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HIV-1相关性神经病变的流行病学及临床特征

Epidemiology and clinical features of HIV-1 associated neuropathies.

作者信息

Verma A

机构信息

Department of Neurology, University of Miami School of Medicine and Jackson Memorial Hospital, Florida, USA.

出版信息

J Peripher Nerv Syst. 2001 Mar;6(1):8-13. doi: 10.1046/j.1529-8027.2001.006001008.x.

Abstract

Peripheral neuropathy is common in human immunodeficiency virus type-1 (HIV-1) infection. Peripheral neuropathies complicate all stages of the HIV-1 disease and cause considerable morbidity and disability in HIV-1 infected individuals and acquired immunodeficiency syndrome (AIDS) patients. Whereas symptomatic neuropathies occur in approximately 10% to 15% of HIV-1-infected patients overall, pathologic evidence of peripheral nerve involvement is present in virtually all end-stage AIDS patients. There are 6 major clinical types of HIV-associated neuropathies that are regularly seen in large HIV-1 clinics. Distal sensory polyneuropathy (DSP) is the most common among the HIV-1-associated neuropathies. DSP generally occurs in later stages of HIV-1 infection and it follows an indolent and protracted clinical course. The dominant clinical features in DSP include distal pain, paresthesia and numbness in a typical length-dependent fashion with proximal to distal gradient. Whereas toxic neuropathies--secondary to certain antiretroviral agents--are clinically similar to DSP, their temporal relation to neurotoxic medication helps distinguish them from other HIV-1-associated neuropathies. DSP and toxic neuropathy may coexist in a single patient. Acute and chronic inflammatory demyelinating polyradiculoneuropathies (AIDP and CIDP) produce global limb weakness. AIDP may occur at seroconversion and it can therefore be the initial manifestation of HIV-1 infection. CIDP generally occurs in the mid to late stages of HIV-1 infection. Progressive polyradiculopathy (PP) occurs in patients with advanced immunodeficiency and is generally caused by the opportunist cytomegalovirus (CMV) infection. Mononeuropathy multiplex (MM) in early stages of HIV-1 infection is immune mediated, whereas in advanced AIDS it is caused by the CMV infection. Finally, subclinical autonomic nervous system involvement is common in all stages of HIV-1 infection. Because HIV-1-associated neuropathies are diverse in their etiology and pathogenesis, a precise clinical diagnosis is required to formulate a rational therapeutic intervention.

摘要

周围神经病变在人类免疫缺陷病毒1型(HIV-1)感染中很常见。周围神经病变使HIV-1疾病的各个阶段复杂化,并在HIV-1感染者和获得性免疫缺陷综合征(AIDS)患者中导致相当高的发病率和残疾率。虽然有症状的神经病变在总体HIV-1感染患者中约占10%至15%,但几乎所有晚期AIDS患者都有周围神经受累的病理证据。在大型HIV-1诊所中经常见到6种主要的与HIV相关的神经病变临床类型。远端感觉性多发性神经病变(DSP)是HIV-1相关神经病变中最常见的。DSP通常发生在HIV-1感染的后期,其临床病程缓慢且迁延。DSP的主要临床特征包括典型的长度依赖性方式的远端疼痛、感觉异常和麻木,呈近端到远端的梯度变化。虽然继发于某些抗逆转录病毒药物的中毒性神经病变在临床上与DSP相似,但它们与神经毒性药物的时间关系有助于将它们与其他HIV-1相关神经病变区分开来。DSP和中毒性神经病变可能在同一患者中并存。急性和慢性炎症性脱髓鞘性多发性神经根神经病(AIDP和CIDP)会导致肢体广泛性无力。AIDP可能在血清转换时发生,因此可能是HIV-1感染的初始表现。CIDP通常发生在HIV-1感染的中晚期。进行性多发性神经根病(PP)发生在免疫缺陷严重的患者中,通常由机会性巨细胞病毒(CMV)感染引起。HIV-1感染早期的多发性单神经病(MM)是免疫介导的,而在晚期AIDS中则由CMV感染引起。最后,亚临床自主神经系统受累在HIV-1感染的所有阶段都很常见。由于HIV-1相关神经病变的病因和发病机制各不相同,需要精确的临床诊断来制定合理的治疗干预措施。

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