Abstract
Objective: Prostate specific antigen (PSA) is an established marker for prostate hypertrophy and cancer. PSA within normal limits reflects both gland hypertrophy and specific inflammation. The aim of the present study was to investigate whether PSA values, within normal levels, are associated with arterial stiffness independently of subclinical inflammation in patients with essential hypertension. Design and Methods: The study comprised 150 consecutive male patients (mean age 60 years) with uncomplicated never-treated essential hypertension. All patients underwent a complete clinical and laboratory evaluation, including PSA levels. Aortic stiffness and arterial wave reflection assessment was made by using carotid femoral (PWVc-f) pulse wave velocity and aortic augmentation index corrected for heart rate (Aix75). Patients with prostate cancer or benign prostate hyperplasia (PSA>4ng/ml) were excluded from the study. Results: PSA levels were positively associated to PWVc-f (r = 0.426, p < 0.001), AIx75 (r = 0.264, p=0.001) and hsCRP (r = 0.376, p < 0.001). When PSA values were grouped in quartiles, patients in the higher quartile presented with higher PWVc-f (p < 0.00001), AIx75 (p < 0.001) and hsCRP (p < 0.001) values. In multivariate analysis after adjustment for the factors affecting arterial stiffness, PSA remained significant determinant of PWVc-f values (R2 = 0.405, p<0.001), while hsCRP was non-significant (p = 0.09). Conclusions: The present study points to an association of PSA levels to aortic stiffness in untreated essential hypertensive males. Potential causal relationships between PSA and arterial stiffness remain to be further explored.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.