Effects of atorvastatin on serum lipids of patients with familial hypercholesterolaemia
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1Department of Internal Medicine III, University Hospital Dijkzigt, Rotterdam, The Netherlands. hoogerbrugge@inw3.azrnl
Insights
Atorvastatin effectively lowered LDL cholesterol in familial hypercholesterolaemia patients. This HMG-CoA reductase inhibitor demonstrated significant reductions, proving valuable for managing severe high cholesterol.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
Background:
- Familial hypercholesterolaemia (FH) is a genetic disorder characterized by high LDL cholesterol levels.
- Standard treatments for FH include diet, simvastatin, colestyramine, and nicotinic acid.
- Patients with FH often require advanced therapeutic options to manage persistent hypercholesterolaemia.
Purpose of the Study:
- To evaluate the efficacy of atorvastatin, a novel HMG-CoA reductase inhibitor, in patients with familial hypercholesterolaemia.
- To assess the effects of atorvastatin on LDL cholesterol levels in patients with high LDLc despite standard therapy.
- To compare the effectiveness of different doses of atorvastatin against existing standard treatments.
Main Methods:
- An open-label study involving FH patients with LDLc > 5.0 mmol/L on standard therapy for at least 3 months.
- Patients received 40 mg atorvastatin daily for 6 weeks, followed by 80 mg atorvastatin daily for another 6 weeks.
- Standard therapy included diet with simvastatin (alone or with colestyramine) or nicotinic acid.
Main Results:
- Treatment with 80 mg atorvastatin resulted in a significant decrease in LDL cholesterol compared to 40 mg simvastatin alone (24% reduction) or with colestyramine (19% reduction).
- LDL cholesterol reduction with 80 mg atorvastatin was comparable to that achieved with simvastatin combined with nicotinic acid.
- Atorvastatin was well-tolerated, with no observed side-effects during the study period.
Conclusions:
- Atorvastatin is a valuable therapeutic option for patients suffering from severe hypercholesterolaemia, such as familial hypercholesterolaemia.
- The study supports the use of atorvastatin in managing high LDL cholesterol levels in challenging patient populations.
- Atorvastatin offers a promising addition to the existing treatment strategies for lipid management in FH.
Objectives:
The effects of atorvastatin, a new synthetic HMG-CoA reductase inhibitor, were investigated in patients with familial hypercholesterolaemia (FH), with high LDLc levels whilst on standard treatment.
Design:
Open treatment with 40 mg atorvastatin daily for 6 weeks, followed by another 6 weeks with 80 mg atorvastatin.
Setting:
Outpatient lipid clinic of a tertiary referral centre.
Subjects:
FH was diagnosed when the untreated LDLc concentration was higher than 6 mmol L-1, tendon xanthomas were present at the participant or a first degree relative, and the family history for hypercholesterolaemia was positive. The FH patients were selected for an LDLc above 5.0 mmol L-1 whilst on standard therapy for at least 3 months. Standard therapy consisted of a diet and 40 mg simvastatin, either alone (n = 17), or in combination with 8-12 g colestyramin (n = 12), or 1800 mg nicotinic acid (n = 12).
Main Outcome Measure:
Effects on LDLc concentration.
Results:
LDLc concentration significantly decreased during treatment with 80 mg atorvastatin as compared to LDLc levels on 40 mg simvastatin alone or in combination with 8-12 g colestyramin, by 24 +/- 14% (P < 0.01) and 19 +/- 22% (P < 0.01), respectively. LDLc concentration was comparable during treatment with 80 mg atorvastatin or 40 mg simvastatin in combination with 1800 mg nicotinic acid. Atorvastatin was tolerated well, no side-effects were observed.
Conclusions:
Atorvastatin is a valuable addition to the treatment possibilities of patients with serious hypercholesterolaemia, like FH.
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