Evidence map›Paper›PMID 34358289›Full record

ArticleClinical chemistry2021

Diagnostic Value of Nucleocapsid Protein in Blood for SARS-CoV-2 Infection.

Yu Zhang, Chui Mei Ong, Cassandra Yun, Weike Mo, Jeffery D Whitman, Kara L Lynch, Alan H B Wu

Open access · bronzeAbstract read
In one paragraph

Article in Clinical chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
3.0field-weighted citation impact, top 7% 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

34 citing papers in PubMed, 55 citations in OpenAlex.

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  15. RAGE Is a Receptor for SARS-CoV-2 N Protein and Mediates N Protein-induced Acute Lung Injury.American journal of respiratory cell and molecular biology · 2023
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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

7 authors at 3 institutions in 2 countries.

Yu ZhangDepartment of Laboratory Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0001-5512-9272
Chui Mei OngDepartment of Laboratory Medicine, University of California, San Francisco, CA, USA.
Cassandra YunDepartment of Laboratory Medicine, University of California, San Francisco, CA, USA.ORCID 0000-0002-6971-2060
Weike MoShanghai East Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.
Jeffery D WhitmanDepartment of Laboratory Medicine, University of California, San Francisco, CA, USA.
Kara L LynchDepartment of Laboratory Medicine, University of California, San Francisco, CA, USA.
Alan H B WuDepartment of Laboratory Medicine, University of California, San Francisco, CA, USA.
University of California, San Francisco · USShanghai East Hospital · CNUniversity of Massachusetts Chan Medical School · US

Funding

Cell Fate Decision by CLV1 in Shoot Apical MeristemF32GM075460 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI QU, XIANG · 2005 to 2007
$143k
NIGMS NIH HHS F32 GM075460
6 · The paper itself

Abstract

backgroundBiomarkers have been widely explored for coronavirus disease 2019 diagnosis. Both viral RNA or antigens (Ag) in the respiratory system and antibodies (Ab) in blood are used to identify active infection, transmission risk, and immune response but have limitations. This study investigated the diagnostic utility of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) nucleocapsid protein (N-Ag) in serum.

methodsWe retrospectively studied 208 randomly selected cases with SARS-CoV-2 infection confirmed by viral RNA test in swabs. N-Ag concentrations were measured in remnant serum samples, compared to viral RNA or Ab results, and correlated to electronic health records for clinical value evaluation.

resultsSerum N-Ag was detected during active infection as early as day 2 from symptom onset with a diagnostic sensitivity of 81.5%. Within 1 week of symptom onset, the diagnostic sensitivity and specificity reached 90.9% (95% CI, 85.1%-94.6%) and 98.3% (95% CI, 91.1%-99.9%), respectively. Moreover, serum N-Ag concentration closely correlated to disease severity, reflected by highest level of care, medical interventions, chest imaging, and the length of hospital stays. Longitudinal analysis revealed the simultaneous increase of Abs and decline of N-Ag.

conclusionsSerum N-Ag is a biomarker for SARS-CoV-2 acute infection with high diagnostic sensitivity and specificity compared to viral RNA in the respiratory system. There is a correlation between serum N-Ag concentrations and disease severity and an inverse relationship of N-Ag and Abs. The diagnostic value of serum N-Ag, as well as technical and practical advantages it could offer, may meet unsatisfied diagnostic and prognostic needs during the pandemic.

Indexed as

COVID-19Antibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19 TestingHumansNucleocapsid ProteinsPhosphoproteinsRetrospective StudiesRNA, ViralSARS-CoV-2Sensitivity and SpecificityAntibodies, ViralCoronavirus Nucleocapsid Proteinsnucleocapsid phosphoprotein, SARS-CoV-2Nucleocapsid ProteinsPhosphoproteinsRNA, ViralbiomarkerCOVID-19SARS-CoV-2serum nucleocapsid protein

Identifiers

PMID34358289
PMCPMC8436384
OpenAlexW3188448296

What OpenQuestion holds

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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.