Acute Myocardial Infarction Clinical Trial
Official title:
Study on CircRNA-Uck2 as a New Diagnostic Marker of Acute Myocardial Infarction
This is an observational diagnostic study that aims to evaluate the diagnostic value of circRNA-Uck2 in Acute Myocardial Infarction (AMI) in adults as compared to healthy and unstable angina controls. Rapid and adequate diagnosis of AMI is of great importance to enable a rapid start of treatment, save large tracts of dying myocardium, reduce the infarct size,and thereby decrease the risk of subsequent heart failure.
RATIONAL acute myocardial infarction (AMI) is the leading cause of sudden death and heart
failure worldwide. And about 10% of all emergency department consultations are with symptoms
suggestive of AMI, however, only 10% to 20% of them are diagnosed as experiencing an AMI.
Rapid and accurate identification of AMI is of paramount clinical importance for subsequent
timely and effectively treatment and management.
Recently, the investigators identified microarray analysis and real-time polymerase chain
reaction (PCR) from AMI animal models and small samples of AMI patients, a molecular
signature of AMI involving 5 circRNAs (circRNA_006877, circRNA_015350, circRNA_002969,
circRNA_013240, circRNA_004682) was found significantly change in AMI patients and likely
serves as candidate serum biomarkers of AMI. Among the 5 circRNAs, circRNA_006877 name of
circRNA-Uck2 (cUck2) has more close association with AMI.
TYPE OF STUDY : multicenter diagnostic evaluation Study MAIN PURPOSE OF THE STUDY : To
evaluate the diagnostic value of circRNAs in AMI in adults as compared to healthy and
unstable angina controls
SECONDARY OBJECTIVES :
assess the ability of cUck2 to discriminate a AMI disease from unstable angina patients in
adults.
explore the relationship between cUck2 and heart function after myocardial infarction
PRODUCTS OF THE STUDY diagnostic kit of AMI in quantitative polymerase chain reaction (qPCR)
NUMBER OF PATIENTS : 3 groups with 169 patients will be included Group 1: 66 AMI adult
patients Group 2: 56 unstable angina adults Group 3: 56 Witnesses healthy adults INCLUSION
LENGTH 36 months DURATION OF THE STUDY 42 months
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