Evidence map›Paper›PMID 33901540›Full record

ReviewImmunology letters2021

Will a little change do you good? A putative role of polymorphisms in COVID-19.

Adriana Alves Oliveira Paim, Ágata Lopes-Ribeiro, Daniele S O Daian E Silva, Luis Adan F Andrade, Thais F S Moraes, Edel F Barbosa-Stancioli, Flávio Guimarães da Fonseca, Jordana G Coelho-Dos-Reis

Open access · greenAbstract readReview
In one paragraph

Review in Immunology letters, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

11 citing papers in PubMed, 17 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

8 authors at 1 institution in 1 country.

Adriana Alves Oliveira PaimLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil.
Ágata Lopes-RibeiroLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil; Biomarkers Research Group, Instituto René Rachou, Osvaldo Cruz Foundation - FIOCRUZ-MINAS, Belo Horizonte, Minas Gerais, Brazil.
Daniele S O Daian E SilvaLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil.
Luis Adan F AndradeLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil; CT Vacinas, BH-TEC Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Rua Professor José Vieira de Mendonça, 770 - Engenho Nogueira, CEP 31310-260, Belo Horizonte, MG, Brazil.
Thais F S MoraesLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil; CT Vacinas, BH-TEC Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Rua Professor José Vieira de Mendonça, 770 - Engenho Nogueira, CEP 31310-260, Belo Horizonte, MG, Brazil.
Edel F Barbosa-StancioliLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil.
Flávio Guimarães da FonsecaLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil; CT Vacinas, BH-TEC Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Rua Professor José Vieira de Mendonça, 770 - Engenho Nogueira, CEP 31310-260, Belo Horizonte, MG, Brazil. Electronic address: fdafonseca@icb.ufmg.br.
Jordana G Coelho-Dos-ReisLaboratório de Virologia Básica e Aplicada, Departamento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Av. Antônio Carlos, 6627, Campus Pampulha, CEP, 31270-901, Belo Horizonte, MG, Brazil; Biomarkers Research Group, Instituto René Rachou, Osvaldo Cruz Foundation - FIOCRUZ-MINAS, Belo Horizonte, Minas Gerais, Brazil. Electronic address: jreis@icb.ufmg.br.
Universidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An alarming disease caused by the new severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) named COVID-19 has emerged as an unprecedented public health problem and ignited a world health crisis. As opposed to what was believed at the beginning of the pandemic, the virus has not only spread but persevere causing secondary waves and challenging the concept of herd immunity against viral infections. While the majority of SARS-CoV-2-infected individuals may remain asymptomatic, a fraction of individuals may develop low to high-grade severity signs and symptoms of COVID-19. The disease is multifactorial and can progress quickly, leading to severe complications and even death in a few days. Therefore, understanding the pre-existing factors for disease development has never been so pressing. In this scenario, the insights on the mechanisms underlying disease allied to the immune response developed during the viral invasion could shed light on novel predictive factors and prognostic tools for COVID-19 management and interventions. A recent genome-wide association study (GWAS) revealed several molecules that significantly impacted critically ill COVID-19 patients, leading to the core mechanisms of COVID-19 pathogenesis. Considering these findings and the fact that ACE-2 polymorphisms alone cannot explain disease progress and severity, this review aims at summarizing the most important and recent findings of the research and expert consensus of possible cytokine-related polymorphisms existing in the differential expression of paramount immune molecules that could be crucial for providing guidelines for decision-making and appropriate clinical management of COVID-19.

Indexed as

Angiotensin-Converting Enzyme 2COVID-19CytokinesPandemicsPolymorphism, GeneticGenome-Wide Association StudyHumansSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2CytokinesCytokine stormPolymorphismSARSSARS-CoV-2

Identifiers

PMID33901540
PMCPMC8064809
OpenAlexW3159165214

What OpenQuestion holds

Textmetadata
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.