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Association between urinary angiotensinogen excretion rates and left ventricular mass index and carotid intima–media thickness in hypertensive kidney transplant recipients
Author(s) -
Tiryaki Ozlem,
Usalan Celalettin
Publication year - 2015
Publication title -
clinical transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.918
H-Index - 76
eISSN - 1399-0012
pISSN - 0902-0063
DOI - 10.1111/ctr.12521
Subject(s) - medicine , left ventricular hypertrophy , blood pressure , urinary system , proteinuria , intima media thickness , creatinine , endocrinology , cardiology , body mass index , muscle hypertrophy , kidney , renin–angiotensin system , risk factor , urology , carotid arteries
Objectives The renin‐angiotensin system (RAS) is thought to regulate blood pressure and to be an independent risk factor for the development of left ventricular hypertrophy (LVH) and carotid intima–media thickness (CIMT). Locally produced RAS in most tissues has been recently described. It has been reported that urinary angiotensinogen levels provide a specific index of the intrarenal RAS status and is significantly correlated with blood pressure and proteinuria. The aim of this study was to evaluate the relationship of local intrarenal RAS with LVH and CIMT in hypertensive renal transplant recipients (RTRs). Results A total of 96 non‐diabetic RTRs (50 hypertensive patients, 46 normotensive patients) were included in this study. Urinary angiotensinogen (UAGT)/urinary creatinine (Ucre) was significantly higher in hypertensive patients compared with normotensive patients (p < 0.01). Left ventricular mass (LVM)I and CIMT were significantly higher in hypertensive patients compared with the normotensive patients (p < 0.01). Importantly, a significant positive correlation was found between UAGT/Ucre levels and LVMI ( r = 0.724, p = 0.012) and also CIMT ( r = 0.452, p = 0.02) in hypertensive RTRs. Conclusions These data indicate that UAGT is increased in hypertensive RTRs, and local RAS may play an important role in the development of cardiovascular abnormalities in hypertensive renal transplant recipients.