Evidence map›Paper›PMID 37332901›Full record

ArticleHeliyon2023

Using a multiplex serological assay to estimate time since SARS-CoV-2 infection and past clinical presentation in malagasy patients.

Mame Diarra Bousso Ndiaye, Lova Tsikiniaina Rasoloharimanana, Solohery Lalaina Razafimahatratra, Rila Ratovoson, Voahangy Rasolofo, Paulo Ranaivomanana, Laurent Raskine, Jonathan Hoffmann, Rindra Randremanana, Niaina Rakotosamimanana and 1 more

Abstract read
In one paragraph

Article in Heliyon, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Mame Diarra Bousso NdiayeInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Lova Tsikiniaina RasoloharimananaInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Solohery Lalaina RazafimahatratraInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Rila RatovosonInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Voahangy RasolofoInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Paulo RanaivomananaInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Laurent RaskineMedical and Scientific Department, Fondation Mérieux, Lyon, France.
Jonathan HoffmannMedical and Scientific Department, Fondation Mérieux, Lyon, France.
Rindra RandremananaInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Niaina RakotosamimananaInstitut Pasteur de Madagascar, Antananarivo, Madagascar.
Matthieu SchoenhalsInstitut Pasteur de Madagascar, Antananarivo, Madagascar.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The world is facing a 2019 coronavirus (COVID-19) pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In this context, efficient serological assays are needed to accurately describe the humoral responses against the virus. These tools could potentially provide temporal and clinical characteristics and are thus paramount in developing-countries lacking sufficient ongoing COVID-19 epidemic descriptions. Methods: We developed and validated a Luminex xMAP® multiplex serological assay targeting specific IgM and IgG antibodies against the SARS-CoV-2 Spike subunit 1 (S1), Spike subunit 2 (S2), Spike Receptor Binding Domain (RBD) and the Nucleocapsid protein (N). Blood samples collected periodically for 12 months from 43 patients diagnosed with COVID-19 in Madagascar were tested for these antibodies. A random forest algorithm was used to build a predictive model of time since infection and symptom presentation. Findings: The performance of the multiplex serological assay was evaluated for the detection of SARS-CoV-2 Interpretation: This study demonstrates that the statistical model predicts time since infection and previous symptom presentation using IgM and IgG response to SARS-CoV2. This tool may be useful for global surveillance, discriminating recent- and past- SARS-CoV-2 infection, and assessing disease severity. Fundings: This study was funded by the French Ministry for Europe and Foreign Affairs through the REPAIR COVID-19-Africa project coordinated by the Pasteur International Network association. WANTAI reagents were provided by WHO AFRO as part of a Sero-epidemiological "Unity" Study Grant/Award Number: 2020/1,019,828-0 P·O 202546047 and Initiative 5% grant n°AP-5PC-2018-03-RO.

Indexed as

COVID-19 seroprevalenceMadagascarPrediction modelSARS-CoV-2 antibodiesSymptom presentationTime since infection

Identifiers

PMID37332901
PMCPMC10263216

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.