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Erschienen in: Current Cardiology Reports 6/2012

01.12.2012 | Lipid Abnormalities and Cardiovascular Prevention (G De Backer, Section Editor)

Management of Dyslipidemias in the Presence of the Metabolic Syndrome or Type 2 Diabetes

verfasst von: Niina Matikainen, Marja-Riitta Taskinen

Erschienen in: Current Cardiology Reports | Ausgabe 6/2012

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Abstract

In the metabolic syndrome and type 2 diabetes, excess energy intake on the background of genetic predisposition and lifestyle factors leads to the dysregulation of fatty acid metabolism and acquired insulin resistance. These initial metabolic defects are reflected to both lipoprotein and glucose metabolism and contribute to increased risk for cardiovascular disease. However, even after controlling for the traditional cardiovascular risk factors, subjects with the metabolic syndrome and type 2 diabetes remain at high residual cardiovascular risk despite of low/normal LDL-cholesterol concentration. For 2 decades, statin therapy has been the cornerstone of treatment of dyslipidemia in these disorders. In the metabolic syndrome and type 2 diabetes, only statin treatment has demonstrated consistently a significant reduction in cardiovascular and all cause mortality in clinical trials. Lately, increased incidence of diabetes especially in the high-risk populations using statins has raised the debate whether statins are indicated for primary prevention especially in the metabolic syndrome. Guidelines recommend intensified lifestyle intervention to those in high risk groups on statin therapy to reduce the residual risk. Despite of the proven efficacy on plasma lipids, fibrate, or niacin as monotherapy, or in combination with statins has failed in reducing cardiovascular mortality. This underlies the fact that improvement in dyslipidemia or other biomarkers is not equal to the reduction in cardiovascular events. However, fibrates in combination with statins seem to be beneficial to reduce CVD events in subjects with low HDL-cholesterol (< 0.9–1.1 mmol/L) and elevated triglycerides (> 2.3 mmol/L), but the data are derived from subgroup analysis of clinical trials. The position of niacin and ezetimibe and omega-3 fatty acids in treatment of dyslipidemia in the metabolic syndrome and type 2 diabetes is even less clear and remains to be established in future clinical trials.
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Zurück zum Zitat Fabbrini E, Mohammed BS, Korenblat KM, et al. Effect of fenofibrate and niacin on intrahepatic triglyceride content, very low-density lipoprotein kinetics, and insulin action in obese subjects with nonalcoholic fatty liver disease. J Clin Endocrinol Metab. 2010;95:2727–35.CrossRefPubMed Fabbrini E, Mohammed BS, Korenblat KM, et al. Effect of fenofibrate and niacin on intrahepatic triglyceride content, very low-density lipoprotein kinetics, and insulin action in obese subjects with nonalcoholic fatty liver disease. J Clin Endocrinol Metab. 2010;95:2727–35.CrossRefPubMed
50.
Zurück zum Zitat Ridker PM, Danielson E, Fonseca FA, et al. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N Engl J Med. 2008;359:2195–207.CrossRefPubMed Ridker PM, Danielson E, Fonseca FA, et al. Rosuvastatin to prevent vascular events in men and women with elevated C-reactive protein. N Engl J Med. 2008;359:2195–207.CrossRefPubMed
51.
Zurück zum Zitat •• Sattar N, Preiss D, Murray HM, et al. Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials. Lancet. 2010;375:735–42. The first meta-analysis of studies on diabetogenic potential of statins. This paper launched the discussion of new onset diabetes being a side-effect of statins and statin use in primary prevention. CrossRefPubMed •• Sattar N, Preiss D, Murray HM, et al. Statins and risk of incident diabetes: a collaborative meta-analysis of randomised statin trials. Lancet. 2010;375:735–42. The first meta-analysis of studies on diabetogenic potential of statins. This paper launched the discussion of new onset diabetes being a side-effect of statins and statin use in primary prevention. CrossRefPubMed
52.
