• Curr Med Res Opin · Jul 2024

    Randomized Controlled Trial

    Association between fatigue and depressive symptoms in persons with post-COVID-19 condition: a post hoc analysis.

    • Kayla M Teopiz, Angela T H Kwan, Gia Han Le, Ziji Guo, Sebastian Badulescu, Felicia Ceban, Shakila Meshkat, Joshua D Di Vincenzo, Giacomo d'Andrea, Bing Cao, Roger Ho, Taeho Greg Rhee, Donovan A Dev, Lee Phan, Mehala Subramaniapillai, Rodrigo B Mansur, Joshua D Rosenblat, and Roger S McIntyre.
    • Brain and Cognition Discovery Foundation, Toronto, ON, Canada.
    • Curr Med Res Opin. 2024 Jul 1; 40 (7): 120312091203-1209.

    ObjectivePost-COVID-19 Condition (PCC) is a prevalent, persistent and debilitating phenomenon occurring three or more months after resolution of acute COVID-19 infection. Fatigue and depressive symptoms are commonly reported in PCC. We aimed to further characterize PCC by assessing the relationship between fatigue and depressive symptom severity in adults with PCC.MethodsA post hoc analysis was conducted on data retrieved from a randomized, double-blinded, placebo-controlled study evaluating vortioxetine for cognitive deficits in persons with PCC. We sought to determine the relationship between baseline fatigue [i.e. Fatigue Severity Scale (FSS) total score] and baseline depressive symptom severity [i.e. 16-item Quick Inventory of Depressive Symptomatology (QIDS-SR-16) total score] in adults with PCC.ResultsThe statistical analysis included baseline data from 142 participants. After adjusting for age, sex, education, employment status, history of major depressive disorder (MDD) diagnosis, self-reported physical activity, history of documented acute SARS-CoV-2 infection and body mass index (BMI), baseline FSS was significantly correlated with baseline QIDS-SR-16 (β = 0.825, p = .001).ConclusionIn our sample, baseline measures of fatigue and depressive symptoms are correlated in persons living with PCC. Individuals presenting with PCC and fatigue should be screened for the presence and severity of depressive symptoms. Guideline-concordant care should be prescribed for individuals experiencing clinically significant depressive symptoms. Fatigue and depressive symptom severity scores were not pre-specified as primary objectives of the study. Multiple confounding factors (i.e. disturbance in sleep, anthropometrics and cognitive impairment) were not collected nor adjusted for in the analysis herein.Trial RegistrationUnrestricted Research Grant from H. Lundbeck A/S, Copenhagen, Denmark. ClinicalTrials.gov Identifier: NCT05047952.

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