Evidence map›Paper›PMID 33531605›Full record

ArticleScientific reports2021

Time course of the sensitivity and specificity of anti-SARS-CoV-2 IgM and IgG antibodies for symptomatic COVID-19 in Japan.

Yuki Nakano, Makoto Kurano, Yoshifumi Morita, Takuya Shimura, Rin Yokoyama, Chungen Qian, Fuzhen Xia, Fan He, Yoshiro Kishi, Jun Okada and 7 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 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
3.7field-weighted citation impact, top 5% 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, 64 citations in OpenAlex.

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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

17 authors at 5 institutions in 2 countries.

Yuki NakanoDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Makoto KuranoDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan. kurano-tky@umin.ac.jp.
Yoshifumi MoritaDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Takuya ShimuraDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Rin YokoyamaDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Chungen QianThe Key Laboratory for Biomedical Photonics of MOE At Wuhan National Laboratory for Optoelectronics - Hubei Bioinformatics and Molecular Imaging Key Laboratory, Systems Biology Theme, Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Hubei, People's Republic of China.
Fuzhen XiaReagent R&D Center, Shenzhen YHLO Biotech Co., Ltd, Shenzhen, Guangdong, People's Republic of China.
Fan HeReagent R&D Center, Shenzhen YHLO Biotech Co., Ltd, Shenzhen, Guangdong, People's Republic of China.
Yoshiro KishiBusiness Planning Department, Sales and Marketing Division, Medical and Biological Laboratories Co, Ltd, Tokyo, Japan.
Jun OkadaBusiness Planning Department, Sales and Marketing Division, Medical and Biological Laboratories Co, Ltd, Tokyo, Japan.
Naoyuki YoshikawaDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Yutaka NaguraDepartment of Blood Transfusion, The University of Tokyo Hospital, Tokyo, Japan.
Hitoshi OkazakiDepartment of Blood Transfusion, The University of Tokyo Hospital, Tokyo, Japan.
Kyoji MoriyaDepartment of Infection Control and Prevention, The University of Tokyo, Tokyo, Japan.
Yasuyuki SetoDepartment of Gastrointestinal Surgery, The University of Tokyo, Tokyo, Japan.
Tatsuhiko KodamaLaboratory for Systems Biology and Medicine, The University of Tokyo, Tokyo, Japan.
Yutaka YatomiDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan. yatoyuta-tky@umin.ac.jp.
University of Tokyo Hospital · JPThe University of Tokyo · JPLifetech Scientific (China) · CNMedical & Biological Laboratories (Japan) · JPWuhan National Laboratory for Optoelectronics · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The accurate and prompt diagnosis of SARS-CoV-2 infection is required for the control and treatment of the coronavirus infection disease 2019 (COVID-19). In this study, we aimed to investigate the time courses of the anti-severe acute corona respiratory syndrome coronavirus 2 (SARS-CoV-2) IgM and IgG titers and to evaluate the sensitivity and specificity of such tests according to the specific day after the onset of COVID-19 among a patient population in Japan. We measured the titers of SARS-CoV-2 IgM and IgG in sera from 105 subjects, including 26 symptomatic COVID-19 patients, using chemiluminescent immunoassay (CLIA) methods utilizing magnetic beads coated with SARS-CoV-2 nucleocapsid protein and spike protein. The results of a ROC analysis suggested the possibility that the cutoff values in Japan might be lower than the manufacturer's reported cutoff (10 AU/mL): 1  AU/mL for IgM and 5  AU/mL for IgG. The sensitivity of the test before Day 8 after symptom onset was less than 50%; at Days 9-10, however, we obtained a much higher sensitivity of 81.8% for both IgM and IgG. At 15 days or later after symptom onset, the SARS-CoV-2 IgG test had a sensitivity of 100%. These results suggest that if the number of days since disease onset is taken into consideration, these antibody tests could be very useful for the diagnosis of COVID-19 and similar diseases.

Indexed as

Antibody SpecificityCOVID-19COVID-19 TestingEnzyme-Linked Immunosorbent AssayHumansImmunoglobulin GImmunoglobulin MJapanSARS-CoV-2Immunoglobulin GImmunoglobulin M

Identifiers

PMID33531605
PMCPMC7854735
OpenAlexW3126786478

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.