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Clinical Trials/NCT02126280
NCT02126280CompletedNot Applicable

Cross-sectional Clinical Study of the Individual Profile of Activation of Circulating Blood Monocytes in Subjects With Preclinical Atherosclerosis.

Institute for Atherosclerosis Research, Russia1 site in 1 country170 target enrollmentStarted: November 2012Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
170
Locations
1
Primary Endpoint
Development and optimization of the method of monocyte-macrophage isolation.

Study Overview

Brief Summary

The study of proinflammatory and anti-inflammatory cytokines and chemokines expression profiles in human monocytes to identify new effective biomarkers that have the best diagnostic potential in asymptomatic atherosclerosis.

Detailed Description

This project is the first step in creating a method for assessing an individual activity of macrophages. The problems addressed in the project are socially significant because of the high incidence of life-threatening diseases and their effects in the population. The method of evaluation of monocyte-macrophages activity in human blood will be based on the analysis of expression of cytokines and chemokines - markers of inflammatory and anti-inflammatory activity of macrophages. The most informative panel of cytokines and chemokines obtained during the project can be further used to create effective diagnostic tests.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
40 Years to 79 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • men and women aged 40 to 74 years
  • arterial normotension or mild arterial hypertension (systolic blood pressure <160 mm Hg, diastolic blood pressure <90 mm Hg)
  • absence of chronic diseases demanding permanent drug administration (more than 2 month per year)

Exclusion Criteria

  • personal history of transient ischemic attacks
  • personal history of chronic diseases demanding permanent drug administration (more than 2 month per year)
  • personal history of life-threatening diseases
  • indications for surgical treatment of atherosclerotic lesions localized in the extracranial brachiocephalic system

Outcomes

Primary Outcomes

Development and optimization of the method of monocyte-macrophage isolation.

Time Frame: up to 1 years

Technique for isolation/separation of monocytes with culture purity more than 95 % CD14-positive cells according to flow cytometry, the share of viable cells at least 98% by trypan blue vital staining, capable of producing TNFa at concentration of at least 50 pg/ml when stimulated with 100 ng/ml IFN-gamma, and CCL18 at concentration at least 30 pg/ml when stimulated with 10 ng/ml interleukin.

Secondary Outcomes

  • Sample processing and parameter measurements.(up to 1 years)

Investigators

Sponsor
Institute for Atherosclerosis Research, Russia
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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