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Hyperlipidemia Management in T2DM Changing Diabetes Mellitus to Diabetes Lipidus Dr.Wehad ALTourah Consultant Internist, Assistant Director Internal Medicine Residency training Program FRCP(London),KBIM Amiri Hospital Outline Cases Epidemiology and cardiovascular risk Lipid pattern & Target in T2DM Screening CV Risk Stratification Treatment Options: Statins,Fibrates,Niacin,Ezetimibe,Omega-3 FA Combination Treatment Drug Monitoring Statin and DM Future Research Conclusion Case 1 45 years-old gentleman T2DM for 3 years, No other significant history Med.: Metformin 1gm /BID BMI 30 Bp 120/80 Total Cholesterol 7mmol/L LDL-C:2.6 mmol/L HDL-C:1.0 mmol/L TG: 2.0 mmol/L Case1 What will be your primary lipid target : LDL-C? HDL-C? TG? Case 2 45 years- old gentleman Current smoker,T2DM for 5 years, hypertension for 10 years He is on lisonpril 10mg OD, metformin 1 gm BID BMI 28 Blood pressure: 135/85 mmHg HA1C 6.5% Total cholesterol: 5 mmol/L LDL-cholesterol: 2.6 mmol/L HDL-cholesterol: 1.2 mmol/L Triglycerides: 2.0 mmol/L Case 2 Would You Initiate a lipid lowering agent in This Patient? OR Would you advise nonpharmacological Treatment? Case 3 50 years-old lady T2DM for 12 years, Hypertension, non-smoker Meds: metformin 1gm BID, lisinopril 20mg/day, simvastatin10mg/day BMI 26.5 Bp: 135/85 mmHg Total cholesterol: 4.7 mmol/l LDL-cholesterol: 2.7 mmol/L HDL-cholesterol: 1.0 mmol/L Triglycerides: 2.4 mmol/L Case 3 Would you Intensify This Patient’s Statin? OR Would you change her statin to more potent agent? Case 4 65year-old lady, T2DM, PCI for STEMI 6 months ago no current CV symptoms Meds: ASA, clopidogrel, lisinopril, atorvastatin 80 mg/day BMI 29.0 Blood pressure: 125/85 mmHg Total cholesterol: 3.1 mmol/L LDL-cholesterol: 0.9 mmol/L HDL-cholesterol: 0.9 mmol/L Triglycerides: 3.4 mmol/L Case 4 Would you decrease this patient’s statin dose? OR Would you add a fibrate? Case 5 50 year-old lady T2DM 5 years, Hypertension 5 years Had pain in her arms and legs for 6 months Meds: Lisinopril 10mg/d, atorvastatin 20mg/d, aspirin 75mg/d LFT:N CK:700 (40-176 IU/L) Total cholesterol:4.0mmol/L LDL-C:1.8mmol/L HDL-C:0.9mmolL TG:2.0mmol/L Case 5 What will be your Approach to Solve this patient’s problem? DM is a Huge Burden IDF Diabetes Atlas, 6th edition Top 10 countries/territories for prevalence(%) of diabetes (20-79),2013 Dm and CVD IDF 2013 Dm is Strong risk Factor for CAD:DM=CHD T2DM is associated with a marked risk of CVD. Individuals with DM have an absolute risk of major coronary events similar to that on nondiabetic individuals with established coronary heart disease Medescape.Treating Dyslipidemia: Recommendations for T2DM 27/9/13 The risk for CVS death is ↑2-3 fold in T2DM. Prevalence of Dyslipidemia is high in Type 2 Diabetes Control of Lipids LDL-C > 100 mg/dL HDL-C < 40 mg/dL (men) < 50 mg/dL (women) Triglycerides > 150 mg/dL Patients With Diabetes, % Patients Without Diabetes, % P Value 74.7 75.7 NS 63.7 40.0 < .001 61.6 25.5 < .001 N = 498 adults (projected to 13.4 million) aged > or = 18 years with diabetes representative of the US population and surveyed within the cross-sectional National Health and Nutrition Examination Survey 1999-2000. Diabetes Res Clin Pract;70:263-269.2005 Lipid Pattern in Diabetes UKPDS Lipid Pattern in Diabetes UKPDS Clinical Diabetes.Vol.24,no.1,2006 The relationship between LDL-C,HDL-C and CVD UKPDS,0.1mmol/L ↑HDL-C was associated with 15% ↓in CVD events UKPDS,1mmol/L ↑LDL-C was associated with 57% ↑risk MI adapted from Gordon T. et al, American Journal of Medicine, 1977;62;707-714 Lipid Pattern in Diabetes Low HDL- C High Small dense LDL High TG Lipoprotein Pattern in Diabetes Diabetes Care.16:434-444.1994 Whom to Screen? How often? ADA Guidelines 2014 -In most adult patients with DM, measure fasting LIPID PROFILE AT LEAST ANNUALLY. (LEVEL B) -In adults with low risk lipid values(LDL-C <2.6mmol/L, HDL-C>1.3mmol/L, and TG<1.7mmol/L),LIPID ASSESSMENT MAY BE REPEATED EVERY 2 YEARS.