Evidence map›Paper›PMID 42384984›Full record

ArticleEinstein (Sao Paulo, Brazil)2026

Influence of inflammatory and reninangiotensin system gene polymorphisms ACE2 rs2285666, IL1A rs1800587, and TNF rs1800629 on COVID-19 severity and the persistence of symptoms in the post-COVID-19 phase: a cross-sectional study.

Matheus Daudt-Lemos, Evelyn Maciel de Oliveira, Alice Ramos-Silva, Natalia Fonseca Rosário, Thays Araújo Gonçalves, Camila de Melo Carvalho Nascimento, Amanda Mendes do Valle, Lialyz Soares Pereira André, Fabio Aguiar-Alves, Jorge Paulo Strogoff de Matos and 5 more

Abstract read
In one paragraph

Article in Einstein (Sao Paulo, Brazil), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Matheus Daudt-LemosMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0009-0004-1952-2914
Evelyn Maciel de OliveiraMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0009-0000-4230-2929
Alice Ramos-SilvaMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0001-6037-8206
Natalia Fonseca RosárioMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0001-5109-085X
Thays Araújo GonçalvesMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0002-3509-1024
Camila de Melo Carvalho NascimentoMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0002-0846-7380
Amanda Mendes do ValleMolecular Epidemiology and Biotechnology Laboratory, School of Pharmacy, Universidade Federal Fluminense, Niteroi, RJ, Brazil.ORCID http://orcid.org/0000-0002-6912-6969
Lialyz Soares Pereira AndréGraduate Program in Pathology, Faculdade de Medicina, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0003-0032-8076
Fabio Aguiar-AlvesGraduate Program in Pathology, Faculdade de Medicina, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0001-6235-9367
Jorge Paulo Strogoff de MatosPostgraduate Program in Medical Science, Faculdade de Medicina, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0003-3518-9803
Jocemir Ronaldo LugonMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0001-6791-3910
Jorge Reis AlmeidaMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0001-6155-7978
Thalia MedeirosMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0002-5642-4027
Fabiana Barzotto KohlrauschHuman Genetic Laboratory, Department of General Biology, Institute of Biology, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0001-5992-2905
Andrea Alice SilvaMultiuser Laboratory for Research Support in Nephrology and Medical Sciences (LAMAP), School of Medicine, Universidade Federal Fluminense, Niterói, RJ, Brazil.ORCID http://orcid.org/0000-0001-5856-6128

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveWe evaluated the influence of single-nucleotide polymorphisms in cytokine, renin-angiotensin-aldosterone system, and uromodulin genes on COVID-19 severity and the persistence of symptoms in the post-COVID phase.

methodsTwo cross-sectional cohort studies were conducted: a retrospective cohort (cohort 1) from early phase of the pandemic and a prospective cohort (cohort 2) including patients with symptoms in the post-COVID phase. Single-nucleotide polymorphism detection was performed using real-time and conventional polymerase chain reaction.

resultsCohort 1 included 112 patients (mean age 57.4±17.5 years, 42% male). ACE rs4646994, ACE2 rs2285666, IL1A rs1800587, and TNF rs1800629 were associated with COVID-19 severity. However, when evaluating more specific outcomes such as intensive care unit admission and the need for invasive mechanical ventilation, associations were observed only for ACE2 and TNF. In women, the ACE2 rs2285666 GG genotype (p=0.003) and G allele (p=0.013) were associated with intensive care unit admission. In addition the A allele of TNF rs1800629 was associated with a higher risk of invasive mechanical ventilation (p<0.001). Cohort 2 included 107 patients (mean age 54.7±15.18 years 27.2% male). The TNF GA genotype was a risk factor for cough (p=0.03) and exertional fatigue (p=0.049). Lastly, IL1A rs1800587 was associated with the risk of persistent respiratory symptoms.

conclusionOur results suggest that single-nucleotide polymorphisms in ACE2, IL1A, and TNF may be associated with an increased risk of severe COVID-19 and persistence of symptoms in affected patients.

Indexed as

Angiotensin-Converting Enzyme 2COVID-19Interleukin-1alphaPolymorphism, Single NucleotideRenin-Angiotensin SystemTumor Necrosis Factor-alphaAdultAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedProspective StudiesRetrospective StudiesSARS-CoV-2ACE2 protein, humanAngiotensin-Converting Enzyme 2IL1A protein, humanInterleukin-1alphaTumor Necrosis Factor-alpha

Identifiers

PMID42384984
PMCPMC13399304

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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.