...
首页> 外文期刊>Acta Neuropathologica >Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA
【24h】

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

机译:人类病毒疾病组织型的共识分类可可靠鉴定分子亚型:欧洲和美国监测中心之间的评估者间研究

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The current classification of human sporadic prion diseases recognizes six major phenotypic subtypes with distinctive clinicopathological features, which largely correlate at the molecular level with the genotype at the polymorphic codon 129 (methionine, M, or valine, V) in the prion protein gene and with the size of the protease-resistant core of the abnormal prion protein, PrPSc (i.e. type 1 migrating at 21 kDa and type 2 at 19 kDa). We previously demonstrated that PrPSc typing by Western blotting is a reliable means of strain typing and disease classification. Limitations of this approach, however, particularly in the interlaboratory setting, are the association of PrPSc types 1 or 2 with more than one clinicopathological phenotype, which precludes definitive case classification if not supported by further analysis, and the difficulty of fully recognizing cases with mixed phenotypic features. In this study, we tested the inter-rater reliability of disease classification based only on histopathological criteria. Slides from 21 cases covering the whole phenotypic spectrum of human sporadic prion diseases, and also including two cases of variant Creutzfeldt–Jakob disease (CJD), were distributed blindly to 13 assessors for classification according to given instructions. The results showed good-to-excellent agreement between assessors in the classification of cases. In particular, there was full agreement (100 %) for the two most common sporadic CJD subtypes and variant CJD, and very high concordance in general for all pure phenotypes and the most common subtype with mixed phenotypic features. The present data fully support the basis for the current classification of sporadic human prion diseases and indicate that, besides molecular PrPSc typing, histopathological analysis permits reliable disease classification with high interlaboratory accuracy.
机译:当前的人类散发性病毒疾病分类识别出六种具有独特临床病理特征的主要表型亚型,它们在分子水平上与the病毒蛋白基因中多态性密码子129(蛋氨酸,M或缬氨酸,V)的基因型相关,并与P病毒异常蛋白PrP Sc 的蛋白酶抗性核心的大小(即1型以21 kDa迁移,2型以19 kDa迁移)。我们先前证明,通过蛋白质印迹法进行的PrP Sc 分型是菌株分型和疾病分类的可靠方法。但是,这种方法的局限性,特别是在实验室间环境中,是PrP Sc 类型1或2与不止一种临床病理表型的关联,如果没有进一步分析的支持,则无法进行明确的病例分类,并且难以完全识别具有混合表型特征的病例。在这项研究中,我们仅根据组织病理学标准测试了疾病分类的评分间可靠性。根据给定的说明,将21例涵盖人类散发性病毒疾病的整个表型谱的幻灯片,还包括2例变异的Creutzfeldt–Jakob疾病(CJD)的幻灯片,盲目分发给13个评估者进行分类。结果表明,评估者之间在案件分类方面达成了良好至卓越的协议。特别是,两种最常见的散发性CJD亚型和变异型CJD完全一致(100%),并且对于所有纯表型和具有混合表型特征的最常见亚型,总体上具有很高的一致性。目前的数据完全支持当前的零星人类病毒疾病分类的基础,并表明,除了分子PrP Sc 分型之外,组织病理学分析还可以实现可靠的疾病分类,并且具有较高的实验室间准确性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号