Pattern electroretinograms and visual evoked potentials in HIV infection: Evidence of asymptomatic retinal and postretinal impairment in the absence of infectious retinopathy

被引:29
作者
Iragui, VJ
Kalmijn, J
Plummer, DJ
Sample, PA
Trick, GL
Freeman, WR
机构
[1] UNIV CALIF SAN DIEGO,SCH MED,DEPT NEUROSCI,LA JOLLA,CA 92093
[2] UNIV CALIF SAN DIEGO,SCH MED,DEPT OPHTHALMOL,LA JOLLA,CA 92093
[3] VET AFFAIRS MED CTR,SAN DIEGO,CA 92161
[4] HENRY FORD HLTH SCI CTR,DEPT OPHTHALMOL,DETROIT,MI
关键词
D O I
10.1212/WNL.47.6.1452
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Retinal microangiopathy associated with HN infection is usually asymptomatic and escapes detection unless funduscopic examination is performed when evanescent cotton-wool spots are present. The aim of this study was to assess retinal and optic nerve/retrochiasmal function in HIV infection by means of electrophysiologic techniques that are sensitive to the detection of subclinical visual impairment. We studied transient and steady state pattern electroretinograms (PERGs) and pattern-reversal visual evoked potentials (PVEPs) in 21 HIV-negative controls and 33 HIV-positive subjects (16 with CD4 greater than or equal to 200/mL and 17 with CD4 < 200/mL) without visual symptoms or infectious retinopathy. HIV-positive subjects with CD4 greater than or equal to 200/mL had reduced amplitude of the transient PERG P1 potential, but no other latency or amplitude abnormalities. The HIV-positive group with CD4 < 200/mL had reduced P1 transient PERG amplitude, as well as latency delay of the transient PVEP. These findings suggest that HIV infection is associated with subclinical retinopathy and that, when severe immunosuppression occurs, both retinopathy and optic nerve/retrochiasmal dysfunction are present. Transient PERGs are more sensitive measures of visual system disease in HIV infection than are steady state responses.
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页码:1452 / 1456
页数:5
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共 32 条
  • [1] EFFECTS OF STIMULUS LOCATION AND PATTERN UPON THE VISUALLY EVOKED CORTICAL POTENTIAL AND THE ELECTRORETINOGRAM
    ARMINGTON, JC
    BRIGELL, M
    [J]. INTERNATIONAL JOURNAL OF NEUROSCIENCE, 1981, 14 (3-4) : 169 - 178
  • [2] ANATOMY AND PHYSIOLOGY OF THE VISUAL-SYSTEM
    CELESIA, GG
    DEMARCO, PJ
    [J]. JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 1994, 11 (05) : 482 - 492
  • [3] DAWSON WW, 1979, INVEST OPHTH VIS SCI, V18, P988
  • [4] FROEHLICH J, 1991, INVEST OPHTH VIS SCI, V32, P310
  • [5] GEIER SA, 1993, J ACQ IMMUN DEF SYND, V6, P252
  • [7] HOLDER GE, 1987, BR J OPHTHALMOL, V71, P2166
  • [8] NEUROLOGICAL DYSFUNCTION IN ASYMPTOMATIC HIV-1-INFECTED MEN - EVIDENCE FROM EVOKED-POTENTIALS
    IRAGUI, VJ
    KALMIJN, J
    THAL, LJ
    GRANT, I
    ATKINSON, JH
    MCCUTCHAN, JA
    SPECTOR, S
    HEATON, RK
    HESSELINK, J
    JERNIGAN, T
    WILEY, CA
    OLSHEN, R
    ABRAMSON, I
    OLDFIELD, EC
    CHANDLER, J
    KENNEDY, CA
    BUTTERS, N
    DUPONT, R
    PATTERSON, T
    ZISOOK, S
    JESTE, D
    SIEBURG, H
    VELIN, RA
    [J]. ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1994, 92 (01): : 1 - 10
  • [9] Keller S K, 1991, Fortschr Ophthalmol, V88, P716
  • [10] KELLER S K, 1989, Investigative Ophthalmology and Visual Science, V30, P512