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Clinical Trial
. 1990 Sep;228(3):261-6.
doi: 10.1111/j.1365-2796.1990.tb00229.x.

The efficacy and safety of pravastatin, compared to and in combination with bile acid binding resins, in familial hypercholesterolaemia

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Clinical Trial

The efficacy and safety of pravastatin, compared to and in combination with bile acid binding resins, in familial hypercholesterolaemia

N Hoogerbrugge et al. J Intern Med. 1990 Sep.

Abstract

Forty patients with familial hypercholesterolaemia (FH) were treated with 40 mg pravastatin once daily. Pravastatin decreased serum total and low density lipoprotein cholesterol (LDL) after 8 weeks of treatment by 28% and 33%, respectively, while high density lipoprotein cholesterol increased by 8% and triglycerides decreased by 14%. In 30 patients LDL cholesterol had not decreased below 5.0 mmol l-1 after 8 weeks of treatment, and in these patients resins were added to pravastatin, resulting in an additional decrease in total and LDL cholesterol of 8% and 12%, respectively. A control group of 22 FH patients was treated with placebo for 10 weeks, after which time resins were added, and they induced a decrease in total and LDL-cholesterol of 17% and 22%, respectively. Our results over a 24-week treatment period indicate that 40 mg pravastatin is more effective than 3 packets of resins in lowering LDL cholesterol, whereas the combination is most effective of all and can be used safely.

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Comment in

  • HMG-CoA reductase inhibitors.
    Grundy SM. Grundy SM. J Intern Med. 1990 Sep;228(3):201-5. doi: 10.1111/j.1365-2796.1990.tb00218.x. J Intern Med. 1990. PMID: 2401870 No abstract available.

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