CARDIOVASCULAR DISEASE AND DIABETES

Diabetes mellitus (DM) refers to a group of common metabolic disorders that share the phenotype of hyperglycemia.
Several distinct types of DM are caused by a complex interaction of genetics and environmental factors.
Depending on the etiology of the DM, factors contributing to hyperglycemia include reduced insulin secretion, decreased glucose utilization, and increased glucose production.
The metabolic dysregulation associated with DM causes secondary pathophysiologic changes in multiple organ systems that impose a tremendous burden on the individual with diabetes and on the health care system.

1. diabetes and cardiovascular disease DR VISHWANATH HESARUR SENIOR RESIDENT DEPARTMENT OF CARDIOLOGY JNMC , BELGAUM

2. Diabetes Mellitus Diabetes mellitus (DM) refers to a group of common metabolic disorders that share the phenotype of hyperglycemia. Several distinct types of DM are caused by a complex interaction of genetics and environmental factors. Depending on the etiology of the DM, factors contributing to hyperglycemia include reduced insulin secretion, decreased glucose utilization, and increased glucose production. The metabolic dysregulation associated with DM causes secondary pathophysiologic changes in multiple organ systems that impose a tremendous burden on the individual with diabetes and on the health care system.

3. Classification DM is classified on the basis of the pathogenic process that leads to hyperglycemia . The two broad categories of DM are designated type 1 and type 2 Spectrum of glucose homeostasis and DM

4. EPIDEMIOLOGY The worldwide prevalence of DM has risen dramatically over the past two decades, from an estimated 30 million cases in 1985 to 285 million in 2010. The International Diabetes Federation projects that 438 million individuals will have diabetes by the year 2030 Indian 40.9 million people in 2001. By the year 2025, 80.9 million will have diabetes in India. There is still inadequate population-based data on the prevalence of CAD in India, particularly comparing diabetic and nondiabetic subjects.

5. Criteria for the Diagnosis of Diabetes Mellitus Symptoms of diabetes plus random blood glucose concentration 11.1 mmol /L (200 mg/ dL ) a or   Fasting plasma glucose 7.0 mmol /L (126 mg/ dL ) b or   A1C > 6.5% c or   Two-hour plasma glucose 11.1 mmol /L (200 mg/ dL ) during an oral glucose tolerance test d  

6. Cardiovascular disease in diabetes Account for most morbidity and mortality in patients with diabetes mellitus. Diabetic subjects are known to have a two to four times increased CAD risk, and CAD has been reported to occur two to three decades earlier in diabetic subjects as opposed to their nondiabetic counterparts. Diabetes causes microvascular diseases, such as nephropathy, neuropathy, and retinopathy, and macrovascular disease (e.g., atherosclerosis). Atherosclerosis of the coronary, cerebral, and peripheral arteries accounts for approximately 80 percent of mortality and for 75 percent of hospitalizations in persons with diabetes.

7. As type 2 diabetes shares several risk factors in common with coronary artery disease (CAD), such as age, hypertension, dyslipidemia , obesity, physical inactivity, and stress, an increase in the prevalence of diabetes indirectly implicates an escalating risk of CAD as well.

8. Indians India is predicted to bear the greatest CAD burden, according to the estimates from the Global Burden of Disease Study. Of the more than 9 million deaths due to CAD in 2005 in developing countries, 2.4 million (25%) occurred in India.  The mortality rates in India due to acute myocardial infarction (MI) were 141 per 100,000 in males and 136 per 100,000 in females A matter of serious concern is that 52% of the CAD deaths in India occurred in people aged below 70 years, while the same was just 22% in developed countries.

9. Atherosclerosis Compared with nondiabetic individuals, patients with diabetes have a twofold to fourfold increased risk for development and dying of CHD Preis SR, Hwang SJ, Coady S, et al: Trends in all-cause and cardiovascular disease mortality among women and men with and without diabetes mellitus in the Framingham Heart Study, 1950 to 2005. Circulation 119:1728, 2009.)

10. Whereas older studies have suggested a diabetes-associated CVD risk similar to that observed among nondiabetic patients with a prior myocardial infarction (MI)—that is, a “coronary disease equivalent”—more recent observations from clinical trials including patients with diabetes suggest a substantially lower CHD risk, most likely reflecting the effectiveness of contemporary therapeutic interventions.

11. Diabetes is associated with an increased risk for MI; and across the spectrum of acute coronary syndrome (ACS) events, in which diabetes may affect more than one in three patients, patients with diabetes have worse CVD outcomes after ACS events TRITON–TIMI 38 randomized trial.

12. Cardiovascular medicine at the turn of the millennium: Triumphs, concerns, and opportunities. N Engl J Med 337:1360, 1997.

13. In addition to CHD, diabetes increases the risks of stroke and peripheral arterial disease. Two fold increased stroke risk compared with nondiabetic individuals , with hyperglycemia affecting approximately one in three patients with acute stroke, associated with a twofold to sixfold increased risk for adverse clinical outcomes after stroke. Among patients with symptomatic peripheral arterial disease, diabetes prevalence ranges from 20% to 30% and accounts for approximately 50% of all lower extremity amputations.

14. Heart Failure Diabetes associates independently with a twofold to fivefold increased risk of heart failure (HF) compared with those without diabetes, comprising both systolic and diastolic HF, and diabetes patients have worse outcomes once HF has developed and an increased HF risk in the setting of ACS events. The increased risk of HF observed in diabetes is multifactorial , caused by ischemic, metabolic, and functional myocardial perturbation.s

15. PATHOPHYSIOLOGY OF DIABETIC VASCULAR DISEASE Adipocyte Biology and Inflammation We increasingly recognize the role of inflammation in the pathogenesis of diabetes and the metabolic syndrome.