Zurück zum Zitat Preiss D, Seshasai SR, Welsh P, et al. Risk of incident diabetes with intensive-dose compared with moderate-dose statin therapy: a meta-analysis. JAMA. 2011;305:2556–64.CrossRefPubMed Preiss D, Seshasai SR, Welsh P, et al. Risk of incident diabetes with intensive-dose compared with moderate-dose statin therapy: a meta-analysis. JAMA. 2011;305:2556–64.CrossRefPubMed
53.
Zurück zum Zitat •• Waters DD, Ho JE, Demicco DA, et al. Predictors of new-onset diabetes in patients treated with atorvastatin results from 3 large randomized clinical trials. J Am Coll Cardiol. 2011;57:1535–45. A meta-analysis of TNT, IDEAL, and SPARCL trials reporting that baseline fasting blood glucose, body mass index, hypertension, and fasting triglycerides are independent predictors of new-onset T2D during statin treatment. Patients without these risk factors had a diabetes risk of 2% or less in each trial, and those with 1 risk factor had a risk of 4% to 5%. When 3 or 4 of the risk factors were present the risk of new-onset T2D exceeded 10%. CrossRefPubMed •• Waters DD, Ho JE, Demicco DA, et al. Predictors of new-onset diabetes in patients treated with atorvastatin results from 3 large randomized clinical trials. J Am Coll Cardiol. 2011;57:1535–45. A meta-analysis of TNT, IDEAL, and SPARCL trials reporting that baseline fasting blood glucose, body mass index, hypertension, and fasting triglycerides are independent predictors of new-onset T2D during statin treatment. Patients without these risk factors had a diabetes risk of 2% or less in each trial, and those with 1 risk factor had a risk of 4% to 5%. When 3 or 4 of the risk factors were present the risk of new-onset T2D exceeded 10%. CrossRefPubMed
54.
Zurück zum Zitat • Sattar N, Taskinen M. Statins are diabetogenic–myth or reality? Atheroscler. Suppl. 2012;13:1–10. An updated review highlighting the current available evidence related to new-onset diabetes as a side-effect of statins and the potential mechanisms of this association. • Sattar N, Taskinen M. Statins are diabetogenic–myth or reality? Atheroscler. Suppl. 2012;13:1–10. An updated review highlighting the current available evidence related to new-onset diabetes as a side-effect of statins and the potential mechanisms of this association.
55.
Zurück zum Zitat Keech A, Simes RJ, Barter P, et al. Effects of long-term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD study): randomised controlled trial. Lancet. 2005;366:1849–61.CrossRefPubMed Keech A, Simes RJ, Barter P, et al. Effects of long-term fenofibrate therapy on cardiovascular events in 9795 people with type 2 diabetes mellitus (the FIELD study): randomised controlled trial. Lancet. 2005;366:1849–61.CrossRefPubMed
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Zurück zum Zitat Scott R, O'Brien R, Fulcher G, et al. Effects of fenofibrate treatment on cardiovascular disease risk in 9795 individuals with type 2 diabetes and various components of the metabolic syndrome: the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study. Diabetes Care. 2009;32:493–8.CrossRefPubMed Scott R, O'Brien R, Fulcher G, et al. Effects of fenofibrate treatment on cardiovascular disease risk in 9795 individuals with type 2 diabetes and various components of the metabolic syndrome: the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study. Diabetes Care. 2009;32:493–8.CrossRefPubMed
57.
Zurück zum Zitat Jun M, Foote C, Lv J, et al. Effects of fibrates on cardiovascular outcomes: a systematic review and meta-analysis. Lancet. 2010;375:1875–84.CrossRefPubMed Jun M, Foote C, Lv J, et al. Effects of fibrates on cardiovascular outcomes: a systematic review and meta-analysis. Lancet. 2010;375:1875–84.CrossRefPubMed
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Zurück zum Zitat Steiner G, Hamsten A, Hosking J, et al. for the Diabetes Atherosclerosis Intervention Study Investigators. Effect of fenofibrate on progression of coronary-artery disease in type 2 diabetes: the Diabetes Atherosclerosis Intervention Study, a randomised study. Lancet. 2001;357:905–10. Steiner G, Hamsten A, Hosking J, et al. for the Diabetes Atherosclerosis Intervention Study Investigators. Effect of fenofibrate on progression of coronary-artery disease in type 2 diabetes: the Diabetes Atherosclerosis Intervention Study, a randomised study. Lancet. 2001;357:905–10.
