Effects on serum lipids, lipoproteins and fat soluble antioxidant concentrations of consumption frequency of margarines and shortenings enriched withplant stanol esters

Citation
J. Plat et al., Effects on serum lipids, lipoproteins and fat soluble antioxidant concentrations of consumption frequency of margarines and shortenings enriched withplant stanol esters, EUR J CL N, 54(9), 2000, pp. 671-677
Citations number
22
Categorie Soggetti
Endocrynology, Metabolism & Nutrition","Endocrinology, Nutrition & Metabolism
Journal title
EUROPEAN JOURNAL OF CLINICAL NUTRITION
ISSN journal
09543007 → ACNP
Volume
54
Issue
9
Year of publication
2000
Pages
671 - 677
Database
ISI
SICI code
0954-3007(200009)54:9<671:EOSLLA>2.0.ZU;2-P
Abstract
Objective: To examine in humans the effects on serum lipids, lipoproteins a nd fat-soluble antioxidants of a daily consumption of 2.5 g plant stanols, consumed either once per day at lunch or divided over the three meals. Design: A randomized, double-blind, placebo-controlled, cross-over design. Subjects: Thirty-nine healthy normocholesterolemic or mildly hypercholester olemic subjects participated. Interventions: Each subject consumed in random order; no plant stanols; 2.5 g plant stanols at lunch; and 2.5 g plant stanols divided over the three m eals (0.42g at breakfast, 0.84g at lunch and 1.25 g at dinner, which is pro portional to dietary cholesterol intake). Each period lasted 4 weeks. Plant stanols were esterified with fatty acids from low erucic rapeseed oil (LEA R) and incorporated into margarines or shortenings. Results: Consumption of 2.5g plant stanols at lunch results in a similar lo w-density lipoprotein (LDL)-cholesterol-lowering efficacy compared to consu mption of 2.5 g plant stanols divided over the three meals (-0.29 mmol/l co mpared with the control period (P < 0.001; 95% CI, -0.19 to -0.39 mmol/l) f or the once per day diet and -0.31 mmol/l (P < 0.001; 95% CI, -0.20 to -0.4 1mmol/l) for the three times per day period). High-density Lipoprotein (HDL ) cholesterol and triacylglycerol concentrations did not change. After stan dardization for LDL cholesterol, the sum of the most lipophylic hydrocarbon carotenoids (ie alpha-carotene, beta-carotene and lycopene) in particular was slightly, though not significantly, lowered by -0.017 +/- 0.018 mu mol/ mmol LDL cholesterol (P = 0.307) after the once per day period and by -0.03 2 +/- 0.016 mu mol/mmol LDL cholesterol (P = 0.049) after the three times p er day period. Conclusions: Our findings suggest that for lowering LDL cholesterol concent rations it is not necessary to consume products rich in plant stanol ester at each meal or simultaneously with dietary cholesterol.