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7 Cardiovascular safety trials involving GLP-1 analogues The US Food and Drug Administration requirement for most new blood glucose-lowering therapies to undergo cardiovascular disease (CVD) safety evaluation has resulted in all the GLP-1 analogues, except twice-daily exenatide, having been assessed in long-term placebo-controlled randomised outcome trials (Table 2)
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GLP-1 is released after eating and has a few important roles in digestion and metabolism
Artificial intelligence-based predictive models and risk stratification tools Conventional scoring systems for AP have inherent limitations in accurately predicting disease severity and clinical outcomes
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