59.
Zurück zum Zitat Meade T, Zuhrie R, Cook C, Cooper J. Bezafibrate in men with lower extremity arterial disease: randomised controlled trial. BMJ. 2002;325:1139.CrossRefPubMed Meade T, Zuhrie R, Cook C, Cooper J. Bezafibrate in men with lower extremity arterial disease: randomised controlled trial. BMJ. 2002;325:1139.CrossRefPubMed
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Zurück zum Zitat Emmerich KH, Poritis N, Stelmane I, et al. Efficacy and safety of etofibrate in patients with non-proliferative diabetic retinopathy. Klin Monbl Augenheilkd. 2009;226:561–7.CrossRefPubMed Emmerich KH, Poritis N, Stelmane I, et al. Efficacy and safety of etofibrate in patients with non-proliferative diabetic retinopathy. Klin Monbl Augenheilkd. 2009;226:561–7.CrossRefPubMed
61.
Zurück zum Zitat ACCORD Study Group, Ginsberg HN, Elam MB, et al. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med. 2010;362:1563–74.CrossRefPubMed ACCORD Study Group, Ginsberg HN, Elam MB, et al. Effects of combination lipid therapy in type 2 diabetes mellitus. N Engl J Med. 2010;362:1563–74.CrossRefPubMed
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Zurück zum Zitat Sacks FM, Carey VJ, Fruchart JC. Combination lipid therapy in type 2 diabetes. N Engl J Med. 2010;363:692–4. author reply 694–5.CrossRefPubMed Sacks FM, Carey VJ, Fruchart JC. Combination lipid therapy in type 2 diabetes. N Engl J Med. 2010;363:692–4. author reply 694–5.CrossRefPubMed
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Zurück zum Zitat Bruckert E, Labreuche J, Deplanque D, et al. Fibrates effect on cardiovascular risk is greater in patients with high triglyceride levels or atherogenic dyslipidemia profile: a systematic review and meta-analysis. J Cardiovasc Pharmacol. 2011;57:267–72.CrossRefPubMed Bruckert E, Labreuche J, Deplanque D, et al. Fibrates effect on cardiovascular risk is greater in patients with high triglyceride levels or atherogenic dyslipidemia profile: a systematic review and meta-analysis. J Cardiovasc Pharmacol. 2011;57:267–72.CrossRefPubMed
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Zurück zum Zitat Lee M, Saver JL, Towfighi A, et al. Efficacy of fibrates for cardiovascular risk reduction in persons with atherogenic dyslipidemia: a meta-analysis. Atherosclerosis. 2011;217:492–8.CrossRefPubMed Lee M, Saver JL, Towfighi A, et al. Efficacy of fibrates for cardiovascular risk reduction in persons with atherogenic dyslipidemia: a meta-analysis. Atherosclerosis. 2011;217:492–8.CrossRefPubMed
65.
