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. 2022 Dec 1;5(12):e2245861.
doi: 10.1001/jamanetworkopen.2022.45861.

Trends in Risk Factors and Symptoms Associated With SARS-CoV-2 and Rhinovirus Test Positivity in King County, Washington, June 2020 to July 2022

Affiliations

Trends in Risk Factors and Symptoms Associated With SARS-CoV-2 and Rhinovirus Test Positivity in King County, Washington, June 2020 to July 2022

Chelsea Hansen et al. JAMA Netw Open. .

Abstract

Importance: Few US studies have reexamined risk factors for SARS-CoV-2 positivity in the context of widespread vaccination and new variants or considered risk factors for cocirculating endemic viruses, such as rhinovirus.

Objectives: To evaluate how risk factors and symptoms associated with SARS-CoV-2 test positivity changed over the course of the pandemic and to compare these with the risk factors associated with rhinovirus test positivity.

Design, setting, and participants: This case-control study used a test-negative design with multivariable logistic regression to assess associations between SARS-CoV-2 and rhinovirus test positivity and self-reported demographic and symptom variables over a 25-month period. The study was conducted among symptomatic individuals of all ages enrolled in a cross-sectional community surveillance study in King County, Washington, from June 2020 to July 2022.

Exposures: Self-reported data for 15 demographic and health behavior variables and 16 symptoms.

Main outcomes and measures: Reverse transcription-polymerase chain reaction-confirmed SARS-CoV-2 or rhinovirus infection.

Results: Analyses included data from 23 498 individuals. The median (IQR) age of participants was 34.33 (22.42-45.08) years, 13 878 (59.06%) were female, 4018 (17.10%) identified as Asian, 654 (2.78%) identified as Black, and 2193 (9.33%) identified as Hispanic. Close contact with an individual with SARS-CoV-2 (adjusted odds ratio [aOR], 3.89; 95% CI, 3.34-4.57) and loss of smell or taste (aOR, 3.49; 95% CI, 2.77-4.41) were the variables most associated with SARS-CoV-2 test positivity, but both attenuated during the Omicron period. Contact with a vaccinated individual with SARS-CoV-2 (aOR, 2.03; 95% CI, 1.56-2.79) was associated with lower odds of testing positive than contact with an unvaccinated individual with SARS-CoV-2 (aOR, 4.04; 95% CI, 2.39-7.23). Sore throat was associated with Omicron infection (aOR, 2.27; 95% CI, 1.68-3.20) but not Delta infection. Vaccine effectiveness for participants fully vaccinated with a booster dose was 93% (95% CI, 73%-100%) for Delta, but not significant for Omicron. Variables associated with rhinovirus test positivity included being younger than 12 years (aOR, 3.92; 95% CI, 3.42-4.51) and experiencing a runny or stuffy nose (aOR, 4.58; 95% CI, 4.07-5.21). Black race, residing in south King County, and households with 5 or more people were significantly associated with both SARS-CoV-2 and rhinovirus test positivity.

Conclusions and relevance: In this case-control study of 23 498 symptomatic individuals, estimated risk factors and symptoms associated with SARS-CoV-2 infection changed over time. There was a shift in reported symptoms between the Delta and Omicron variants as well as reductions in the protection provided by vaccines. Racial and sociodemographic disparities persisted in the third year of SARS-CoV-2 circulation and were also present in rhinovirus infection. Trends in testing behavior and availability may influence these results.

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Conflict of interest statement

Conflict of Interest Disclosures: Ms Hansen reported receiving personal fees from Sanofi outside the submitted work. Ms Kuchta reported receiving grants from Pierce County during the conduct of the study. Dr Waghmare reported receiving clinical trial support to their institution from Pfizer, Ansun Biopharma, Allovir, and GlaxoSmithKline/Vir; receiving personal fees from Kyorin Pharmaceuticals; and receiving grants from Amazon and VB Tech outside the submitted work. Dr Englund reported receiving grants from Pfizer, AstraZeneca, Merck, and GlaxoSmithKline and receiving personal fees from Pfizer, AstraZeneca, Meissa Vaccines, Moderna, and Sanofi Pasteur outside the submitted work. Dr Chu reported receiving personal fees from Ellume, the Bill and Melinda Gates Foundation, Vindico, Abbvie, Merck, and Pfizer; receiving research funding from Gates Ventures and Sanofi Pasteur and receiving support and reagents from Ellume and Cepheid outside the submitted work. Dr Viboud reported receiving honoraria from Elsevier outside the submitted work. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Total Enrollments, Excluded Enrollments, and Final Sample Size
Figure 2.
Figure 2.. Trends in Viral Circulation, Nonpharmaceutical Interventions, and Vaccination
A, The 5-week moving average of the percentage of samples positive for SARS-CoV-2 and rhinovirus in the Seattle Coronavirus Assessment Network (SCAN) study population over time, the square root of the reported SARS-CoV-2 cases in King County divided by 3 (for easier visualization), and the percentage of positive rhinovirus tests in the Pacific Northwest (PNW) surveillance system. Vertical dashed lines separate time-periods (wild-type variant, pre-Omicron variants, Omicron variants). B, The percentage of SCAN study participants by vaccination status (not fully vaccinated includes unvaccinated or received an incomplete primary schedule) and the weekly average of the Oxford Stringency Index in Washington State, which reflects the strength of interventions on a scale of 0% to 100%. Dashed lines separate time-periods (wild-type variant, pre-Omicron variants, Omicron variants).
Figure 3.
Figure 3.. Risk Factors and Symptoms Associated With SARS-CoV-2 and Rhinovirus Infection
A, Adjusted odds ratios (aORs) and 95% CIs for risk factors associated with SARS-CoV-2 and rhinovirus positivity. Odds ratios are ordered from highest to lowest for SARS-CoV-2. Missing bars indicate the variable was not included in the model a priori or dropped during model selection. Bars touching the dashed vertical line are not statistically significant. B, Separate models were run for the risk of test positivity with Delta and Omicron. aOther race and ethnicity includes American Indian or Alaska Native, Native Hawaiian and other Pacific Islander, other, and 2 or more races.

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