Nolano Maria, Manganelli Fiore, Provitera Vincenzo, Pisciotta Chiara, Stancanelli Annamaria, Caporaso Giuseppe, Iodice Rosa, Shy Michael E, Santoro Lucio
From the Neurology Division (M.N., V.P., A.S., G.C.), "Salvatore Maugeri" Foundation, Institute of Telese Terme; the Department of Neurosciences, Reproductive and Odontostomatological Sciences (F.M., C.P., R.I., L.S.), University Federico II of Naples, Italy; and the Department of Neurology (M.E.S.), University of Iowa, Iowa City.
Neurology. 2015 Jan 27;84(4):407-14. doi: 10.1212/WNL.0000000000001188. Epub 2014 Dec 24.
To assess the involvement of small nerve fibers in Charcot-Marie-Tooth type 1A (CMT1A).
We used indirect immunofluorescence and confocal microscopy on punch biopsies from glabrous (fingertip) and hairy (thigh and leg) skin of 20 unrelated patients with CMT1A to quantify somatic and autonomic nerve fibers. In particular, we quantified epidermal nerve fibers (ENF), Meissner corpuscles (MC), intrapapillary myelinated endings (IME), and sudomotor nerves. We correlated morphologic data with findings from quantitative sensory testing, sudomotor output, sympathetic skin response, and cardiovascular reflexes. A control population of healthy age- and sex-matched controls was included with a matching ratio of 1:2.
We found a length-dependent loss of ENFs that worsened with aging. We also observed a loss of MCs, IMEs, and sudomotor nerves. The loss of ENF at distal leg correlated with the increase in heat-pain thresholds (p < 0.05) and with tactile thresholds (p < 0.05). Sudomotor nerve fiber loss correlated with ENF density (p < 0.05) and sweating output (p < 0.001).
We demonstrated through morphologic, physical, and psychophysical testing that small somatic and autonomic fibers are abnormal and cause symptoms in patients with CMT1A. Awareness of such symptoms by the clinician could lead to better treatment.
评估小神经纤维在1A型遗传性运动感觉神经病(CMT1A)中的受累情况。
我们对20例无亲缘关系的CMT1A患者的无毛(指尖)和有毛(大腿和小腿)皮肤进行打孔活检,采用间接免疫荧光和共聚焦显微镜技术对躯体和自主神经纤维进行定量分析。具体而言,我们对表皮神经纤维(ENF)、迈斯纳小体(MC)、乳头内有髓神经末梢(IME)和汗腺运动神经进行了定量分析。我们将形态学数据与定量感觉测试、汗腺运动输出、交感皮肤反应和心血管反射的结果进行了关联分析。纳入了年龄和性别匹配的健康对照人群,匹配比例为1:2。
我们发现ENF存在长度依赖性丢失,且随着年龄增长而加重。我们还观察到MC、IME和汗腺运动神经的丢失。小腿远端ENF的丢失与热痛阈值升高(p < 0.05)和触觉阈值升高(p < 0.05)相关。汗腺运动神经纤维丢失与ENF密度(p < 0.05)和出汗量(p < 0.001)相关。
我们通过形态学、物理和心理物理学测试证明,CMT1A患者的小躯体和自主神经纤维异常并导致症状。临床医生意识到这些症状可能会带来更好的治疗效果。