Evidence map›Paper›PMID 26541494›Full record

ArticleJournal of clinical neurology (Seoul, Korea)2016

Real-Time Quaking-Induced Conversion Analysis for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease in Korea.

Jeong Ho Park, Yeong Gon Choi, Yun Jung Lee, Seok Joo Park, Hong Seok Choi, Kyung Chan Choi, Eun Kyoung Choi, Yong Sun Kim

Open access · diamondAbstract read
In one paragraph

Article in Journal of clinical neurology (Seoul, Korea), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 10% of its field
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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

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  16. RT-QuIC: a new test for sporadic CJD.Practical neurology · 2019
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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

8 authors at 3 institutions in 1 country.

Jeong Ho ParkKorea CJD Diagnostic Center, Hallym University, Anyang, Korea.
Yeong Gon ChoiLaboratory of Transmissible Spongiform Encephalopathy, Ilsong Institute of Life Science, Hallym University, Anyang, Korea.
Yun Jung LeeLaboratory of Transmissible Spongiform Encephalopathy, Ilsong Institute of Life Science, Hallym University, Anyang, Korea.
Seok Joo ParkLaboratory of Transmissible Spongiform Encephalopathy, Ilsong Institute of Life Science, Hallym University, Anyang, Korea.
Hong Seok ChoiLaboratory of Transmissible Spongiform Encephalopathy, Ilsong Institute of Life Science, Hallym University, Anyang, Korea.
Kyung Chan ChoiDepartment of Pathology, Chuncheon Sacred Heart Hospital, Hallym University College of Medicine, Chuncheon, Korea.
Eun Kyoung ChoiDepartment of Biomedical Gerontology, Graduate School of Hallym University, Chuncheon, Korea.
Yong Sun KimKorea CJD Diagnostic Center, Hallym University, Anyang, Korea.
Hallym University · KRHallym University Medical Center · KRHallym University Chuncheon Sacred Heart Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeThe level of 14-3-3 protein in the cerebrospinal fluid (CSF) is increased in Creutzfeldt-Jakob disease (CJD) patients, which has led to it being used as a clinical biomarker for the ante-mortem diagnosis of human prion diseases. However, the specificity of the 14-3-3 protein is less reliable for CJD diagnosis. Newly developed assays including real-time quaking-induced conversion (RT-QuIC) have made it possible to detect the PrPSc-like abnormal prion isoform with a high sensitivity in animal and human specimens that might contain a minute amount of PrP(Sc) due to in vitro prion replication.

methodsThis study applied a highly sensitive RT-QuIC assay using recombinant human PrP to detect PrP(Sc) in the CSF of 81 patients with sporadic CJD (sCJD) in Korea.

resultsRT-QuIC analysis of the CSF samples based on the expression levels of 14-3-3 and total tau proteins revealed positivity in 62 of 81 sCJD patients (sensitivity of 76.5%) but no positive results in the 100 non-CJD patients.

conclusionsThe sensitivity of the RT-QuIC in this study was similar to that in some previous reports, and the specificity of RT-QuIC was higher than that of 14-3-3 in CSF, suggesting that RT-QuIC analysis can complement the weakness of the specificity of 14-3-3 for the diagnosis of sCJD. These results indicate that RT-QuIC might be very useful for the rapid and specific diagnosis of sCJD and provide a practical novel method for the ante-mortem diagnosis of human prion diseases.

Indexed as

14-3-3cerebrospinal fluidCreutzfeldt-Jakob diseaseRT-QuICtotal tau protein

Identifiers

PMID26541494
PMCPMC4712274
OpenAlexW2130288198

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LicenceCC BY-NC
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Registered trials

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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.