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在快速进展性痴呆的临床队列中,脑脊液 SNAP-25 和神经颗粒蛋白在克雅氏病中的诊断和预后价值。

Diagnostic and prognostic value of cerebrospinal fluid SNAP-25 and neurogranin in Creutzfeldt-Jakob disease in a clinical setting cohort of rapidly progressive dementias.

机构信息

Department of Biomedical and Neuromotor Sciences (DiBiNeM), University of Bologna, Bologna, Italy.

IRCCS, Istituto delle Scienze Neurologiche di Bologna, Programma Neuropatologia delle Malattie Neurodegenerative, Bologna, Italy.

出版信息

Alzheimers Res Ther. 2023 Sep 8;15(1):150. doi: 10.1186/s13195-023-01300-y.

Abstract

BACKGROUND

The levels of synaptic markers synaptosomal-associated protein 25 (SNAP-25) and neurogranin (Ng) have been shown to increase early in the cerebrospinal fluid (CSF) of patients with Creutzfeldt-Jakob disease (CJD) and to have prognostic potential. However, no validation studies assessed these biomarkers' diagnostic and prognostic value in a large clinical setting cohort of rapidly progressive dementia.

METHODS

In this retrospective study, using commercially available immunoassays, we measured the levels of SNAP-25, Ng, 14-3-3, total-tau (t-tau), neurofilament light chain (NfL), and phospho-tau181 (p-tau) in CSF samples from consecutive patients with CJD (n = 220) or non-prion rapidly progressive dementia (np-RPD) (n = 213). We evaluated and compared the diagnostic accuracy of each CSF biomarker and biomarker combination by receiver operating characteristics curve (ROC) analyses, studied SNAP-25 and Ng CSF concentrations distribution across CJD subtypes, and estimated their association with survival using multivariable Cox regression analyses.

RESULTS

CSF SNAP-25 and Ng levels were higher in CJD than in np-RPD (SNAP-25: 582, 95% CI 240-1250 vs. 115, 95% CI 78-157 pg/ml, p < 0.0001; Ng: 841, 95% CI 411-1473 vs. 390, 95% CI 260-766 pg/ml, p < 0.001). SNAP-25 diagnostic accuracy (AUC 0.902, 95% CI 0.873-0.931) exceeded that of 14-3-3 (AUC 0.853, 95% CI 0.816-0.889), t-tau (AUC 0.878, 95% CI 0.845-0.901), and the t-tau/p-tau ratio (AUC 0.884, 95% CI 0.851-0.916). In contrast, Ng performed worse (AUC 0.697, 95% CI 0.626-0.767) than all other surrogate biomarkers, except for NfL (AUC 0.649, 95% CI 0.593-0.705). SNAP-25 maintained a relatively high diagnostic value even for atypical CJD subtypes (AUC 0.792, 95% CI 0.729-0.854). In Cox regression analyses, SNAP-25 levels were significantly associated with survival in CJD (hazard ratio [HR] 1.71 95% CI 1.40-2.09). Conversely, Ng was associated with survival only in the most rapidly progressive CJD subtypes (sCJD MM(V)1 and gCJD M1) (HR 1.81 95% CI 1.21-2.93).

CONCLUSIONS

In the clinical setting, CSF SNAP-25 is a viable alternative to t-tau, 14-3-3, and the t-tau/p-tau ratio in discriminating the CJD subtypes from other RPDs. Additionally, SNAP-25 and, to a lesser extent, Ng predict survival in CJD, showing prognostic power in the range of CSF t-tau/14-3-3 and NfL, respectively.

摘要

背景

突触相关蛋白 25(SNAP-25)和神经颗粒蛋白(Ng)的突触水平已在克雅氏病(CJD)患者的脑脊液(CSF)中早期升高,并具有预后潜力。然而,没有验证研究评估这些生物标志物在快速进行性痴呆的大型临床队列中的诊断和预后价值。

方法

在这项回顾性研究中,我们使用商业上可获得的免疫测定法,测量了连续的 CJD 患者(n=220)或非朊病毒快速进行性痴呆(np-RPD)患者(n=213)的 CSF 样本中 SNAP-25、Ng、14-3-3、总 tau(t-tau)、神经丝轻链(NfL)和磷酸化 tau181(p-tau)的水平。我们通过接收者操作特征曲线(ROC)分析评估和比较每个 CSF 生物标志物和生物标志物组合的诊断准确性,研究了 CJD 亚型之间 SNAP-25 和 Ng CSF 浓度的分布,并使用多变量 Cox 回归分析估计了它们与存活的相关性。

结果

CJD 患者的 CSF SNAP-25 和 Ng 水平高于 np-RPD(SNAP-25:582,95%CI 240-1250 与 115,95%CI 78-157 pg/ml,p<0.0001;Ng:841,95%CI 411-1473 与 390,95%CI 260-766 pg/ml,p<0.001)。SNAP-25 的诊断准确性(AUC 0.902,95%CI 0.873-0.931)超过了 14-3-3(AUC 0.853,95%CI 0.816-0.889)、t-tau(AUC 0.878,95%CI 0.845-0.901)和 t-tau/p-tau 比值(AUC 0.884,95%CI 0.851-0.916)。相比之下,除了 NfL(AUC 0.649,95%CI 0.593-0.705)外,Ng 的表现(AUC 0.697,95%CI 0.626-0.767)比所有其他替代生物标志物都差。即使对于非典型 CJD 亚型,SNAP-25 也保持了相对较高的诊断价值(AUC 0.792,95%CI 0.729-0.854)。在 Cox 回归分析中,SNAP-25 水平与 CJD 患者的存活显著相关(HR 1.71,95%CI 1.40-2.09)。相反,Ng 仅与最快速进展性 CJD 亚型(sCJD MM(V)1 和 gCJD M1)相关(HR 1.81,95%CI 1.21-2.93)。

结论

在临床环境中,CSF SNAP-25 是区分 CJD 亚型与其他 RPD 的 t-tau、14-3-3 和 t-tau/p-tau 比值的可行替代物。此外,SNAP-25 和在较小程度上 Ng 预测了 CJD 的存活,分别在 CSF t-tau/14-3-3 和 NfL 的范围内显示出预后能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5705/10485978/b5d81aa4e5d5/13195_2023_1300_Fig1_HTML.jpg

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