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Published on: November 17, 2018
[Effectiveness and tolerance of atorvastatin for antiretroviral therapy-secondary dyslipemia]
Anna Soler1, Elisabet Deig, Josep Guil
1Unitat de Malalties Infeccioses-VIH, Fundació Hospital-Asil de Granollers, Granollers, Barcelona, Spain.
Insights
Atorvastatin effectively treated hypercholesterolemia in HIV patients on antiretroviral therapy. The drug demonstrated good tolerance and safety, with a high success rate in achieving therapeutic goals.
Area of Science:
- Cardiology
- Infectious Diseases
- Pharmacology
Background:
- Hypercholesterolemia is a common complication in patients with Human Immunodeficiency Virus (HIV) undergoing antiretroviral treatment.
- Secondary dyslipidemia in HIV patients requires effective and safe management strategies.
Purpose of the Study:
- To evaluate the effectiveness and tolerance of atorvastatin in managing hypercholesterolemia in HIV-positive patients.
- To assess the safety profile of atorvastatin in this specific patient population.
Main Methods:
- A prospective study involving HIV+ patients with secondary dyslipidemia meeting NCEP-III criteria.
- Patients received 10 mg/day of atorvastatin, with a potential dose increase to 20 mg/day.
- Follow-up duration was 6 months.
Main Results:
- The study included 32 patients.
- Therapeutic objectives were achieved in 62% of cases.
- Atorvastatin demonstrated good clinical tolerance, with only one adverse event requiring drug discontinuation.
Conclusions:
- Atorvastatin is an effective treatment for dyslipidemia in HIV patients.
- Atorvastatin is safe and well-tolerated in this population.
- The findings support the use of atorvastatin for managing hypercholesterolemia in HIV-infected individuals on antiretroviral therapy.
Background And Objective:
We investigated atorvastatin effectiveness and tolerance in HIV patients with hypercholesterolemia related to antiretroviral treatment.
Patients And Method:
Prospective study that included HIV+ patients under antiretroviral treatment who displayed secondary dyslipemia and medical treatment criteria (according to NCEP-III). These patients were given 10 mg/day atorvastatin and hygienic-dietetic measures. If the therapeutic objectives were not achieved, the dose of atorvastatin was increased to 20 mg/day. Patients were followed up for 6 months.
Results:
32 patients were included. In 5 cases it was necessary to increase the dose from 10 mg atorvastatin to 20 mg. The therapeutic objective was obtained in 62% cases, with a good clinical tolerance. Only one adverse effect was noticed, which forced the removal of the drug.
Conclusion:
In our study atorvastatin was effective for the treatment of dyslipemia in HIV patients, and it was safe and well tolerated.
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