This prospective cohort study aims to establish a lifespan cohort of myocardial infarction and build a standardized, multidimensional, and shareable disease-specific database by systematically integrating clinical phenotypes, multi-omics data, and longitudinal follow-up information. Based on artificial intelligence and multi-omics integration, the study further seeks to develop a precision prevention and control framework for acute myocardial infarction covering the full continuum from early risk warning and accurate diagnosis to individualized treatment and long-term risk management. The study will enroll adults aged 18 to 74 years, including two major populations: individuals at high risk of acute myocardial infarction, such as those with stable or unstable angina, and patients with confirmed acute myocardial infarction diagnosed according to the Fourth Universal Definition of Myocardial Infarction. Biospecimens, including venous blood, urine, and feces, will be collected, and participants will undergo standardized baseline assessment and follow-up. The primary outcome is all-cause mortality during follow-up. Secondary outcomes include cardiovascular death, recurrent myocardial infarction, readmission due to heart failure, revascularization, stroke, stent thrombosis, and severe bleeding. This study is expected to provide scientific evidence and technical support for precision prevention, diagnosis, treatment, and long-term management of myocardial infarction.
Study Type
OBSERVATIONAL
Enrollment
6,000
Fuzhou University Affiliated Provincial Hospital
Fuzhou, Fujian, China
Rate of all-cause mortality
Time frame: From enrollment to the end of study follow-up, up to 5 years
Rate of cardiovascular death
Time frame: From enrollment to the end of study follow-up, up to 5 years
Rate of recurrent myocardial infarction
Time frame: From enrollment to the end of study follow-up, up to 5 years
Rate of readmission due to heart failure
Time frame: From enrollment to the end of study follow-up, up to 5 years
Rate of target vessel or non-target vessel revascularization
Time frame: From enrollment to the end of study follow-up, up to 5 years
Rate of stroke
Time frame: From enrollment to the end of study follow-up, up to 5 years
Rate of definite or probable stent thrombosis
Time frame: From enrollment to the end of study follow-up, up to 5 years
Rate of severe bleeding
Time frame: From enrollment to the end of study follow-up, up to 5 years
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