(Level E) Diabetes Care,volume 37,Supp 1,January 2014 What are the additional predictors beyond LDL and HDL To be assessed? 1-Apo lipoprotein B: No evidence yet for regular screening. Very strong predictor for cardiovascular disease in DM. Has less biologic variation, reliable measures. Non fasting sample. High cost. ESC/EAS 2011 What are the additional predictors beyond LDL and HDL to be assessed? 2-Highly sensitive CRP -These additional inflammatory markers are helpful in intermediate risk patients but proven to be unhelpful for the very high risk patients. Risk Stratification? Is it important? What are the risk scoring systems? Total cardiovascular risk estimation 1- Framingham Risk Score. 2- Systemic Coronary Risk Estimation(SCORE). 3- Atherosclerotic cardiovascular disease risk (ASCVD).(ACC/AHA) 4- QRISK Lifetime cardiovascular risk (Joint British Societies in 2014). SCORE Framingham Risk Score Total cardiovascular risk estimation Very High Risk Risk Level SCORE 10yrs CVD Risk ≥ 10% CVD/PAD/ Stroke + T2DM + CKD + Risk Factors (FH/Severe HTN) ESC/EAS Guidelines 2011 High Risk Moderate Risk ≤10% - ≥5% ≤5% - ≥1% ++ +++ Low Risk ≤1% ASCVD 10-year Risk ACC/AHA Guidelines 2013 Cumulative Incidence of CVD Adjusted for the Competing Risk of Death According to Risk Factor Burden at Age 50 Lloyd-Jones DM et al, Circulation 2006;113:791 Management of Hyperlipidemia in DM? Management Of Hyperlipidemia in T2DM? 1-Whom should we treat? 2-What are the important targets? 3-What are the target Levels? 4-What are the treatment Strategies? Q1: Whom Should we Treat? Whom Should we Treat? ADA Guidelines 2014 1-Diabetic patients <40years,without CVD,LDL cholesterol>2.6mmol/L(low risk) after failure of life style modifications, or with multiple CVD risk factors(level C). ADA Guidelines, January 2014 Whom Should we Treat? ADA Guidelines 2014 2- Patients without CVD,>40years,having one or more other CVD risk factors(family history of CVD, hypertension,smoking,albuminuria) regardless of the LDL(level A). 3-Diabetic patients with overt CVD, regardless of the LDL level(High risk patients),(level A). ADA Guidelines,January 2014 Q2:Which target is the most important? LDL Othe rs HDL TG UKPDS - LDL cholesterol was the strongest independent predictor of CHD, followed by HDL.TG level did not predict CHD events. Clinical Diabetes.Vol.24,no. 1,2006 Q3: What Are the Lipid’s Target Level? ADA Guidelines 2014 In individuals without overt CVD, the goal is LDL-C <2.6mmol/L.(Level B) Individuals with overt CVD, a lower LDL-C goal of < 1.8mmol/L with a high dose statin. (Level B) If maximum tolerated statin therapy, a reduction in LDL-C of 30-40-% from baseline is an alternative goal.(Level B) Diabetes Care,vol.37,Supp 1,January 2014 ADA Guidelines 2014 TG <1.7mmol/L and HDL cholesterol>1.0mmo/L in men and > 1.3mmo/L in women. LDL-C -targeted statin therapy remains the preferred strategy.(Level A) ADA Guidelines,January 2014 Q4:What are the Treatment Options or Strategies? Treatment Options Life Style Exercise Diet Pharmacological Lipid Management Statins Fibrates Niacin Ezetimibe Non-Lipid Interventions Intensive Glycemic Control Intensive Blood Pressure Control Life style modification is critical component Weight Loss Exercise Diet Life Style Intervention ESC/EAS 2011 >5% weight loss if BMI>25 Level I 30min.moderate physical activity on most days/ wk. Level II Serves up 8,000 calorie burger meal... the equivalent of FIVE DAYS worth of food Life Style Intervention Diet 1-High polyunsaturated fatty acids diet – saturated fat< 7% of daily calories +↓intake of cholesterol to 200mg/day(Level II). 