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Published on: November 10, 2017
Greater remnant lipoprotein cholesterol reduction with pitavastatin compared with pravastatin in HIV-infected
Parag H Joshi1, P Elliott Miller, Seth S Martin
1aDivision of Cardiology, University of Texas Southwestern Medical Center, Dallas, Texas bJohns Hopkins Ciccarone Center for the Prevention of Heart Disease, Baltimore cDepartment of Critical Care Medicine, National Institutes of Health, Bethesda, Maryland dDepartment of Biostatistics, Boston University School of Public Health, Boston, Massachusetts eAtherotech Diagnostics Laboratory, Birmingham fKowa Pharmaceuticals America, Inc., Montgomery, Alabama gCGH Medical Center, University of Illinois School of Medicine, Peoria, Illinois, USA.
Insights
Pitavastatin significantly reduced remnant lipoprotein cholesterol (RLP-C) and other cardiovascular disease risk factors in HIV patients more than pravastatin. Further study is needed on RLP-C reduction
Area of Science:
- Cardiology
- HIV Medicine
- Lipidology
Background:
- Cardiovascular disease (CVD) is a major cause of death in HIV patients.
- Elevated remnant lipoprotein cholesterol (RLP-C) is an emerging CVD risk factor in this population.
- The effect of statins on RLP-C in HIV dyslipidemia is not well understood.
Purpose of the Study:
- To compare the effects of pitavastatin and pravastatin on lipoprotein subfractions, including RLP-C, in HIV patients with dyslipidemia.
- To evaluate changes in atherogenic lipid profiles over 12 weeks.
Main Methods:
- Post hoc analysis of the randomized INTREPID trial.
- Comparison of pitavastatin 4 mg/day versus pravastatin 40 mg/day in HIV patients.
- Measurement of apolipoproteins and lipoprotein cholesterol subfractions at baseline and 12 weeks.
Main Results:
- Pitavastatin demonstrated significantly greater reductions in RLP-C compared to pravastatin (-11.6 mg/dL vs. -8.5 mg/dL; P=0.01).
- Greater reductions in risk ratios (ApoB/ApoAI, TC/HDL-C) were observed with pitavastatin (P<0.05).
- No significant differences were found in HDL-C, its subfractions, or lipoprotein(a) cholesterol levels between the groups.
Conclusions:
- Pitavastatin 4 mg/day effectively lowered RLP-C and other established cardiovascular risk markers more than pravastatin 40 mg/day in HIV patients.
- The clinical impact of RLP-C reduction on CVD risk in HIV dyslipidemia warrants further investigation.
Objective:
Cardiovascular disease (CVD) is a leading cause of morbidity and mortality in those with HIV. An emerging CVD risk factor is triglyceride-rich remnant lipoprotein cholesterol (RLP-C: the sum of intermediate-density lipoprotein and very low-density lipoprotein cholesterol). The effects of statin therapy on lipoprotein subfractions, including RLP-C, in HIV dyslipidemia are unknown.
Methods:
This is a post hoc analysis of the randomized INTREPID trial (NCT 01301066) comparing pitavastatin 4 mg daily vs. pravastatin 40 mg daily in study participants with HIV. We measured apolipoproteins AI and B and lipoprotein cholesterol subfractions separated by density gradient ultracentrifugation at baseline and 12 weeks. We compared changes in atherogenic subfractions over 12 weeks in INTREPID participants using analysis of covariance.
Results:
Lipoprotein subfraction data were available for 213 study participants (pitavastatin n = 104, pravastatin n = 109). Baseline characteristics were similar between treatment groups. Reductions in RLP-C were significantly greater in the pitavastatin group compared with pravastatin group (-11.6 mg/dl vs. -8.5 mg/dl; P = 0.01). Similarly, ratios of risk [apolipoproteins B/apolipoproteins AI, total cholesterol/high-density lipoprotein cholesterol (HDL-C)] showed greater reductions with pitavastatin (P < 0.05). There were no differences in changes in HDL-C, HDL-C subfractions or lipoprotein(a) cholesterol levels.
Conclusion:
In patients with HIV, pitavastatin 4 mg/dl lowered both RLP-C and established apolipoprotein and lipid risk ratios more so than pravastatin 40 mg/dl. The impact of RLP-C reduction on CVD in HIV dyslipidemic patients merits further study.
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