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Clinical Trials/NCT05680844
NCT05680844
Completed
Not Applicable

Observational Study of the Correlation Between Peripheral Treg Cell Senescence and Serum Total Cholesterol Level

Tianjin Medical University1 site in 1 country200 target enrollmentJanuary 1, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hypercholesterolemia
Sponsor
Tianjin Medical University
Enrollment
200
Locations
1
Primary Endpoint
Treg cell senescence
Status
Completed
Last Updated
last year

Overview

Brief Summary

Hypercholesterolemia is a risk factor for the occurrence and development of atherosclerosis. Recent animal studies have found that increased serum cholesterol level is associated with peripheral Treg cell senescence, but clinical evidence is still lacking. The purpose of this study is to analyze the correlation between human peripheral Treg cell senescence and serum total cholesterol level using clinical blood samples, thus laying a foundation for the establishment of novel therapeutic strategies for atherosclerosis based on the regulation of Treg cell senescence.

Detailed Description

Hypercholesterolemia is a risk factor for the occurrence and development of atherosclerosis. Recent animal studies have found that increased serum cholesterol level is associated with peripheral Treg cell senescence, but clinical evidence is still lacking. The purpose of this study is to analyze the correlation between human peripheral Treg cell senescence and serum total cholesterol level using clinical blood samples, thus laying a foundation for the establishment of novel therapeutic strategies for atherosclerosis based on the regulation of Treg cell senescence.

Registry
clinicaltrials.gov
Start Date
January 1, 2023
End Date
December 31, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
Tianjin Medical University
Responsible Party
Principal Investigator
Principal Investigator

Xintong Ge

Professor

Tianjin Medical University General Hospital

Eligibility Criteria

Inclusion Criteria

  • Age ≥ 30 and ≤ 60 years old with independent behavior ability.
  • The participants need to fully understand the purpose and content of the study, and voluntarily participate in the study and sign the informed consent.

Exclusion Criteria

  • Pregnant or lactating women.
  • Acute and severe diseases in the last 3 months, including but not limited to, acute myocardial infarction, acute cerebral infarction, cerebral hemorrhage, circulatory failure, respiratory failure (internal diseases), trauma requiring hospitalization, or undergoes surgery under general anesthesia (surgical diseases).
  • History of severe diseases, including but not limited to, tumors, serious hematological diseases, serious cardiopulmonary diseases (interventional therapy for coronary artery disease, atrial fibrillation, chronic obstructive pulmonary disease, etc.), renal failure, liver failure, old stroke with serious sequelae.
  • Have participated in clinical trials in the past 3 months.
  • The investigator considers that not appropriate for inclusion.

Outcomes

Primary Outcomes

Treg cell senescence

Time Frame: After confirming the subject has signed the informed consent, and recorded the past medical history and medication (especially hypolipidemic drugs) in the past 3 months.

Treg cell senescence will be evaluated by the beta-galactosidase (SA-betagal) activity test

Study Sites (1)

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