Study on the Mechanism of Multi-group Analysis of the Influence of Depression on Common Cardiovascular Diseases
NCT ID: NCT06975592
Last Updated: 2025-05-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
NOT_YET_RECRUITING
300 participants
OBSERVATIONAL
2025-05-25
2029-07-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Depression is a health problem as common as cardiovascular disease, and it has been proved to be an important risk factor of cardiovascular disease. Previous studies have shown that depression is related to the increased risk of subsequent cardiovascular events, including myocardial infarction, angina pectoris, stroke and cardiovascular mortality. The risk of cardiovascular disease in patients with major depression is about 72% higher than that in healthy control group.
Previous studies have shown that compared with healthy people, the intestinal microbial composition of patients with major depression, especially the microbial diversity and the relative abundance of specific bacterial groups, has changed significantly. Many studies have also confirmed that dysbacteriosis may be an important cause of MDD, and with the passage of time, the pathological changes caused by MDD will further destroy the intestinal environment and lead to dysbacteriosis. In addition, intestinal microflora can also produce a variety of important mediators, such as metabolites produced by bacterial fermentation of food, host molecules modified by bacteria (bile acids, etc.) or direct products of bacteria, which also play an important role in the pathogenesis of MDD. In recent years, both population studies and animal experiments have found that the changes in the composition and function of intestinal flora (that is, the imbalance of intestinal microbial flora) will accelerate the occurrence and development of cardiovascular diseases. Intestinal flora will metabolize the food ingested by the host into a series of metabolites, including trimethylamine oxide, short-chain fatty acids, secondary bile acids and indole sulfate, etc. These metabolites will affect the physiological process of the host by activating various signal pathways, thus affecting the occurrence and development of cardiovascular diseases (such as coronary heart disease, hypertension, arrhythmia and heart failure).
All the above results suggest that intestinal flora and its metabolites play an important role in promoting the occurrence and development of cardiovascular diseases in depression, but its internal mechanism is not completely clear. Therefore, it is of great significance to deeply explore the pathophysiological mechanism of depression on cardiovascular diseases for guiding the prevention and treatment of cardiovascular diseases.
A total of 300 people were enrolled in this study, which were divided into healthy control group, depression group and depression combined with cardiovascular disease group, with 100 cases in each group. Samples of patients' feces, urine peripheral blood and oral secretions were collected and analyzed by multi-omics. Subsequently, after 6 months, 1 year, 2 years and 5 years after discharge, the clinical prognosis of the patients was obtained and recorded.
The purpose of this study is to discover and deeply explore the pathophysiological mechanism of depression on common cardiovascular diseases (coronary heart disease, hypertension, arrhythmia or heart failure) through the research methods of 16S rDNA sequencing, metagenome sequencing and metabonomics, so as to provide theoretical basis for comprehensive treatment of cardiovascular diseases caused by depression, and at the same time provide potential biomarkers and prevention targets for cardiovascular diseases caused by depression.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Hostility, Depression, Social Environment and CHD Risk
NCT00005533
Major Depressive Disorder - Understanding The Link Between The Brain And The Heart
NCT01568307
Depression Care for Hospitalized Coronary Heart Disease Patients: Prospective Cohort Study
NCT01626027
Cardiac Markers in Depressed Patients With Coronary Heart Disease - R01HL147862
NCT04682769
The Impact of Depression and/or Anxiety on PCI Patients
NCT03057691
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
OTHER
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Healthy control group
1\) Good health and no gastrointestinal diseases; 2) No previous history of mental illness; 2) No previous history of cardiovascular disease;
No interventions assigned to this group
Depression group
1. Meet the diagnostic criteria of the latest guidelines for depression, and be clinically diagnosed by at least two psychiatrists;
2. Patients with first-episode depression;
3. Have not taken any psychoactive drugs before or have not taken any psychoactive drugs within 4 weeks.
No interventions assigned to this group
Depression with cardiovascular disease group
1. Meet the diagnostic criteria of the latest guidelines for depression, and be clinically diagnosed by at least two psychiatrists;
2. Patients with first-episode depression;
3. Have not taken any psychoactive drugs before or have not taken any psychoactive drugs within 4 weeks.
4. There is definite clinical evidence of heart failure, coronary heart disease, hypertension or arrhythmia.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Depression group
1\) Meet the diagnostic criteria of the latest guidelines for depression, and be clinically diagnosed by at least two psychiatrists; 2) Patients with first-episode depression; 3) Have not taken any psychoactive drugs before or have not taken any psychoactive drugs within 4 weeks.
3\. Depression with cardiovascular disease group
1. Meet the diagnostic criteria of the latest guidelines for depression, and be clinically diagnosed by at least two psychiatrists;
2. Patients with first-episode depression;
3. Have not taken any psychoactive drugs before or have not taken any psychoactive drugs within 4 weeks.
4. There is definite clinical evidence of heart failure, coronary heart disease, hypertension or arrhythmia.
Exclusion Criteria
2. Long-term use of psychoactive drugs/use of psychoactive drugs within 4 weeks;
3. Patients with thyroid dysfunction
4. Patients with severe liver and kidney dysfunction;
5. Patients with chronic obstructive pulmonary disease, interstitial pulmonary fibrosis and pulmonary hypertension;
6. Patients with autoimmune diseases and tumors;
7. used antibiotics, yogurt or other drugs or foods that affect intestinal flora within 4 weeks;
8. Pregnant or lactating women;
9. There is a serious impairment of cognitive function, which makes it impossible to cooperate with the research procedure;
10. Have received invasive medical procedures such as gastroscopy and colonoscopy in the past three months;
11. The diet has changed greatly in the past week;
12. Participate in simultaneous clinical trials;
13. Refuse to sign the informed consent for participating in the experiment.
85 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
First Affiliated Hospital of Harbin Medical University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
The First Affiliated Hospital of Harbin Medical University
Harbin, Heilongjiang, China
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Depression and CVD
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.