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Published on: August 15, 2019
TAS2R38 Genotype Does Not Affect SARS-CoV-2 Infection in Primary Ciliary Dyskinesia
Gioia Piatti1, Giorgia Girotto2, Maria Pina Concas3
1Department of Pathophysiology and Transplantation, University of Milan and Unit of Bronchopneumology, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Via Francesco Sforza 35, 20122 Milan, Italy.
Individuals with Primary Ciliary Dyskinesia (PCD) do not appear to face a higher risk of severe COVID-19 outcomes. The TAS2R38 bitter taste receptor genotype also does not influence SARS-CoV-2 infection susceptibility in this population.
Area of Science:
- Genetics
- Immunology
- Pulmonology
Background:
- Primary Ciliary Dyskinesia (PCD) is a rare inherited disorder affecting respiratory cilia, leading to recurrent infections.
- Chronic respiratory conditions are potential risk factors for SARS-CoV-2 acquisition.
Purpose of the Study:
- To investigate if individuals with PCD have increased susceptibility to SARS-CoV-2 infection.
- To determine if TAS2R38 bitter taste receptor gene polymorphisms correlate with SARS-CoV-2 infection prevalence and symptom severity in PCD patients.
Main Methods:
- A cohort of 40 adult PCD patients completed questionnaires regarding SARS-CoV-2 infection, symptoms, and vaccination status.
- COVID-19 positive patients also completed SNOT-22 and ARTIQ questionnaires.
- Genotyping for TAS2R38 polymorphisms was performed.
Main Results:
- 30% of PCD patients reported a COVID-19 diagnosis, mostly with mild symptoms.
- A statistically significant difference in Body Mass Index (BMI) was observed, higher in the COVID-19 positive group (p=0.03).
- No protective role of the PAV allele of TAS2R38 against SARS-CoV-2 infection was found.
Conclusions:
- PCD patients may not be at increased risk for severe COVID-19.
- TAS2R38 bitter taste receptor genotype does not appear to influence SARS-CoV-2 infection in individuals with PCD.
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