Comparison of efficacy of plant stanol ester and sterol ester: Short-term and longer-term studies

被引:60
作者
O'Neill, FH [1 ]
Sanders, TAB [1 ]
Thompson, GR [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Sch Med, Hammersmith Hosp, Dept Metab Med,Div Investigat Sci, London W12 0NN, England
关键词
D O I
10.1016/j.amjcard.2005.03.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Published data suggest that the cholesterol-lowering effect of dietary plant sterol esters is less marked in longer-term than in short-term studies, whereas plant stanol esters maintain their efficacy. To investigate this further, healthy subjects and patients with familial hypercholesterolemia (FH) receiving statins were randomized to receive plant sterol ester 1.6 g/day or plant stanol ester 1.6 g/day or 2.6 g/day for 2 months. There was no difference among the 3 groups in the pooled low-density lipoprotein (LDL)-lowering response of FH patients and healthy subjects, but the effect of plant sterol diminished at 2 months and was not significantly different from baseline. This was accompanied by increases in serum plant sterols and a significant decrease in 7 alpha -hydroxy-4-cholesten-3-one, a marker of bile acid synthesis, especially in FH patients not taking bile acid sequestrants. In contrast, plant stanol esters lowered significantly both LDL cholesterol and plant sterols at 2 months and had no effect on bile acid synthesis. Slight decreases in serum lipid-soluble antioxidants occurred with both plant sterol and stanol esters. Our findings suggest that absorption of dietary plant sterols downregulates bile acid synthesis, which attenuates their cholesterol-lowering efficacy. We conclude that plant stanol esters are preferable for the long-term management of hypercholesterolemia. (c) 2005 Elsevier Inc. All rights reserved.
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页码:29D / 36D
页数:8
相关论文
共 50 条
[1]   Plant sterol ester-enriched spread lowers plasma total and LDL cholesterol in children with familial hypercholesterolemia [J].
Amundsen, ÅL ;
Ose, L ;
Nenseter, MS ;
Ntanios, FY .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 76 (02) :338-344
[2]  
Andersson A, 1999, EUR HEART J SUPPL, V1, pS80
[3]   THE PLASMA-LEVEL OF 7-ALPHA-HYDROXY-4-CHOLESTEN-3-ONE REFLECTS THE ACTIVITY OF HEPATIC CHOLESTEROL 7-ALPHA-HYDROXYLASE IN MAN [J].
AXELSON, M ;
BJORKHEM, I ;
REIHNER, E ;
EINARSSON, K .
FEBS LETTERS, 1991, 284 (02) :216-218
[4]   LEVELS OF 7-ALPHA-HYDROXY-4-CHOLESTEN-3-ONE IN PLASMA REFLECT RATES OF BILE-ACID SYNTHESIS IN MAN [J].
AXELSON, M ;
ALY, A ;
SJOVALL, J .
FEBS LETTERS, 1988, 239 (02) :324-328
[5]   INFLUENCE OF BETA-SITOSTEROL ON BILIARY CHOLESTEROL SATURATION AND BILE-ACID KINETICS IN MAN [J].
BEGEMANN, F ;
BANDOMER, G ;
HERGET, HJ .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1978, 13 (01) :57-63
[6]  
Berge KE, 2002, J LIPID RES, V43, P486
[7]   Incremental reduction of serum total cholesterol and low-density lipoprotein cholesterol with the addition of plant stanol ester-containing spread to statin therapy [J].
Blair, SN ;
Capuzzi, DM ;
Gottlieb, SO ;
Nguyen, T ;
Morgan, JM ;
Cater, NB .
AMERICAN JOURNAL OF CARDIOLOGY, 2000, 86 (01) :46-52
[8]  
BRINK EJ, 2000, LONG TERM FOLLOW UP, P99
[9]  
BRYNES AE, 2003, LIPIDS ATHEROSCLEROS, P119
[10]   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