16. The adipocyte , long regarded as a storage depot for triglycerides, actually can generate substantial quantities of proinflammatory mediators, such as tumor necrosis factor-alpha (TNF-α) TNF-α can cause insulin resistance and can thus causally link adiposity to diabetes. TNF-α and allied proinflammatory cytokines derived from the adipocyte can activate vascular endothelial and smooth muscle cells to provoke aspects of vascular dysfunction. In this manner, adipocyte products can directly promote vascular dysfunction and hasten atherogenesis

17. ROLE OF ADIPONECTIN

18. Diabetic Metabolic and Vascular Dysfunction Diabetes causes metabolic abnormalities, including hyperglycemia, dyslipidemia , and insulin resistance, that disrupt normal arterial function and render arteries susceptible to atherosclerosis. It specifically alters the function of vascular endothelium and smooth muscle cells, as well as platelets, in ways that promote atherogenesis . Diabetes impairs the vasodilator function of endothelial cells and decreases the bioavailability of nitric oxide (NO).

19. Orasanu G, Plutzky J: The pathologic continuum of diabetic vascular disease. J Am Coll Cardiol 53:S35, 2009

20. Hyperglycemia decreases NO production from endothelial nitric oxide synthase ( eNOS ) and increases its degradation via generation of reactive oxygen species (ROS). Recent evidence suggests that hyperglycaemia -induced ROS generation is involved in the persistence of vascular dysfunction despite normalization of glucose levels. This phenomenon has been called ’metabolic memory’ and may explain why macro- and microvascular complications progress, despite intensive glycaemic control, in patients with DM. Hyperglycemia triggers the production of ROS in vascular cells through enzymatic (protein kinase C and the reduced form of nicotinamide adenine dinucleotide phosphate [NADPH] oxidases ) and nonenzymatic sources of oxidant stress (e.g., the formation of advanced glycation end products, AGEs).

21. As oxidative stress increases, the eNOS cofactor tetrahydrobiopterin becomes oxidized and uncouples eNOS , which cause the enzyme to produce superoxide anion instead of NO Superoxide anion quenches NO in a diffusion-limited reaction to produce peroxynitrite . Peroxynitrite inhibits prostacyclin synthase and endothelium-dependent hyperpolarizing factor activity. Similar to the effects of hyperglycemia, free fatty acids activate intracellular enzymatic oxidant sources, including protein kinase C, NADPH oxidases , and eNOS , yielding analogous increases in superoxide anion

22. The excess adipose tissue that usually accompanies type 2 diabetes mellitus releases excess fatty acids. Free fatty acids attenuate prostacyclin bioavailability by inhibiting prostacyclin synthase . [34] Moreover, free fatty acids interfere with intracellular signaling pathways to cause not only muscle and visceral insulin resistance but also vascular insulin resistance. In diabetes, hyperglycemia and increased free fatty acids increase the concentration in the cell of the metabolite diacylglycerol . Diacylglycerol , in turn, activates a family of enzymes known as protein kinase C (PKC), that perform key regulatory functions by phosphorylating proteins important in metabolic control .

23. Activation of PKC can inhibit the expression of eNOS , augment cytokine-induced tissue factor gene expression and procoagulant activity in human endothelial cells, and increase the production of proinflammatory cytokines, proliferation of vascular wall cells, and production of extracellular matrix macromolecules that accumulate during atherosclerotic lesion formation.

24. Diabetes also disturbs vascular function through nonenzymatic glycation of macromolecules. In states of hyperglycemia and increased oxidative stress, many proteins and even lipids undergo nonenzymatic glycation Glycated proteins can form structures known as AGEs that cause the macromolecule to take on a brown hue, similar to burnt sugar. AGEs accumulate in the vessel wall and appear to contribute to the pathobiology of complications of diabetes, notably the accelerated vascular disease characteristic of this condition.

25. Phospholipids and apolipoproteins can form AGEs and AGE-modified proteins can accumulate in diabetic subjects. The presence of glycated forms of low-density lipoproteins (LDLs) can engender an immune response and contribute to macrovascular disease. AGE-modified LDL apoprotein and LDL lipid levels increase in diabetic subjects compared with nondiabetics Increased AGE production is associated with reduced nitric oxide bioavailability through impairment of eNOS transcription and activity, production of oxygen-derived free radicals, and activation of NF- kB .

26. Diabetes impairs vascular smooth muscle function and augments the production of vasoconstrictor mediators, angiotensin II and vasoconstrictor prostanoids , including endothelin-1, which causes vascular smooth muscle growth and inflammation. However, most diabetics have peripheral autonomic impairment at the time of diagnosis, and vascular beds regulated by these nerves have decreased arterial resistance

27. Similar to endothelial cells, diabetes activates atherogenic mechanisms within vascular smooth muscle cells, including protein kinase C, RAGE, NF- kB and the production of oxidative stress. [30] Diabetes heightens vascular smooth muscle cell migration in atherosclerotic lesions. Advanced atherosclerotic lesions have fewer vascular smooth muscle cells in diabetic patients than nondiabetic patients, possibly resulting in decreased resiliency of the fibrous cap and thereby increasing the risk of rupture and luminal thrombi

28. Platelet abnormalities Colwell JA, Nesto RW: The platelet in diabetes: Focus on prevention of ischemic events. Diabetes Care 26:2181, 2003.

29. Type 2 diabetes and its associated metabolic abnormalities favor an imbalance in the coagulation and fibrinolytic systems that support clot formation and stability. Type 2 diabetes increases plasminogen activator inhibitor type 1 (PAI-1) levels, impairing fibrinolytic capacity in atherosclerotic lesions. Moreover, diabetes increases the expression of tissue factor and levels of plasma coagulation factors, and decreases levels of endogenous anticoagulant.

30. These abnormalities include increased circulating tissue factor, factor VII, von Willebrand factor, and plasminogen activator inhibitor 1, with decreased levels of antithrombin III and protein C. In addition, disturbances of platelet activation, aggregation, morphology, and life span further contribute to increased thrombotic potential, as well as to the acceleration of atherosclerosis

31. Anatomic characteristics of atherosclerotic disease development Postmortem studies have documented a more diffuse distribution of atherosclerotic changes with increased overall atherosclerotic disease burden in subjects who had diabetes The qualitative morphologic differences between plaques in diabetic and nondiabetic subjects are believed to be small, however .

