Use este identificador para citar ou linkar para este item: http://hdl.handle.net/1843/60395
Tipo: Artigo de Periódico
Título: Negative correlation between ACE2 gene expression levels and loss of taste in a cohort of COVID-19 hospitalized patients: New clues to long-term cognitive disorders
Autor(es): Isabela Braga-Paz
João Locke Ferreira de Araújo
Hugo José Alves
Renata Eliane de Ávila
Gustavo Gomes Resende
Mauro Martins Teixeira
Renato Santana de Aguiar
Renan Pedra de Souza
Diana Bahia
Resumo: In early 2020, one of the most prevalent symptoms of SARS-CoV-2 infection was the loss of smell (anosmia), found in 60-70% of all cases. Anosmia used to occur early, concomitantly with other symptoms, and often persisted after recovery for an extended period, sometimes for months. In addition to smell disturbance, COVID-19 has also been associated with loss of taste (ageusia). The latest research suggests that SARS-CoV-2 could spread from the respiratory system to the brain through receptors in sustentacular cells localized to the olfactory epithelium. The virus invades human cells via the obligatory receptor, angiotensin-converting enzyme II (ACE2), and a priming protease, TMPRSS2, facilitating viral penetration. There is an abundant expression of both ACE2 and TMPRSS2 in sustentacular cells. In this study, we evaluated 102 COVID-19 hospitalized patients, of which 17.60% presented anosmia and 9.80% ageusia. ACE1, ACE2, and TMPRSS2 gene expression levels in nasopharyngeal tissue were obtained by RT-qPCR and measured using ΔCT analysis. ACE1 Alu287bp association was also evaluated. Logistic regression models were generated to estimate the effects of variables on ageusia and anosmia Association of ACE2 expression levels with ageusia. was observed (OR: 1.35; 95% CI: 1.098-1.775); however, no association was observed between TMPRSS2 and ACE1 expression levels and ageusia. No association was observed among the three genes and anosmia, and the Alu287bp polymorphism was not associated with any of the outcomes. Lastly, we discuss whetherthere is a bridge linking these initial symptoms, including molecular factors, to long-term COVID-19 health consequences such as cognitive dysfunctions.
Assunto: COVID-19
Genética
Disfunção Cognitiva
Idioma: eng
País: Brasil
Editor: Universidade Federal de Minas Gerais
Sigla da Instituição: UFMG
Departamento: ICB - INSTITUTO DE CIÊNCIAS BIOLOGICAS
Tipo de Acesso: Acesso Aberto
Identificador DOI: https://doi.org/10.3389/fcimb.2022.905757
URI: http://hdl.handle.net/1843/60395
Data do documento: 29-Set-2022
metadata.dc.url.externa: https://www.frontiersin.org/articles/10.3389/fcimb.2022.905757/full
metadata.dc.relation.ispartof: Frontiers in Cellular and Infection Microbiology
Aparece nas coleções:Artigo de Periódico



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