2-↑the amount of soluble dietary fibers to 10-25g/day(level II). →associated with 5-15% ↓in the LDL-C. 3- limits the carbohydrates to <60% in individuals with ↑TG/ ↓HDL→ short term effect /OR replace the saturated fat with carbohydrates /monosaturated fat(Level I). National Evidence Based Guidelines for the Management of Type 2 Diabetes Mellitus. the Australian Centre for Diabetes Strategies.Part7.2004 ADA.2014 Dietary Recommendation to TC and LDL-C ESC,EAS Guidelines2011 Effects of Drug Therapy and Diet on Lipids Pre-drug Drug Drug + diet 325 300 275 250 TC 225 (mg/dL) 200 175 150 125 100 1° Prevention (n=40) * 84% reached NCEP LDL target (<130 mg/dL) † 63% reached NCEP LDL-C target (<100 mg/dL) Barnard RJ, et al. Exerpta Medica Brief Reports. 1997;1112-1114. 2° Prevention (n=53) Pharmacological Lipid Management Statins Combina tions Fibrates Ezetimibe Niacin Use Statins To Treat the Risk Not Cholesterol Clinical Trial Evidence Primary Prevention Secondary Prevention Study Intervention Baseline LDLcholesterol (mg/dl) Number Diabetes/ Total CVD Out come RRR Diabetes (%) RRR NonDiabetes (%) Primary Prevention CARDS Atorvastatin 10mg 117 2838 Acute Coronary Events Stroke 36* - Primary secondary Prevention HPS ALLHAT Primary Prevention CARDS Simvastatin 20mg 5963/20536 Major CHD event Primary&124Secondary Prevention Any major CVS event HPS Pravastatin 129 3635/10357 Major CHD event 48* 27* 22* 27* 24* 11 8 16 23* 44* 20* Total mortality Major CHD event 43 55* 29* 23* 10mg ASCOT-LLA Atorvastatin 10mg Secondary Prevention 128 2532/10305 Major CHD event Secondary Prevention Total CVS events and procedures 4S 4S Simvastatin 10-40mg 186 202/4444 CTT CARE Pravastatin 40mg 136 586/4159 Major CHD Expanded endpoint 13 25* 26* 23* LIPID Pravastatin 40mg 143 1077/9014 Major CHD event Any CVS event 19 21* 23* 13* Clinical Diabetes.Vol.24.no.1,2006 Collaborative Atorvastatin Diabetes Study(CARDS) First RCT statin trial conducted only in diabetic subjects 2838 patients 40-75 yrs T2DM 1428 Atorvastatin 10mg 1410 placebo LDL-C <4.4 +at least one risk factor Primary endpoint Time to first CV event/revascularization/stroke FU 3.9 yrs Lancet.364:685-696.2004 CARDS The trial was terminated 2 years earlier than expected 40% reduction LDL-C CARDS Conclusion: Atorvastatin 10 mg daily is safe and efficacious in reducing the risk of first cardiovascular disease events, including stroke, in patients with T2DM without high LDL-cholesterol. Lancet.364:685-696.2004 Heart Protection Study(HPS) The Largest sub-analysis of statins in patients with DM ( 2912 T2DM ) Composite primary end point 33 Effect of Statins in the 4S trial in patients with and without Diabetes *There was 55%reduction in the incidence of CVD events(P0.002) CTT Meta-analysis 18686 patients with diabetes from 14 RCTs primary& secondary CVD prevention, follow-up 4.3 years 21%reduction in the incidence of major vascular events/1mmol LDL-C reduction Lancet.366.1267-1278.2005 Is intensive Lipid Lowering Beneficial? Is intensive Lipid Lowering Beneficial? Treating to New Targets Study (TNT) Pravastatin or Atorvastatin Evaluation and Infection Therapy- Thrombolysis in Myocardial Infarction 22 (PROVE IT-TIMI22) Incremental Decrease in Endpoints Through Aggressive Lipid Lowering(IDEAL) :103 patients :80mg/D,135 :10mg/D *Significant differences in favour of atorvastatin 80 mg were also observed for time to CVA event (P 0.037) and any CV event (P 0.044). *LDL cholesterol levels were significantly lowered in patients receiving atorvastatin 80mg (P <0.0001). Diabetes Care,Vol.29,no.6,January2006 -No significant difference between the treatment groups in the rate of treatment related adverse events and persistent elevation in liver enzymes. Diabetes Care,Vol.29,no.6,January2006 Diabetes Care,Vol.29,no.6,January2006 PROVE IT –TIMI 22 To determine the impact of intensive lipid lowering therapy versus standard therapy with statins on the outcome in acute coronary syndrome(ACS) patients with diabetes. 