Evidence map›Paper›PMID 35126396›Full record

ArticleFrontiers in immunology2022

Measurement of SARS-CoV-2 Antibody Titers Improves the Prediction Accuracy of COVID-19 Maximum Severity by Machine Learning in Non-Vaccinated Patients.

Makoto Kurano, Hiroko Ohmiya, Yoshiro Kishi, Jun Okada, Yuki Nakano, Rin Yokoyama, Chungen Qian, Fuzhen Xia, Fan He, Liang Zheng and 6 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Observational
  8. Article
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

16 authors.

Makoto KuranoDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.
Hiroko OhmiyaBusiness Planning Department, Sales & Marketing Division, Medical & Biological Laboratories Co., Ltd, Tokyo, Japan.
Yoshiro KishiBusiness Planning Department, Sales & Marketing Division, Medical & Biological Laboratories Co., Ltd, Tokyo, Japan.
Jun OkadaBusiness Planning Department, Sales & Marketing Division, Medical & Biological Laboratories Co., Ltd, Tokyo, Japan.
Yuki NakanoDepartment 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 Ministry of Education at Wuhan National Laboratory for Optoelectronics - Hubei Bioinformatics & Molecular Imaging Key Laboratory, Systems Biology Theme, Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.
Fuzhen XiaReagent R&D Center, Shenzhen YHLO Biotech Co., Ltd, Shenzhen, China.
Fan HeReagent R&D Center, Shenzhen YHLO Biotech Co., Ltd, Shenzhen, China.
Liang ZhengReagent R&D Center, Shenzhen YHLO Biotech Co., Ltd, Shenzhen, China.
Yi YuReagent R&D Center, Shenzhen YHLO Biotech Co., Ltd, Shenzhen, China.
Daisuke JubishiDepartment of Infection Control and Prevention, The University of Tokyo, Tokyo, Japan.
Koh OkamotoDepartment of Infection Control and Prevention, The University of Tokyo, Tokyo, Japan.
Kyoji MoriyaDepartment of Infection Control and Prevention, The University of Tokyo, Tokyo, Japan.
Tatsuhiko KodamaLaboratory for Systems Biology and Medicine, Research Center for Advanced Science and Technology, The University of Tokyo, Tokyo, Japan.
Yutaka YatomiDepartment of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous studies have suggested that the titers of antibodies against SARS-CoV-2 are associated with the COVID-19 severity, however, the types of antibodies associated with the disease maximum severity and the timing at which the associations are best observed, especially within one week after symptom onset, remain controversial. We attempted to elucidate the antibody responses against SARS-CoV-2 that are associated with the maximum severity of COVID-19 in the early phase of the disease, and to investigate whether antibody testing might contribute to prediction of the disease maximum severity in COVID-19 patients. We classified the patients into four groups according to the disease maximum severity (severity group 1 (did not require oxygen supplementation), severity group 2a (required oxygen supplementation at low flow rates), severity group 2b (required oxygen supplementation at relatively high flow rates), and severity group 3 (required mechanical ventilatory support)), and serially measured the titers of IgM, IgG, and IgA against the nucleocapsid protein, spike protein, and receptor-binding domain of SARS-CoV-2 until day 12 after symptom onset. The titers of all the measured antibody responses were higher in severity group 2b and 3, especially severity group 2b, as early as at one week after symptom onset. Addition of data obtained from antibody testing improved the ability of analysis models constructed using a machine learning technique to distinguish severity group 2b and 3 from severity group 1 and 2a. These models constructed with non-vaccinated COVID-19 patients could not be applied to the cases of breakthrough infections. These results suggest that antibody testing might help physicians identify non-vaccinated COVID-19 patients who are likely to require admission to an intensive care unit.

Indexed as

Severity of Illness IndexVaccination HesitancyAntibodies, ViralAntibody FormationBreakthrough InfectionsCoronavirus Nucleocapsid ProteinsCOVID-19COVID-19 VaccinesHumansImmunoglobulin AImmunoglobulin GImmunoglobulin MMachine LearningProtein DomainsSARS-CoV-2Spike Glycoprotein, CoronavirusAntibodies, ViralCoronavirus Nucleocapsid ProteinsCOVID-19 VaccinesImmunoglobulin AImmunoglobulin GImmunoglobulin MN protein, SARS-CoVSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19IgAIgGIgMmachine learningnucleocapsid proteinseverityspike protein

Identifiers

PMID35126396
PMCPMC8814445

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.