Endothelial Activation Microparticles and Inflammation Status Improve with Exercise Training in African Americans

Author:

Babbitt Dianne M.1,Diaz Keith M.12,Feairheller Deborah L.13,Sturgeon Kathleen M.14,Perkins Amanda M.15,Veerabhadrappa Praveen16,Williamson Sheara T.1,Kretzschmar Jan17,Ling Chenyi17,Lee Hojun17,Grimm Heather17,Thakkar Sunny R.1,Crabbe Deborah L.8,Kashem Mohammed A.8,Brown Michael D.17

Affiliation:

1. Hypertension, Molecular and Applied Physiology Laboratory, Department of Kinesiology, Temple University, 1800 N. Broad Street, Philadelphia, PA 19122, USA

2. Center for Behavioral Cardiovascular Health, Department of Medicine, Columbia University Medical Center, New York, NY 10027, USA

3. ECRI Institute, Health Technology Assessment Group, Plymouth Meeting, PA 19462, USA

4. Institute of Translational Medicine and Therapeutics, University of Pennsylvania, Philadelphia, PA 19104, USA

5. Department of Kinesiology, Missouri State University, Springfield, MO 65897, USA

6. Department of Exercise Science, College of Education, Shippensburg University, Shippensburg, PA 17257, USA

7. Vascular Health Laboratory, Department of Kinesiology & Nutrition, University of Illinois at Chicago, Chicago, IL 60607, USA

8. Division of Cardiology, Department of Medicine, School of Medicine, Temple University, Philadelphia, PA 19140, USA

Abstract

African Americans have the highest prevalence of hypertension in the world which may emanate from their predisposition to heightened endothelial inflammation. The purpose of this study was to determine the effects of a 6-month aerobic exercise training (AEXT) intervention on the inflammatory biomarkers interleukin-10 (IL-10), interleukin-6 (IL-6), and endothelial microparticle (EMP) CD62E+ and endothelial function assessed by flow-mediated dilation (FMD) in African Americans. A secondary purpose was to evaluate whether changes in IL-10, IL-6, or CD62E+ EMPs predicted the change in FMD following the 6-month AEXT intervention. A pre-post design was employed with baseline evaluation including office blood pressure, FMD, fasting blood sampling, and graded exercise testing. Participants engaged in 6 months of AEXT. Following the AEXT intervention, all baseline tests were repeated. FMD significantly increased, CD62E+ EMPs and IL-6 significantly decreased, and IL-10 increased but not significantly following AEXT. Changes in inflammatory biomarkers did not significantly predict the change in FMD. The change inVO2 maxsignificantly predicted the change in IL-10. Based on these results, AEXT may be a viable, nonpharmacological method to improve inflammation status and endothelial function and thereby contribute to risk reduction for cardiovascular disease in African Americans.

Funder

National Heart, Lung, and Blood Institute

Publisher

Hindawi Limited

Subject

Internal Medicine

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