Diagnostic value of cerebrospinal fluid tau and real⁃time quaking⁃induced conversion in sporadic Creutzfeldt⁃Jakob disease

Objective To explore the diagnostic value of cerebrospinal fluid (CSF) biomarkers, total tau protein (t‑tau), phosphorylated tau protein 181 (p‑tau181) and real‑time quaking‑induced conversion (RT ‑QuIC) in sporadic Creutzfeldt‑Jakob disease (sCJD). Methods A retrospective study was conducted on 30 patients diagnosed with probable sCJD at Huashan Hospital, Fudan University from April 2020 to November 2022, serving as the sCJD group. Meanwhile, 25 patients diagnosed with rapidly progressive Alzheimer's disease (AD) and 23 patients diagnosed with autoimmune encephalitis (AE), matched for gender and age with the sCJD group, were selected as the AD group and AE group, respectively. CSF t‑tau, p ‑ tau181 and t‑tau/p‑tau181 ratio were collected from the 3 groups. The auxiliary examination data of the sCJD group, including typical manifestations of electroencephalography (EEG) and head MRI, as well as RT‑ QuIC results, were collected with emphasis. Results There were statistically significant differences in CSF t‑tau (χ2 = 38.247, P = 0.000), p‑tau181 (χ2 = 22.855, P = 0.000) and t‑tau/p‑tau181 ratio (χ2 = 43.780, P = 0.000) among 3 groups. Further pairwise comparisons revealed that the t‑tau in the sCJD group was higher than that in the AD group (Z = ‑ 4.392, P = 0.000) and AE group (Z = ‑ 5.852, P = 0.000); the p‑tau181 in the AD group was higher than that in the sCJD group (Z = 2.830, P = 0.014) and AE group (Z = 4.758, P = 0.000); the t‑tau/p‑tau181 ratio in the sCJD group was higher than that in the AD group (Z = ‑ 6.601, P = 0.000) and AE group (Z = ‑ 3.339, P = 0.003), and the t‑tau/p‑tau181 ratio in the AE group was higher than that in the AD group (Z = ‑ 2.984, P = 0.009). Among the 30 patients in the sCJD group, 70% (21/30) exhibited abnormal MRI findings in the brain, all displaying the typical cortical "lace sign"; 40% (12/30) showed typical triphasic waves on EEG. In the sCJD group, 7 cases underwent CSF RT ‑ QuIC, and pathogenic prion protein was detected in 5 patients. Conclusions Elevated CSF t‑tau and t‑tau/p‑tau181 ratio, as well as positive RT‑QuIC results, hold certain diagnostic value for sCJD.

Institutions

Publication Details

Journal
SHILAP Revista de lepidopterología
Published
2025-04-01
DOI
https://doi.org/10.3969/j.issn.1672‑6731.2025.04.008
Primary Topic
Prion Diseases and Protein Misfolding
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Diagnostic value of cerebrospinal fluid tau and real⁃time quaking⁃induced conversion in sporadic Creutzfeldt⁃Jakob disease

SHILAP Revista de lepidopterología
Prion Diseases and Protein Misfolding
article

Diagnostic value of cerebrospinal fluid tau and real⁃time quaking⁃induced conversion in sporadic Creutzfeldt⁃Jakob disease

article en

Abstract

Objective To explore the diagnostic value of cerebrospinal fluid (CSF) biomarkers, total tau protein (t‑tau), phosphorylated tau protein 181 (p‑tau181) and real‑time quaking‑induced conversion (RT ‑QuIC) in sporadic Creutzfeldt‑Jakob disease (sCJD). Methods A retrospective study was conducted on 30 patients diagnosed with probable sCJD at Huashan Hospital, Fudan University from April 2020 to November 2022, serving as the sCJD group. Meanwhile, 25 patients diagnosed with rapidly progressive Alzheimer's disease (AD) and 23 patients diagnosed with autoimmune encephalitis (AE), matched for gender and age with the sCJD group, were selected as the AD group and AE group, respectively. CSF t‑tau, p ‑ tau181 and t‑tau/p‑tau181 ratio were collected from the 3 groups. The auxiliary examination data of the sCJD group, including typical manifestations of electroencephalography (EEG) and head MRI, as well as RT‑ QuIC results, were collected with emphasis. Results There were statistically significant differences in CSF t‑tau (χ2 = 38.247, P = 0.000), p‑tau181 (χ2 = 22.855, P = 0.000) and t‑tau/p‑tau181 ratio (χ2 = 43.780, P = 0.000) among 3 groups. Further pairwise comparisons revealed that the t‑tau in the sCJD group was higher than that in the AD group (Z = ‑ 4.392, P = 0.000) and AE group (Z = ‑ 5.852, P = 0.000); the p‑tau181 in the AD group was higher than that in the sCJD group (Z = 2.830, P = 0.014) and AE group (Z = 4.758, P = 0.000); the t‑tau/p‑tau181 ratio in the sCJD group was higher than that in the AD group (Z = ‑ 6.601, P = 0.000) and AE group (Z = ‑ 3.339, P = 0.003), and the t‑tau/p‑tau181 ratio in the AE group was higher than that in the AD group (Z = ‑ 2.984, P = 0.009). Among the 30 patients in the sCJD group, 70% (21/30) exhibited abnormal MRI findings in the brain, all displaying the typical cortical "lace sign"; 40% (12/30) showed typical triphasic waves on EEG. In the sCJD group, 7 cases underwent CSF RT ‑ QuIC, and pathogenic prion protein was detected in 5 patients. Conclusions Elevated CSF t‑tau and t‑tau/p‑tau181 ratio, as well as positive RT‑QuIC results, hold certain diagnostic value for sCJD.

SHILAP Revista de lepidopterología
Fudan University (CN), First People's Hospital of Yunnan Province (CN), Huashan Hospital (CN)
Gender equality
Openalex Percentile: Top 59%
Prion Diseases and Protein Misfolding
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.