TY - JOUR TI - Free androgen index as a predictor of blood pressure progression and accelerated vascular aging in menopause AU - Georgiopoulos, G.A. AU - Lambrinoudaki, I. AU - Athanasouli, F. AU - Armeni, E. AU - Rizos, D. AU - Kazani, M. AU - Karamanou, M. AU - Manios, E. AU - Augoulea, A. AU - Stellos, K. AU - Papamichael, C. AU - Stamatelopoulos, K. JO - Atherosclerosis PY - 2016 VL - 247 TODO - null SP - 177-183 PB - Elsevier Ireland Ltd SN - 0021-9150 TODO - 10.1016/j.atherosclerosis.2016.02.021 TODO - testosterone; vasoactive agent; androgen; biological marker; hormone, adult; aging; arterial stiffness; Article; blood pressure; cardiovascular disease; clinical assessment; diastolic blood pressure; endothelium; flow mediated dilation; follow up; free androgen index; hemodynamics; human; hypertension; major clinical study; menopause; postmenopause; priority journal; pulse pressure; pulse wave; risk factor; systolic blood pressure; vascular aging; vasodilatation; age; blood; blood pressure; disease course; female; hypertension; middle aged; pathophysiology; predictive value; register; time factor; vascular endothelium, Age Factors; Aging; Androgens; Biomarkers; Blood Pressure; Disease Progression; Endothelium, Vascular; Female; Follow-Up Studies; Hormones; Humans; Hypertension; Middle Aged; Postmenopause; Predictive Value of Tests; Pulse Wave Analysis; Registries; Risk Factors; Time Factors; Vascular Stiffness TODO - Background and aims: We aimed to assess the prognostic value of free androgen index (FAI) and its change over time in arterial stiffness progression, endothelial function and hypertension in postmenopausal women. Methods: Postmenopausal women (n = 180) without clinically overt cardiovascular disease or diabetes were consecutively recruited and followed for a median of 29 months. The main outcome measures were changes over time in endothelial function (FMD), reflected waves, localized and systemic (PWV) arterial stiffness and hypertension. Results: Increased baseline FAI was significantly associated with new onset hypertension (OR for each SD, 2.71, 95% CI 1.14-6.41, p = 0.024), deterioration of pulse wave velocity (PWV) (0.414 m/s per SD), flow-mediated dilation (FMD) (-0.42% per SD), systolic (2.5 mmHg per SD) and pulse pressure progression (2.3 mmHg per SD, p < 0.05 for all). Baseline FAI remained an independent predictor of changes in PWV (p = 0.006), FMD (p = 0.02), peripheral pulse pressure (p = 0.028), transition to new onset hypertension (p = 0.001) and higher BP category (p = 0.012), after adjustment for age, changes in systolic blood pressure, traditional risk factors, vasoactive medication or total testosterone. Baseline FAI improved reclassification for the risk of transition into higher BP category (NRI = 47.5 ± 20.3%, p = 0.02) and abnormal PWV (NRI = 53.4 ± 23.2%, p = 0.021). Similarly, in a subgroup of patients with measured FAI at follow-up, its changes over time predicted changes in PWV, peripheral pulse pressure and hypertension status (p < 0.05 for all). Conclusions: In apparently healthy postmenopausal women, FAI could be a novel biomarker superior to total testosterone for accelerated vascular aging and hypertension status. © 2016 Elsevier Ireland Ltd. ER -