Why the study?
Long-term patterns of depressive symptoms among patients with HFpEF and their relationship with prognoses are not well studied.
Does a recurrent deterioration depression trajectory increase the risk of all-cause mortality in patients with HFpEF?
Does a recurrent deterioration depression trajectory increase the risk of all-cause mortality in patients with HFpEF?
Monitoring depression trajectories over time in HFpEF patients reveals that recurrent deterioration of depressive symptoms is associated with a significantly increased risk of all-cause mortality.
Depressive symptom trajectories may refine HFpEF prognosis; hypothesis-generating and should not yet change practice.
BACKGROUND: Long-term patterns of depressive symptoms among patients with heart failure, specifically those with a preserved ejection fraction (HFpEF), and their relationship with prognoses are not well studied. METHODS: This analysis included 609 participants from the TOPCAT (Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist) trial. Depressive symptoms were assessed using the Patient Health Questionnaire-9 (PHQ-9) at baseline and at 1-year, 2-year and 3-year intervals. Individual trajectory patterns based on PHQ-9 scores during the first 3 years were identified using latent class trajectory models, and their associations with clinical outcomes were evaluated using Cox regression models. RESULTS: Among the 609 participants, 316 (51.9%) were female, with a median age of 74 years (IQR: 66, 80). Four distinct depression trajectory patterns were identified: low (consistently low scores; 349, 57.3%), mild (sustained mild elevation; 110, 18.1%), high (sustained moderate-severe elevation; 52, 8.5%) and recurrent deterioration (high baseline scores, remission, then escalation; 98, 16.1%). According to the multivariate Cox model, recurrent deterioration was associated with a significantly greater risk of all-cause mortality (HR: 2.05; 95% CI 1.16, 3.64) than the low trajectory pattern. No significant differences were found among the low, mild and high trajectory groups. CONCLUSIONS: Four distinct depression trajectory patterns were identified among patients with HFpEF. Notably, patients who experienced a recurrent deterioration trajectory presented a significantly increased risk of all-cause mortality. Our findings highlight the importance of monitoring patients' depressive symptoms over time rather than focusing on a single timepoint. TRIAL REGISTRATION NUMBER: NCT00094302.
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Xing et al. (2025) studied this question.
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