Evidence map›Paper›PMID 33661132›Full record

ArticleJMIR research protocols2021

Molecular and Cellular Biomarkers of COVID-19 Prognosis: Protocol for the Prospective Cohort TARGET Study.

Patricia Kurizky, Otávio T Nóbrega, Alexandre Anderson De Sousa Munhoz Soares, Rodrigo Barbosa Aires, Cleandro Pires De Albuquerque, André Moraes Nicola, Patrícia Albuquerque, Andréa Teixeira-Carvalho, Luciana Ansaneli Naves, Wagner Fontes and 9 more

Open access · goldAbstract read
In one paragraph

Article in JMIR research protocols, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 48% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Observational
  3. Observational
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

19 authors at 4 institutions in 1 country.

Patricia Kurizky *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-5759-2727
Otávio T Nóbrega *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0003-1775-7176
Alexandre Anderson De Sousa Munhoz Soares *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0003-4716-9543
Rodrigo Barbosa Aires *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0003-3044-2064
Cleandro Pires De Albuquerque *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-9245-7504
André Moraes Nicola *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0001-8656-5835
Patrícia Albuquerque *Faculdade de Ceilândia, University of Brasília, Brasília, Brazil.ORCID https://orcid.org/0000-0001-8160-7784
Andréa Teixeira-Carvalho *Fundação Oswaldo Cruz, FIOCRUZ-Minas, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0003-2814-5183
Luciana Ansaneli Naves *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-3363-3803
Wagner Fontes *Instituto de Ciências Biológicas, University of Brasília, Brasília, Brazil.ORCID https://orcid.org/0000-0001-5140-8573
Isabelle Souza LuzInstituto de Ciências Biológicas, University of Brasília, Brasília, Brazil.ORCID https://orcid.org/0000-0001-8722-5103
Liza Felicori *Instituto de Ciências Biológicas, Federal University of Minas Gerais, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0002-3240-9658
Ana Paulo Monteiro Gomides *Centro Universitário de Brasília, Brasília, Brazil.ORCID https://orcid.org/0000-0003-2884-2210
Dayde Lane Mendonça-Silva *Hospital Universitário de Brasília, University of Brasília, Brasília, Brazil.ORCID https://orcid.org/0000-0001-5653-7411
Laila Salmen Espindola *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-1886-868X
Olindo Assis Martins-Filho *Fundação Oswaldo Cruz, FIOCRUZ-Minas, Belo Horizonte, Brazil.ORCID https://orcid.org/0000-0002-5494-4889
Sheila Maria Barbosa de Lima *Instituto de Tecnologia em Imunobiológicos Bio-Manguinhos, FIOCRUZ, Rio de Janeiro, Brazil.ORCID https://orcid.org/0000-0001-9234-1678
Licia Maria Henrique Mota *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-8182-5121
Ciro Martins Gomes *Programa de Pós-graduação em Ciências Médicas da Faculdade de Medicina, University of Brasília, Brasilia, Brazil.ORCID https://orcid.org/0000-0002-3069-6884
Universidade de Brasília · BRFundação Oswaldo Cruz · BRUniversidade Federal de Minas Gerais · BRUniversity Center of Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSince the beginning of the COVID-19 pandemic, the world's attention has been focused on better understanding the relation between the human host and the SARS-CoV-2 virus, as its action has led to hundreds of thousands of deaths.

objectiveIn this context, we decided to study certain consequences of the abundant cytokine release over the innate and adaptive immune systems, inflammation, and hemostasis, comparing mild and severe forms of COVID-19.

methodsTo accomplish these aims, we will analyze demographic characteristics, biochemical tests, immune biomarkers, leukocyte phenotyping, immunoglobulin profile, hormonal release (cortisol and prolactin), gene expression, thromboelastometry, neutralizing antibodies, metabolic profile, and neutrophil function (reactive oxygen species production, neutrophil extracellular trap production, phagocytosis, migration, gene expression, and proteomics). A total of 200 reverse transcription polymerase chain reaction-confirmed patients will be enrolled and divided into two groups: mild/moderate or severe/critical forms of COVID-19. Blood samples will be collected at different times: at inclusion and after 9 and 18 days, with an additional 3-day sample for severe patients. We believe that this information will provide more knowledge for future studies that will provide more robust and useful clinical information that may allow for better decisions at the front lines of health care.

resultsThe recruitment began in June 2020 and is still in progress. It is expected to continue until February 2021. Data analysis is scheduled to start after all data have been collected. The coagulation study branch is complete and is already in the analysis phase.

conclusionsThis study is original in terms of the different parameters analyzed in the same sample of patients with COVID-19. The project, which is currently in the data collection phase, was approved by the Brazilian Committee of Ethics in Human Research (CAAE 30846920.7.0000.0008).

trial registrationBrazilian Registry of Clinical Trials RBR-62zdkk; https://ensaiosclinicos.gov.br/rg/RBR-62zdkk. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/24211.

Indexed as

biomarkercohortCOVID-19cytokine profiledesigngeneticsimmune systemimmunologymetabolomicsneutralizing antibodiesneutrophil functionprognosisproteomicsTARGETthromboelastometryvirus

Identifiers

PMID33661132
PMCPMC7935398
OpenAlexW3132739362

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.