Enhanced blood pressure variability in a high cardiovascular risk group of African Americans: FIT4Life Study.
Publication/Presentation Date
1-1-2010
Abstract
High blood pressure (BP) levels in African Americans elicit vascular inflammation resulting in vascular remodeling. BP variability (BPV) correlates with target organ damage. We aimed to investigate the relationship between inflammatory markers and BPV in African Americans. Thirty-six African Americans underwent 24-hour ambulatory BP monitoring (ABPM). BPV was calculated using the average real variability index. Fasting blood samples were assayed for high-sensitivity C-reactive protein (hs-CRP), tumor necrosis factor-alpha (TNF-alpha), and white blood cell (WBC) count. Significant associations between hs-CRP and 24-hour systolic variability (r=0.50; P=.012) and awake systolic variability (r=0.45; P=.02) were identified after adjusting for age, body mass index, and 24-hour mean BP. ABPM variables were compared between the hs-CRP tertile groups. In post-hoc analysis, there was a significant difference in 24-hour and awake periods for both systolic and diastolic variability among the groups. TNF-alpha and WBC count showed no associations with ABPM variables. hs-CRP was associated with systolic variability, and higher levels of hs-CRP were related with greater BPV. Higher inflammatory status influences wider fluctuations in systolic BP, which in turn could facilitate early progression to target organ damage independent of absolute BP levels in African Americans.
Volume
4
Issue
4
First Page
187
Last Page
195
ISSN
1933-1711
Published In/Presented At
Veerabhadrappa, P., Diaz, K. M., Feairheller, D. L., Sturgeon, K. M., Williamson, S., Crabbe, D. L., Kashem, A., Ahrensfield, D., & Brown, M. D. (2010). Enhanced blood pressure variability in a high cardiovascular risk group of African Americans: FIT4Life Study. Journal of the American Society of Hypertension : JASH, 4(4), 187–195. https://doi.org/10.1016/j.jash.2010.04.005
Disciplines
Medicine and Health Sciences
PubMedID
20885987
Department(s)
Department of Medicine
Document Type
Article