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CLN3 病的诊断置信度方案。

A diagnostic confidence scheme for CLN3 disease.

机构信息

Department of Neurology, University of Rochester, Rochester, New York, USA.

Kennedy Krieger Institute, Baltimore, Maryland, USA.

出版信息

J Inherit Metab Dis. 2021 Nov;44(6):1453-1462. doi: 10.1002/jimd.12429. Epub 2021 Sep 7.

Abstract

Over the past 20 years, diagnostic testing for genetic diseases has evolved, leading to variable diagnostic certainty for individuals included in long-term natural history studies. Using genotype and phenotype data from an ongoing natural history study of CLN3 disease, we developed a hierarchical diagnostic confidence scheme with three major classes: Definite, Probable, or Possible CLN3 disease. An additional level, CLN3 Disease PLUS, includes individuals with CLN3 disease plus an additional disorder with a separate etiology that substantially affects the phenotype. Within the Definite and Probable CLN3 disease classes, we further divided individuals into subclasses based on phenotype. After assigning participants to classes, we performed a blinded reclassification to assess the reliability of this scheme. A total of 134 individuals with suspected CLN3 disease were classified: 100 as Definite, 21 as Probable, and 7 as Possible. Six individuals were classified as CLN3-PLUS. Phenotypes included the classical juvenile-onset syndromic phenotype, a "vision loss only" phenotype, and an atypical syndromic phenotype. Some individuals were too young to fully classify phenotype. Test-retest reliability showed 96% agreement. We created a reliable diagnostic confidence scheme for CLN3 disease that has excellent face validity. This scheme has implications for clinical research in CLN3 and other rare genetic neurodegenerative disorders.

摘要

在过去的 20 年中,遗传性疾病的诊断检测技术不断发展,导致长期自然病史研究中纳入的个体的诊断确定性存在差异。我们利用正在进行的 CLN3 疾病自然病史研究中的基因型和表型数据,制定了一个三级诊断置信方案,分为三个主要类别:明确的、可能的或可能的 CLN3 疾病。另外一个级别 CLN3 疾病 PLUS,包括 CLN3 疾病加上另一种具有独立病因的疾病的个体,该疾病对表型有实质性影响。在明确和可能的 CLN3 疾病类别中,我们根据表型进一步将个体分为亚类。在为参与者分配类别后,我们进行了盲法重新分类,以评估该方案的可靠性。共有 134 名疑似 CLN3 疾病的个体被分类:100 名明确,21 名可能,7 名可能。有 6 名被归类为 CLN3-PLUS。表型包括经典的青少年发病综合征表型、“仅视力丧失”表型和非典型综合征表型。一些个体年龄太小,无法完全分类表型。测试-重测可靠性显示 96%的一致性。我们为 CLN3 疾病制定了一个可靠的诊断置信方案,具有极好的表面效度。该方案对 CLN3 及其他罕见遗传性神经退行性疾病的临床研究具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d90/9248362/d82486527414/nihms-1761222-f0001.jpg

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