4162 patients 739 DM ACS Atorvastatin 80mg Pravastatin 40mg FU 18-36months Primary endpoint death, MI, unstable angina requiring hospitalization, revascularization with PCI or CABG at least 30 days following randomization or stroke, Triple endpoint: acute cardiac events(death, MI, unstable angina requiring hospitalization) PROVE IT –TIMI 22 PROVE IT-TIMI 22 *Rate of events was higher in diabetic patients and the rate of acute cardiac events was reduced with the intensive therapy P(0.03) PROVE IT –TIMI 22 Conclusion: In ACS patients with DM, intensive statins therapy reduces the acute cardiac events as it does in those without DM. Despite intensive therapy, the majority of diabetics did not reach the dual goal of LDL-C< 1.8mmol/L. Statins? Which Dose? ADA Guidelines 2014 Maximum tolerated drug dose that will lead to the target LDL,OR 30-40%rduction in LDL-C from baseline. (Level B) ACC/AHA Guideline 2013 ACC/AHA Guidelines 2013 Are All Statin the Same? Which Statin? The CURVES Trial Comparison of LDL-C among Statins *At doses of 10, 20, and 40 mg, atorvastatin produced reductions in LDL-C of -38%, -46%, and -51%, respectively (P>0.01). Am J Cardiol.81:582-587.1998 Residual CV Risk Remains? Treatment Beyond LDL-Cholesterol? Beyond LDL-Cholesterol: Triglyceride(TG) HDL-Cholesterol (Guidelines for the HDL-C target levels were not established) What are the target levels According to the Guidelines? ADA 2014: TG level<150mg/dl(1.7mmol/L) and HDL-Cholesterol >40mg/dl(1.0mmol/L)in men and >50mg/dl(1.3mmol/L) in women are desirable.(Level C). HDL-C raising strategies may be considered in high-risk individuals with HDL-C < 40mg/dl(<50mg/dl in women). What are the available agents? Fibrates Niacin Ezetimibe Omega 3 What is the evidence from the trials? Fibrates FIELD VA-HIT ACCORD Fenofibrate Intervention and Event Lowering in DM study (FIELD) -FIELD is primary prevention , double-blind, placebocontrolled trial in 63 centres in 3 countries. -Examining the effects of long-term fibrate therapy on coronary heart disease (CHD) event rates in patients with T2DM regardless of the lipid profile. Lancet,366:1849.2005 FIELD Primary end point: CAD death, non-fatal MI Significant reduction in all CV death& secodary end point (P0.035).Effect is more in mixed lipidemia. ADA Guidelines 2014 - Hypertriglyceridemia dietary and life style changes. -Severe hypertriglyceridemia is absent therapy targeting HDL-C or TG lacks the strong evidence base of statin therapy. - Severe hypertriglyceridemia <1000mg/dl(11mmol/L) immediate pharmacological therapy may be warranted with fibtares, niacin or fish oil. Is Combination therapy Beneficial? The Action to Control Cardiovascular Risk in Diabetes-Lipid trial(ACCORD) ACCORD -Investigated whether combination therapy with a statin plus a fibrate, as compared with statin monotherapy, would reduce the risk of cardiovascular disease in patients with T2DM at high risk for CVD. NEJM. Vol. 362. no.17.April 29,2010 ACCORD 5518 patients T 2 DM 2765received fenofibrate &simvastatin 2753 received Simvastatin& placebo Secondary outcomes included the combination of the primary outcome plus revascularization or hospitalization for congestive heart failure FU 4.7 years primary outcome was the first occurrence of a major cardiovascular event NEJM.vol.362no.17.April 29.2010 ACCORD: Results NEJM.vol.362.no.17.April 29.2010 ACCORD: Results NEJM.vol.362.no.17.April 29.2010 ACCORD “The combination of fenofibrate and simvatatin did not reduce the rate of fatal cardiovascular events, non-fatal MI or non-fatal stroke, as compared with simvatatin alone.” NEJM, April 29,2010.vol.362no.17 ADA Guidelines 2014 Combination therapy with statin and fibrates maybe efficacious for treatment for all three lipid fractions, but this combination is associated with an increased risk of abnormal transaminase levels, myositis or rhabdomyolysis and does not provide additional CVS benefit. Hence, combination therapy can not be broadly recommended.