Extended‐release niacin increases anti‐apolipoprotein A‐I antibodies that block the antioxidant effect of high‐density lipoprotein–cholesterol: the EXPLORE clinical trial. (18th January 2017)

• Record Type: Journal Article
• Authors: Batuca, Joana R.; Amaral, Marta C.; Favas, Catarina; Paula, Filipe S.; Ames, Paul R. J.; Papoila, Ana L.; Delgado Alves, José
• Is Part Of: British journal of clinical pharmacology. Volume 83:Number 5(2017:May)
• Page Start: 1002
• Page End: 1010
• Publication Date: 2017-01-18
• Subjects: antibodies -- antioxidant -- apoliproteins -- high‐density lipoprotein -- immune system; Pharmacology -- Periodicals; Drugs -- Periodicals; 615.1
• DOI: 10.1111/bcp.13198
• Languages: English
• ISSNs: 0306-5251

Abstract

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 –1 (men) or ≤50 mg dl –1 (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 –1, 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 –1, 95% CI 1.16 to 9.25; P = 0.012) and its subclasses HDL2 (coefficient estimate 2.46 mg dl –1, 95% CI 0.57 to 4.34; P = 0.011) and HDL3 (coefficient estimate 2.73 mg dl –1, 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 –1, 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.