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Atorvastatin in dyslipidaemia of the nephrotic syndrome
Pedro Valdivielso1, Manuel Moliz, Alfonso Valera
1Department of Internal Medicine, Nephrology and Lipid Unit, Hospital Clínico Universitario Virgen de la Victoria, Servicio Andaluz de Salud y Universidad de Málaga, Málaga, Spain. valdivielso@uma.es
Insights
Low-dose atorvastatin effectively manages dyslipidaemia in nephrotic syndrome patients, reducing cardiovascular risk. This study found atorvastatin safe, well-tolerated, and even beneficial for renal function, decreasing proteinuria.
Area of Science:
- Nephrology
- Cardiology
- Pharmacology
Background:
- Nephrotic syndrome is associated with dyslipidaemia, increasing cardiovascular risk and potentially worsening renal function.
- Effective management of dyslipidaemia is crucial for improving outcomes in patients with nephrotic syndrome.
Purpose of the Study:
- To evaluate the efficacy and safety of 10 mg atorvastatin in controlling dyslipidaemia in patients with nephrotic syndrome.
- To assess the impact of atorvastatin on lipid profiles, safety parameters, and renal function.
Main Methods:
- A prospective, open-label, 6-month study involving 10 patients with nephrotic syndrome.
- Patients received 10 mg of atorvastatin daily, with measurements of lipids, lipoproteins, safety markers, and renal function.
Main Results:
- Atorvastatin significantly reduced LDL cholesterol by 41% and triglycerides by 31% (P < 0.05).
- HDL cholesterol increased by 15% (NS).
- The drug was well-tolerated, with no adverse effects on safety markers or renal function; proteinuria decreased in most patients.
Conclusions:
- Low-dose atorvastatin (10 mg daily) is a safe and effective treatment for dyslipidaemia in nephrotic syndrome.
- Atorvastatin therapy may also offer renal benefits by reducing proteinuria in these patients.
Abstract:
The combined dyslipidaemia that accompanies the nephrotic syndrome increases the cardiovascular risk and appears to worsen long-term renal function. Our aim was to determine the efficacy and safety of 10 mg atorvastatin in the control of dyslipidaemia in these patients. We carried out a prospective, open, 6 month study of 10 patients with primary or secondary nephrotic syndrome (proteinuria >3.5 g/day, hypoalbuminaemia, oedema and hyperlipidaemia). The changes in lipids and plasma lipoproteins were measured, as well as the safety profile (transaminases, creatine phosphokinase, fibrinogen and antithrombin III activity) and parameters of renal function. The addition of 10 mg atorvastatin daily for 6 months resulted in a 41% reduction in low density lipoprotein (LDL) cholesterol and 31% in triglycerides (both P < 0.05), and a 15% increase in high density lipoprotein (HDL) cholesterol (NS). The drug was well tolerated and there was no change in the safety profile or deterioration in renal function. In fact, the levels of proteinuria fell in all but one patient (6.2 +/- 2.6 vs 4.8 +/- 2.5 g/24 h; P < 0.05). Atorvastatin, at the above dose, and for the time used proved to be a safe drug that effectively reduced dyslipidaemia in patients with nephrotic syndrome.
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