Literature DB >> 2232062

Primary hypertriglyceridemia with borderline high cholesterol and elevated apolipoprotein B concentrations. Comparison of gemfibrozil vs lovastatin therapy.

G L Vega1, S M Grundy.   

Abstract

A common pattern of dyslipidemia is elevated levels of plasma triglyceride, borderline high total cholesterol, reduced high-density lipoprotein, and increased apolipoprotein B. This pattern of dyslipidemia frequently is associated with premature coronary heart disease. Nicotinic acid is the drug of first choice for this pattern. In this study, gemfibrozil and lovastatin were compared for their effects on the overall lipoprotein profile in 13 men with this type of dyslipidemia. Both drugs significantly reduced very-low-density lipoprotein and intermediate-density lipoprotein cholesterol levels, and both modestly raised high-density lipoprotein cholesterol levels. Gemfibrozil therapy, however, failed to reduce total cholesterol or total apolipoprotein B levels, whereas lovastatin therapy lowered levels of total cholesterol by 28%, low-density lipoprotein cholesterol by 33%, and total apolipoprotein B by 32%. Moreover, lovastatin therapy caused greater declines in lipoprotein cholesterol ratios than gemfibrozil therapy. Lovastatin thus seems to have certain advantages over gemfibrozil for treatment of elevated plasma triglyceride levels accompanied by borderline high total cholesterol and raised apolipoprotein B levels; therefore, lovastatin therapy should be considered as one approach for management of this condition.

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Year:  1990        PMID: 2232062

Source DB:  PubMed          Journal:  JAMA        ISSN: 0098-7484            Impact factor:   56.272


  7 in total

Review 1.  Statins: definitive translational research.

Authors:  Scott M Grundy
Journal:  Mol Med       Date:  2014-12-16       Impact factor: 6.354

2.  Lipoprotein composition and oxidative modification during therapy with gemfibrozil and lovastatin in patients with combined hyperlipidaemia.

Authors:  M Vázquez; D Zambón; Y Hernández; T Adzet; M Merlos; E Ros; J C Laguna
Journal:  Br J Clin Pharmacol       Date:  1998-03       Impact factor: 4.335

3.  Atorvastatin versus Bezafibrate in Mixed Hyperlipidaemia : Randomised Clinical Trial of Efficacy and Safety (the ATOMIX Study).

Authors:  Emilio Ros; Josefina Oliván; José M Mostaza; Miquel Vilardell; Xavier Pintó; Fernando Civeira; A Hernández; Pedro Marqués da Silva; A Rodriguez-Botaro; Daniel Zambón; Joan Lima; José A Gómez-Gerique; Cristina Díaz; Rosa Arístegui; José M Sol; Gonzalo Hernández
Journal:  Clin Drug Investig       Date:  2003       Impact factor: 2.859

4.  Plasma triglycerides determine low density lipoprotein composition, physical properties, and cell-specific binding in cultured cells.

Authors:  B J McKeone; J R Patsch; H J Pownall
Journal:  J Clin Invest       Date:  1993-05       Impact factor: 14.808

5.  Pravastatin treatment in combined hyperlipidaemia. Effect on plasma lipoprotein levels and size.

Authors:  S Zambon; A Cortella; G Sartore; G Baldo-Enzi; E Manzato; G Crepaldi
Journal:  Eur J Clin Pharmacol       Date:  1994       Impact factor: 2.953

Review 6.  Gemfibrozil. A reappraisal of its pharmacological properties and place in the management of dyslipidaemia.

Authors:  C M Spencer; L B Barradell
Journal:  Drugs       Date:  1996-06       Impact factor: 9.546

7.  Native low-density lipoprotein-dependent interleukin-8 production through pertussis toxin-sensitive G-protein coupled receptors and hydrogen peroxide generation contributes to migration of human aortic smooth muscle cells.

Authors:  Hyun Kyo Lim; Sungwoo Ryoo
Journal:  Yonsei Med J       Date:  2011-05       Impact factor: 2.759

  7 in total

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