Zurück zum Zitat Awan Z, Seidah NG, MacFadyen JG, et al. Rosuvastatin, proprotein convertase subtilisin/kexin type 9 concentrations, and LDL cholesterol response: the JUPITER trial. Clin Chem. 2012;58:183–9.CrossRefPubMed Awan Z, Seidah NG, MacFadyen JG, et al. Rosuvastatin, proprotein convertase subtilisin/kexin type 9 concentrations, and LDL cholesterol response: the JUPITER trial. Clin Chem. 2012;58:183–9.CrossRefPubMed
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Zurück zum Zitat Farnier M. The role of proprotein convertase subtilisin/kexin type 9 in hyperlipidemia: focus on therapeutic implications. Am J Cardiovasc Drugs. 2011;11:145–52.CrossRefPubMed Farnier M. The role of proprotein convertase subtilisin/kexin type 9 in hyperlipidemia: focus on therapeutic implications. Am J Cardiovasc Drugs. 2011;11:145–52.CrossRefPubMed
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Zurück zum Zitat Rosenblit PD. Do persons with diabetes benefit from combination statin and fibrate therapy? Curr Cardiol Rep. 2012;14:112–24.CrossRefPubMed Rosenblit PD. Do persons with diabetes benefit from combination statin and fibrate therapy? Curr Cardiol Rep. 2012;14:112–24.CrossRefPubMed
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Zurück zum Zitat Canner PL, Berge KG, Wenger NK, et al. Fifteen year mortality in Coronary Drug Project patients: long-term benefit with niacin. J Am Coll Cardiol. 1986;8:1245–55.CrossRefPubMed Canner PL, Berge KG, Wenger NK, et al. Fifteen year mortality in Coronary Drug Project patients: long-term benefit with niacin. J Am Coll Cardiol. 1986;8:1245–55.CrossRefPubMed
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Zurück zum Zitat Chapman MJ, Redfern JS, McGovern ME, Giral P. Niacin and fibrates in atherogenic dyslipidemia: pharmacotherapy to reduce cardiovascular risk. Pharmacol Ther. 2010;126:314–45.CrossRefPubMed Chapman MJ, Redfern JS, McGovern ME, Giral P. Niacin and fibrates in atherogenic dyslipidemia: pharmacotherapy to reduce cardiovascular risk. Pharmacol Ther. 2010;126:314–45.CrossRefPubMed
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Zurück zum Zitat Boden WE, Probstfield JL, et al. AIM-HIGH Investigators; niacin in patients with low HDL cholesterol levels receiving intensive statin therapy. N Engl J Med. 2011;365:2255–67.CrossRefPubMed Boden WE, Probstfield JL, et al. AIM-HIGH Investigators; niacin in patients with low HDL cholesterol levels receiving intensive statin therapy. N Engl J Med. 2011;365:2255–67.CrossRefPubMed
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Zurück zum Zitat Leiter LA, Betteridge DJ, Farnier M, et al. Lipid-altering efficacy and safety profile of combination therapy with ezetimibe/statin vs statin monotherapy in patients with and without diabetes: an analysis of pooled data from 27 clinical trials. Diabetes Obes Metab. 2011;13:615–28.CrossRefPubMed Leiter LA, Betteridge DJ, Farnier M, et al. Lipid-altering efficacy and safety profile of combination therapy with ezetimibe/statin vs statin monotherapy in patients with and without diabetes: an analysis of pooled data from 27 clinical trials. Diabetes Obes Metab. 2011;13:615–28.CrossRefPubMed
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Zurück zum Zitat Fleg JL, Mete M, Howard BV, et al. Effect of statins alone vs statins plus ezetimibe on carotid atherosclerosis in type 2 diabetes: the SANDS (Stop Atherosclerosis in Native Diabetics Study) trial. J Am Coll Cardiol. 2008;52:2198–205.CrossRefPubMed Fleg JL, Mete M, Howard BV, et al. Effect of statins alone vs statins plus ezetimibe on carotid atherosclerosis in type 2 diabetes: the SANDS (Stop Atherosclerosis in Native Diabetics Study) trial. J Am Coll Cardiol. 2008;52:2198–205.CrossRefPubMed
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Zurück zum Zitat Baigent C, Landray M, Reith T, et al. for the Sharp Collaborative Group. Study of Heart and Renal Protection (SHARP): randomized trial to assess the effects of lowering low-density lipoprotein cholesterol among 9438 patients with chronic kidney disease. Am Heart J. 2010;160:785–94.e10.CrossRef Baigent C, Landray M, Reith T, et al. for the Sharp Collaborative Group. Study of Heart and Renal Protection (SHARP): randomized trial to assess the effects of lowering low-density lipoprotein cholesterol among 9438 patients with chronic kidney disease. Am Heart J. 2010;160:785–94.e10.CrossRef
74.
