Acute Coronary Syndrome Genetic Study

• Conditions: Acute Coronary Syndrome

• Registration Number: NCT01964313
• Lead Sponsor: Peking University First Hospital

Brief Summary

To describe the role of genetic factors and its relationship and interaction with environmental factors in the recurrence of cardiac events in Chinese patients with acute coronary syndrome.

Detailed Description

* Research cohort: Patients diagnosed with acute coronary syndrome are enrolled and to be followed up for 2 years.

* Baseline and follow up variables include patients' demographics, medical history, ACS event characteristics, clinical treatment options (interventional cardiology, drug therapy: antithrombotic therapy, other treatments recommended by guidelines ) and follow up events information.

* Blood Sample collection 4ml of vein blood will be drawed. Centrifugation of plasma and WBC will be done on-site within 30 minutes for DNA extraction. Samples will be stored at -80℃ freezer for subsequent applications.

* A nested case-controlled study is designed for the genetic analysis:

1. Cases: Patients suffered from death, myocardial infarction, stroke and coronary revascularization and bleeding during the 2-year follow up. We expected to get 600 cases in the study cohort;

2. Controls: among patients without any of the above events during follow, matched controls of 1:1 ratio will be selected according to date of admission (± 1 month), age (± 5 years), sex, baseline ACS diagnosis, whether treated with PCI , the same pattern of antithrombotic therapy and the study center.

* Genotyping Genotype testing using exome DNA chips (Exome Beadchip). Exome Beadchip is a high-throughput DNA chip designed by Illumina's, containing 240,000 SNP on exons in the genome that may lead to functional changes.

* Analysis:

1. To analysis the impact of genetic characteristics on selection of treatment strategy in ACS patients, and its interaction with other baseline clinical variables.

2. To analysis the impact of genetic characteristics on patient outcomes, and its interaction with clinical characteristics and management patterns.

Study Timeline

• Study Start: 2012-07
• Study First Submitted: 2013-10-14
• Study First Submitted QC: 2013-10-14
• Study First Posted: 2013-10-17
• Status Verified: 2016-06
• Last Update Submitted: 2016-06-20
• Last Update Posted: 2016-06-21
• Primary Completion: 2016-12
• Study Completion: 2016-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 3422

Inclusion Criteria

• Written informed consent has been provided.

• Contact Order Form has been provided.

• Aged 18 years or older.

• Diagnosis of STEMI, NSTEMI or UA using the following definitions:

  1. Criteria for STEMI diagnosis:

     1. History of chest pain/discomfort and
     2. Persistent ST-segment elevation (> 30 min) of ≥ 0.1 mV in 2 or more contiguous ECG leads or presumed new left bundle branch block (LBBB) on admission and
     3. Elevation of cardiac biomarkers (CK-MB, troponins): at least one value above the 99th percentile of the local laboratory upper reference limit.

  2. Criteria for NSTEMI diagnosis:

     1. History of chest pain/discomfort and
     2. Lack of persistent ST-segment elevation, LBBB or intraventricular conduction disturbances and
     3. Elevation of cardiac biomarkers (CK-MB, troponins): at least one value above the 99th percentile of the local laboratory upper reference limit.

  3. Criteria for Unstable Angina diagnosis:

     1. Symptoms of angina at rest or on minimal exercise and
     2. At least 0.5mm ST deviation in at least 2 leads and
     3. No increase in biomarkers of necrosis
     4. OR objective evidence of ischaemia by non-invasive imaging OR significant coronary stenosis as determined by the treating physician at angiography if this is standard practice in study site.

• Hospitalized within 48 hours of onset of symptoms.

Exclusion Criteria

Patients will not be eligible to participate if any of the following exclusion criteria are present:

• UA, STEMI and NSTEMI precipitated by or as a complication of surgery, trauma, or GI bleeding or post-PCI.
• UA, STEMI and NSTEMI occurring in patients already hospitalized for other reasons.
• Presence of any condition/circumstance which in the opinion of the investigator could significantly limit the complete follow up of the patient (e.g. tourist, non-native speaker or does not understand the local language, psychiatric disturbances).
• Presence of serious/severe co-morbidities in the opinion of the investigator which may limit short term (i.e. 6 month) life expectancy.
• Current participation in a randomised interventional clinical trial.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Major adverse cardiovascular events	2 year	Death, Myocardial infarction, stroke, coronary revascularization

Trial Locations

Locations (1)

Peking University First hospital; 🇨🇳 Beijing, Beijing, China