CSF Tau proteins reduce misdiagnosis of sporadic Creutzfeldt-Jakob disease suspected cases with inconclusive 14-3-3 result

被引:5
作者
Leito, M. J. [1 ,5 ]
Baldeiras, I. [1 ,4 ,5 ]
Almeida, M. R. [5 ]
Ribeiro, M. H. [1 ,4 ]
Santos, A. C. [5 ]
Ribeiro, M. [5 ]
Tomas, J. [2 ]
Rocha, S. [3 ]
Santana, I. [2 ,4 ,5 ]
Oliveira, C. R. [1 ,2 ,4 ,5 ]
机构
[1] Ctr Hosp & Univ Coimbra, Dept Neurol, Univ Hosp Coimbra, Neurochem Lab, Praceta Mota Pinto, P-3000075 Coimbra, Portugal
[2] Ctr Hosp & Univ Coimbra, Dept Neurol, Univ Hosp Coimbra, P-3000075 Coimbra, Portugal
[3] St Marcos Hosp, Dept Neurol, P-4710243 Braga, Portugal
[4] Univ Coimbra, Fac Med, Polo 3, P-3000548 Coimbra, Portugal
[5] Univ Coimbra, CNC IBILI Ctr Neurosci & Cell Biol, Rua Larga,1st Floor, P-3004504 Coimbra, Portugal
关键词
sCJD; CSF; 14-3-3; protein; Biomarkers; Tau protein; Phosphorylated Tau protein; CEREBROSPINAL-FLUID; DIFFERENTIAL-DIAGNOSIS; 14-3-3-PROTEIN; MARKERS; ASSAY; ASSOCIATION; VARIANT; CJD;
D O I
10.1007/s00415-016-8209-x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Cerebrospinal fluid (CSF) 14-3-3 protein supports sporadic Creutzfeldt-Jakob (sCJD) diagnosis, but often leads to weak-positive results and lacks standardization. In this study, we explored the added diagnostic value of Total Tau (t-Tau) and phosphorylated Tau (p-Tau) in sCJD diagnosis, particularly in the cases with inconclusive 14-3-3 result. 95 definite sCJD and 287 patients without prion disease (non-CJD) were included in this study. CSF samples were collected in routine clinical diagnosis and analysed for 14-3-3 detection by Western blot (WB). CSF t-Tau and p-Tau were quantified by commercial ELISA kits and PRNP and APOE genotyping assessed by PCR-RFLP. In a regression analysis of the whole cohort, 14-3-3 protein revealed an overall accuracy of 82 % (sensitivity = 96.7 %; specificity = 75.6 %) for sCJD. Regarding 14-3-3 clear positive results, we observed no added value either of t-Tau alone or p-Tau/t-Tau ratio in the model. On the other hand, considering 14-3-3 weak-positive cases, t-Tau protein increased the overall accuracy of 14-3-3 alone from 91 to 94 % and specificity from 74 to 93 % (p < 0.05), with no sensitivity improvement. However, inclusion of p-Tau/t-Tau ratio did not significantly improve the first model (p = 0.0595). Globally, t-Tau protein allowed a further discrimination of 65 % within 14-3-3 inconclusive results. Furthermore, PRNP MV genotype showed a trend to decrease 14-3-3 sensitivity (p = 0.051), but such effect was not seen on t-Tau protein. In light of these results, we suggest that t-Tau protein assay is of significant importance as a second marker in identifying 14-3-3 false-positive results among sCJD probable cases.
引用
收藏
页码:1847 / 1861
页数:15
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