Literature DB >> 17142146

Lipoprotein effects of combined ezetimibe and colesevelam hydrochloride versus ezetimibe alone in hypercholesterolemic subjects: a pilot study.

Robert H Knopp1, Christine Tsunehara, Barbara M Retzlaff, Brian Fish, Hien Nguyen, Susan Anderson, Thuy Nguyen.   

Abstract

Two drug classes act in the intestine to lower cholesterol. Ezetimibe inhibits cholesterol absorption, whereas bile acid-binding resins enhance cholesterol excretion via enhanced conversion to bile acids. Combining these 2 classes may be beneficial, but cholestyramine binds ezetimibe, and the combined effect of colesevelam hydrochloride and ezetimibe was little studied. The aim of the study was to determine if adding colesevelam HCl to ezetimibe provides additional lowering of low-density lipoprotein- and apolipoprotein B-containing lipoproteins or alters ezetimibe levels. Twenty subjects with low-density lipoprotein cholesterol (LDL-C) levels of 130 mg/dL or higher were enrolled and taught a National Cholesterol Education Program Step I diet. At a second baseline visit, lipoproteins were measured and subjects were randomly allocated to (1) ezetimibe 10 mg daily with placebo colesevelam HCl twice daily (E) or (2) ezetimibe 10 mg daily with 1.875 g colesevelam HCl twice daily (E + C). Lipoproteins were measured 6 and 12 weeks after initiating treatment. Baseline characteristics (mean +/- SD) were statistically indistinguishable in E vs E + C: LDL-C (mg/dL), 167 +/- 26 and 158 +/- 27; triglyceride, 134 +/- 75 and 140 +/- 67; and BMI, 29.4 +/- 4.9 and 27.8 +/- 6.6 kg/m(2), respectively. Percent changes after 12 weeks in E vs E + C were as follows: LDL-C, -24 +/- 12 vs -30 +/- 11 (P = .102); triglyceride, -19 +/- 34 vs 36 +/- 85 (P = .054; at 6 weeks, P = .009); total cholesterol, -19 +/- 9 vs -15 +/- 8 (P = .50); non-high-density lipoprotein cholesterol, -25 +/- 10 vs -21 +/- 11 (P = .70); apolipoprotein B, -31 +/- 14 vs -22 +/- 14 (P = .41). Plasma ezetimibe levels at 12 weeks were 21% lower in E + C vs E, a nonsignificant difference (P = .54). In conclusion, in the short term, colesevelam HCl may not consistently add cholesterol-lowering benefit to ezetimibe. This observation requires confirmation.

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Year:  2006        PMID: 17142146     DOI: 10.1016/j.metabol.2006.08.013

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  6 in total

Review 1.  Use and indications of cholestyramine and bile acid sequestrants.

Authors:  Franco Scaldaferri; Marco Pizzoferrato; Francesca Romana Ponziani; Giovanni Gasbarrini; Antonio Gasbarrini
Journal:  Intern Emerg Med       Date:  2011-07-08       Impact factor: 3.397

Review 2.  Management of the patient with statin intolerance.

Authors:  Byron F Vandenberg; Jennifer Robinson
Journal:  Curr Atheroscler Rep       Date:  2010-01       Impact factor: 5.113

Review 3.  LDL reduction: how low should we go and is it safe?

Authors:  Jennifer G Robinson
Journal:  Curr Cardiol Rep       Date:  2008-11       Impact factor: 2.931

4.  Colesevelam hydrochloride: evidence for its use in the treatment of hypercholesterolemia and type 2 diabetes mellitus with insights into mechanism of action.

Authors:  Michael James Zema
Journal:  Core Evid       Date:  2012-07-12

5.  Anti-oxidant and Anti-hypercholesterolemic Activities of Wasabia japonica.

Authors:  Young Sun Lee; Jae Ha Yang; Man Jong Bae; Wang Keun Yoo; Shen Ye; Charlie C L Xue; Chun Guang Li
Journal:  Evid Based Complement Alternat Med       Date:  2008-06-12       Impact factor: 2.629

Review 6.  Role of colesevelam in combination lipid-lowering therapy.

Authors:  Michael R Jones; Oliseyenum M Nwose
Journal:  Am J Cardiovasc Drugs       Date:  2013-10       Impact factor: 3.571

  6 in total

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