Department of Microbiology, Immunology, and Molecular Genetics, David Geffen School of Medicine and College of Letters and Sciences, University of California, Los Angeles, Los Angeles, California, USA.
Department of Pediatrics, University of California, Los Angeles, Los Angeles, California, USA.
Muscle Nerve. 2020 Dec;62(6):688-698. doi: 10.1002/mus.27041. Epub 2020 Sep 20.
Serial muscle biopsies within clinical trials for Duchenne muscular dystrophy (DMD) are critical to document therapeutic responses. Less invasive means of sampling muscle are needed. We analyzed a retrospective consecutive case-series cohort of vacuum-assisted core needle muscle biopsy procedures performed on healthy and dystrophic individuals at a single institution assessing for safety and reliability of obtaining sufficient high-quality biopsy tissue for histologic assessment in adult and pediatric subjects. Of 471 muscle cores from 128 biopsy procedures, 377-550 mg of total muscle tissue was obtained per procedure with mean core weight of 129 mg (SD, 25.1 mg). All biopsies were adequate for histological assessment. There were no significant adverse events. This core needle biopsy approach, when combined with improved sample processing, provides a safe means to consistently obtain muscle samples for diagnostic and clinical trial applications.
在针对杜氏肌营养不良症 (DMD) 的临床试验中进行连续肌肉活检对于记录治疗反应至关重要。需要更微创的肌肉采样方法。我们分析了单家机构进行的真空辅助核心针肌肉活检程序的回顾性连续病例系列队列,以评估在成人和儿科受试者中获取足够高质量活检组织进行组织学评估的安全性和可靠性。在 128 次活检程序中,共获得了 471 个肌肉核心,每个程序获得的总肌肉组织量为 377-550mg,平均核心重量为 129mg(标准差,25.1mg)。所有活检均足以进行组织学评估。没有发生重大不良事件。这种核心针活检方法与改进的样本处理相结合,为诊断和临床试验应用提供了一种安全的方法来持续获得肌肉样本。