Pfister H W, Einhäupl K M, Wick M, Fateh-Moghadam A, Huber M, Schielke E, Goebel F D, Matuschke A, Heinrich B, Bogner J R
Neurologische Klinik, Universität München, Federal Republic of Germany.
J Neurol. 1989 Jul;236(5):288-91. doi: 10.1007/BF00314458.
The major pathological abnormalities of HIV encephalopathy are infiltrates of macrophages, multinucleated giant cells, microglial nodules and demyelination. Elevated myelin basic protein (MBP) levels in the cerebrospinal fluid (CSF) provide a marker for central nervous system demyelination. The purpose of this study was to investigate the possible role of CSF MBP as a useful and early marker for HIV encephalopathy. The CSF of 40 consecutive patients with HIV infection of various clinical stages was investigated, including 13 patients with clinical signs of HIV encephalopathy. CSF MBP was elevated in 2 patients (5.0 and 5.3 ng/ml), both of whom had moderate to severe HIV encephalopathy. The course of the disease was rapid in both patients. In the remaining 38 patients, CSF MBP levels were marginally elevated (n = 12) or normal (n = 26). Our results suggest that CSF MBP is not a sensitive marker for the diagnosis and evaluation of HIV encephalopathy, but may be an indicator of prognosis for the course of the disease. There were only few findings of elevated CSF MBP levels in patients with HIV encephalopathy in the current study, and this may be because the disorder progressed slowly in most patients. It is possible that CSF MBP levels in HIV encephalopathy may only be elevated with acute clinical deterioration but are normal in slowly progressive forms of demyelination, as seen in multiple sclerosis.
HIV 脑病的主要病理异常包括巨噬细胞浸润、多核巨细胞、小胶质细胞结节和脱髓鞘。脑脊液(CSF)中髓鞘碱性蛋白(MBP)水平升高是中枢神经系统脱髓鞘的一个标志物。本研究的目的是探讨脑脊液MBP作为HIV脑病有用的早期标志物的可能作用。对40例不同临床阶段的HIV感染连续患者的脑脊液进行了研究,其中包括13例有HIV脑病临床体征的患者。2例患者(5.0和5.3 ng/ml)的脑脊液MBP升高,这2例患者均患有中度至重度HIV脑病。两名患者的病程均进展迅速。在其余38例患者中,脑脊液MBP水平轻度升高(n = 12)或正常(n = 26)。我们的结果表明,脑脊液MBP不是诊断和评估HIV脑病的敏感标志物,但可能是疾病病程预后的一个指标。在本研究中,HIV脑病患者脑脊液MBP水平升高的发现很少,这可能是因为大多数患者病情进展缓慢。HIV脑病患者的脑脊液MBP水平可能仅在急性临床恶化时升高,而在缓慢进展的脱髓鞘形式(如多发性硬化症)中正常。