TACS on High-inflammatory and Refractory Depression

Overview

This study is a randomized controlled trial with a duration of 12 weeks (4 weeks of intervention + 8 weeks of follow-up). The participants are patients with treatment-resistant depression (TRD) and high inflammatory activity (n=52). The study aims to clarify the effectiveness of 15mA, 77.5Hz transcranial alternating current stimulation (tACS) in treating TRD with high inflammatory activity by comparing the changes in depressive symptoms and biological markers after active tACS stimulation versus sham stimulation. Additionally, the study seeks to explore potential underlying mechanisms of action.

This experiment is a randomized controlled trial lasting 12 weeks (4 weeks of intervention + 8 weeks of follow-up), with participants being patients with treatment-resistant depression (TRD) and high inflammatory activity (n=52). The study aThis study plans to include 52 patients with treatment-resistant depression (TRD) and high inflammatory activity who meet the inclusion and exclusion criteria. Participants will be randomly assigned to either the active stimulation group (active group, n=26) or the sham stimulation group (sham group, n=26). During the baseline phase, basic information (e.g., gender, age, age of onset, family history of mental illness) will be collected, and assessments using scales (as detailed in the experimental methods) will be completed. EDTA blood collection tubes will be used to collect 10ml of fasting peripheral venous blood (-80°C for storage). The intervention will begin the following day with either tACS or sham stimulation. Before the first tACS or sham treatment, participants will undergo resting-state electroencephalogram (EEG) recordings to assess brain wave activity in different brain regions. Participants will receive a total of 20 sessions of tACS or sham intervention (5 sessions per week, with a break on weekends). At the end of weeks 2 and 4, the scales will be reassessed. After the 4-week intervention period ends, another EEG will be recorded, and fasting peripheral venous blood (10ml) will be collected the following morning for storage. After the intervention phase, participants will enter an 8-week follow-up period. At the 8th and 12th weeks, all participants will undergo a reassessment using the HAMD-17 scale and provide 10ml of peripheral venous blood for analysis. The data from the scales, blood analysis, and EEG will be summarized and used for statistical analysis. Throughout the study, participants' antidepressant medication will remain unchanged. The specific details are as follows: 1. Assessment of Treatment Efficacy: The changes in depressive symptoms before and after treatment will be compared within groups using the HAMD-17 scale, allowing the quantification of the clinical effect of tACS treatment. Between-group comparisons will be made between the active tACS group and the sham stimulation group to evaluate the difference in actual therapeutic efficacy versus placebo effect. 2. Analysis of Changes in Peripheral Blood Biomarkers: Blood samples will be analyzed for levels of inflammatory factors and glial cell activity markers before and after treatment. This will help explore the correlation between these biomarkers and depressive symptoms. It may provide insights into whether the antidepressant effects of tACS are mediated by biological changes, specifically whether tACS works by modulating immune-inflammatory responses. 3. Assessment of Electroencephalogram (EEG) Changes: EEG recordings will be analyzed to assess brain wave activity in different brain regions before and after treatment. This will help explore the relationship between changes in brain wave power in specific regions and the improvement in depressive symptoms, as well as how these changes relate to the levels of biological markers. 4. Long-Term Follow-Up Results: Follow-up at 8 weeks and 12 weeks after treatment will provide data on the durability of the tACS treatment effect. This will help assess the potential long-term value of tACS in the management of treatment-resistant depression. 5. Insights into Mechanisms of Action and Etiology: The models established through data analysis may reveal how tACS affects the underlying etiology of depression, particularly the role of immune-inflammatory responses. These insights could help identify new therapeutic targets for treatment-resistant depression and facilitate the development of novel treatment strategies.