Effect of alirocumab on specific lipoprotein non-high-density lipoprotein cholesterol and subfractions as measured by the vertical auto profile method: analysis of 3 randomized trials versus placebo

Autor: James M. McKenney, Krishnaji R. Kulkarni, Poulabi Banerjee, Corinne Hanotin, Peter P. Toth, Eli M. Roth, Seth S. Martin, Steven R. Jones, Parag H. Joshi, Sara Hamon
Jazyk: angličtina
Rok vydání: 2016
Předmět:
Adult
Male
medicine.medical_specialty
Clinical chemistry
Endocrinology
Diabetes and Metabolism

Lipoproteins
Clinical Biochemistry
Hypercholesterolemia
030204 cardiovascular system & hematology
Lipoproteins
VLDL

Placebo
Bioinformatics
Antibodies
Monoclonal
Humanized

Gastroenterology
PCSK9
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Endocrinology
Double-Blind Method
Internal medicine
Medicine
Humans
030212 general & internal medicine
Triglycerides
Alirocumab
Hypercholesterolaemia
Randomized Controlled Trials as Topic
Biochemistry
medical

business.industry
Cholesterol
Research
Biochemistry (medical)
Lipoprotein subfraction
Antibodies
Monoclonal

Cholesterol
LDL

Middle Aged
Vertical auto profile
Lipid Metabolism
chemistry
VAP
lipids (amino acids
peptides
and proteins)

Female
business
Lipoproteins
HDL

Lipoprotein
Lipidology
Zdroj: Lipids in Health and Disease
ISSN: 1476-511X
Popis: Background The effect of alirocumab on potentially atherogenic lipoprotein subfractions was assessed in a post hoc analysis using the vertical auto profile (VAP) method. Methods Patients from three Phase II studies with low-density lipoprotein cholesterol (LDL-C) ≥2.59 mmol/L (100 mg/dL) at baseline on stable statin therapy were randomised to receive subcutaneous alirocumab 50–150 mg every 2 weeks (Q2W) or 150–300 mg every 4 weeks (according to study) or placebo for 8–12 weeks. Samples from patients treated with alirocumab 150 mg Q2W (n = 74; dose common to all three trials) or placebo (n = 71) were analysed by VAP. Percent change in lipoprotein subfractions with alirocumab vs. placebo was analysed at Weeks 6, 8 or 12 using analysis of covariance. Results Alirocumab significantly reduced LDL-C and the cholesterol content of subfractions LDL1, LDL2 and LDL3+4. Significant reductions were also observed in triglycerides, apolipoproteins CII and CIII and the cholesterol content of very low-density, intermediate-density, and remnant lipoproteins. Conclusion Alirocumab achieved reductions across a spectrum of atherogenic lipoproteins in patients receiving background statin therapy. Trial registration Clinicaltrials.gov identifiers: NCT01288443, NCT01288469, NCT01266876 Electronic supplementary material The online version of this article (doi:10.1186/s12944-016-0197-4) contains supplementary material, which is available to authorized users.
Databáze: OpenAIRE