(Level A) *Gemfibrozil is not preferably combined with statins ACC/AHA 2013 Guidelines Niacin: -Niacin is the most effective drug for raising HDL-C. -Niacin Trials: ARBITER 6-HALTSNIA-Plaque,AIM-HIGH, -HPS2-THRIVE showed disappointing results. Diabetes&Vascular Disease Research.10(2) 99-114.2012 Niacin: -NO COMPLETED RCT with clinical endpoints are available yet to guide practice on addition of niacin to statin therapy. -Until the results of the ongoing trials are reported, a consensus suggested to add niacin to statin in very high risk group. Medescape .15.3.2011 ADA Guidelines 2014 If the HDL-C<1mmol/L and the LDL-C between 2.6mmol/L and 3.3mmol/L , a fibrate or niacin might be used especially if a patient is intolerant to statins. Ezetimibe The Improved Reduction of Outcomes: Vytorin Efficacy International Trial: IMPROVE-IT Trial: -The trial is investigating the effect of simvastatin 40mg/d with or without ezetimibe 10mg/d in patients with ACS. Outcome: -Effect of treatment on CVD death, non-fatal stroke and mom-fatal MI -The results will be released in September 2014 Diabetes&Vascular Disease Research.10(2) 99-114.2012 Omega- 3 Fatty Acids - Omega-3 PUFAs can be used to ↓ TG levels. Trials: ORIGIN GISSI-P JELIS -There were differences in the outcomes seen in the various PUFA studies. -Further studies are needed to confirm the benefit of omega -3 FA in patients with DM and dyslipidemia. Pharmacotherapy.24(12):1692-1713.2004 How would you monitor Lipid Lowering Therapy? How Would You Treat Intolerability to Lipid Lowering Agents? ESC/EAS Guidelines 2011 Statins are safe but nothing is without risk: Review of 35 statin therapy trials FDA-approved statin* monotherapy vs placebo (N = 74,102) Outcome Statin Placebo (%) (%) RD P value Myalgias 15.4 18.7 2.7 0.37 CK elevations 0.9 0.4 0.2 0.64 Rhabdomyolysis 0.2 0.1 0.4 0.13 LFT elevation 1.4 1.1 4.2 <0.01 AE discontinuation 5.6 6.1 -0.5 0.80 *Atorvastatin, fluvastatin, lovastatin, pravastatin, rosuvastatin, simvastatin.AE:adverse events. Circulation;114:2788-97.2006 ESC/EAS Guidelines 2011 Statin Diabetogenicity Remaining Question -JUPITER Trial: 26% higher incidence of DM in the rosuvastatin group. -A meta-analysis of 13 RC statin trials with 91140 participants showed that treatment of 255 patients with statins for 4 years resulted in one additional case of DM while preventing 5.4 vascular events among 255 patients. -Future studies should continue to assess the effects of end organ dysfunction related to long-term hyperglycemia from statin therapy. Am J Cardiovasc Drugs.14:79-87(2014) Curr Opin Cardio.28:554-560.2013/ Lancet.375:75-742.2010. Future Research New LDL-C lowering drugs Phase III trials: 1-Microsomal transfer protein inhibitors(MTP). 2-Thyroid hormone mimetics with liver selectivity. 3-Oligonucleotides suppressing Apo B. ESC/EAS Guidelines 2011 CASES Case 1 What will be your primary lipid target : LDL-C? HDL-C? TG? 45 years-old gentleman T2DM for 3 years, No other significant history Med.: Metformin 1gm /BID BMI30 Bp 120/80 Total Cholesterol 7mmol/L LDL-C:2.6 mmol/L HDL-C: 1 mmol/L TG: 2 mmol/L Case 1 UKDP: LDL cholesterol was the strongest independent predictor of CHD, followed by HDL.TG level did not predict CHD events. -LDL-C remains the primary goal in the treatment of dyslipidemia according to ADA,ACC,ESC and NCEP. -Targeting HDL-C may be useful in high risk patients but still the evidence is lacking. Diabetes&Vascular Disease Research.10(2).99-114.2012 British Journal of Diabetes and Vascular