Literature DB >> 6109940

Colestipol plus nicotinic acid in treatment of heterozygous familial hypercholesterolaemia.

D R Illingworth, B E Phillipson, J H Rapp, W E Connor.   

Abstract

Thriteen patients with heterozygous familial hypercholesterolaemia (FH) were sequentially treated with: a low-cholesterol, fat-restricted diet; diet and colestipol; and diet and colestipol and nicotinic acid. Concentrations of plasma cholesterol decreased from 415 +/- 69 mg/dl on diet alone to 327 +/- 54 mg/dl on colestipol and fell to 246 +/- 49 mg/dl on the combined drug regimen. Plasma concentrations of LDL cholesterol declined 24% on colestipol; the subsequent addition of nicotinic acid resulted in a further 31% fall so that values on the combined drug regimen were 47% below those seen on diet alone. HDL cholesterol levels were similar on both the diet (40 mg/dl) and colestipol (43 mg/dl) treatment periods but increased to 53 mg/dl on the combined drug regimen. Treatment resulted in significant decreases in the LDL:HDL ratio which fell from 8.4 on diet to 3.3 on the colestipol plus nicotinic acid regimen. In most patients with heterozygous FH, combined use of a bile acid sequestrant and nicotinic acid affords the opportunity to maintain a normal lipid profile. Prolonged use of this regimen may reduce the incidence of premature coronary atherosclerosis which naturally occurs in these patients.

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Year:  1981        PMID: 6109940     DOI: 10.1016/s0140-6736(81)91910-3

Source DB:  PubMed          Journal:  Lancet        ISSN: 0140-6736            Impact factor:   79.321


  10 in total

Review 1.  A comparative review of the adverse effects of treatments for hyperlipidaemia.

Authors:  A Steiner; B Weisser; W Vetter
Journal:  Drug Saf       Date:  1991 Mar-Apr       Impact factor: 5.606

2.  Clinical and laboratory responses to niceritrol in the treatment of hypercholesterolaemia.

Authors:  L D Curtis; J P Reckless; A F Winder; D J Betteridge
Journal:  Postgrad Med J       Date:  1988-09       Impact factor: 2.401

Review 3.  Treatment of hypercholesterolemia in black patients.

Authors:  J T Wright; J M McKenney; A J Wasserman
Journal:  J Natl Med Assoc       Date:  1988-09       Impact factor: 1.798

4.  Lack of pharmacokinetic interaction between cholestyramine and acipimox, a new lipid lowering drug.

Authors:  C de Paolis; R Farina; E Pianezzola; G Valzelli; F Celotti; A E Pontiroli
Journal:  Br J Clin Pharmacol       Date:  1986-10       Impact factor: 4.335

5.  Combination treatment with cholestyramine and bezafibrate for heterozygous familial hypercholesterolaemia.

Authors:  L D Curtis; A C Dickson; K L Ling; J Betteridge
Journal:  BMJ       Date:  1988-07-16

Review 6.  Lipid-lowering drugs. An overview of indications and optimum therapeutic use.

Authors:  D R Illingworth
Journal:  Drugs       Date:  1987-03       Impact factor: 9.546

7.  Effects of hypolipidemic therapy on cholesterol homeostasis in freshly isolated mononuclear cells from patients with heterozygous familial hypercholesterolemia.

Authors:  E E Sundberg; D R Illingworth
Journal:  Proc Natl Acad Sci U S A       Date:  1983-12       Impact factor: 11.205

8.  Hypocholesterolemic effects of mevinolin in patients with heterozygous familial hypercholesterolemia.

Authors:  D R Illingworth; G J Sexton
Journal:  J Clin Invest       Date:  1984-12       Impact factor: 14.808

9.  Effects of acipimox and cholestyramine on serum lipoproteins, non-cholesterol sterols and cholesterol absorption and elimination.

Authors:  H Gylling; H Vanhanen; T A Miettinen
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

10.  Partial ileal bypass in treatment of familial hypercholesterolaemia.

Authors:  L J Chalstrey; A F Winder; D J Galton
Journal:  J R Soc Med       Date:  1982-11       Impact factor: 18.000

  10 in total

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