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Pre-clinical and clinical studies have demonstrated that melatonin has cardio-protection effects. Melatonin has anti-inflammatory, antioxidant, antihypertensive, antithrombotic and antilipaemic properties, which plays important roles in a variety of cardiovascular pathophysiologic processes. Nocturnal melatonin levels decreased after AMI, and lower serum melatonin concentrations after AMI are associated with more heart failure and cardiac death and left ventricular remodeling. Moreover in women with increased BMI, lower melatonin secretion is associated with higher risks of MI. Early-morning blood collection is easier in clinical practice. Therefore, the investigators carried out a cohort study to evaluate the prognostic value of plasma soluble melatonin in hospitalized patients with acute myocardial infarction (AMI).
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| plasma melatonin levels | Diagnostic Test |
| Measure | Description | Time Frame |
|---|---|---|
| cardiovascular mortality | The median follow-up was 31.6 months |
| Measure | Description | Time Frame |
|---|---|---|
| non-cardiovascular mortality | The median follow-up was 31.6 months | |
| Myocardial infarction | The median follow-up was 31.6 months | |
| heart failure readmission |
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Inclusion Criteria:
Exclusion Criteria:
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A single center study on PCI-treated myocardial infarction patients
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| ID | Term |
|---|---|
| D009203 | Myocardial Infarction |
| ID | Term |
|---|---|
| D017202 | Myocardial Ischemia |
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D014652 | Vascular Diseases |
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readmission to any hospital due to diagnosed heart failure |
| The median follow-up was 31.6 months |
| Stroke | defined using the World Health Organization criteria | The median follow-up was 31.6 months |
| D007238 |
| Infarction |
| D007511 | Ischemia |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D009336 | Necrosis |