32. In atherectomy specimens of coronary arteries’ cell-rich areas, the extent of the necrotic plaque core, calcification, and thrombus were increased in patients who had type 2 diabetes These characteristics are likely associated with the formation of vulnerable plaques and plaque rupture; diabetes also affects repair mechanisms after plaque disruption . Postmortem studies demonstrated an increased frequency of healed ruptures in patients who had type 2 diabetes and died from acute coronary events

33. Macroscopic postmortem studies documented the earlier and more diffuse distribution of atherosclerotic changes in subjects who had diabetes The atherosclerotic changes in diabetic subjects are not fundamentally different from those in nondiabetics , but occur at younger age and progress more rapidly. The traditionally angiographic observation of ‘‘small coronary vessels’’ in diabetics likely reflects the advanced, diffuse involvement of these patients at the time of coronary angiography.

34. The anatomic characteristics of advanced, stenotic CAD are not fundamentally different between diabetic and nondiabetic subjects The relation between atherosclerotic changes of coronary vessels and myocardial changes in diabetic subjects is controversial. In laboratory animals, alterations in myocytes are observed before any damage to the intramural arteries Similarly, in autopsy studies of diabetic subjects, characteristic findings of a so-called ‘‘diabetic cardiomyopathy ’’ have been described. These include widespread regions of myocardial fibrosis, intimal proliferation of small myocardial arterioles, and accumulation of interstitial glycoprotein and collagen; all of these lead to decreased ventricular compliance and contractility [86–88]. In addition, advance glycation end products may be an important pathophysiologic mechanism for diastolic dysfunction in these patients

35. Clinical Manifestations of Atherosclerosis in Diabetes Coronary Artery Disease 2- to 4-fold increase in the risk of developing coronary artery disease. type 2 diabetes mellitus was accorded a coronary artery disease risk-equivalent. In patients with known coronary artery disease and diabetes, the rates of death approach 45% over 7 years and 75% over 10 years. Outcomes are worse in diabetic patients for each manifestation of coronary artery disease.

36. In the Organization to Assess Strategies for Ischemic Syndromes (OASIS) registry, a 6-nation unstable angina outcome study, diabetes increased mortality by 57%. The SHOCK ( SHould we emergently revascularize Occluded Coronaries for cardiogenic shocK ) trial of revascularization found a 36% increase in death in diabetic patients with cardiogenic shock complicating myocardial infarction. After myocardial infarction has occurred, the 1-month mortality rate is increased in diabetic patients by 58%. Approximately 50% of diabetic patients die 5 years after a myocardial infarction, double the rate found in nondiabetic patients.

37. Cerebrovascular Disease Diabetes increases the risk of stroke. For example, the risk of stroke among patients taking hypoglycemic medications was increased 3-fold among the nearly 350 000 men in the Multiple Risk Factor Intervention Trial. In the Baltimore-Washington Cooperative Young Stroke Study, stroke risk increased more than 10-fold in diabetic patients younger than 44 years of age, ranging as high as 23-fold in young white men. Diabetes also increases stroke related mortality, doubles the rate of recurrent stroke, and trebles the frequency of stroke-related dementia.

38. Peripheral Arterial Disease Diabetes increases the incidence and severity of limb ischemia approximately 2- to 4-fold. Data from the Framingham cohort and Rotterdam studies show increased rates of absent pedal pulses, femoral bruits, and diminished ankle-brachial indices. Diabetic peripheral arterial disease often affects distal limb vessels, such as the tibial and peroneal arteries, limiting the potential for collateral vessel development and reducing options for revascularization. As such, patients with diabetes are more likely to develop symptomatic forms of the disease, such as intermittent claudication and critical limb ischemia, and undergo amputation.

39. In the Framingham cohort, the presence of diabetes increased the frequency of intermittent claudication by more than 3-fold in men and more than 8-fold in women. Diabetes is the most common cause of nontraumatic amputations in the United States.

40. DIABETIC DYSLIPIDEMIA

41. Lipid and lipoprotein abnormalities in NIDDM VLDL More of large VLDL consequent of poor clearance- more of circulatingApoB100 IDL increased LDL More of unesterified cholesterol, prolonged half ,life higher quantities of circulating small dense LDL HDL Normal or raised but may be low in obese patients with hypercholesterolemia Triglycerides Increased Cholesterol May be increased or normal

42. Lipid and lipoprotein abnormalities in IDDM VLDL Increased LDL Marginally raised HDL Low or Normal Triglycerides Increased Cholesterol Esterified Cholesterol is diminished

43. Prevention of Coronary Heart Disease and Its Complications in the Setting of Diabetes Therapeutic lifestyle interventions The ADA/AHA overarching therapeutic lifestyle targets include

44. Alcohol : Moderate amounts, not exceeding two glasses or 20 g/day for men and one glass or 10 g/day for women. Beyond lifestyle Lipid management Blood pressure control Aspirin therapy Glucose managemaent

45. Lipid Therapy Insulin resistance and type 2 diabetes – dyslipidemia Despite extensive research in modifying triglyceride and HDL cholesterol levels with a variety of pharmacologic agents, however, the net influence on CVD risk of these strategies remains uncertain, and the modification of LDL cholesterol remains the cornerstone of therapeutic lipid intervention in patients with diabetics

46. Guidelines of the ADA/AHA The target lipid values in diabetic individuals (age >40 years) without cardiovascular disease should be as follows: LDL < 2.6 mmol /L (100 mg/ dL ) HDL >1 mmol /L (40 mg/ dL ) in men and >1.3 mmol /L (50 mg/ dL ) in women; and Triglycerides < 1.7 mmol /L (150 mg/ dL ). In patients >40 years, addition of a statin , regardless of the LDL level in patients with CHD & those without CHD, but who have CHD risk factors. If the patient is known to have CHD, the LDL goal of <1.8 mmol /L (70 mg/ dL ) as an "option"

47. ADA guidelines: Major statin trials or sub-studies in diabetic patients Lancet 2004;364:685 Diabetes Care 2006;29:1220 Lancet 2003;361:2005 Diabetes Care 2006;7:1478 Diabetes Care 1997;20:614 *Num. needed to treat (NNT) for moderate-high risk DM to avoid one death or MI: 3-50 ADA Standards of Care; Diabetes Care, January 2011

48. Omega-3 Fatty Acids Predominantly fish oil preparations – lower triglycerides by up to 40% Absence of interactions with statins Add-on therapy to statins Minimal effects on HDL and total cholesterol and modestly raises LDL with no adverse glycemic effects.

