Background: The relationship between the imbalance of TH1-TH2 cytokine levels in the early stages of acute ischemic stroke (AIS) and the subsequent development of post-stroke depression (PSD) remains unclear. Early detection of PSD and understanding its progression hold critical clinical significance.
Methods: A prospective cohort study was conducted involving 119 patients with AIS admitted to Suzhou Municipal Hospital. Th1/Th2 cytokines (TNF-α, IL-2, IFN-γ, IL-4, IL-6, IL-10) were measured within 24 h of admission. PSD was assessed at 3 months using the Hamilton Depression Rating Scale (HAMD). Logistic regression analysis was used to identify factors associated with PSD.
Results: The PSD group exhibited higher HAMD scores and modified Rankin Scale (mRS) scores at 3 months (P < 0.001). The Th1 cytokine TNF-α was elevated, while the Th2 cytokine IL-4 was decreased in the PSD group (P < 0.05). The TNF-α/IL-4 ratio was significantly elevated in the PSD group (P < 0.001). Multivariate regression analysis confirmed that Th1-Th2 cytokine imbalance in the early stages of AIS was an independent predictor of PSD at 3 months (P-trend<0.001), with the TNF-α/IL-4 ratio demonstrating the highest predictive value (AUC = 0.741, sensitivity 57.9 %, specificity 85.2 %, P < 0.001).
Conclusion: Early Th1-Th2 cytokine imbalance in AIS patients serves as a significant predictor of PSD at 3 months. These findings suggest that immune dysfunction during the early stage may aid in identifying patients at higher risk for developing PSD.
Keywords: Acute ischemic stroke; Post-stroke depression; Th1-Th2 imbalance.
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