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Extended-release niacin increases anti-apolipoprotein A-I antibodies that block the antioxidant effect of high-density lipoprotein-cholesterol: the EXPLORE clinical trial.
- Source :
- British Journal of Clinical Pharmacology; May2017, Vol. 83 Issue 5, p1002-1010, 9p, 1 Diagram, 2 Charts, 1 Graph
- Publication Year :
- 2017
-
Abstract
- Aims Extended-release niacin (ERN) is the most effective agent for increasing high-density lipoprotein-cholesterol (HDL-C). Having previously identified anti-HDL antibodies, we investigated whether ERN affected the antioxidant capacity of HDL and whether ERN was associated with the production of antibodies against HDL (aHDL) and apolipoprotein A-I (aApoA-I). Methods Twenty-one patients older than 18 years, with HDL-C ≤40 mg dl<superscript>-1</superscript> (men) or ≤50 mg dl<superscript>-1</superscript> (women) were randomly assigned to receive daily ERN ( n = 10) or placebo ( n = 11) for two sequential 12-week periods, with 4 weeks of wash-out before cross-over. Primary outcome was change of paraoxonase-1 (PON1) activity and secondary outcomes were changes in aHDL and aApoA-I antibodies. Clinical Trial Unique Identifier: EudraCT 2006-006889-42. Results The effect of ERN on PON1 activity was nonsignificant (coefficient estimate 20.83 U l<superscript>-1</superscript>, 95% confidence interval [CI] -9.88 to 51.53; P = 0.184). ERN was associated with an increase in HDL-C levels (coefficient estimate 5.21 mg dl<superscript>-1</superscript>, 95% CI 1.16 to 9.25; P = 0.012) and its subclasses HDL2 (coefficient estimate 2.46 mg dl<superscript>-1</superscript>, 95% CI 0.57 to 4.34; P = 0.011) and HDL3 (coefficient estimate 2.73 mg dl<superscript>-1</superscript>, 95% CI 0.47 to 4.98; P = 0.018). ERN was significantly associated with the production of aApoA-I antibodies (coefficient estimate 0.25 μg ml<superscript>-1</superscript>, 95% CI 0.09-0.40; P = 0.001). aApoA-I titres at baseline were correlated with decreased PON activity. Conclusions The rise in HDL-C achieved with ERN was not matched by improved antioxidant capacity, eventually hampered by the emergence of aApoA-I antibodies. These results may explain why Niacin and other lipid lowering agents fail to reduce cardiovascular risk. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 03065251
- Volume :
- 83
- Issue :
- 5
- Database :
- Complementary Index
- Journal :
- British Journal of Clinical Pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 122635366
- Full Text :
- https://doi.org/10.1111/bcp.13198