Effects of fenofibrate on plasma oxidized LDL and 8-isoprostane in a sub-cohort of GOLDN participants

Yan Dong, Brian T. Steffen, Jing Cao, Alexander K. Tsai, Jose Ordovas, Robert Straka, Xia Zhou, Edmond Kabagambe, Naomi Q. Hanson, Donna Arnett, Michael Y. Tsai

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Background: Fenofibrate significantly reduces circulating triglyceride (TG) concentrations, particularly in individuals with elevated levels. The purpose of the current study was to determine whether fenofibrate treatment reduces markers of oxidative stress, oxidized low density lipoprotein (ox-LDL) and 8-isoprostane (8-isoP), in a manner similar to TG where those with the highest levels show the greatest reductions. Materials/methods: The concentrations of TG, 8-isoP, and ox-LDL were measured in plasma before and after 3 weeks of fenofibrate treatment (160. mg/d) in a sub-cohort (n = 187) of the Genetics of Lipid Lowering Drugs and Diet Network (GOLDN) study. Results: Data were divided into tertiles as determined by pre-treatment values of the respective target. Fenofibrate treatment resulted in significant reductions in TG concentrations by 24.2% (p< 0.0001), 41.9% (p< 0.0001), and 46.6% (p< 0.0001) in tertiles 1, 2, and 3, respectively. Significant reductions were also observed in ox-LDL of 7.2% (p = 0.0096), 8.5% (p = 0.0019) and 12.1% (p< 0.0001) in tertiles 1, 2, and 3, respectively. Finally, fenofibrate treatment resulted in a 32.7% increase (p = 0.0201) in 8-isoP levels in tertile 1, but a significant decrease of 34.4% (p< 0.0001) in tertile 3. Conclusions: This study is the largest to date to demonstrate that fenofibrate reduces oxidative stress and the first to show a suppressive effect on 8-isoP levels in individuals with a high oxidative burden following short term (3 wk) drug therapy. Those with the highest baseline levels of ox-LDL and 8-isoP showed the greatest reductions following fenofibrate treatment. Given the role of oxidative stress in atherosclerosis and coronary heart disease, our observations may partially explain the efficacy of fenofibrate in reducing cardiovascular events in select patients.

Original languageEnglish
Pages (from-to)422-425
Number of pages4
JournalAtherosclerosis
Volume214
Issue number2
DOIs
StatePublished - Feb 2011

Bibliographical note

Funding Information:
This study is a sub-population of the GOLDN study. GOLDN is a multi-center study in families with 3-generation pedigree. The study is funded by NIH and has two centers, one in Minneapolis, MN and the other in Salt Lake City, UT with the majority of the population as European Caucasians. The primary purpose is to investigate the interaction of genetic and environmental factors on response to fenofibrate treatment. The detailed design of the study is described elsewhere [17] .

Funding

This study is a sub-population of the GOLDN study. GOLDN is a multi-center study in families with 3-generation pedigree. The study is funded by NIH and has two centers, one in Minneapolis, MN and the other in Salt Lake City, UT with the majority of the population as European Caucasians. The primary purpose is to investigate the interaction of genetic and environmental factors on response to fenofibrate treatment. The detailed design of the study is described elsewhere [17] .

FundersFunder number
National Institutes of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)U01HL072524

    Keywords

    • Atherosclerosis
    • Fenofibrate
    • GOLDN
    • Isoprostane
    • Ox-LDL
    • Triglyceride

    ASJC Scopus subject areas

    • Cardiology and Cardiovascular Medicine

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