Lipohydroxy acid has a chemical structure similar to salicylic acid
GLP-1 receptor agonists mimic the action of the natural hormone GLP-1, enhancing insulin secretion in response to meals, inhibiting glucagon release, slowing gastric emptying, and promoting satiety
At MPR 0.5, the adjusted HR was quite similar to that in the main analysis (HR 0.87 [0.71-1.06]), but this became lower at MPR 0.75 (HR 0.75 [0.60 0.95]) and lower yet at MPR 0.95 (HR 0.62 [0.46 0.84]) When excluding subjects with follow-up times shorter than 6 months, 25,390 individuals remained, and the unadjusted HR for MOF was found to be 0.86 [0.731.02] for GLP-1 RAs compared to DPP-4is
Nothing else is even close. The very same class of medications, GLP-1 agonists, that he promoted comes from government funded science that started in the 1980s with curious scientists testing a variety of venoms on guinea pig pancreases