigan, T
Hesselink, J
Hansen, L
Abramson, I
Masys, D
机构
[1] Univ Calif San Diego, Dept Neurosci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Pathol, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Psychiat, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[5] Vet Affairs Med Ctr, Psychiat Serv, San Diego, CA 92161 USA
[6] Presbyterian Univ Hosp, Div Neuropathol, Pittsburgh, PA 15213 USA
[7] USN Hosp, San Diego, CA 92161 USA
关键词
D O I
10.1002/ana.410420618
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
To determine the neuropathological substrate of human immunodeficiency virus (HIV)-associated neurocognitive disorders, we examined persons with acquired immunodeficiency syndrome before their death and related their antemortem neuropsychological performance to postmortem indicators of HIV encephalitis, viral burden, and presynaptic and postsynaptic neuronal injury. Of 20 prospectively examined cases, 9 were neurocognitively normal, 5 showed neuropsychological impairment, 5 had minor cognitive/motor disorder, and 1 was demented. Degree of neurocognitive impairment was strongly related to the amount of dendritic simplification based on microtubule-associated protein 2 immunohistochemical staining, somewhat less so to a semiquantitative viral burden score based on numbers of HIV gp41-immunoreactive cells, and much less so to the presence of multinucleated giant cells or microglial nodules. It appears that even milder neurocognitive impairment reflects microneuroanatomical injury to synaptic structures.
引用
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页码:963 / 972
页数:10
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共 53 条
[41]  
MASLIAH E, 1994, RES P ARNMD, V72, P119
[42]   THE DIAGNOSTIC UTILITY OF ELEVATION IN CEREBROSPINAL-FLUID BETA-2-MICROGLOBULIN IN HIV-1 DEMENTIA [J].
MCARTHUR, JC ;
NANCESPROSON, TE ;
GRIFFIN, DE ;
HOOVER, D ;
SELNES, OA ;
MILLER, EN ;
MARGOLICK, JB ;
COHEN, BA ;
FARZADEGAN, H ;
SAAH, A .
NEUROLOGY, 1992, 42 (09) :1707-1712
[43]  
MILLER SW, 1997, J INT NEUROPSYCH SOC, V3, P49
[44]   THE AIDS DEMENTIA COMPLEX .2. NEUROPATHOLOGY [J].
NAVIA, BA ;
CHO, ES ;
PETITO, CK ;
PRICE, RW .
ANNALS OF NEUROLOGY, 1986, 19 (06) :525-535
[45]   THE AIDS DEMENTIA COMPLEX [J].
PRICE, RW ;
BREW, BJ .
JOURNAL OF INFECTIOUS DISEASES, 1988, 158 (05) :1079-1083
[46]  
SACKTOR DA, 1996, J NEUROVIROL, V2, P404
[47]   Pathogenic and protective correlates of T cell proliferation in AIDS [J].
Schrier, RD ;
Wiley, CA ;
Spina, C ;
McCutchan, JA ;
Grant, I .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 98 (03) :731-740
[48]   MORPHOLOGICAL-CHANGES ASSOCIATED WITH STAGES OF MEMORY FORMATION IN THE CHICK FOLLOWING PASSIVE-AVOIDANCE TRAINING [J].
STEWART, MG ;
RUSAKOV, DA .
BEHAVIOURAL BRAIN RESEARCH, 1995, 66 (1-2) :21-28
[49]   CENTRAL-NERVOUS-SYSTEM DAMAGE PRODUCED BY EXPRESSION OF THE HIV-1 COAT PROTEIN GP120 IN TRANSGENIC MICE [J].
TOGGAS, SM ;
MASLIAH, E ;
ROCKENSTEIN, EM ;
RALL, GF ;
ABRAHAM, CR ;
MUCKE, L .
NATURE, 1994, 367 (6459) :188-193
[50]  
WEIS S, 1993, ACTA NEUROPATHOL, V85, P185