Journal of hypertension | 2019
Impact of kidney transplantation on aortic stiffness and aortic stiffness index β0.
Abstract
BACKGROUND\nIn chronic kidney disease, the enhanced aortic stiffness increases risk of cardiovascular events. Kidney transplantation (KTx) may improve aortic stiffness; however, it is unclear whether the improvement of aortic stiffness is merely the outcome of the reduction of blood pressure (BP) post-KTx. Furthermore, the long-term trajectory of aortic stiffness remains uncertain, as activation of the immune system may have a negative long-term impact on arterial wall property.\n\n\nMETHOD\nUsing aortic stiffness β0 as a BP-independent stiffness parameter, and a statistical adjustment for BP, we aimed to examine the early vs. late changes in aortic stiffness, and to define the characteristics of patients with favourable and unfavourable long-term trajectories of aortic stiffness. In this longitudinal study, aortic stiffness was assessed before, 3, 6 and 24 months after KTx in 79 individuals. Aortic stiffness was determined by carotid-femoral pulse wave velocity (cf-PWV), and aortic stiffness index β0 was obtained by applying the stiffness parameter β0 theory to cf-PWV based on Bramwell-Hill s equation using a reference pressure.\n\n\nRESULTS\nThere was an early reduction of β0 3 months after KTx (29.0\u200a±\u200a2.0 to 25.8\u200a±\u200a1.2, P\u200a=\u200a0.033) followed by a gradual increase at 6 (28.0\u200a±\u200a1.4, P\u200a=\u200a0.005 vs. 3 months) and 24 months (28.3\u200a±\u200a1.3, P\u200a=\u200a0.003 vs. 3 months). A late increase in β0 was associated with higher levels of the interleukin-6 (P\u200a=\u200a0.029) even after adjustment for potential cofounders. Using statistical adjustments for BP showed similar results.\n\n\nCONCLUSION\nReduction of aortic stiffness index β0 3 months after KTx suggests that KTx leads to an early de-stiffening of the intrinsic mechanical properties of aorta. However, this improvement is followed by a later stiffening, which is associated with increased interleukin-6, suggesting that activation of the immune system may be involved in arterial wall remodelling in kidney recipients.