49. The Japan EPA Lipid Intervention Study (JELIS) 4565 patients Randomized trial comparing treatment with 1800 mg of eicosapentaenoic acid (EPA) plus simvastatin 5mg daily versus simvastatin 5mg alone. In this subset, EPA treatment conferred a 22% risk reduction ( P = 0.048) for major adverse CVD events compared with simvastatin alone. On the basis of the accumulated data, fish oil has emerged as the primary consideration for add-on therapy in patients with diabetes who do not achieve non-HDL targets with maximally tolerated statin monotherapy .

50. Fibric Acid Derivatives ( Fibrates ) Agonists of PPAR α that lower triglycerides and modestly increase HDL cholesterol. The Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) trial 9795 patients with type 2 diabetes fenofibrate versus placebo failed to demonstrate a statistically significant reduction in the primary endpoint of coronary death or nonfatal MI, despite accumulating 544 primary outcome events for evaluation (5.2% versus 5.9%; HR = 0.89; 95% CI, 0.75-1.05).

51. ACCORD-Lipid trial 5518 patients with type 2 diabetes at high cardiovascular risk Fenofibrate , compared with placebo each added to simvastatin background therapy, Failed to yield significant improvements on MACE despite the accumulation of 601 primary endpoint events of CV death, MI, and stroke

52. ACCORD LIPID: Lipid parameters

53. Summary - fibrates remain an option Intolerance to statin medications Isolated hypertriglyceridemia in diabetic patients at otherwise low CVD risk, and As add-on therapy to maximally tolerated statin monotherapy when patients do not achieve therapeutic targets (noting some increased myopathy risk).

54. Niacin Potent modulator of lipid metabolism Greatest effect : Increases HDL-cholesterol while lowering triglycerides. However, the net CVD effects and safety of niacin, especially in the context of background statin therapy, remain to be determined. A recent meta-analysis estimated a 27% relative risk reduction associated with niacin in the absence of statin background therapy.

55. Summary - niacin remains an option Intolerance to statin medications Isolated hypertriglyceridemia in diabetic patients with an otherwise low CVD risk, and As add-on therapy to maximally tolerated statin monotherapy when patients do not achieve therapeutic targets

56. Recommendations on management of dyslipidaemia in diabetes

57. The incremental CVD efficacy and safety of niacin added to simvastatin therapy, compared with simvastatin alone, are presently being evaluated in two large, ongoing randomized trials: the National Heart, Lung, and Blood Institute (NHLBI)–sponsored Atherothrombosis Intervention in Metabolic Syndrome with Low HDL/High Triglycerides and Impact on Global Health Outcomes (AIM HIGH) trial, comprising 3300 patients with vascular disease and atherogenic dyslipidemia ; and the Heart Protection Study 2-Treatment of HDL to Reduce the Incidence of Vascular Events (HPS2-THRIVE) trial, coordinated by the Oxford University Clinical Trial Service Unit, that has completed enrollment of over 25,000 patients with CVD. .

58. Blood pressure The prevalence of hypertension is higher in patients with T1DM than in the general population (up to 49% in DCCT/EDIC)and more than 60% of patients diagnosed with T2DM have arterial hypertension. According to current pathophysiological considerations, this is related to: ( i ) hyperinsulinaemia linked to increased renal reabsorption of sodium; (ii) increased sympathetic tone and (iii) increased renin-angiotensin-aldosterone system activity. Obesity, aging and the appearance of renal disease further increase the prevalence of hypertension. DM and hypertension are additive risk factors for CVD. While the development of T2DM doubles the cardiovascular risk in men and more than triples the risk in women, hypertension causes a four-fold increase in cardiovascular risk in people with DM

59. Hypertension Hypertension affects approximately 70% of diabetic patients with a steep graded association between blood pressure and adverse cardiovascular outcomes Numerous classes of antihypertensive medications reduce both macrovascular and microvascular disease complications, blood pressure management is of principal importance in this high-risk population. Blood pressure goal of <130/80 mm Hg.

60. Adler AI, Stratton IM, Neil HA, et al: Association of systolic blood pressure with macrovascular and microvascular complications of type 2 diabetes [UKPDS 36]: Prospective observational study. BMJ 321:412, 2000.

61. Hypertension Optimal Treatment (HOT) trial

62. ACCORD trial 4700 patients were assigned to intensive- (achieved mean systolic blood pressure 119 mm Hg) or standard treatment [mean systolic blood pressure (BP) 134 mmHg] mean follow-up of 4.7 years

63. ACCORD BP: Using an average of 3 drugs, the authors achieved a SBP of 119 mmHg vs. 133 mmHg

64. ACCORD BP: Results Conclusions : “In patients with type 2 diabetes at high risk for cardiovascular events, targeting a systolic blood pressure of less than 120 mmHg, as compared with less than 140 mmHg, did not reduce the rate of fatal and nonfatal major CVD events.”

65. Antagonists of the Renin-Angiotensin-Aldosterone System (RAAS) ACE inhibitors and ARBs have become keystones of therapy for hypertension in diabetes ACE Inhibitors The recommendation for ACE inhibitors as first-line hypertension therapy in the setting of diabetes is supported by data from randomized trials of patients with and without hypertension.

66. In the Heart Outcomes Prevention Evaluation (HOPE) study R amipril versus placebo among patients at increased risk for CVD, Ramipril was superior to placebo in the diabetes subset of 3577 HOPE patients for the primary outcome of cardiovascular death, MI, and stroke (25% RRR; P = 0.004) and for overt nephropathy (24% RRR; P = 0.027). Similar observations derive from the diabetes subanalysis of the EUROPA trial , Perindopril versus placebo 19% RRR among the 1502 participants with diabetes was similar to the 20% risk reduction observed in the overall trial.

67. Angiotensin II Receptor Blockers The Telmisartan Randomized AssessmeNt Study in ACE iNtolerant subjects with cardiovascular Disease (TRANSCEND) trial 5926 patients with intolerance to ACE inhibitors, Randomized to telmisartan 80 mg daily versus placebo, including 2118 patients with diabetes. In the overall trial, telmisartan failed to achieve statistical superiority over placebo in reducing the primary composite of CVD death, MI, stroke, or HF hospitalization (HR = 0.92; 95% CI, 0.81-1.05), But it significantly reduced the secondary composite of CV death, MI, or stroke (HR = 0.87; 95% CI, 0.76-1.00).

