Yellow V: Rosuvastatin and Evolocumab for Coronary Artery Disease

Sponsor
Icahn School of Medicine at Mount Sinai (Other)
Overall Status
Completed
CT.gov ID
NCT05984953
Collaborator
(none)
195
1
110.9
1.8

Study Details

Study Description

Brief Summary

The aim of the retrospective study is to characterize the molecular mechanisms responsible for the effect of statins and evolocumab in patients with stable coronary artery disease. The research team will retrieve and review intravascular imaging and gene expression data previously collected in the catheterization laboratory during the following time-period: 8/1/2013-4/14/2015 and 5/4/2021 - 10/28/2022.

Condition or Disease Intervention/Treatment Phase

Detailed Description

The researchers will use the previously collected transcriptomic and intravascular imaging data collected from subjects between 8/1/2013-4/14/2015 (statin group) and subjects who participated in YELLOW III study (evolocumab group). The analyses will allow us detect common and unique pathways for each drug. The researchers will use intravascular imaging findings (optical coherence tomography, OCT) to characterize patient's individual response to treatment as beneficial, if OCT fibrous cap thickness (FCT) increased at follow-up and develop machine-learning models to predict the individual response using baseline gene expression.

The researchers hypothesize that the analyses will uncover unique gene panels predicting beneficial response to statin and evolocumab allowing to select the best treatment approach for an individual patient. The total number of subjects will be 195. Transcriptomic profile of PBMC at baseline and follow-up will be compared between the groups to establish the common and distinctive molecular mechanisms of the effect of statins and evolocumab.

Study Design

Study Type:
Observational
Actual Enrollment :
195 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Effect of Statins and Evolocumab on Peripheral Blood Mononuclear Cell Gene Expression in Patients With Coronary Artery Disease: Yellow V
Actual Study Start Date :
Aug 1, 2013
Actual Primary Completion Date :
Oct 28, 2022
Actual Study Completion Date :
Oct 28, 2022

Arms and Interventions

Arm Intervention/Treatment
Statin

85 patients treated with statin

Drug: statin
40 mg of rosuvastatin daily for 8-12 weeks

Evolocumab

110 patients treated with evolocumab in addition to statin or evolocumab alone

Drug: statin
40 mg of rosuvastatin daily for 8-12 weeks

Drug: evolocumab
140 mg evolocumab every 2 weeks (26 weeks)

Outcome Measures

Primary Outcome Measures

  1. Expression levels of mRNA in blood cells [18 month]

    Expression levels of mRNA in blood cells of the patients to be measured to identify the genes which are associated with a beneficial response to treatment using transcriptomic analysis of PBMC to find the key genes (biomarkers) responsible for effective therapy.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Subjects with coronary artery disease who underwent cardiac catheterization with or without PCI

  • Patients from 8/1/2013-4/14/2015 and YELLOW III with both visits available, baseline and follow-up

Exclusion Criteria:
  • patients from 8/1/2013-4/14/2015 and YELLOW III lost to follow-up

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mount Sinai Hospital New York New York United States 10029

Sponsors and Collaborators

  • Icahn School of Medicine at Mount Sinai

Investigators

  • Principal Investigator: Annapoorna Kini, MD, MOUNT SINAI HOSPITAL

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Annapoorna Kini, Professor, Icahn School of Medicine at Mount Sinai
ClinicalTrials.gov Identifier:
NCT05984953
Other Study ID Numbers:
  • STUDY-22-01743
First Posted:
Aug 9, 2023
Last Update Posted:
Aug 9, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Product Manufactured in and Exported from the U.S.:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 9, 2023