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    Eur J Clin Nutr. 2002 Apr;56(4):352-7.

    Soy in hypercholesterolaemia: a double-blind, placebo-controlled trial.

    Source

    North Karelia Project, National Public Health Institute, Helsinki, Finland. pekka.puska@ktl.fi

    Abstract

    OBJECTIVE:

    To study whether Abacor, a product based on isolated soy protein with high and standardised levels of isoflavones and cotyledon soy fibres, was more effective in lowering total and LDL cholesterol than placebo.

    DESIGN:

    Randomised, placebo-controlled, double-blind, parallel group, single centre study.

    SETTING:

    Primary care in Joensuu, North Karelia, Finland.

    SUBJECTS:

    Subjects were screened from the patient database of the health centre; 30 were randomised to the Abacor group and 30 subjects to placebo. Eight subjects were withdrawn, six from the active group, two from the placebo group.

    INTERVENTION:

    The preparations were given as two daily liquid supplements in addition to the subjects' regular diets for 6 weeks.

    RESULTS:

    Abacor showed a statistically significant lipid-lowering effect as compared to placebo, although an unexpected reduction was seen in the placebo group. The estimated difference between active treatment and placebo was 0.25 mmol/l (95% CI 0.01, 0.50; P=0.049) for total cholesterol, corresponding to reductions of 8.3 and 5.1%, respectively. The difference in reduction of LDL-cholesterol was 0.27 mmol/l (95% CI 0.06, 0.49; P=0.014) and corresponded to a reduction of 13.2% in the active treatment group, and 8.0% in the placebo group. Abacor showed a rapid onset of effect, as compared with placebo. During a wash-out period of 4 weeks after treatment, the subjects returned to pre-treatment cholesterol levels.

    CONCLUSION:

    Added to a regular diet, Abacor significantly reduced LDL-cholesterol and total cholesterol. These beneficial effects occurred within 6 weeks of treatment.

    PMID:
    11965512
    [PubMed - indexed for MEDLINE]
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