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TAS2R38 haplotypes, COVID-19 infection, and symptomatology: a cross-sectional analysis of data from the Canadian Longitudinal Study on Aging.
Meng, Tongzhu; Nielsen, Daiva E.
Afiliación
  • Meng T; School of Human Nutrition, McGill University, 21,111 Lakeshore Rd., Room MS2-035, Saint-Anne-de-Bellevue, QC, H9X 3V9, Canada.
  • Nielsen DE; School of Human Nutrition, McGill University, 21,111 Lakeshore Rd., Room MS2-035, Saint-Anne-de-Bellevue, QC, H9X 3V9, Canada. daiva.nielsen@mcgill.ca.
Sci Rep ; 14(1): 4673, 2024 02 26.
Article en En | MEDLINE | ID: mdl-38409357
ABSTRACT
The TAS2R38 gene is well known for its function in bitter taste sensitivity, but evidence also suggests a role in innate immunity. TAS2R38 may be relevant in coronavirus disease 2019 (COVID-19), but research findings are inconsistent. The objective of this study was to explore whether common TAS2R38 haplotypes are associated with COVID-19 infection and symptomatology in the Canadian Longitudinal Study on Aging (CLSA). Data from the CLSA COVID-19 Questionnaire and Seroprevalence sub-studies were utilized with CLSA genetic data for common TAS2R38 haplotypes related to bitter taste sensitivity. Haplotypes were categorized into three diplotype groups [P]AV homozygotes, [P]AV/[A]VI heterozygotes, and [A]VI homozygotes. No significant differences were observed between diplotypes and COVID-19 infection frequency. Among self-reported COVID-19 cases (n = 76), and in uncorrected exploratory analyses, heterozygotes were less likely to report experiencing sinus pain compared to [P]AV homozygotes. Among seroprevalence-confirmed cases (n = 177), [A]VI homozygotes were less likely to report experiencing a sore/scratchy throat compared to [P]AV homozygotes. However, both observations were non-significant upon correction for multiple testing. In this study, TAS2R38 haplotypes were not significantly associated with COVID-19 infection or symptomatology. Nevertheless, in light of some exploratory patterns and conflicting evidence, additional research is warranted to evaluate links between TAS2R38 and innate immunity.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Receptores Acoplados a Proteínas G / COVID-19 Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Receptores Acoplados a Proteínas G / COVID-19 Límite: Humans País/Región como asunto: America do norte Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article País de afiliación: Canadá