Evidence map›Paper›PMID 35721829›Full record

ArticleCommunications medicine2022

Prediction of SARS-CoV-2-positivity from million-scale complete blood counts using machine learning.

Gianlucca Zuin, Daniella Araujo, Vinicius Ribeiro, Maria Gabriella Seiler, Wesley Heleno Prieto, Maria Carolina Pintão, Carolina Dos Santos Lazari, Celso Francisco Hernandes Granato, Adriano Veloso

Open access · goldAbstract read
In one paragraph

Article in Communications medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 22 citations in OpenAlex.

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  6. Serum Thyrotropin and Triiodothyronine Levels in Levothyroxine-treated Patients.The Journal of clinical endocrinology and metabolism · 2023
    Observational
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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

9 authors at 2 institutions in 1 country.

Gianlucca ZuinUniversidade Federal de Minas Gerais, CS Dept., Belo Horizonte, Brazil.ORCID 0000-0002-0429-3280
Daniella AraujoUniversidade Federal de Minas Gerais, CS Dept., Belo Horizonte, Brazil.
Vinicius RibeiroHuna, São Paulo, Brazil.
Maria Gabriella SeilerKunumi, Belo Horizonte, Brazil.
Wesley Heleno PrietoGrupo Fleury, São Paulo, Brazil.
Maria Carolina PintãoGrupo Fleury, São Paulo, Brazil.ORCID 0000-0002-6452-7931
Carolina Dos Santos LazariGrupo Fleury, São Paulo, Brazil.ORCID 0000-0002-1418-1880
Celso Francisco Hernandes GranatoGrupo Fleury, São Paulo, Brazil.
Adriano VelosoUniversidade Federal de Minas Gerais, CS Dept., Belo Horizonte, Brazil.
Fleury S.A. (Brazil) · BRUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Complete Blood Count (CBC) is a commonly used low-cost test that measures white blood cells, red blood cells, and platelets in a person's blood. It is a useful tool to support medical decisions, as intrinsic variations of each analyte bring relevant insights regarding potential diseases. In this study, we aimed at developing machine learning models for COVID-19 diagnosis through CBCs, unlocking the predictive power of non-linear relationships between multiple blood analytes. Methods: We collected 809,254 CBCs and 1,088,385 RT-PCR tests for SARS-Cov-2, of which 21% (234,466) were positive, from 900,220 unique individuals. To properly screen COVID-19, we also collected 120,807 CBCs of 16,940 individuals who tested positive for other respiratory viruses. We proposed an ensemble procedure that combines machine learning models for different respiratory infections and analyzed the results in both the first and second waves of COVID-19 cases in Brazil. Results: We obtain a high-performance AUROC of 90 + % for validations in both scenarios. We show that models built solely of SARS-Cov-2 data are biased, performing poorly in the presence of infections due to other RNA respiratory viruses. Conclusions: We demonstrate the potential of a novel machine learning approach for COVID-19 diagnosis based on a CBC and show that aggregating information about other respiratory diseases was essential to guarantee robustness in the results. Given its versatile nature, low cost, and speed, we believe that our tool can be particularly useful in a variety of scenarios-both during the pandemic and after.

Indexed as

BiomarkersDiagnosisViral infection

Identifiers

PMID35721829
PMCPMC9199341
OpenAlexW4282967107

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.