Evidence map›Paper›PMID 42376321›Full record

ArticleFrontiers in cellular and infection microbiology2026

Genetic association between LONG COVID and TMPRSS2 polymorphisms (rs12329760 and rs2070788) in Brazilian healthcare professionals.

Alysson Fellipe Costa Telles, Bearli Souza Menezes Junior, Cliomar Alves Dos Santos, Ludmila Oliveira Carvalho Sena, Maria Rosa Melo Alves, Maria Luiza Aguiar Martins Moraes, Rosana Cipolotti

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Alysson Fellipe Costa TellesPostgraduate Program in Health Sciences at the Federal University of Sergipe, Aracaju, Brazil.
Bearli Souza Menezes JuniorParreiras Horta Health Foundation, Aracaju, Brazil.
Cliomar Alves Dos SantosParreiras Horta Health Foundation, Aracaju, Brazil.
Ludmila Oliveira Carvalho SenaPostgraduate Program in Health Sciences at the Federal University of Sergipe, Aracaju, Brazil.
Maria Rosa Melo AlvesPostgraduate Program in Health Sciences at the Federal University of Sergipe, Aracaju, Brazil.
Maria Luiza Aguiar Martins MoraesPostgraduate Program in Health Sciences at the Federal University of Sergipe, Aracaju, Brazil.
Rosana CipolottiPostgraduate Program in Health Sciences at the Federal University of Sergipe, Aracaju, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long COVID syndrome has a multifactorial cause that is not fully understood and may be influenced by both external and intrinsic factors. In this context, a Genome-Wide Association Study (GWAS) was proposed to evaluate the association between Single Nucleotide Polymorphisms (SNPs) in TMPRSS2 (rs12329760 and rs2070788) and the occurrence of Long COVID in 363 Brazilian healthcare professionals, recruited using a non-probabilistic method. The study employed a self-report questionnaire to collect sociodemographic and clinical data from both the acute and chronic phases and also collected oral mucosa cells for genotypic analysis by qPCR using Taqman probes. The categorized information was analyzed using the PSPP software using Pearson's chi-square test in three genetic statistical models: additive, dominant, and recessive. Assessing long COVID in general, only clinical variables such as increased susceptibility, presence of symptoms, and severity influenced the occurrence of the syndrome. When specifying the main reported symptom, brain fog, females and young adults (18 to 29 years old) are the most vulnerable, and rs2070788 in the recessive model proved to be relevant. This association is more evident when evaluating only the symptomatic group in the post-COVID period, as the additive model also influences the groups. rs12329760 showed no relevant influence on the groups. Therefore, this study provides unprecedented evidence of the association between brain fog and rs2070788, requiring case-control studies to better clarify how this association occurs.

Indexed as

COVID-19Genetic Predisposition to DiseaseHealth PersonnelPolymorphism, Single NucleotideSerine EndopeptidasesAdolescentAdultBrazilFemaleGenome-Wide Association StudyGenotypeHumansMaleMiddle AgedPost-Acute COVID-19 SyndromeSARS-CoV-2Serine EndopeptidasesTMPRSS2 protein, humanenzymological regulation of gene expressiongenetic susceptibilitylong Covidoccupational healthsingle nucleotide polymorphism

Identifiers

PMID42376321
PMCPMC13311128

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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 Socratic graph.