Zurück zum Zitat Harris WS, Miller M, Tighe AP, et al. Omega-3 fatty acids and coronary heart disease risk: clinical and mechanistic perspectives. Atherosclerosis. 2008;197:12–24.CrossRefPubMed Harris WS, Miller M, Tighe AP, et al. Omega-3 fatty acids and coronary heart disease risk: clinical and mechanistic perspectives. Atherosclerosis. 2008;197:12–24.CrossRefPubMed
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Zurück zum Zitat Skulas-Ray AC, Kris-Etherton PM, Harris WS, et al. Dose-response effects of omega-3 fatty acids on triglycerides, inflammation, and endothelial function in healthy persons with moderate hypertriglyceridemia. Am J Clin Nutr. 2011;93:243–52.CrossRefPubMed Skulas-Ray AC, Kris-Etherton PM, Harris WS, et al. Dose-response effects of omega-3 fatty acids on triglycerides, inflammation, and endothelial function in healthy persons with moderate hypertriglyceridemia. Am J Clin Nutr. 2011;93:243–52.CrossRefPubMed
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Zurück zum Zitat Kromhout D, Yasuda S, Geleijnse JM, Shimokawa H. Fish oil and omega-3 fatty acids in cardiovascular disease: do they really work? Eur Heart J. 2012;33:436–43.CrossRefPubMed Kromhout D, Yasuda S, Geleijnse JM, Shimokawa H. Fish oil and omega-3 fatty acids in cardiovascular disease: do they really work? Eur Heart J. 2012;33:436–43.CrossRefPubMed
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Zurück zum Zitat Abeywardena MY, Patten GS. Role of Omega3 Longchain polyunsaturated fatty acids in reducing cardio-metabolic risk factors. Endocrin Metab Immune Disord Drug Targets. 2011;11:232–46. Abeywardena MY, Patten GS. Role of Omega3 Longchain polyunsaturated fatty acids in reducing cardio-metabolic risk factors. Endocrin Metab Immune Disord Drug Targets. 2011;11:232–46.
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Zurück zum Zitat Wierzbicki AS, Clarke RE, Viljoen A, Mikhailidis DP. Triglycerides: a case for treatment? Curr Opin Cardiol. 2012;27:398–404.CrossRefPubMed Wierzbicki AS, Clarke RE, Viljoen A, Mikhailidis DP. Triglycerides: a case for treatment? Curr Opin Cardiol. 2012;27:398–404.CrossRefPubMed
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Zurück zum Zitat • Kwak SM, Myung SK, Lee YJ, et al. Efficacy of Omega-3 fatty acid supplements (eicosapentaenoic acid and docosahexaenoic acid) in the secondary prevention of cardiovascular disease: a meta-analysis of randomized, double-blind, placebo-controlled trials. Arch Intern Med. 2012;172:686–94. A thorough meta-analysis of 13 RCTs demonstrating insufficient evidence of omega-3 fatty acid supplements to reduce overall cardiovascular events in patients with a history of cardiovascular disease. CrossRefPubMed • Kwak SM, Myung SK, Lee YJ, et al. Efficacy of Omega-3 fatty acid supplements (eicosapentaenoic acid and docosahexaenoic acid) in the secondary prevention of cardiovascular disease: a meta-analysis of randomized, double-blind, placebo-controlled trials. Arch Intern Med. 2012;172:686–94. A thorough meta-analysis of 13 RCTs demonstrating insufficient evidence of omega-3 fatty acid supplements to reduce overall cardiovascular events in patients with a history of cardiovascular disease. CrossRefPubMed
80.
