Oxidative Stress and Cardiovascular Risk Factors: The Coronary Artery Risk Development in Young Adults (CARDIA) Study

Author:

Heravi Amir S.1,Zhao Di2,Michos Erin D.1ORCID,Doria De Vasconcellos Henrique1ORCID,Ambale-Venkatesh Bharath1ORCID,Lloyd-Jones Donald3,Schreiner Pamela J.4,Reis Jared P.5,Shikany James M.6,Lewis Cora E.7ORCID,Ndumele Chiadi E.1,Guallar Eliseo2ORCID,Ouyang Pamela1ORCID,Hoogeveen Ron C.8ORCID,Lima Joao A. C.1,Post Wendy S.1,Vaidya Dhananjay1

Affiliation:

1. School of Medicine, Johns Hopkins University, Baltimore, MD 21287, USA

2. Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD 21287, USA

3. Feinberg School of Medicine, Northwestern University, Chicago, IL 60208, USA

4. School of Public Health, University of Minnesota, Minneapolis, MN 55455, USA

5. National Heart, Lung, and Blood Institute, Bethesda, MD 20892, USA

6. School of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA

7. School of Public Health, University of Alabama at Birmingham, Birmingham, AL 35294, USA

8. Baylor College of Medicine, Houston, TX 77030, USA

Abstract

Introduction—Oxidative stress is linked to cardiovascular diseases (CVD) and is suggested to vary by sex. However, few population-level studies have explored these associations and the majority comprise populations with advanced CVD. We assessed urinary isoprostane concentrations, a standard measure of oxidative stress, in a relatively young and healthy cohort, hypothesizing that higher oxidative stress is associated with an adverse cardiometabolic profile and female sex. Methods—Oxidative stress was measured in 475 women and 266 men, aged 48–55 years, from the Coronary Artery Risk Development in Young Adults (CARDIA) study using urinary 8-isoprostane (IsoP) and 2,3-dinor-8-isoprostane (IsoP-M). Multivariable-adjusted regression was used to evaluate cross-sectional associations. As secondary analysis, previously measured plasma F2-isoprostanes (plasma IsoP) from another CARDIA subset was similarly analyzed. Results—Mean (SD) ages for men and women were 52.1(2.3) and 52.2(2.2) years, respectively (p = 0.46), and 39% of the participants self-identified as Black (vs. White). Before adjustments, female sex was associated with higher median urinary IsoP (880 vs. 704 ng/g creatinine in men; p < 0.01) and IsoP m (1675 vs. 1284 ng/g creatinine in men; p < 0.01). Higher body mass index (BMI), high-density cholesterol (HDL-C), and triglycerides, current smoking, and less physical activity were associated with higher oxidative stress. Diabetes was not associated with urinary IsoP but was associated with lower IsoP m and plasma IsoP. Higher serum creatinine showed diverging associations with higher plasma and lower urinary isoprostane concentrations. Conclusions—Different isoprostane entities exhibit varying association patterns with CVD risk factors, and therefore are complementary, rather than interchangeable, in assessment of oxidative stress. Still, consistently higher isoprostanes among women, smokers, less active persons, and those with higher BMI and plasma triglycerides could reflect higher oxidative stress among these groups. While urinary isoprostanes are indexed to urinary creatinine due to variations in concentration, caution should be exercised when comparing groups with differing serum creatinine.

Funder

National Heart, Lung, and Blood Institute (NHLBI) in collaboration with the University of Alabama at Birmingham

Northwestern University

University of Minnesota

YALTA study

Kaiser Foundation Research Institute

American Heart Association Go Red for Women Strategically Focused Research Network

Blumenthal Scholars Award in Preventive Cardiology at Johns Hopkins University

Publisher

MDPI AG

Subject

Cell Biology,Clinical Biochemistry,Molecular Biology,Biochemistry,Physiology

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