68. Calcium Channel Blockers Dihydropyridine calcium channel blockers, such as nifedipine , nitrendipine , and amlodipine , are well tolerated and effective at lowering blood pressure. In active controlled comparisons, amlodipine has been proven superior to hydrochlorothiazide when it is added to a background of benazepril therapy, But in randomized trials directly comparing the efficacy of calcium channel blockers versus ACE inhibitors, superior outcomes were observed with ACE inhibitors

69. Beta Blockers Another key component of effective CVD risk reduction in diabetes. Mask hypoglycemia symptoms and adverse effects on glucose and lipid metabolism. These concerns have been mitigated by the results of CVD outcomes trials supporting the benefit of beta blockers for patients with diabetes in the chronic ambulatory setting and in the post-ACS population. Metabolic effects of various beta blockers differ, which suggests improved metabolic parameters with non cardioselective beta blockers that also have alpha receptor–blocking properties; the clinical relevance of these differential effects remains to be determined.

70. Combination Therapy for Hypertension In the Action in Diabetes and Vascular disease: preterAx and diamicroN -MR Controlled Evaluation (ADVANCE) trial 11,140 patients with type 2 diabetes Compared combination therapy with perindopril and indapamide versus placebo 9% relative reduction in a composite primary outcome combining microvascular and macrovascular disease endpoints, compared with placebo.

71. In the Anglo-Scandinavian Cardiac Outcomes Trial–Blood Pressure Lowering Arm (ASCOT-BPLA ), 923 patients which randomized treatment to amlodipine with perindopril added as needed versus atenolol with bendroflumethiazide added as needed, The amlodipine-perindopril combination yielded a significant 13% relative risk reduction ( P = 0.028) in major CVD outcomes in with diabetes, compared with atenolol-bendroflumethiazide .

72. The Avoiding Cardiovascular Events through Combination Therapy in Patients Living with Systolic Hypertension (ACCOMPLISH) trial the 6946 patients with diabetes A ll patients were treated with benazepril , with randomization to add-on amlodipine versus add-on hydrochlorothiazide, treatment with benazepril-amlodipine versus benazepril -hydrochlorothiazide was associated with a 21% reduction in CVD outcomes among (60.4% of the study cohort; P = 0.003). Therefore, in combination with thiazide diuretics and with amlodipine , ACE inhibitors are associated with improved CVD outcomes, with the combination with amlodipine proving superior in head-to-head comparison.

73. Likewise, the average systolic blood pressure achieved in the diabetic subset of HOPE (139/77 mm Hg) and in the ADVANCE trial (136/73 mm Hg) provide further support for the safety and efficacy of such intensified blood pressure targets in the high-risk population of patients with DM.

74. Antihypertensive Therapy Summary In summary, five classes of medications have substantial evidence basis for CVD efficacy in the setting of diabetes, including ACE inhibitors, calcium channel blockers, beta blockers, thiazide diuretics, and ARBs. Evidence supports an aggressive blood pressure target of <130/80 mm Hg for patients with diabetes to achieve optimal CVD risk mitigation, with most patients requiring a combination of multiple blood pressure medications to achieve such targets.

75. Recommendations for blood pressure control in diabetes

76. Antiplatelet Therapy Patients with diabetes have a number of aberrations of platelet structure, function, and activity, yielding in aggregate a prothrombotic milieu. Aspirin Therapy The ADA/AHA presently recommend daily aspirin (75 to 162 mg/day) for all patients with diabetes who have prevalent CVD or for primary prevention in all patients older than 40 years with additional CVD risk factors (or younger in the presence of prevalent CVD risk).

77. Absolute or relative aspirin resistance- 40% of patients with increasing prevalence associated with poor metabolic control. On the basis of this ongoing uncertainty with regard to the role of aspirin in the setting of primary CVD risk prevention in type 2 diabetes, two large-scale randomized clinical trials are currently under way

78. A Study of Cardiovascular Events In Diabetes (ASCEND) plans to enroll 10,000 patients with type 1 or type 2 diabetes without CVD, randomized factorially to treatment with 100 mg acetylsalicylic acid (ASA) daily versus placebo or with omega-3 fatty acid 1 g daily versus placebo, with a primary endpoint of major adverse cardiovascular events . The Aspirin and Simvastatin Combination for Cardiovascular Events Prevention Trial in Diabetes (ACCEPT-D) plans to enroll 4700 patients with type 1 or type 2 diabetes to receive 100 mg ASA plus simvastatin versus simvastatin alone in a prospective, open-label, blinded endpoint evaluation (PROBE) design trial to assess the cardiovascular efficacy of ASA in primary prevention for patients with diabetes that has been treated with statins

79. Thienopyridines The thienopyridines irreversibly bind to P2Y 12 ADP receptors and inhibit ADP-induced activation of glycoprotein (GP) IIb / IIIa , preventing the binding of fibrinogen and platelet thrombus formation, thus yielding more potent antiplatelet effects than achieved with aspirin alone.

80. The CAPRIE trial Compared outcomes in patients with NSTEMI , ischemic stroke, or established PAD randomized to treatment with aspirin versus clopidogrel , 3866 patients with diabetes were enrolled. In the subset of patients with diabetes, the 12.5% reduction in major adverse CVD events with clopidogrel versus aspirin was comparable to the effect observed in the overall study cohort. Given the incremental expense of clopidogrel and its associated increment in bleeding risk, however, this strategy is not routinely recommended over the use of aspirin alone for most patients.

81. Increased prevalence of resistance to clopidogrel , a prodrug requiring metabolic conversion that appears to be impaired in diabetes, resulting in decreased circulating active metabolite. These observations have led some investigators to explore the effects of increased dosing of clopidogrel in patients with diabetes, with preliminary data suggesting increased antiplatelet effects with such a strategy. However, the net clinical safety and efficacy of increased dosing of clopidogrel requires further evaluation before application in clinical practice.