Zurück zum Zitat • The ORIGIN Trial Investigators. n-3 Fatty Acids and Cardiovascular Outcomes in Patients with Dysglycemia. N Engl J Med. 2012. Latest large outcome trial testing lipid lowering in glycemic subjects to reduce CVD endpoints. Supplementation with 1 g of omega-3 fatty acids did not affect CVD mortality, death from arrhythmia, or rates of major cardiovascular events compared with among over 12.000 subjects with dysglycemia and additional risk factors and therefore at high risk for T2D. About half of the study population received statins. • The ORIGIN Trial Investigators. n-3 Fatty Acids and Cardiovascular Outcomes in Patients with Dysglycemia. N Engl J Med. 2012. Latest large outcome trial testing lipid lowering in glycemic subjects to reduce CVD endpoints. Supplementation with 1 g of omega-3 fatty acids did not affect CVD mortality, death from arrhythmia, or rates of major cardiovascular events compared with among over 12.000 subjects with dysglycemia and additional risk factors and therefore at high risk for T2D. About half of the study population received statins.
81.
Zurück zum Zitat Barter PJ, Caulfield M, Eriksson M, et al. Effects of torcetrapib in patients at high risk for coronary events. N Engl J Med. 2007;357:2109–22.CrossRefPubMed Barter PJ, Caulfield M, Eriksson M, et al. Effects of torcetrapib in patients at high risk for coronary events. N Engl J Med. 2007;357:2109–22.CrossRefPubMed
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Zurück zum Zitat Barter PJ, Rye KA, Tardif JC, et al. Effect of torcetrapib on glucose, insulin, and hemoglobin A1c in subjects in the Investigation of Lipid Level Management to Understand its Impact in Atherosclerotic Events (ILLUMINATE) trial. Circulation. 2011;124:555–62.CrossRefPubMed Barter PJ, Rye KA, Tardif JC, et al. Effect of torcetrapib on glucose, insulin, and hemoglobin A1c in subjects in the Investigation of Lipid Level Management to Understand its Impact in Atherosclerotic Events (ILLUMINATE) trial. Circulation. 2011;124:555–62.CrossRefPubMed
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Zurück zum Zitat •• Drew BG, Rye KA, Duffy SJ, et al. The emerging role of HDL in glucose metabolism. Nat Rev Endocrinol. 2012;8:237–45. A thorough review discussing the emerging role of HDL in glucose metabolism and potential therapeutic options achieved by raising HDL. The authors highlight that classical anti-atherogenic and anti-inflammatory properties as well as other actions of HDL may affect insulin secretion from the β-cell, direct glucose uptake by the muscle, and insulin sensitivity. CrossRefPubMed •• Drew BG, Rye KA, Duffy SJ, et al. The emerging role of HDL in glucose metabolism. Nat Rev Endocrinol. 2012;8:237–45. A thorough review discussing the emerging role of HDL in glucose metabolism and potential therapeutic options achieved by raising HDL. The authors highlight that classical anti-atherogenic and anti-inflammatory properties as well as other actions of HDL may affect insulin secretion from the β-cell, direct glucose uptake by the muscle, and insulin sensitivity. CrossRefPubMed
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Zurück zum Zitat • Fryirs MA, Barter PJ, Appavoo M, et al. Effects of high-density lipoproteins on pancreatic beta-cell insulin secretion. Arterioscler Thromb Vasc Biol. 2010;30:1642–8. This study utilized rat primary islets and Min6 cell to examine in vitro the effects of human HDL to stimulate insulin secretion in a ABCG1-dependent mechanism, both in basal, and high-glucose conditions. The key finding was that HDL as well as apoproteins apoA-I and apoA-II increased β-cell insulin secretion. The authors suggest that raising HDL levels may be beneficial in T2D. CrossRefPubMed • Fryirs MA, Barter PJ, Appavoo M, et al. Effects of high-density lipoproteins on pancreatic beta-cell insulin secretion. Arterioscler Thromb Vasc Biol. 2010;30:1642–8. This study utilized rat primary islets and Min6 cell to examine in vitro the effects of human HDL to stimulate insulin secretion in a ABCG1-dependent mechanism, both in basal, and high-glucose conditions. The key finding was that HDL as well as apoproteins apoA-I and apoA-II increased β-cell insulin secretion. The authors suggest that raising HDL levels may be beneficial in T2D. CrossRefPubMed
