非艾滋病HIV感染的神经系统表现:一组同性恋和双性恋男性的随访。

C M Marra, W T Longstreth, H H Handsfield, B D Townes, R W Coombs, V L Murphy, A C Collier, C L Maxwell, K Claypoole, K R Maravilla, R Sloan, W A Cohen, S B Ross
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引用次数: 1

摘要

为了确定HIV感染的神经系统异常,159名HIV血清阳性的无艾滋病男性和76名血清阴性的对照者接受了标准化的全身和神经系统检查、腰椎穿刺(LP)、神经心理学(NP)评估和脑磁共振(MR)成像。病史、体格和实验室评估每六个月重复一次。每6-12个月重复一次NP测试(所有受试者)和MR成像(仅血清阳性);每年重复LP(仅血清阳性)。平均随访24.6个月。157例血清阳性患者中有60例(38.2%)出现神经异常,76例对照患者中有23例(30.3%)出现神经异常,多数与听力有关(p = NS)。随访期间,136例血清阳性患者中有43例(31.6%)出现持续性听力异常,64例血清阴性患者中有9例(14.1%)出现持续性听力异常(p = 0.008)。7例hiv血清阳性患者出现周围神经病变;这在听力异常的人群中更为常见(p = 0.03)。hiv血清阳性患者在NP测试中的表现不如对照组好,但总体表现并未下降。MR成像导致的脑萎缩恶化或脑脊液异常在hiv血清阳性患者中比血清阴性患者更常见,并且可能与周围神经病变有共同的机制。需要进一步的研究来确定这些异常是否预示着更严重的神经系统疾病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurologic Manifestations
of HIV Infection Without AIDS:Follow-UP of a Cohort
of Homosexual and Bisexual Men.

To identify neurological abnormalities in HIV infection, 159 HIV-seropositive men without AIDS and 76 seronegative controls underwent standardized general and neurological examinations, lumbar puncture (LP), neuropsychological (NP) assessment, and brain magnetic resonance (MR) imaging. History, physical, and laboratory evaluations were repeated every six months. NP tests (all subjects) and MR imaging (seropositives only) was repeated every 6-12 months; LP (seropositives only) was repeated yearly. Mean follow-up was 24.6 months. Neurological abnormalities, most related to hearing, were seen in 60 (38.2%) of 157 seropositives and 23 (30.3%) of 76 controls at baseline (p = NS). During follow-up, 43 (31.6%) of 136 seropositives had persistent hearing abnormalities compared to 9 (14.1%) of 64 seronegatives (p = 0.008). Seven HIV-seropositives developed peripheral neuropathy; this was more common among those with hearing abnormalities (p = 0.03). HIV-seropositives performed less well on NP tests than controls, but overall performance did not decline. Worsening brain atrophy by MR imaging or cerebrospinal fluid abnormalities are more common in HIV-seropositives than seronegatives and may share a common mechanism with peripheral neuropathy. Further study is needed to determine whether these abnormalities portend more serious neurological disease.

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