82. Recommendationsfor antiplatelet therapy in patients with diabetes

83. Glucose management Drug classes - oral and injectable glucose-lowering medications approved for clinical use These drugs work by Stimulating endogenous insulin release, Impairing hepatic glucose production, Improving the body's response to insulin, or Delaying intestinal carbohydrate absorption.

84. UKPDS 34, Lancet 352: 854, 1998 UKPDS Metformin Sub-Study: CHD Events Myocardial Infarction 5 10 15 20 Incidence per 1000 patient years Conventional Diet Insulin SU’s Metformin p=0.01 NS 39% Reduction Coronary Deaths 2 4 6 8 10 p=0.02 50% Reduction Metformin Incidence per 1000 patient years Conventional Diet n= 411 951 342 411 342 #Events 73 139 39 36 16

85. Cardiovascular Effects of Intensive Glucose Control Strategies UKPDS randomized 5102 patients with newly diagnosed type 2 diabetes to intensive glucose control with sulfonylurea or insulin compared with diet alone; those overweight at study entry (n = 795) could also be randomized in the intensive arm to receive metformin .

86. Type 2 Diabetes: A1C Predicts CHD CHD Mortality Incidence (%) in 3.5 Years All CHD Events Incidence (%) in 3.5 Years A1C=hemoglobin A1C * P <0.01 vs lowest tertile ** P <0.05 vs lowest tertile 2 4 6 8 10 12 Low <6% High >7.9% * Middle 6-7.9% 5 10 15 20 25 Middle 6-7.9% High >7.9% ** Low <6% Adapted with permission from Kuusisto J et al. Diabetes . 1994;43:960-967.

87. % relative risk reduction P=0.03 P<0.01 P<0.01 P=0.05 P=0.02 UKPDS Group. Lancet. 1998;352:837-853. UKPDS Relative Risk Reduction for Intensive vs. Less Intensive Glucose Control Over 10 years, HbA 1c was 7.0% (6.2-8.2) in the intensive group (n=2,729) compared with 7.9% (6.9-8.8) in the conventional group (n=1,138).

88. Recently, three trials assessing the CVD effects of more intensive glucose control among patients with type 2 diabetes at high CVD risk showed no significant CVD benefit of intensified glucose control.

89. Conclusion. A meta-analysis of cardiovascular outcomes based on VADT, ACCORD and ADVANCE HbA1c reduction of 1% was associated with a 15% RRR in nonfatal MI but without benefits on stroke or all-cause mortality. However, patients with a short duration of T2DM, lower baseline HbA1c at randomization, and without a history of CVD seemed to benefit from more-intensive glucose-lowering strategies.

90. Other Glucose-Lowering Medications Few data are available with regard to the CVD effects of other glucose-lowering medications. [46] Suggested CVD benefits with insulin derive from selected trials including both type 2 and type 1 diabetes, but these studies all had limited statistical power to assess such effects. [4,54] On this backdrop, and in the wake of increased regulatory scrutiny with regard to safety and efficacy assessment of drugs being developed for diabetes, [44] numerous randomized CVD clinical outcomes trials are currently under way or in advanced planning.

91. Acute Coronary Syndromes Insulin and Glucose Control The myocardium preferentially metabolizes FFA under physiologic conditions ,but it can also metabolize a variety of substrates during periods of stress (such as ischemia), and glucose is principal among these. Countering the metabolic switch to glucose metabolism during ischemia, the myocardium develops a relative insulin resistance Underpinning extensive research into metabolic modulation of the ischemic myocardium, with insulin as the primary focus of investigation.

92. Glucose-Insulin-Potassium Therapy The use of insulin for ACS was first described in 1963 by Sodi-Pallares , with the intention of facilitating potassium flux in the ischemic myocardium, the so-called polarizing therapy. After decades of investigation, this combination of glucose, insulin, and potassium has become known as GIK therapy, and the focus of attention has shifted from the polarizing effects to the direct effects of insulin

93. Summary of Selected Randomized Trials Assessing the Effect of Insulin Infusion on Major Adverse Cardiovascular Outcomes Among Patients with Acute Coronary Syndrome Events DIGAMI = Diabetes Mellitus Insulin-Glucose Infusion in Acute Myocardial Infarction trial [60] ; ECLA = Estudios Cardiol?gicos Latinoam?rica glucose-insulin-potassium pilot trial [110] ; GIPS = glucose-insulin-potassium study [111] ; CREATE = Clinical Trial of REviparin and Metabolic Modulation in Acute Myocardial Infarction Treatment Evaluation [59] ; Hi-5 = The Hyperglycemia: Intensive Insulin Infusion in Infarction study [112] ; Pol -GIK = The Poland glucose-insulin-potassium trial [113] ; units/hr = units per hour of intravenous insulin.

94. R evascularization Revascularization in these patients is challenged by Diffuse atherosclerotic involvement of epicardial vessels, higher propensity to develop re- stenosis after PCI and Saphenous graft occlusion after CABG and Unremitting atherosclerotic progression causing new stenosis . Co morbidity ( PVD, CRF ) Periprocedural complications Worse longterm clinical outcones

95. OUTCOMES COMPARED TO PATIENTS WITHOUT DIABETES   Often worse in diabetic patients . With PCI  —  Procedural success rates are similar. Higher rates of restenosis and lower rates of event-free survival .

96. Restenosis   Diabetic patients –increased restenosis and progression of coronary disease. The following studies illustrate the magnitude of the increase in restenosis risk : In an analysis of 3090 patients who underwent PCI with BMS, 418 of whom (14 %) had diabetes . 6 month angiographic follow-up, the rate of restenosis was significantly higher in the diabetic patients (31 % vs 21 in non DM patients).

97. In an analysis of 10,778 patients in the j- Cypher registry who underwent PCI with SES, there were 966 patients with insulin-dependent diabetes, 3404 with noninsulin-dependent diabetes, and 6378 without diabetes . At 3 years - rate of TLR was significantly higher in the insulin-dependent and noninsulin-dependent groups compared to those without diabetes (19, 14, and 10 % , respectively).

