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Current testing for SARS-CoV-2 focuses on detection of the pathogen via isolated nucleic acids, routinely from nasopharyngeal swabs. To our knowledge, no approved clinical SARS-CoV-2 diagnostic tests using nasopharyngeal swabs incorporate measurements of host responses at the time of diagnosis. Monitoring host responses during SARS-CoV-2 infection is important, as stratification of COVID-19 patients based on host responses is predictive of mortality. Conveniently, host nucleic acids can be isolated from the same swab used for SARS-CoV-2 diagnosis, providing an efficient means for early and simultaneous measurement of both host and viral transcripts.
We will generate algorithms for predicting patient morbidity/mortality and healthcare system utilization by correlating host transcriptome profile from COVID-19 diagnostic swabs with clinical outcomes of cases and controls.
Our results will define the relationship between host transcriptome responses and COVID-19 disease progression will i) identify high-risk patients that would benefit from early intervention strategies and ii) provide predictive capacity for hospitals to efficiently prepare and allocate resources for optimal patient health.
Jeremy Hirota
Dayna Mikkelsen
Incubate Innovate Network of Canada
Medicine
Professional, scientific and technical services
McMaster University
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