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Clinical Trials/NCT02857387
NCT02857387
Completed
N/A

Markers of Vascular Aging and Coronary Syndrome

CHU de Reims1 site in 1 country65 target enrollmentOctober 2015

Overview

Phase
N/A
Intervention
Not specified
Conditions
Acute Coronary Syndrome
Sponsor
CHU de Reims
Enrollment
65
Locations
1
Primary Endpoint
Post-translational modifications of Proteins quantification assessed by Liquid chromatography-mass spectrometry
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

Atherosclerosis and aging are associated to the raise of biochemical alterations of proteins grouped under the name of " non-enzymatic post-translational modifications ". They often correspond to the irreversible binding of glucose or other oses (glycation) or urea derivatives (carbamylation) on proteins and lead to the formation of complex compounds (post-translational modifications derived products, PTMD) that can accumulate in tissues and be responsible for deleterious effects. The specific role of these compounds in the pathophysiology of aging and atherosclerosis remains unknown, as are the molecular and cellular mechanisms implicated.

This project is based on the hypothesis that non-enzymatic post-translational modifications may cause changes in the genesis of complication of coronary atherosclerosis and that PTMD could therefore constitute relevant biomarkers in this specific clinical situation.

To explore these potential new biomarkers, the investigators designed a study in patients having experienced an acute coronary syndrome and followed during a year. The concentrations of PTMD assayed at 0, 1, 3, 12 months, will be correlated to clinical (severity and evolution) and paraclinical (cutaneous autofluorescence) data and the effect of cardiac rehabilitation will be assessed.

This should help to identify new (and non-traditional) biomarkers of coronary heart disease and determine some of the implicated pathophysiological mechanisms.

Registry
clinicaltrials.gov
Start Date
October 2015
End Date
August 27, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • acute coronary heart syndrome
  • included during hospitalization, usual cardiologic follow-up planned in Reims university hospital

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Post-translational modifications of Proteins quantification assessed by Liquid chromatography-mass spectrometry

Time Frame: up to 1 year

Study Sites (1)

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