Abstract
Background The hallmark of vascular inflammation is the recruitment of circulating leucocytes, primarily monocytes, macrophages and T lymphocytes, into the vascular wall; however, the link between monocyte/macrophage activation and hypertension has not been established as yet. In this study, we determined how sCD163, a monocyte/macrophage soluble scavenger receptor and immunomodulator, relates to arterial blood pressure (BP) in hypertensive Saudi individuals. Materials and methods A total of 90 (30 non-hypertensive obese, 30 hypertensive obese and 30 lean normotensive controls) adult Saudi subjects, aged 40-60years, participated in this cross-sectional study. Serum fasting blood glucose, triglycerides, total cholesterol, HDL-cholesterol (HDL-C), LDL-cholesterol (LDL-C), leptin, adiponectin, resistin, insulin, tumour necrosis factor-alpha (TNF-α), PAI-1, angiotensin II, high-sensitivity C-reactive protein (hsCRP) and sCD163 were measured in all subjects studied. Results sCD163 concentrations were significantly increased in obese hypertensive patients compared to controls (P=0·016). Positive correlations between sCD163 and body mass index (BMI) (r=0·27, P=0·01), systolic BP (r=0·25, P=0·01), diastolic BP (r=0·33, P=0·001), LDL-C (r=0·21, P=0·04), TNF-α (r=0·23, P=0·02) and hsCRP (r=0·33, P=0·008) were observed. Positive correlations between sCD163 and diastolic BP (r=0·23, P=0·04) and LDL-C (r=0·22, P=0·03) remained significant after controlling for BMI. Conclusions Taken together, these data demonstrate that the monocyte/macrophage activation-related sCD163 is positively associated with BMI and increased arterial BP with the elevation in diastolic BP being independent of the BMI. © 2012 Stichting European Society for Clinical Investigation Journal Foundation.
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Al-Daghri, N. M., Al-Attas, O. S., Bindahman, L. S., Alokail, M. S., Alkharfy, K. M., Draz, H. M., … Chrousos, G. P. (2012). Soluble CD163 is associated with body mass index and blood pressure in hypertensive obese Saudi patients. European Journal of Clinical Investigation, 42(11), 1221–1226. https://doi.org/10.1111/j.1365-2362.2012.02714.x
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