Evidence map›Paper›PMID 39932589›Full record

ArticleJournal of neurology2025

Isolated CSF RT-QuIC positivity associates with a less aggressive disease course and decreased levels of neuronal/glial damage biomarkers in patients with sporadic Creutzfeldt-Jakob disease.

Laura Naranjo, Jordi Sarto, Carlos Nos, Daniel Alcolea, Iñigo Rodríguez-Baz, Irene Navalpotro-Gómez, Aída Fernández-Lebrero, Bernat Bertrán-Recasens, María Elena Erro, Ana Lara Pelayo-Negro and 16 more

Abstract readMulticenter Study
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In one paragraph

Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Laura NaranjoImmunology Department, Biomedical Diagnostic Center, Hospital Clínic de Barcelona, Barcelona, Spain.
Jordi SartoAlzheimer's Disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Carlos NosGeneral Subdirectorate of Surveillance and Response to Emergencies in Public Health, Department of Public Health in Catalonia, Barcelona, Spain.
Daniel AlcoleaSant Pau Memory Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Barcelona, Spain.
Iñigo Rodríguez-BazSant Pau Memory Unit, Neurology Department, Hospital de la Santa Creu i Sant Pau, Biomedical Research Institute Sant Pau, Barcelona, Spain.
Irene Navalpotro-GómezCognitive Decline and Movement Disorders Unit, Neurology Department, Hospital del Mar-Hospital del Mar Research Institute, Barcelona, Spain.
Aída Fernández-LebreroCognitive Decline and Movement Disorders Unit, Neurology Department, Hospital del Mar-Hospital del Mar Research Institute, Barcelona, Spain.
Bernat Bertrán-RecasensNeuromuscular Diseases Unit, Neurology Department, Hospital del Mar, Barcelona, Spain.
María Elena ErroNeurology Department and Brain Biobank, Navarrabiomed-Universidad Pública de Navarra (UPNA)-Hospital Universitario de Navarra (HUN), IdiSNA, Pamplona, Spain.
Ana Lara Pelayo-NegroNeurology Department, University Hospital Marqués de Valdecilla-IDIVAL, Santander, Spain.
Clara EsteveImmunology Department, CLILAB Diagnòstics, Vilafranca del Penedès, Spain.
Susana FernándezNeurology Department, Hospital de Sant Joan Despi - Moises Broggi, Barcelona, Spain.
Andreu Massot-TarrúsNeurology Department, F. Ass. Mútua Terrassa, Terrassa, Spain.
Anuncia BoltesNeurology Department, Hospital General de Granollers, Barcelona, Spain.
Albert TorrentsReference Laboratory, Barcelona, Spain.
Nicolau GuanyabensNeurology Department, Hospital de Mataró, Barcelona, Spain.
Alfredo Palomino-GarcíaNeurology Department, Hospital Universitario Virgen del Rocío, Seville, Spain.
Natalia EgriImmunology Department, Biomedical Diagnostic Center, Hospital Clínic de Barcelona, Barcelona, Spain.
Albert LladóAlzheimer's Disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
Mircea BalasaAlzheimer's Disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain.
María Antonia RomeraImmunology Department, Biomedical Diagnostic Center, Hospital Clínic de Barcelona, Barcelona, Spain.
María Del Carmen AntónImmunology Department, Biomedical Diagnostic Center, Hospital Clínic de Barcelona, Barcelona, Spain.
Rocío Soledad CousoImmunology Department, Biomedical Diagnostic Center, Hospital Clínic de Barcelona, Barcelona, Spain.
Raquel Sánchez-Valle *Alzheimer's Disease and Other Cognitive Disorders Unit, Neurology Service, Hospital Clínic de Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Universitat de Barcelona, Barcelona, Spain. rsanchez@clinic.cat.
Raquel Ruiz-García *Immunology Department, Biomedical Diagnostic Center, Hospital Clínic de Barcelona, Barcelona, Spain. rruizg@clinic.cat.ORCID http://orcid.org/0000-0002-8403-3613
Spanish sCJD Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Discrepancies in results between cerebrospinal fluid (CSF) 14-3-3 protein and prion protein detection using real-time quaking-induced conversion (RT-QuIC) might limit the confidence in ante-mortem clinical diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD). We aimed to evaluate the concordance and diagnostic performance of 14-3-3 protein and RT-QuIC in a real clinical practice cohort, and to analyze neuronal/glial damage biomarkers in sCJD patients based on their diagnostic assay results. A retrospective multicentre study was conducted on 157 suspected sCJD patients from 38 Spanish hospitals in a 4-year period. CSF 14-3-3 protein and RT-QuIC were simultaneously evaluated in a single laboratory. A diagnosis of probable sCJD was established in 63 patients (40.1%), of which 12 (19.0%) were ultimately diagnosed with definite sCJD. Forty-one sCJD patients (65.1%) were positive for both 14-3-3 protein and RT-QuIC, 17 (27.0%) isolated positive for RT-QuIC, and 5 (7.9%) isolated positive for 14-3-3 protein. RT-QuIC demonstrated higher sensitivity (92.1%) and specificity (98.9%) compared to 14-3-3 (73.0% and 62.8%) for the diagnosis of sCJD. Isolated RT-QuIC positivity was associated with longer disease duration (median: 10.5 months, IQR: 8.8-15.7), higher frequency of Met/Val cases (75.0%), lower prevalence of periodic sharp-wave complexes (5.9%), and lower levels of GFAP (3967.4 pg/mL), UCH-L1 (2218.1 pg/mL), and t-Tau (228.8 pg/mL) compared to double-positive and isolated 14-3-3-positive patients. In conclusion, CSF RT-QuIC is a highly specific and sensitive biomarker for ante-mortem sCJD diagnosis and should be considered as the preferred CSF ancillary test. Isolated RT-QuIC positivity indicates a less aggressive biological disease in sCJD patients.

Indexed as

14-3-3 ProteinsCreutzfeldt-Jakob SyndromeAdultAgedAged, 80 and overBiomarkersDisease ProgressionFemaleHumansMaleMiddle AgedNeurogliaNeuronsPrion ProteinsRetrospective Studiestau Proteins14-3-3 ProteinsBiomarkersPrion Proteinstau Proteins14-3-3 proteinDiagnostic performanceNeuronal/glial damage biomarkersReal-time quaking-induced conversionSporadic Creutzfeldt–Jakob disease

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.