National Prion Clinic, University College London (UCL) Hospitals NHS Foundation Trust, London, UK.
MRC Prion Unit at UCL, Institute of Prion Diseases, 33 Cleveland Street, London, W1W 7FF, UK.
Eur J Hum Genet. 2022 Oct;30(10):1167-1170. doi: 10.1038/s41431-022-01132-8. Epub 2022 Jun 27.
Inherited prion diseases (IPD) are a set of rare neurodegenerative diseases that are always caused by mutation of the prion protein gene (PRNP). These are highly heterogeneous in clinical presentation and best described by the specific gene mutation, but traditionally include the canonical syndromes familial Creutzfeldt-Jakob disease, Gerstamann-Straussler-Scheinker syndrome, and fatal familial insomnia. In the UK, care of IPD patients and clinical PRNP sequencing have been carried out almost exclusively by the National Prion Clinic and affiliated laboratories since the disease gene was discovered in 1989. Using data obtained over 30 years (1990-2019), this study aimed to provide a greater understanding of the genetic prevalence of IPD using multiple complementary methods. A key source of bias in rare disorders is ascertainment, so we included an analysis based on capture-recapture techniques that may help to minimise ascertainment bias. 225 patients, with 21 different IPD mutations were identified, varying in frequency (with 8/21 mutations comprising over 90% observed cases), derived from 116 kindreds and 151 3-generation families. We estimated a total of 303 UK families (95% CI = 222, 384) segregate IPD mutations, 1091 (95% CI = 720, 1461) UK mutation carriers and a lifetime risk of approximately 1 in 60,000. Simpler methods of measuring prevalence based on extrapolation from the annual incidence of disease, and large scale genomic studies, result in similar estimates of prevalence. These estimates may be of value for planning preventive trials of therapeutics in IPD mutation carriers, prevention of prion disease transmission and provision of specialist services.
遗传性朊病毒病(IPD)是一组罕见的神经退行性疾病,始终由朊病毒蛋白基因(PRNP)突变引起。这些疾病在临床表现上高度异质,最好通过特定的基因突变来描述,但传统上包括经典综合征家族性克雅氏病、Gerstamann-Straussler-Scheinker 综合征和致命性家族性失眠症。自 1989 年发现疾病基因以来,英国的 IPD 患者护理和临床 PRNP 测序几乎完全由国家朊病毒诊所和附属实验室进行。利用 30 多年(1990-2019 年)获得的数据,本研究旨在使用多种互补方法,更好地了解 IPD 的遗传流行率。在罕见疾病中,偏倚的一个关键来源是确定,因此我们进行了基于捕获-再捕获技术的分析,这可能有助于最小化确定偏倚。确定了 225 名患者,其中有 21 种不同的 IPD 突变,其频率各不相同(8/21 种突变占观察到的病例的 90%以上),源自 116 个家系和 151 个 3 代家族。我们估计共有 303 个英国家族(95%CI=222,384)遗传 IPD 突变,1091 个(95%CI=720,1461)英国突变携带者,终生风险约为每 60000 人中有 1 人。基于疾病年发病率推断的简单流行率测量方法和大规模基因组研究,得出的流行率估计相似。这些估计可能对规划 IPD 突变携带者的治疗预防性试验、预防朊病毒病传播和提供专业服务具有价值。