TY - JOUR
T1 - Enhanced blood pressure variability in a high cardiovascular risk group of african Americans
T2 - FIT4Life Study
AU - Veerabhadrappa, Praveen
AU - Diaz, Keith M.
AU - Feairheller, Deborah L.
AU - Sturgeon, Kathleen M.
AU - Williamson, Sheara
AU - Crabbe, Deborah L.
AU - Kashem, Abul
AU - Ahrensfield, Debra
AU - Brown, Michael D.
PY - 2010
Y1 - 2010
N2 - 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 highsensitivity C-reactive protein (hs-CRP), tumor necrosis factor-alpha (TNF-α), 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-α 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.
AB - 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 highsensitivity C-reactive protein (hs-CRP), tumor necrosis factor-alpha (TNF-α), 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-α 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.
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U2 - 10.1016/j.jash.2010.04.005
DO - 10.1016/j.jash.2010.04.005
M3 - Article
C2 - 20885987
AN - SCOPUS:77957719578
SN - 1933-1711
VL - 4
SP - 187
EP - 195
JO - Journal of the American Society of Hypertension
JF - Journal of the American Society of Hypertension
IS - 4
ER -