98. Predictors of restenosis in diabetic patients Smaller vessel caliber Greater length of the stented segment Lower body mass index It is unclear why diabetic patients are more prone to restenosis after PCI. Exaggerated intimal hyperplasia has been demonstrated, possibly due to the stimulatory effect on vascular smooth muscle of growth factors, such as insulin-like growth factor-I .

99. Event-free survival     Event-free survival (events such as death or MI) is worse after revascularization with PCI The following observations illustrate the range of findings : In a consecutive series of patients with successful stent placement, comprising 715 patients with DM vs 2839 without DM.

100. In the j- Cypher registry - cardiovascular event at 3 years was significantly greater in the insulin-dependent group (hazard ratio 1.12, 95% CI 1.03-1.23), but not the noninsulin-dependent group, compared to those without diabetes . The SYNTAX trial compared PCI with drug eluting stents (DES) versus CABG in patients with complex coronary artery disease (left main and/or three vessel disease). 452 patients with DM. At 5 year follow-up, The rate of repeat revascularization of patients undergoing PCI (n = 231) was higher in patients with diabetes (29 versus 19 % ). Mortality was also increased in the diabetic population (20 versus 12 %)

101. With CABG ---   Procedural success rates are similar Follow-up - death and adverse nonfatal outcomes higher in patients with diabetes Mortality   No affect in-hospital mortality after CABG , short- and long-term survival after CABG are significantly reduced . In different large observational studies, diabetic patients had higher mortality rates at 30 days (5 versus 2.5 percent) and at five and ten years (22 versus 12 percent and 50 versus 29 percent, respectively) .

102. OUTCOMES AFTER PCI   The rates of TLR ,MI or survival may be influenced by the stent type as well as diabetes-related factors. Stent type     DES now preferred to BMS Reductions in restenosis and TLR or TVR.

103. The individual trials are limited in their ability to compare two stent designs due to relatively small number of enrolled patients The following summarizes the results of those studies: BMS versus first generation stents : Significantly lower rates of TLR with first generation stents compared to BMS in subgroup analyses of major trials such as SIRIUS , DIABETES, that enrolled only patients with diabetes , and in a pooled analysis from the first five TAXUS trials

104. CYPHER Pooled: Diabetic Subgroup Angiographic Restenosis P<0.001 P<0.001  79%  80%

105. Pooled TAXUS Trials (II, IV, VI) Overall Diabetic Subset: Angiographic Restenosis  87% P<0.001  80% P<0.001 (n=263) (n=264)

106. SES versus PES : The DES-DIABETES trial 400 patient Primary endpoint - insegment stenosis At 6 months - significantly lower in the SES group (4.0 versus 20.8 percent, respectively) and At 9 months - there was no significant difference in the incidence or MI or death . At 4 years - there was no significant difference in the rates of MACE (11.0 versus 16 percent ) or TVR (7.5 versus 12 percent) . 

107. ISAR-DIABETES 250 patients 125 were randomly assigned to receive PES and 125 to receive SESs . nine-month follow-up period The primary end point was in-segment late luminal loss. Secondary end points were angiographic restenosis and the need for revascularization of the target lesion In-segment restenosis - 16.5 percent vs 6.9 percent (P=0.03). TLR - performed in 12.0 vs 6.4 percent (P=0.13).  

108. Second versus first generation stents : SPIRIT IV trial  3687 subgroup analysis which randomly assigned patients to second generation everolimus -eluting stents (EES) or PES , No significant difference in the primary outcome of target vessel failure between the EES and PES groups in patients with diabetes (6.4 versus 6.9 percent, )

109. Best available evidence - relative efficacy and safety of the various DES or BMS comes from a 2012 mixed treatment comparison analysis of 42 randomized trials with 22,844 patients with years of follow-up. Compared to bare metal stents, SES, PES, EES, and ZES were associated with : A significant reduction in TVR, with EES having the highest probability of being the best (with limited usable data for the ZES-resolute stent). No increased risk of any safety outcome (death, MI, or probable/definite stent thrombosis). For these outcomes, the EES had the highest probability of being the best stent.

110. Diabetes-related factors   Nephropathy   Important predictor of risk after PCI. Observational study of 537 diabetic patients in with proteinuria had a significantly higher two-year mortality rate following PCI (20 versus 9 percent in those without proteinuria , adjusted hazard ratio 1.8 ).

111. Glycemic control   Rate of restenosis after PCI - lower if optimal glycemic control is achieved . In a study of 239 patients, 179 with DM, who underwent elective PCI (67 percent with stenting ) after measurement of glycosylated hemoglobin (HbA1c ). Preprocedural HbA1c ≤7 percent had a rate TVR at 12 months that was comparable to that in non DM patients (15 versus 18 percent ), HbA1c >7 percent had a significantly higher rate of target vessel revascularization (34 percent).

112. Thiazolidinediones   Inhibit vascular smooth muscle cell proliferation and migration and Reduce intimal proliferation after vascular injury This approach has been evaluated in two, small randomize trials who underwent PCI with stenting were randomly assigned to either a thiazolidinedione ( pioglitazone or   rosiglitazone ) or placebo . The rate of angiographic restenosis was lower in the thiazolidinedione group . Further studies are required to confirm the efficacy and safety of this approach, particularly with the use of drug-eluting stents.

113. Glycoprotein IIb / IIIa inhibitors   Reduce the risk of ischemic complications - undergoing PTCA including those with an ACS & higher-risk patients with stable angina . On the other hand, in lower-risk patients undergoing elective stenting , a GP  IIb / IIIa  inhibitor may not provide any additional benefit if the patient is pretreated with  clopidogrel  (600 mg) as shown in the ISAR-REACT trial

114. Indication is more compelling in diabetic patients, since pooled analyses or meta-analyses of trials of patients undergoing elective or urgent PCI or those with an acute coronary syndrome suggested a significant mortality benefit at 30 days and one year in the subset of patients with diabetes .

115. ISAR-SWEET trial 701 diabetic patients undergoing elective PCI were randomly assigned to either  abciximab  plus heparin (70 U/kg) or placebo plus heparin (140 U/kg).  All patients were pretreated with 600 mg of  clopidogrel  at least two hours before the procedure. Patients were treated with balloon angioplasty, bare metal stents, or drug-eluting stents (10, 80, and 10 percent, respectively).