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Zurück zum Zitat Liu K, Daviglus ML, Loria CM, et al. Healthy lifestyle through young adulthood and the presence of low cardiovascular disease risk profile in middle age: the Coronary Artery Risk Development in (Young) Adults (CARDIA) study. Circulation. 2012;125:996–1004.CrossRefPubMed Liu K, Daviglus ML, Loria CM, et al. Healthy lifestyle through young adulthood and the presence of low cardiovascular disease risk profile in middle age: the Coronary Artery Risk Development in (Young) Adults (CARDIA) study. Circulation. 2012;125:996–1004.CrossRefPubMed
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Zurück zum Zitat Seidah NG, Prat A. The biology and therapeutic targeting of the proprotein convertases. Nat Rev Drug Discov. 2012;11:367–83.CrossRefPubMed Seidah NG, Prat A. The biology and therapeutic targeting of the proprotein convertases. Nat Rev Drug Discov. 2012;11:367–83.CrossRefPubMed
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Zurück zum Zitat Chan DC, Watts GF. Dyslipidaemia in the metabolic syndrome and type 2 diabetes: pathogenesis, priorities, pharmacotherapies. Expert Opin Pharmacother. 2011;12:13–30.CrossRefPubMed Chan DC, Watts GF. Dyslipidaemia in the metabolic syndrome and type 2 diabetes: pathogenesis, priorities, pharmacotherapies. Expert Opin Pharmacother. 2011;12:13–30.CrossRefPubMed
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Zurück zum Zitat Karpe F, Dickmann JR, Frayn KN. Fatty acids, obesity, and insulin resistance: time for a reevaluation. Diabetes. 2011;60:2441–9.CrossRefPubMed Karpe F, Dickmann JR, Frayn KN. Fatty acids, obesity, and insulin resistance: time for a reevaluation. Diabetes. 2011;60:2441–9.CrossRefPubMed
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Zurück zum Zitat Chapman MJ, Ginsberg HN, Amarenco P, et al. for the European Atherosclerosis Society Consensus Panel. Triglyceride-rich lipoproteins and high-density lipoprotein cholesterol in patients at high risk of cardiovascular disease: evidence and guidance for management. Eur Heart J. 2011;32:1345–61. Chapman MJ, Ginsberg HN, Amarenco P, et al. for the European Atherosclerosis Society Consensus Panel. Triglyceride-rich lipoproteins and high-density lipoprotein cholesterol in patients at high risk of cardiovascular disease: evidence and guidance for management. Eur Heart J. 2011;32:1345–61.
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Zurück zum Zitat Grundy SM, Becker D, Clark LT, et al. for the National Cholesterol Education Program (NCEP). Expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). Third report of the National Cholesterol Education Program (NCEP). Circulation. 2002;106:3143–3421. Grundy SM, Becker D, Clark LT, et al. for the National Cholesterol Education Program (NCEP). Expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III). Third report of the National Cholesterol Education Program (NCEP). Circulation. 2002;106:3143–3421.
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Zurück zum Zitat ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. The antihypertensive and lipid-lowering treatment to prevent heart attack trial. Major outcomes in moderately hypercholesterolemic, hypertensive patients randomized to pravastatin vs usual care: The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT-LLT). JAMA. 2002;288:2998–3007.CrossRef ALLHAT Officers and Coordinators for the ALLHAT Collaborative Research Group. The antihypertensive and lipid-lowering treatment to prevent heart attack trial. Major outcomes in moderately hypercholesterolemic, hypertensive patients randomized to pravastatin vs usual care: The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT-LLT). JAMA. 2002;288:2998–3007.CrossRef
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Metadaten
Titel
Management of Dyslipidemias in the Presence of the Metabolic Syndrome or Type 2 Diabetes
verfasst von
Niina Matikainen
Marja-Riitta Taskinen
Publikationsdatum
01.12.2012
Verlag
Current Science Inc.
Erschienen in
Current Cardiology Reports / Ausgabe 6/2012
Print ISSN: 1523-3782
Elektronische ISSN: 1534-3170
DOI
https://doi.org/10.1007/s11886-012-0309-3

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