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FKRP 相关肌营养不良症患者的诊断延误。

Diagnostic delay in patients with FKRP-related muscular dystrophy.

机构信息

University of Iowa Carver College of Medicine, 375 Newton Rd, Iowa City, IA 52242, USA.

Department of Pediatrics, University of Iowa Carver College of Medicine, 200 Hawkins Drive Iowa City, IA 52242, USA.

出版信息

Neuromuscul Disord. 2021 Dec;31(12):1235-1240. doi: 10.1016/j.nmd.2021.08.013. Epub 2021 Sep 6.

Abstract

Diagnostic journey for people with FKRP mutations participating in a dystroglycanopathy natural history study (n = 68; NCT00313677) was analyzed. Earliest symptoms and age at muscular dystrophy diagnosis were abstracted from subject-reported medical history and record review. Initial signs/symptoms were classified as chronic motor dysfunction (e.g., delayed motor milestones, weakness, falling; n = 40, 59%), elevated transaminases (n = 7, 10%), or acute/intermittent symptoms (myoglobinuria, myalgia, febrile illness-associated acute weakness; n = 21, 31%). Median time from sign/symptom onset to diagnosis was 6.5 years and differed by symptom group: 7.5 years for motor group, 9 years for acute/intermittent group, and 4 years for elevated transaminases group. The sign/symptom category that most commonly resulted in a diagnosis was chronic motor dysfunction (n = 45). Of those without clear weakness as first symptom (n = 55), 36.4% were not diagnosed with MD until weakness became apparent. Median time to diagnosis was shortest for those with febrile illness-associated acute weakness (0.25 years). Median time from first sign/symptom to MD diagnosis has decreased incrementally from 18.8 years for those with onset in the 1970s to < 10 years for symptom onset occurring after 2000. Awareness of disease presentation variability will aid in earlier diagnosis, which is increasingly important with treatments in development.

摘要

对参与肌营养不良聚糖病自然史研究的 FKRP 基因突变患者(n=68;NCT00313677)的诊断过程进行了分析。从受试者报告的病史和记录回顾中提取最早的症状和肌营养不良症诊断年龄。初始体征/症状分为慢性运动功能障碍(例如,运动发育迟缓、无力、跌倒;n=40,59%)、转氨酶升高(n=7,10%)或急性/间歇性症状(肌红蛋白尿、肌痛、发热性疾病相关急性无力;n=21,31%)。从出现症状到诊断的中位时间为 6.5 年,且因症状组而异:运动组为 7.5 年,急性/间歇性组为 9 年,转氨酶升高组为 4 年。最常导致诊断的症状类别是慢性运动功能障碍(n=45)。在没有明显无力作为首发症状的患者中(n=55),36.4%的患者直到明显出现无力才被诊断为肌营养不良症。发热性疾病相关急性无力患者的诊断中位时间最短(0.25 年)。从首次出现症状到肌营养不良症诊断的中位时间从 20 世纪 70 年代发病的患者的 18.8 年逐渐缩短到 21 世纪后发病的患者的<10 年。了解疾病表现的变异性将有助于更早地诊断疾病,这在治疗方法不断发展的情况下变得越来越重要。

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