GLP-1(9-36) amide and (9-37), which was previously thought to be the inactive metabolite of GLP-1, also exerts cardioprotective effects. Direct administration of GLP-1(9-36) during reperfusion reduced ischaemic damage in isolated hearts and increased cGMP release, vasodilatation and coronary flow in AMI mouse model, one may speculate that total GLP-1 level may associate with adverse cardiovascular events in AMI patients, the hypothesis is therefore tested in this study.
Study Type
OBSERVATIONAL
Enrollment
709
The plasma GLP-1 levels was determined by enzymatic assays.
all-cause mortality
Time frame: The median follow-up was 29 months
cardiovascular mortality
Time frame: The median follow-up was 29 months
non-cardiovascular mortality
Time frame: The median follow-up was 29 months
Myocardial infarction
Time frame: The median follow-up was 29 months
heart failure readmission
readmission to any hospital due to diagnosed heart failure
Time frame: The median follow-up was 29 months
Stroke
defined using the World Health Organization criteria
Time frame: The median follow-up was 29 months
repeated revascularization
defined as repeated PCI or bypass grafting of not only infarct related artery
Time frame: The median follow-up was 29 months
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