Abstract:Objective To investigate the effects of repetitive transcranial magnetic stimulation (rTMS) on hippocampal structural alterations and emotion regulation ability in patients with depression.Methods Between January 2024 and June 2025, 98 patients with depression in our hospital were enrolled and randomly assigned to a control group (n = 49), which received conventional antidepressant therapy, or an observation group (n = 49), which received rTMS in addition to conventional treatment. Clinical efficacy, symptom severity, cerebral perfusion parameters, emotion regulation ability, hippocampal volume, and adverse reactions were compared between the two groups.Results The overall effective rate was higher in the observation group than in the control group (P < 0.05). After treatment, the Hamilton Depression Rating Scale-17 items (HAMD-17) score was significantly lower in the observation group than in the control group (P < 0.05). The change in HAMD-17 score from baseline to post-treatment was significantly greater in the observation group than in the control group (P < 0.05). The changes in CBF, CBV, and MTT from baseline were also significantly greater in the observation group than in the control group (P < 0.05). After treatment, the cognitive reappraisal score was significantly higher and the expressive suppression score was significantly lower in the observation group than in the control group (P < 0.05). The changes in both scores from baseline were significantly greater in the observation group than in the control group (P < 0.05). After treatment, left, right, and bilateral hippocampal volumes were significantly higher in the observation group than in the control group (P < 0.05). The increases in hippocampal volumes from baseline were also significantly greater in the observation group than in the control group (P < 0.05). The overall incidence of adverse events showed no significant difference between the two groups (P > 0.05).Conclusion The addition of TMS to standard antidepressant therapy improves depressive symptoms and emotion regulation ability, enhances hippocampal structural plasticity, and is safe, supporting its clinical applicability.