Tanveer Nadeem, Sharma Mehar C, Sarkar Chitra, Gulati Sheffali, Kalra Veena, Singh Sumit, Bhatia Rohit
Department of Pathology, All India Institute of Medical Sciences (AIIMS), New Delhi 110029, India.
Clin Neurol Neurosurg. 2009 Jul;111(6):496-502. doi: 10.1016/j.clineuro.2009.01.011. Epub 2009 Feb 28.
Muscle biopsy is an important diagnostic modality and screening test for the diagnosis of dystrophinopathies. Sometimes muscle biopsies are needed for the diagnosis when genetic tests are inconclusive and are also useful for immunoblotting assay of the dystrophin protein. However, the procedure is painful, requires anesthesia and sometimes needs to be repeated. This study was undertaken to elucidate the role of skin biopsy in the diagnosis of dystrophinopathies and to validate if it can be utilized as a useful adjunct/replacement for the muscle biopsy.
Paired skin and muscle biopsies were studied from 39 patients with Duchenne muscular dystrophy (DMD), 4 patients with Becker's muscular dystrophy (BMD) and 37 controls. Immunostaining for dystrophin and utrophin was done on frozen sections of the test group and controls and their staining pattern in skin biopsies was compared with corresponding muscle biopsies.
Immunostaining for dystrophin was negative in the skin biopsies of all patients (39/39, 100%) with DMD and was only weakly expressed in skin of BMD patients (4/4, 100%). Dystrophin was strongly expressed on arrector pili muscle cells of all control patients (94.6%) except two cases in whom it was weakly expressed. Utrophin was expressed on the arrector pili muscle cells of DMD patients (39/39, 100%) as well as controls (30/37, 81.1%).
Our study suggests that skin biopsy is very useful for the diagnosis of dystrophinopathies and their differentiation from other muscle diseases. It has high degrees of sensitivity, specificity, and positive and negative predictive values. It can be a useful adjunct/replacement for the muscle biopsy especially when repeated biopsies are required for monitoring therapy or in patients with advanced DMD where extreme fibrosis, adipose tissue infiltration and inflammation make interpretation of the muscle biopsy difficult. Skin biopsy is a simple, cost effective, less invasive and less traumatic diagnostic procedure when compared with muscle biopsy. This is even more pertinent because patients with muscular dystrophies have a higher risk for any form of general anesthesia. A smaller scar and fewer chances of infection at the site of biopsy are other additional advantages of skin biopsy over muscle biopsy.
肌肉活检是诊断肌营养不良症的重要诊断方法和筛查试验。当基因检测结果不明确时,有时需要进行肌肉活检来辅助诊断,并且肌肉活检对于肌营养不良蛋白的免疫印迹分析也很有用。然而,该操作会带来疼痛,需要麻醉,有时还需要重复进行。本研究旨在阐明皮肤活检在肌营养不良症诊断中的作用,并验证其是否可作为肌肉活检的有用辅助手段/替代方法。
对39例杜氏肌营养不良症(DMD)患者、4例贝克型肌营养不良症(BMD)患者和37例对照者进行了配对的皮肤和肌肉活检。对试验组和对照组的冰冻切片进行肌营养不良蛋白和抗肌萎缩蛋白聚糖的免疫染色,并将皮肤活检中的染色模式与相应的肌肉活检进行比较。
所有DMD患者(39/39,100%)的皮肤活检中肌营养不良蛋白免疫染色均为阴性,而BMD患者的皮肤中仅微弱表达(4/4,100%)。除两例微弱表达外,所有对照患者(94.6%)的立毛肌细胞上肌营养不良蛋白均呈强表达。抗肌萎缩蛋白聚糖在DMD患者(39/39,100%)以及对照者(30/37,81.1%)的立毛肌细胞上均有表达。
我们的研究表明,皮肤活检对于肌营养不良症的诊断及其与其他肌肉疾病的鉴别非常有用。它具有高度的敏感性、特异性以及阳性和阴性预测值。它可以作为肌肉活检的有用辅助手段/替代方法,特别是在需要重复活检以监测治疗时,或者在晚期DMD患者中,极度纤维化、脂肪组织浸润和炎症使肌肉活检的解读变得困难时。与肌肉活检相比,皮肤活检是一种简单、经济有效、侵入性较小且创伤较小的诊断方法。这一点更为重要,因为肌营养不良症患者接受任何形式全身麻醉的风险更高。皮肤活检在活检部位留下的疤痕较小且感染几率较低,这是相对于肌肉活检的其他额外优势。