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Depressive symptoms are highly prevalent in long COVID (LC) and may shape its symptom burden. As hypothalamic–pituitary–adrenal (HPA) axis and autonomic nervous system (ANS) alterations have been implicated in both LC and depressive disorders, this overlap raises the question of whether both conditions share psychobiological activity patterns or show distinct profiles. The present study compared these systems between youth with LC and depressive disorders during a developmental period of heightened mental health vulnerability. Thirty-four participants were included ( n = 17 per subgroup; LC: M age = 16.3 years; depressive disorders: M age = 18.8 years). Cumulative HPA axis activity was indexed via hair cortisol concentration (HCC). Basal ANS activity was assessed via five-minute resting-state heart rate variability. Fatigue, perceived stress, and psychological distress were self-reported. Group differences were analysed using Mann–Whitney U tests, with correlational analyses. Participants with depressive disorders exhibited higher HCC than those with LC ( p = .004, r = .69). In contrast, participants with LC showed reduced parasympathetic activity (lower HFnu; p = .018, r = .57) and diminished autonomic adaptability (higher DFA-α1, p = .013, r = −.60). Within LC, fatigue and psychological distress were associated with attenuated parasympathetic indices, while fatigue was also linked to lower HCC. Despite overlapping symptom profiles, LC and depressive disorders showed distinct psychobiological signatures, alongside divergent autonomic and endocrine correlates of subjective symptom burden. Longitudinal mechanistic studies are needed to clarify the development and specificity of these alterations following SARS-CoV-2 infection.
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“Nonlinear HRV metrics (DFA-α1, SampEn) combined with hair cortisol can discriminate long COVID from depressive disorders in youth even with small samples, supporting their use in differential assessment and potentially in monitoring intervention response.”
“Without a healthy reference, it cannot be determined whether HCC or HRV indices in either clinical group deviate from normative physiological levels, nor whether the observed patterns are specific to LC or depressive disorders. Accordingly, the present findings should be understood as relative differences between the two clinical groups.”
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Oehlke et al. (2026) studied this question.
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