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Study on the Mechanism of Immune Inflammation in Cognitive Impairment of Depression (depression)

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Xi'an Jiaotong University

Status

Enrolling

Conditions

Depression

Treatments

Other: no-intervention

Study type

Observational

Funder types

Other

Identifiers

NCT06100302
XJTU1AF2022LSK-249

Details and patient eligibility

About

The patients with depression were observed and followed up to evaluate the changes of symptoms and cognitive function in patients with depression at different time points before and after drug treatment. At the same time, immunometabolism indicators in serum, urine and stool were detected to screen out immunoinflammatory markers related to cognitive function and treatment response in patients with depression, hoping to provide a new strategy for optimal treatment of depression.

Full description

  1. Participants were included according to the inclusion and exclusion criteria, and demographic data of depressed patients and healthy controls were recorded, including age, sex, ethnicity, occupation, etc. Subjects in the depression group were treated with antidepressants (as recommended by the guidelines) and were followed up baseline, 2 weeks, 8 weeks, 12 weeks, and 24 weeks after treatment, respectively. At each follow-up point, symptoms were assessed using Hamilton Depression Scale (HAMD), Hamilton Anxiety Scale (HAMA), Depression Screening Scale (PHQ-9) and Generalized Anxiety Scale (GAD-7), and cognitive function was assessed using Thinc-it at three follow-up points: baseline, 12 weeks after treatment, and 24 weeks after treatment. General data were compared between patients with depression and healthy controls at baseline.
  2. The depression group was followed up. Serum and fecal of patients with depression were collected at 5 follow-up points at baseline, 2 weeks, 8 weeks, 12weeks and 24 weeks after treatment, and serum metabolic indexes and fecal metagenome were detected.

Enrollment

400 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18-60 years old, male or female;
  • Meet the diagnostic criteria for depression in the International Classification of Diseases-10 (ICD-10), and the Hamilton Depression Scale (HAMD) score ≥18 points;
  • Junior high school education and above, can cooperate with the completion of relevant scales and sample collection;
  • did not receive antidepressant therapy at admission or took medication for less than 14 days; And the duration of drug withdrawal ≥3 months;
  • No history of infection and taking hormones, antibiotics or anti-inflammatory drugs in the past 1 month;
  • History of physical diseases such as centerless, liver, kidney and gastrointestinal tract, active infection, active or chronic inflammation, autoimmune diseases, etc.

Exclusion criteria

  • Pregnant and lactating women;
  • Clinically significant or unstable medical conditions, including congestive heart failure, liver and kidney failure, cancer, immune and metabolic endocrine diseases;
  • Patients with acute or chronic infection, taking anti-inflammatory drugs, cortisol hormones, and receiving antibiotics for 3 consecutive days in the past 1 month;
  • Patients with neuropsychiatric diseases other than depression.

Trial design

400 participants in 2 patient groups

MD group
Description:
Patients with depression who met the inclusion criteria
Treatment:
Other: no-intervention
HC group
Description:
Healthy subjects meeting enrollment criteria
Treatment:
Other: no-intervention

Trial contacts and locations

1

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Central trial contact

Jia M; Ma q y

Data sourced from clinicaltrials.gov

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