Hypertriglyceridemia: a too long unfairly neglected major cardiovascular risk factor

被引:150
作者
Tenenbaum, Alexander [1 ,2 ,3 ]
Klempfner, Robert [1 ,2 ]
Fisman, Enrique Z. [2 ,3 ]
机构
[1] Sheba Med Ctr, Cardiac Rehabil Inst, IL-52621 Tel Hashomer, Israel
[2] Tel Aviv Univ, Sackler Fac Med, IL-69978 Tel Aviv, Israel
[3] Cardiovasc Diabetol Res Fdn, IL-58484 Holon, Israel
关键词
Cardiovascular risk; Cholesterol; Fibrates; Hypertriglyceridemia; Insulin resistance; Metabolic syndrome; Obesity; Statins; Triglycerides; Type; 2; diabetes; FREE FATTY-ACIDS; CORONARY-HEART-DISEASE; TRIGLYCERIDE-RICH LIPOPROTEINS; APOLIPOPROTEIN-C-III; ENDOPLASMIC-RETICULUM STRESS; HIGH-DENSITY-LIPOPROTEINS; TYPE-2; DIABETIC-PATIENTS; GLUT4; GENE-EXPRESSION; ALL-CAUSE MORTALITY; PROTEIN-KINASE-C;
D O I
10.1186/s12933-014-0159-y
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
The existence of an independent association between elevated triglyceride (TG) levels, cardiovascular (CV) risk and mortality has been largely controversial. The main difficulty in isolating the effect of hypertriglyceridemia on CV risk is the fact that elevated triglyceride levels are commonly associated with concomitant changes in high density lipoprotein (HDL), low density lipoprotein (LDL) and other lipoproteins. As a result of this problem and in disregard of the real biological role of TG, its significance as a plausible therapeutic target was unfoundedly underestimated for many years. However, taking epidemiological data together, both moderate and severe hypertriglyceridaemia are associated with a substantially increased long term total mortality and CV risk. Plasma TG levels partially reflect the concentration of the triglyceride-carrying lipoproteins (TRL): very low density lipoprotein (VLDL), chylomicrons and their remnants. Furthermore, hypertriglyceridemia commonly leads to reduction in HDL and increase in atherogenic small dense LDL levels. TG may also stimulate atherogenesis by mechanisms, such excessive free fatty acids (FFA) release, production of proinflammatory cytokines, fibrinogen, coagulation factors and impairment of fibrinolysis. Genetic studies strongly support hypertriglyceridemia and high concentrations of TRL as causal risk factors for CV disease. The most common forms of hypertriglyceridemia are related to overweight and sedentary life style, which in turn lead to insulin resistance, metabolic syndrome (MS) and type 2 diabetes mellitus (T2DM). Intensive lifestyle therapy is the main initial treatment of hypertriglyceridemia. Statins are a cornerstone of the modern lipids-modifying therapy. If the primary goal is to lower TG levels, fibrates (bezafibrate and fenofibrate for monotherapy, and in combination with statin; gemfibrozil only for monotherapy) could be the preferable drugs. Also ezetimibe has mild positive effects in lowering TG. Initial experience with en ezetimibe/fibrates combination seems promising. The recently released IMPROVE-IT Trial is the first to prove that adding a non-statin drug (ezetimibe) to a statin lowers the risk of future CV events. In conclusion, the classical clinical paradigm of lipids-modifying treatment should be changed and high TG should be recognized as an important target for therapy in their own right. Hypertriglyceridemia should be treated.
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页数:10
相关论文
共 174 条
[1]
Genetic analysis of haptoglobin polymorphisms with cardiovascular disease and type 2 diabetes in the diabetes heart study [J].
Adams, Jeremy N. ;
Cox, Amanda J. ;
Freedman, Barry I. ;
Langefeld, Carl D. ;
Carr, J. Jeffrey ;
Bowden, Donald W. .
CARDIOVASCULAR DIABETOLOGY, 2013, 12
[2]
Overproduction of VLDL1 driven by hyperglycemia is a dominant feature of diabetic dyslipidemia [J].
Adiels, M ;
Borén, J ;
Caslake, MJ ;
Stewart, P ;
Soro, A ;
Westerbacka, J ;
Wennberg, B ;
Olofsson, SO ;
Packard, C ;
Taskinen, MR .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2005, 25 (08) :1697-1703
[3]
Harmonizing the Metabolic Syndrome A Joint Interim Statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity [J].
Alberti, K. G. M. M. ;
Eckel, Robert H. ;
Grundy, Scott M. ;
Zimmet, Paul Z. ;
Cleeman, James I. ;
Donato, Karen A. ;
Fruchart, Jean-Charles ;
James, W. Philip T. ;
Loria, Catherine M. ;
Smith, Sidney C., Jr. .
CIRCULATION, 2009, 120 (16) :1640-1645
[4]
Factors associated with postprandial lipemia and apolipoprotein A-V levels in individuals with familial combined hyperlipidemia [J].
Almeda-Valdes, Paloma ;
Cuevas-Ramos, Daniel ;
Mehta, Roopa ;
Munoz-Hernandez, Liliana ;
Cruz-Bautista, Ivette ;
Perez-Mendez, Oscar ;
Teresa Tusie-Luna, Maria ;
Gomez-Perez, Francisco J. ;
Pajukanta, Paivi ;
Matikainen, Niina ;
Taskinen, Marja-Riitta ;
Aguilar-Salinas, Carlos A. .
BMC ENDOCRINE DISORDERS, 2014, 14
[5]
Insulin resistance predicts progression of de novo atherosclerotic plaques in patients with coronary heart disease: a one-year follow-up study [J].
An, Xuanqi ;
Yu, Dong ;
Zhang, Ruiyan ;
Zhu, Jinzhou ;
Du, Run ;
Shi, Yuhang ;
Xiong, Xiaowei .
CARDIOVASCULAR DIABETOLOGY, 2012, 11
[6]
Which features of the metabolic syndrome predict the prevalence and clinical outcomes of angiographic coronary artery disease? [J].
Anderson, JL ;
Horne, BD ;
Jones, HU ;
Reyna, SP ;
Carlquist, JF ;
Bair, TL ;
Pearson, RR ;
Lappé, DL ;
Muhlestein, JB .
CARDIOLOGY, 2004, 101 (04) :185-193
[7]
High-Density Lipoproteins - Multifunctional but Vulnerable Protections from Atherosclerosis [J].
Annema, Wijtske ;
von Eckardstein, Arnold .
CIRCULATION JOURNAL, 2013, 77 (10) :2432-2448
[8]
[Anonymous], CEREBROVASC DIS S1
[9]
Free fatty acids repress the GLUT4 gene expression in cardiac muscle via novel response elements [J].
Armoni, M ;
Harel, C ;
Bar-Yoseph, F ;
Milo, S ;
Karnieli, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (41) :34786-34795
[10]
Arner P, 2001, DIABETES OBES METAB, V3, pS11, DOI 10.1046/j.1463-1326.2001.00031.x