Herrmann D N, McDermott M P, Sowden J E, Henderson D, Messing S, Cruttenden K, Schifitto G
Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Neurology. 2006 Mar 28;66(6):857-61. doi: 10.1212/01.wnl.0000203126.01416.77.
To investigate whether serially assessed epidermal nerve fiber (ENF) density and quantitative sensory thresholds (QSTs) are associated with the clinical transition from HIV infection with no neuropathy or asymptomatic neuropathy to symptomatic distal sensory neuropathy (SDSP).
Identifying predictors of transition to SDSP would enable identification of subjects at enhanced risk for development of HIV-SDSP and facilitate intervention studies with the ultimate goal of disease prevention. Asymptomatic signs of sensory dysfunction in the feet have been shown to be weakly predictive of SDSP; however, bedside evaluation of small sensory fibers is limited. Abnormality of these fibers may play an important role in the genesis of SDSP.
Fifty-eight HIV-infected subjects underwent serial clinical, virologic, immunologic, skin biopsy, and QST assessments. Cox proportional hazards modeling was used to examine the associations of serial ENF density and QST assessments with the risk of development of SDSP among the subset of 26 subjects who had asymptomatic or no neuropathy at study entry.
Median follow-up was 2.9 years (range 6 months to 4.5 years) during which 19 of 26 subjects transitioned to SDSP. Using a model where ENF density and QST measures from the study visit before potential transition were examined, a lower leg ENF density, a higher cooling threshold, and a higher heat pain threshold for minimal pain (HP 0.5) were associated with a greater risk of SDSP in univariate analyses. In multiple regression analyses, leg ENF density but not QST measures were significantly associated with SDSP. A leg ENF density of 10 fibers/mm or less conferred a 14-fold greater risk of SDSP than a leg ENF density greater than 10 fibers/mm.
Measures of small sensory fibers (leg epidermal nerve fiber density, cooling and heat pain thresholds) seem to be associated with transition to symptomatic HIV-associated distal sensory neuropathy 6 to 12 months later.
研究连续评估的表皮神经纤维(ENF)密度和定量感觉阈值(QST)是否与从无神经病变或无症状神经病变的HIV感染向有症状的远端感觉神经病变(SDSP)的临床转变相关。
识别向SDSP转变的预测因素将有助于确定发生HIV-SDSP风险增加的受试者,并促进以疾病预防为最终目标的干预研究。足部感觉功能障碍的无症状体征已被证明对SDSP的预测性较弱;然而,床边对小感觉纤维的评估有限。这些纤维的异常可能在SDSP的发生中起重要作用。
58名HIV感染受试者接受了系列临床、病毒学、免疫学、皮肤活检和QST评估。采用Cox比例风险模型,在研究开始时无症状或无神经病变的26名受试者亚组中,检验系列ENF密度和QST评估与发生SDSP风险之间的关联。
中位随访时间为2.9年(范围6个月至4.5年),在此期间,26名受试者中有19名转变为SDSP。在一个模型中,对潜在转变前研究访视时的ENF密度和QST测量值进行了检查,在单变量分析中,小腿ENF密度降低、冷觉阈值升高和最小疼痛热痛阈值(HP 0.5)升高与SDSP风险增加相关。在多元回归分析中,小腿ENF密度而非QST测量值与SDSP显著相关。小腿ENF密度为10根纤维/mm或更低时,发生SDSP的风险比小腿ENF密度大于10根纤维/mm时高14倍。
小感觉纤维测量值(小腿表皮神经纤维密度、冷觉和热痛阈值)似乎与6至12个月后向有症状的HIV相关远端感觉神经病变的转变相关。