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Therefore, statements about BPC-157 and angiogenesis should remain tied to the specific experimental model and measured endpoint rather than being generalized into broad claims about biological benefit

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While overall MACE risk was similar for both agents, risk gradients by eGFR differed: liraglutides cardiovascular risk increased as kidney function declined ( p for trend = 0.0079), whereas dulaglutide maintained a stable risk profile across CKD stages ( p = 0.19)