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https://www.selleckchem.com/products/Staurosporine.html 28-1.71%)). Independent origin of the RIPA and LIPA were present in 75.8%. The RIPA arose from the aorta (49.6%, 95% CI 43.2%-55.9%), coeliac trunk (35.7%, 95% CI 28.7-42.6%), right renal artery (10.3%, 95% CI 7.27-13.3%) and left gastric artery (2.07%, 95% CI 0.97-3.16%). Other less common origins had a pooled prevalence of 2.07% (95% CI 0.97-3.16%). The LIPA arose from the aorta (46.8%, 95% CI 39.1-54.6%), coeliac trunk (46.1%, 95 CI 38.6-53.5%), left renal artery (1.47%, 95% CI 0.78-2.15%) and left gastric artery (1.07%, 95% CI 0.25-1.89%). Other less common origins had a pooled prevalence of 1.29% (95% CI 0.44-2.14%). The inferior phrenic arteries express a wide range of variations in origin. Knowledge of their origins are important in interventional radiology, gastroenterology, surgery and traumatology. The inferior phrenic arteries express a wide range of variations in origin. Knowledge of their origins are important in interventional radiology, gastroenterology, surgery and traumatology. The aim of this real-world study is to evaluate the effect of glucagon-like peptide1 receptor-agonist (GLP1 RA) and sodium-glucose co-transporter2 inhibitor (SGLT2i) on coronary heart disease (CHD) risk, in patients with type 2 diabetes (T2D) in primary cardiovascular prevention. Data from 312 patients with T2D, without CHD history, starting treatment with GLP1 RA (n=174) or SGLT2i (n=138), were retrospectively collected. UKPDS-RE score was used to estimate 10-years risk for CHD before and 6, 12 and 24months after prescription. The 10-year CHD risk significantly decreased over 24months in both GLP1 RA and SGLT2i groups (p=0.037 and p<0.001, respectively), with 3% and 7% CHD risk reduction already obtained after the first 6months of GLP1 RA and SGLT2i therapy respectively (p<0.001 in both groups. Analyses by categories of baseline CHD risk showed significant reductions of CHD risk in the severe risk categories of both gro

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