Disease.Vol.5.issue2.56-62.2005 Case 2: Would You Initiate a lipid lowering agent in This Patient? OR Would you advise non-pharmacological Treatment 45 years- old gentleman Current smoker, 10 year history of hypertension He is on lisonpril 10mg OD BMI 28 Blood pressure: 135/85 mmHg HA1C 6.5% Total cholesterol: 5 mmol/L LDL-cholesterol: 2.6 mmol/L HDL-cholesterol: 1.2 mmol/L Triglycerides: 2.0 mmol/L Whom Should we Treat? ADA Guidelines 2014 1-Diabetic patients <40years,without CVD,LDL cholesterol>2.6mmol/L(low risk) after failure of life style modifications, or with multiple CVD risk factors(level C). ADA Guidelines, January 2014 Whom Should we Treat? ADA Guidelines 2014 2- Patients without CVD,>40years,having one or more other CVD risk factors(family history of CVD, hypertension,smoking,albuminuria) regardless of the LDL(level A). 3-Diabetic patients with overt CVD, regardless of the LDL level(High risk patients),(level A). ADA Guidelines,January 2014 Case 3: Would you Intensify This Patient’s Statin? OR Would you change her statin to more potent agent 50 years-old lady T2DM for 12 years, Hypertension, non-smoker Meds: metformin 1gm BID, lisinopril 20mg/day, simvastatin10mg/day BMI 26.5 Bp: 135/85 mmHg Total cholesterol: 6 mmol/l LDL-cholesterol: 2.7 mmol/L HDL-cholesterol: 1.0 mmol/L Triglycerides: 2.4 mmol/L Case 3 DM, age 40-75,LDL-C 1.8-4.9mmol/L: Framingham CV Risk Score= 3.44% moderate intensityrisk= statin unless score>7.5%,then high –intensity SCORE 1% statin The patient will be in the moderate risk group Case 4: Would you decrease this patient’s statin dose? OR Would you add a fibrate? 65year-old lady, T2DM, PCI for STEMI 6 months ago no current CV symptoms Meds: ASA, clopidogrel, lisinopril, atorvastatin 80 mg/day BMI 29.0 Blood pressure: 125/85 mmHg Total cholesterol: 3.1 mmol/L LDL-cholesterol: 0.9 mmol/L HDL-cholesterol: 0.9 mmol/L Triglycerides: 3.4 mmol/L Total cardiovascular risk estimation Risk Level Very High Risk SCORE 10yrs CVD Risk ≥ 10% CVD/PAD/ Stroke + T2DM + CKD + Risk Factors (FH/Severe HTN) ESC/EAS Guidelines 2011 High Risk Moderate Risk ≤10%≥5% ≤5%≥1% ++ +++ Low Risk ≤1% Case 4: ADA Guidelines 2014 Combination therapy with statin and fibrates or statin and niacin maybe efficacious for treatment for all three lipid fractions, but this combination is associated with an increased risk of abnormal transaminase levels, myositis or rhabdomyolysis and does not provide additional CVS benefit. Hence, combination therapy can not be broadly recommended.(Level A) ACC/AHA Guidelines 2013 Case 5: What will be your Approach to Solve this patient problem? 50 year-old lady T2DM 5 years, Hypertension 5 years Had pain in her arms and legs for 6 months Meds: Lisinopril 10mg/d, atorvastatin 20mg/d,aspirin 75mg/d LFT:N CK:700 (40-176 IU/L) Total cholesterol:4.0mmol/L LDL-C:1.8mmol/L HDL-C:0.9mmolL TG:2.0mmol/L Case5:ESC/EASGuidelines 2011 Conclusion -The prevalence of T2DM is continuing to rise. - Diabetes increases the risk of CVD which is the major cause of death in this population, and is treated as CVD equivalent. -Dyslipidemia should be the key management target. -There is little evidence for any threshold below which the lower LDL-C is not associated with lower risk. Conclusion - Life style measures are an important cornerstone in the management. -Glycemic Control can also beneficially modify plasma lipid levels particularly in patients with very high TG. -Statin therapy is highly effective at reducing the risk of CVD in primary & secondary prevention trials. Conclusion -Combination therapy of statins and other lipid lowering agents can not be broadly recommended. -Despite statin therapy, high CVD risk persists suggesting that further intervention in addition to intensive statin therapy are needed in the very high-risk diabetic patients. Thank you