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Substitution of nevirapine or raltegravir for protease inhibitor vs. rosuvastatin treatment for the management of dyslipidaemia in HIV-infected patients on stable antiretroviral therapy (Nevrast study).

AbstractOBJECTIVES:
An observational, prospective, cohort study was performed to compare efficacy and safety of a switch from ritonavir-boosted protease inhibitor (PI/r) to nevirapine or raltegravir with that of rosuvastatin addition to current antiretroviral therapy in HIV-infected patients with hyperlipidaemia.
METHODS:
All HIV-infected patients receiving a stable PI/r-based antiretroviral regimen, with persistently suppressed viremia, naïve to non-nucleoside analogues and to integrase strand transfer inhibitors, with mixed hyperlipidaemia, and who underwent a switch from PI/r to nevirapine (Group A) or raltegravir (Group B) or who started rosuvastatin at 10 mg daily (group C) with unchanged antiretroviral regimen were enrolled into the study.
RESULTS:
Overall, 136 patients were enrolled: 43 patients were included in the group A, 46 in the group B, and 47 in the group C. The mean age was 46.6 years, and 108 (79.4%) were males. After 48 weeks of follow-up, a significantly greater reduction in the mean low-density lipoprotein (LDL) cholesterol level was reported in group C (-28.2%) than in group A (-10.2%; p < .001) and B (-12.4%; p = .021), while a significantly greater reduction in the mean concentration of triglycerides was observed in group A (-31.2%) and B (-35.5%) than in group C (-11.9%; p = .034 and p = .004, respectively). The incidence of adverse events was <10% and comparable across the three groups.
CONCLUSION:
In HIV-positive subjects receiving a PI/r, the initiation of rosuvastatin treatment after 48 weeks yielded a greater decline in LDL cholesterol, while the switch from PI/r to nevirapine or raltegravir led to a greater decline in triglycerides.
AuthorsLeonardo Calza, Eleonora Magistrelli, Vincenzo Colangeli, Marco Borderi, Linda Bussini, Isabella Bon, Maria Carla Re, Pierluigi Viale
JournalInfectious diseases (London, England) (Infect Dis (Lond)) Vol. 49 Issue 10 Pg. 737-747 (Oct 2017) ISSN: 2374-4243 [Electronic] England
PMID28683645 (Publication Type: Comparative Study, Journal Article, Observational Study)
Chemical References
  • Anti-HIV Agents
  • Anticholesteremic Agents
  • Cholesterol, LDL
  • HIV Integrase Inhibitors
  • HIV Protease Inhibitors
  • Raltegravir Potassium
  • Rosuvastatin Calcium
  • Nevirapine
  • Ritonavir
Topics
  • Adult
  • Anti-HIV Agents (administration & dosage, adverse effects, therapeutic use)
  • Anticholesteremic Agents (administration & dosage, adverse effects, therapeutic use)
  • Antiretroviral Therapy, Highly Active
  • Cholesterol, LDL (blood)
  • Cohort Studies
  • Drug Substitution
  • Female
  • HIV Infections (complications, drug therapy, virology)
  • HIV Integrase Inhibitors (administration & dosage, adverse effects, therapeutic use)
  • HIV Protease Inhibitors (administration & dosage, adverse effects, therapeutic use)
  • HIV-1 (drug effects)
  • Humans
  • Hyperlipidemias (drug therapy)
  • Male
  • Middle Aged
  • Nevirapine (administration & dosage, adverse effects, therapeutic use)
  • Prospective Studies
  • Raltegravir Potassium (administration & dosage, adverse effects, therapeutic use)
  • Ritonavir
  • Rosuvastatin Calcium (administration & dosage, adverse effects, therapeutic use)
  • Viral Load
  • Viremia (drug therapy)

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