116. Primary endpoint at one year did not differ between the two groups (8.3 versus 8.6 percent with placebo ) No difference in mortality at one year (4.8 versus 5.1 percent ). Follow-up angiography at 7 months - a reduction in the rate of angiographic restenosis with  abciximab  (29 versus 38 % with placebo) and, At one year, a significantly lower rate of target lesion revascularization (23.2 versus 30.4 percent).

117. OUTCOMES AFTER CABG   Internal thoracic artery grafts   All patients undergoing CABG, including those with diabetes, should receive an internal thoracic (mammary) artery (ITA), to improve survival. In addition , prefer bilateral to single ITA grafting for many patients with diabetes based on two observational studies.

118. Perioperative glycemic control   Outcomes are worse in patients with significant hyperglycemia Intensive glycemic control - improve both cardiac and noncardiac outcomes in diabetic patients after CABG . The following observations illustrate the range of findings: In a prospective trial, 141 patients with diabetes who were undergoing CABG were randomly assigned to tight glycemic control (125 to 200  mg/ dL ) with a GIK infusion or standard therapy with intermittent subcutaneous insulin .

119. Patients treated with GIK had lower mean serum glucose concentrations in the perioperative period (138 versus 260 mg/ dL  [7.7 versus 14.4 mg/ dL ]).  At two years, GIK patients had significantly lower rates of wound infections (1 versus 10 percent ), recurrent ischemia (5 versus 19 percent), and mortality (2 versus 10 percent).

120. PCI VERSUS CABG   Multivessel or left main coronary artery disease who require revascularization, the evidence suggests better outcomes with CABG rather than PCI with stenting . Supporting evidence Early trials comparing balloon angioplasty to CABG in patients with diabetes suggested higher rates of revascularization and mortality with the former particularly in patients with multivessel disease. Early trials of PCI with stenting , including those using DES, showed similar survival rates but a persistent increased need for revascularization.

121. FREEDOM trial ( Future REvascularization Evaluation in patients with Diabetes mellitus: Optimal management of Multivessel disease ) 1900 pts with DM and multivessel CAD (83 percent three-vessel disease) were randomly assigned to either PCI with drug-eluting stents ( paclitaxel  or  sirolimus ) or CABG. Both groups received optimal medical therapies for the secondary prevention of cardiovascular disease. Median follow-up- 3.8 years.

122. At one year, there was a higher rate of repeat revascularization in the PCI group (12.6 versus 4.8 percent; hazard ratio 2.74, 95% CI 1.91-3.89).

123. Very early studies evaluated outcomes in patients treated with either bare metal stents (BMS) or CABG in patients with diabetes. Subset analyses from two smaller randomized trials, ARTS-I and AWESOME, showed a higher rate of repeat revascularization with BMS. Mortality was not significantly different, but these studies were severely underpowered to assess mortality.

124. The first evidence comparing DES to CABG was observational and suggested that DES diminished the advantage of CABG compared to PCI seen when BMS are used in diabetic patients . ARTS II study, which was a single-arm study of 607 patients (including 159 with diabetes) who were treated with  sirolimus  eluting stents; the outcomes were compared to the CABG arm in the ARTS I trial . At 3 years , primary combined endpoint of death, stroke ,MI and repeat revascularization with DES was not significantly different from the CABG arm of ARTS I after adjustment for independent predictors (27.7 versus 17.7 percent for CABG).

125. More evidence comparing DES to CABG came from the CARDia and SYNTAX trials, which came to similar conclusions . CARDia trial (The Coronary Artery Revascularization in Diabetes ) Randomly assigned 510 patients with diabetes and symptomatic, multivessel , or complex single vessel CAD to either stenting (31 % were BMS & 69% DES) or CABG .

126. % 5 15 2.0 9.9 20 CARDia Trial design: Diabetic p atients with multi-vessel disease or complex single-vessel disease, but not left main disease, were randomized to either CABG or PCI . Clinical outcomes were compared at 12 months. (p = 0.63) CABG (n = 254) PCI (n = 256) (p = 0.001) 5 10 15 20 10.2 11.6 % Primary endpoint Repeat revascularization 10

127. CARDia Conclusion - Similar incidence of death, MI, or stroke in diabetics with CABG or PCI CABG was associated with fewer repeat revascularizations compared with PCI No difference in death, MI, but trend toward increased stroke with CABG, as suggested by other studies

128. In subgroup analysis of the 452 patients with diabetes in SYNTAX, which compared CABG to DES ( paclitaxel -eluting stents ) in patients with multivessel or left main coronary artery disease

129. % 5 15 5.9 13.7 20 SYNTAX Trial design: Patients with severe three-vessel disease or left main (LM) disease were randomized to either CABG or DES-PCI with paclitaxel -eluting stents . Clinical outcomes were compared at 12 months. (p = 0.0015) CABG (n = 897) DES-PCI (n = 903) (p = 0.0001) 5 10 15 20 12.1 17.8 % MACCE Repeat revascularization 10

130. SYNTAX Conclusion CABG was associated with fewer repeat revascularizations compared with DES-PCI in patients with LM or three-vessel disease, but a higher rate of stroke No difference in death, MI, or thrombosis Diabetics are especially more likely to benefit with CABG compared with DES-PCI

131.                                                                                                                                                                                                                     CABG v/s PCI in Diabetics

132. MEDICAL THERAPY VERSUS REVASCULARIZATION In BARI 2D trial 2368 patients with type 2 DM and stable ischemic heart disease Randomized to receive prompt revascularization plus intensive medical therapy compared with intensive medical therapy alone.

133. During 5 years - overall mortality rates between the two groups did not differ significantly—11.7% vs 12.2% ( P = 0.97). In secondary analyses stratified according to the mode of revascularization, all cardiovascular outcomes were statistically similar between the PCI and medical therapy groups, but CABG compared with medical therapy was associated with a significant reduction in major adverse cardiovascular events (22.4% versus 30.5%; P = 0.01).

134. These data provide support for a primary strategy of intensive medical therapy, as well as additional suggestion of the benefit of bypass surgery, although direct comparisons between PCI and CABG are not possible from this study design.

135. THANK U