Department of Neurosciences, Biomedicine, and Movement Sciences, University of Verona, Policlinico G. B. Rossi, Verona, Italy.
Laboratory of Persistent Viral Diseases, Rocky Mountain Laboratories, National Institute for Allergy and Infectious Diseases, National Institutes of Health, Hamilton, Montana.
JAMA Neurol. 2017 Feb 1;74(2):155-162. doi: 10.1001/jamaneurol.2016.4614.
Early and accurate in vivo diagnosis of Creutzfeldt-Jakob disease (CJD) is necessary for quickly distinguishing treatable from untreatable rapidly progressive dementias and for future therapeutic trials. This early diagnosis is becoming possible using the real-time quaking-induced conversion (RT-QuIC) seeding assay, which detects minute amounts of the disease-specific pathologic prion protein in cerebrospinal fluid (CSF) or olfactory mucosa (OM) samples.
To develop an algorithm for accurate and early diagnosis of CJD by using the RT-QuIC assay on CSF samples, OM samples, or both.
DESIGN, SETTING, AND PARTICIPANTS: In this case-control study, samples of CSF and OM were collected from 86 patients with a clinical diagnosis of probable (n = 51), possible (n = 24), or suspected (n = 11) CJD and 104 negative control samples (54 CSF and 50 OM). The CSF and OM samples were analyzed using conventional RT-QuIC. The CSF samples underwent further testing using improved RT-QuIC conditions. In addition, the diagnostic performance of a novel, easy-to-use, gentle flocked swab for sampling of OM was evaluated. Data were collected from January 1 to June 30, 2015.
Correlations between RT-QuIC results and the final diagnosis of recruited patients.
Among the 86 patients (37 men [43%] and 49 women [57%]; mean [SD] age, 65.7 [11.5] years) included for analysis, all 61 patients with sporadic CJD had positive RT-QuIC findings using OM or CSF samples or both for an overall RT-QuIC diagnostic sensitivity of 100% (95% CI, 93%-100%). All patients with a final diagnosis of non-prion disease (71 CSF and 67 OM samples) had negative RT-QuIC findings for 100% specificity (95% CI, 94%-100%). Of 8 symptomatic patients with various mutations causing CJD or Gerstmann-Sträussler-Scheinker syndrome, 6 had positive and 2 had negative RT-QuIC findings for a sensitivity of 75% (95% CI, 36%-96%).
A proposed diagnostic algorithm for sporadic CJD combines CSF and OM RT-QuIC testing to provide virtually 100% diagnostic sensitivity and specificity in the clinical phase of the disease.
快速准确的体内诊断克雅氏病(CJD)对于快速区分可治疗和不可治疗的快速进行性痴呆症以及未来的治疗试验非常必要。这种早期诊断使用实时震颤诱导转换(RT-QuIC)种子测定法成为可能,该方法可以检测到脑脊液(CSF)或嗅粘膜(OM)样本中微量的疾病特异性病理朊病毒蛋白。
通过使用 CSF 样本、OM 样本或两者的 RT-QuIC 测定法开发用于 CJD 准确和早期诊断的算法。
设计、地点和参与者:在这项病例对照研究中,从 86 名临床诊断为可能(n=51)、可能(n=24)或疑似(n=11)CJD 的患者和 104 名阴性对照样本(54 个 CSF 和 50 个 OM)中收集了 CSF 和 OM 样本。CSF 和 OM 样本使用常规 RT-QuIC 进行分析。CSF 样本进一步使用改良的 RT-QuIC 条件进行测试。此外,还评估了一种新型、易于使用、温和的植绒拭子用于 OM 采样的诊断性能。数据收集于 2015 年 1 月 1 日至 6 月 30 日。
RT-QuIC 结果与招募患者的最终诊断之间的相关性。
在纳入分析的 86 名患者(37 名男性[43%]和 49 名女性[57%];平均[标准差]年龄 65.7[11.5]岁)中,所有 61 名散发型 CJD 患者的 OM 或 CSF 样本或两者的 RT-QuIC 结果均为阳性,总体 RT-QuIC 诊断敏感性为 100%(95%CI,93%-100%)。所有非朊病毒疾病(71 个 CSF 和 67 个 OM 样本)的最终诊断患者的 RT-QuIC 结果均为阴性,特异性为 100%(95%CI,94%-100%)。在 8 名有各种导致 CJD 或 Gerstmann-Straussler-Scheinker 综合征的基因突变的有症状患者中,6 名患者的 RT-QuIC 结果为阳性,2 名患者的 RT-QuIC 结果为阴性,敏感性为 75%(95%CI,36%-96%)。
针对散发型 CJD 的拟议诊断算法结合了 CSF 和 OM RT-QuIC 检测,在疾病的临床阶段提供了几乎 100%的诊断敏感性和特异性。