Colesevelam HCl: a non-systemic lipid-altering drug

被引:60
作者
Bays, H
Dujovne, C
机构
[1] Kansas Fdn Clin Pharmacol, Radiant Res, Overland Pk, KS 66215 USA
[2] Louisville Metab & Atherosclerosis Res Ctr, Louisville, KY 40213 USA
关键词
bile acid; bile acid sequestrant; cholesterol; cholestyramine; colesevelam HCl; colestipol; high density lipoprotein; low density lipoprotein; polymer; resin;
D O I
10.1517/eoph.4.5.779.22219
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Colesevelam HCl (WelChol(R), Sankyo Pharmaceuticals Inc.) is a bile acid sequestrant polymer, which has been shown to significantly lower low density lipoprotein cholesterol and favourably affect high-density lipoprotein cholesterol blood levels in monotherapy and in combination with statins (HMG-CoA reductase inhibitors). Although it is similar to other bile acid sequestrants in that it binds bile acids and is non-systemic, colesevelam HCl differs in that it has a unique polymer structure that allows for greater tolerability with less potential drug interactions than with resins. Currently, statins are the most commonly prescribed lipid-altering drugs. However, it is not uncommon that patients demonstrate true or perceived intolerances to statin therapy, that are often dose-related and may include elevations in liver or muscle enzyme blood levels, or myalgias or muscle weakness without muscle enzyme elevation. In rare circumstances, myopathy and even rhabdomyolysis can occur with statins. In addition, many statins also have important potential drug interactions. Finally, statin monotherapy is often not sufficient in achieving lipid treatment goals in many severely dyslipidaemic patients and the availability of colesevelam HCl provides a lipid-altering treatment addition to other lipid-altering drugs. From a clinical perspective, such combination therapy is often required to achieve treatment goals [1] in patients with more complicated or severe dyslipidaemia. Colesevelam HCl may also be an alternative in monotherapy for many patients with mild-to-moderate hypercholesterolaemia, as well as in some patients at potential risk from systemic exposure to alternative lipid-altering drugs (such as young children and fertile women).
引用
收藏
页码:779 / 790
页数:12
相关论文
共 37 条
[11]  
CASHINHEMPHILL L, JAMA, V264, P3013
[12]   Executive summary of the Third Report of the National Cholesterol Education Program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (Adult Treatment Panel III) [J].
Cleeman, JI ;
Grundy, SM ;
Becker, D ;
Clark, LT ;
Cooper, RS ;
Denke, MA ;
Howard, WJ ;
Hunninghake, DB ;
Illingworth, DR ;
Luepker, RV ;
McBride, P ;
McKenney, JM ;
Pasternak, RC ;
Stone, NJ ;
Van Horn, L ;
Brewer, HB ;
Ernst, ND ;
Gordon, D ;
Levy, D ;
Rifkind, B ;
Rossouw, JE ;
Savage, P ;
Haffner, SM ;
Orloff, DG ;
Proschan, MA ;
Schwartz, JS ;
Sempos, CT ;
Shero, ST ;
Murray, EZ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 285 (19) :2486-2497
[13]  
Davidson MH, 2002, AM J CARDIOL, V90, p50K
[14]   Colesevelam hydrochloride: a non-absorbed, polymeric cholesterol-lowering agent [J].
Davidson, MH ;
Dicklin, MR ;
Maki, KC ;
Kleinpell, RM .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2000, 9 (11) :2663-2671
[15]   Colesevelam hydrochloride (Cholestagel) - A new, potent bile acid sequestrant associated with a low incidence of gastrointestinal side effects [J].
Davidson, MH ;
Dillon, MA ;
Gordon, B ;
Jones, P ;
Samuels, J ;
Weiss, S ;
Isaacsohn, J ;
Toth, P ;
Burke, SK .
ARCHIVES OF INTERNAL MEDICINE, 1999, 159 (16) :1893-1900
[16]  
Dietschy JM, 1997, AM J CLIN NUTR, V65, P1581
[17]  
DIETSCHY JM, 1993, J LIPID RES, V34, P1637
[18]   Drug interactions with colesevelam hydrochloride, a novel, potent lipid-lowering agent [J].
Donovan, JM ;
Stypinski, D ;
Stiles, MR ;
Olson, TA ;
Burke, SK .
CARDIOVASCULAR DRUGS AND THERAPY, 2000, 14 (06) :681-690
[19]   Side effects of statins: Hepatitis versus "transaminitis" - Myositis versus "CPKitis" [J].
Dujovne, CA .
AMERICAN JOURNAL OF CARDIOLOGY, 2002, 89 (12) :1411-1413
[20]   Efficacy and safety of Ezetimibe added to ongoing statin therapy for treatment of patients with primary hypercholesterolemia [J].
Gagné, C ;
Bays, HÉ ;
Weiss, SR ;
Mata, P ;
Quinto, K ;
Melino, M ;
Cho, M ;
Musliner, TA ;
Gumbiner, B .
AMERICAN JOURNAL OF CARDIOLOGY, 2002, 90 (10) :1084-1091