McArthur J C, Stocks E A, Hauer P, Cornblath D R, Griffin J W
Department of Neurology, The Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Arch Neurol. 1998 Dec;55(12):1513-20. doi: 10.1001/archneur.55.12.1513.
The sensitivity of neuron-specific antibodies permit the identification of the small unmyelinated nerve fibers within the skin.
To develop a reference range of epidermal nerve fiber density in humans, and to evaluate their diagnostic efficiency for sensory neuropathies.
Ninety-eight normal controls (age range, 13-82 years) were examined with both directed neurologic examinations and quantitative sensory testing. The diagnostic utility was examined in 20 patients with sensory neuropathies. Each subject had 2 punch biopsies performed at each site in the thigh and distal part of the leg (total of 392 biopsies). After formalin fixation, 50-microm-thick free-floating sections were stained with a polyclonal antibody to neuron-specific ubiquitin hydrolase, anti-protein gene product 9.5. We enumerated intraepidermal nerve fibers per millimeter to derive a "linear density." The linear density technique was validated against a stereological technique that used the fractionator to measure the total length of intraepidermal nerve fibers per 3-mm punch.
The biopsy technique was well tolerated, with no notable complications. The linear density quantitation was rapid and had high intraobserver and interobserver reliability. We determined that the density of intraepidermal fibers in normal controls was 21.1+/-10.4 per millimeter (mean +/- SD) in the thigh (fifth percentile, 5.2 per millimeter), and was 13.8+/-6.7 per millimeter at the distal part of the leg (fifth percentile, 3.8 per millimeter). Significantly higher intraepidermal fiber densities were seen in the youngest group (P = .004), and we observed no significant effect of race, sex, height, or weight. The density at the thigh was significantly correlated with that at the distal part of the leg (P = .01) and was consistently higher by about 60%, a reflection of the normal proximal-distal gradient. The results obtained with stereology and the linear density correlated significantly (P=.001), providing internal validation for the technique. Epidermal nerve fiber density was significantly reduced (P = .001) in patients with sensory neuropathies. With a cutoff derived from the fifth percentile of the normative range for the distal part of the leg, the technique had a positive predictive value of 75%, a negative predictive value of 90%, and a diagnostic efficiency of 88%.
We have established a reference range for intraepidermal nerve fiber density in normal humans by means of a simple quantitation method based on enumeration of individual intraepidermal nerve fibers on vertical sections of punch skin biopsy specimens stained with the sensitive panaxonal marker anti-protein gene product 9.5. The utility of the density measurement was confirmed for sensory neuropathy with a diagnostic efficiency of 88%. Skin biopsies may be useful to assess the spatial distribution of involvement in peripheral nerve disease and the response to neurotrophic and other restorative therapies.
神经元特异性抗体的敏感性使得能够识别皮肤内的无髓小神经纤维。
建立人类表皮神经纤维密度的参考范围,并评估其对感觉神经病的诊断效能。
对98名正常对照者(年龄范围13 - 82岁)进行定向神经学检查和定量感觉测试。对20例感觉神经病患者进行诊断效用评估。每位受试者在大腿和小腿远端的每个部位进行2次钻孔活检(共392次活检)。经福尔马林固定后,用抗神经元特异性泛素水解酶的多克隆抗体、抗蛋白基因产物9.5对50微米厚的游离漂浮切片进行染色。我们计算每毫米表皮内神经纤维数量以得出“线性密度”。线性密度技术与使用分样器测量每3毫米钻孔中表皮内神经纤维总长度的体视学技术进行了验证。
活检技术耐受性良好,无明显并发症。线性密度定量快速,观察者内和观察者间可靠性高。我们确定正常对照者大腿表皮内纤维密度为每毫米21.1±10.4(均值±标准差)(第五百分位数为每毫米5.2),小腿远端为每毫米13.8±6.7(第五百分位数为每毫米3.8)。最年轻组的表皮内纤维密度显著更高(P = 0.004),且我们未观察到种族、性别、身高或体重有显著影响。大腿处的密度与小腿远端的密度显著相关(P = 0.01),且始终高出约60%,反映了正常的近端 - 远端梯度。体视学和线性密度获得的结果显著相关(P = 0.001),为该技术提供了内部验证。感觉神经病患者的表皮神经纤维密度显著降低(P = 0.001)。以小腿远端正常范围第五百分位数得出的临界值,该技术的阳性预测值为75%,阴性预测值为90%,诊断效能为88%。
我们通过一种基于对用敏感的全轴突标记物抗蛋白基因产物9.5染色的钻孔皮肤活检标本垂直切片上的单个表皮内神经纤维进行计数的简单定量方法,建立了正常人类表皮内神经纤维密度的参考范围。密度测量对感觉神经病的效用得到证实,诊断效能为88%。皮肤活检可能有助于评估周围神经疾病受累的空间分布以及对神经营养和其他修复性治疗的反应。