Factors associated with phenotypes of dyspnea in post-COVID-19 condition: a cross-sectional study
- PMID: 38862585
- PMCID: PMC11167032
- DOI: 10.1038/s41598-024-64370-4
Factors associated with phenotypes of dyspnea in post-COVID-19 condition: a cross-sectional study
Abstract
Post-COVID-19 condition (PCC) is defined as the persistence of symptoms, like fatigue and dyspnea, at least 3 months post-COVID infection. As dyspnea is a common symptom, we attempted to further clinically phenotype those with PCC-associated dyspnea. 1642 adults (average age of 49.6y with 63% female-predominance and BMI of 31.2 kg/m2) with physician confirmed diagnosis of PCC from June 2020-April 2023 in Alberta, Canada were included. Those with dyspnea were more likely to be female (56.5%, p = 0.005) and have higher BMI (31.3 kg/m2 vs. 29.5 kg/m2; p = 0.0008), history of asthma (21.1% vs. 12.3%; p < 0.001), more persistent PCC symptoms (p = 0.0001), more functional limitations, as well as lower quality of life (p < 0.0001). Multivariable-adjusted logistic regression analysis demonstrated dyspnea was independently associated with fatigue (OR = 4.20; CI = 2.71,6.59) and inversely associated with hospitalization for COVID-19 (OR = 0.53; CI = 0.32,0.91), age (OR = 0.98 per one year of age; CI = 0.96,0.99) and 6-min-walk-distance per 10 m difference (OR = 0.98, CI = 0.96,1.0). Fatigue was a predictor of dyspnea, and was associated with milder infection, higher BMI, and reduced 6-min-walk-distance despite normal pulmonary function. Reduced TLC or DLCO was associated with more severe infection and reduced 6-min-walk-distance. Thus, we speculate there are at least two dyspnea-associated phenotypes: phenotype with pronounced fatigue (normal PFT) and phenotype with pronounced pulmonary abnormalities (abnormal PFT). Improved understanding of the dyspnea-associated phenotypes may allow for better targeted rehabilitation.
© 2024. The Author(s).
Conflict of interest statement
GYL has received research funding from Roche Diagnostics, Alberta Lung and the Canadian Institutes for Health Research and has received honoraria for educational activities from Boehringer Ingelheim, Alberta Lung, Pfizer, and Canadian Thoracics Society/Respiplus. GF has received honoraria for lectures or presentations from Boehringer Ingelheim, AstraZeneca and Roche and is on an advisory board for Boehringer Ingelheim and Roche. MKS has received funding from the Canadian Institutes for Health Research, Natural Sciences and Engineering Council and the University of Alberta Hospital. The remaining authors declare that they have no competing interests.
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