Department of Neurology, Case Western Reserve University & University Hospitals Cleveland Medical, Cleveland, OH 44106, USA.
Department of Pathology, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.
Viruses. 2021 Sep 8;13(9):1794. doi: 10.3390/v13091794.
Genetic prion disease accounts for 10-15% of prion disease. While insertion of four or more octapeptide repeats are clearly pathogenic, smaller repeat insertions have an unclear pathogenicity. The goal of this case series was to provide an insight into the characteristics of the 2-octapeptide repeat genetic variant and to provide insight into the risk for Creutzfeldt-Jakob disease in asymptomatic carriers. 2-octapeptide repeat insertion prion disease cases were collected from the National Prion Disease Pathology Surveillance Center (US), the National Prion Clinic (UK), and the National Creutzfeldt-Jakob Disease Registry (Australia). Three largescale population genetic databases were queried for the 2-octapeptide repeat insertion allele. Eight cases of 2-octapeptide repeat insertion were identified. The cases were indistinguishable from the sporadic Creutzfeldt-Jakob cases of the same molecular subtype. Western blot characterization of the prion protein in the absence of enzymatic digestion with proteinase K revealed that 2-octapeptide repeat insertion and sporadic Creutzfeldt-Jakob disease have distinct prion protein profiles. Interrogation of large-scale population datasets suggested the variant is of very low penetrance. The 2-octapeptide repeat insertion is at most a low-risk genetic variant. Predictive genetic testing for asymptomatic blood relatives is not likely to be justified given the low risk.
遗传性朊病毒病占朊病毒病的 10-15%。虽然插入四个或更多八肽重复显然是致病性的,但较小的重复插入的致病性尚不清楚。本病例系列的目的是深入了解 2-八肽重复遗传变异体的特征,并深入了解无症状携带者患克雅氏病的风险。从美国国家朊病毒疾病病理学监测中心、英国国家朊病毒临床中心和澳大利亚国家克雅氏病登记处收集了 2-八肽重复插入朊病毒病病例。对三个大规模人群遗传数据库进行了 2-八肽重复插入等位基因的查询。鉴定出 8 例 2-八肽重复插入病例。这些病例与同一分子亚型的散发性克雅氏病病例无法区分。在没有用蛋白酶 K 进行酶消化的情况下对朊病毒蛋白进行 Western blot 特征分析表明,2-八肽重复插入和散发性克雅氏病具有不同的朊病毒蛋白谱。对大规模人群数据集的查询表明,该变体的外显率非常低。鉴于风险较低,对于无症状血液亲属进行预测性遗传检测不太可能合理。