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Diabetes Mellitus 101 for Cardiologists (and Alike): 2015 Stan Schwartz MD,FACP Affiliate, Main Line Health System Emeritus, Clinical Associate Professor of Medicine, U of Pa. 6105472000 An Aggressive Pathophysiologic Approach to Therapy of Type 2 Diabetes in Cardiometabolic Patients: Looking at Diabetes Medications with a Cardiologists Eye Part 14
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Glycemic Benefit of Ranolazine Proportional to Baseline HgA1c
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INFLUENCE OF FASTING GLUCOSE AT BASELINE ON THE EFFECT OF RANOLAZINE TO LOWER GLYCEMIC VARIABLES IN ALL PATIENTS AT 4 MONTHS- Implies glucose-dependent Insulin Release. Chisholm, Dhalla, Karwatowska-Prokopczuk and Belardinelli (2008). CVT unpublished MERLIN data Change in FPG as a function of baseline FPG <126126-400 -50 -25 0 25 Baseline FPG (mg/dl) 570553 229 232 (n) Change from baseline in fasting glucose (mg/dl)
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PATIENTS WITH DIABETES WERE MORE LIKELY TO ACHIEVE HbA1c < 7% WITH RANEXA VS PLACEBO CARISA MERLIN TIMI-36 Timmis AD, et al. Eur Heart J. 2006;27:42-48. 0 20 40 60 80 100 Baseline 12 Weeks 38% Percent With HbA1c < 7% Placebo (n = 37) Ranexa (n = 47) 43% 26% 55%* 0 20 40 60 80 100 Placebo (n = 770) Ranexa (n = 707) Baseline 4 Months 44% 49% 43% 59% † *p = 0.004 vs placebo † p < 0.001 vs placebo.
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Safety of Ranexa in Patients With Diabetes HR 95% CI p Value* Recurrent ischemia Overall cohort vs placebo0.870.76–0.990.03 Patients with diabetes vs placebo 0.750.61–0.930.008* Patients with diabetes vs without diabetes 0.950.80–1.110.10 Death, any cause0.980.70–1.360.91 CV death or MI1.090.86–1.380.46* New or worsening heart failure1.010.73–1.390.95 † Sudden cardiac death0.760.41–1.390.37 *p for interaction = 0.29. † p for interaction = 0.68. Morrow DA, et al. Circulation. 2009;119:2032-2039. NOTE: Data Not Included in New Label MERLIN TIMI-36
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Recurrent Ischemia in Patients with Diabetes Mellitus RANOLAZINE (N=1104) Results PLACEBO (N=1116) Days after Randomization Recurrent Ischemia (%) Hazard Ratio 0.75 (95% CI 0.61 to 0.93) P =0.008 0 5 10 15 20 090180270360 19.2% 15.1% Morrow DA et al. Circulation 2009; epub
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OTHER GLYCOMETABOLIC PARAMETERS IN PATIENTS WITH DIABETES MELLITUS Body weight (kg) 0.43-0.06 LDL (mmol/L) -0.2-0.2 Trig (mmol/L) -0.1-0.1 HDL (mmol/L) 0.10.1 Hypoglycemia (%) 33 MEDIAN CHANGE FROM BASELINE PLACEBO N=1117 RANOLAZINE N=1098 Morrow DA, AHA 2007, Orlando, FL
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RANEXA CAN BE USED IN PATIENTS WITH CAD AND DIABETES ● Ranexa does not increase the incidence of hypoglycemia compared with placebo ● Ranexa does not increase the incidence of: ─ Weight gain ─ Cardiovascular adverse events ─ Dyslipidemia (LDL, HDL, total cholesterol, and triglycerides) ─ Clinically relevant changes in blood pressure or heart rate Timmis AD, et al. Eur Heart J 2006;27:42-48
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SUMMARY ● Ranolazine significantly and dose- dependently reduces HbA1c. ● The magnitude of HbA1c lowering by ranolazine is correlated with the levels of HbA1c and FPG at baseline. ● There was no increase in the incidence of hypoglcyemia in ranolazine-treated patients
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EFFECT OF RANOLAZINE ON PLASMA INSULIN RESPONSE DURING AN IVGTT IN NORMAL RATS 0 600 1200 1800 0 10 20 30 Ranolazine (15mg/kg) Vehicle Plasma Insulin (% of baseline) Time (min) Dhalla et al, unpubl data (on file, CVT Pharm)
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EFFECT OF RANOLAZINE AND GLYBURIDE ON PLASMA GLUCOSE AND INSULIN CONCENTRATIONS IN NORMAL RATS: eg: GLUCOSE DEPENDENT INSULIN RELEASE 0 30 60 90 120 0 1 2 3 GLYBURIDE RANOLAZINE Glucose (mg/dl) Plasma Insulin (mg/dl) GLYBURIDERANOLAZINE 030 0 0 0 TIME (min) Dhalla et al, unpubl data (on file, CVT Pharm) Normal glycemia- no insulin release- eg: GLUCOSE DEPENDENT INSULIN RELEASE
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GLUCOSE DEPENDENCE OF THE EFFECT OF RANOLAZINE ONINSULIN SECRETION FROM HUMAN PANCREATIC ISLETS Insulin Release (% of control) Glucose-3mMGlucose-20mM P<0.05 0 100 200 300 400 Dhalla et al, unpubl data (on file, CVT Pharm) RAN CON
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CONCENTRATION DEPENDENT EFFECT OF RANOLAZINE ON INSULIN SECRETION FROM HUMAN PANCREATIC ISLETS Insulin Release (% of control) Dhalla et al, unpubl data (on file, CVT Pharm) Glucose-3mM Glucose-25mM 0 150 300 450 P<0.05 P<0.01 RAN 0 M RAN 0 M RAN 100 M RAN 5 M
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