Patange Amit R, Valentini Rudolph P, Du Wei, Pettersen Michael D
Carmen and Ann Adams Department of Pediatrics, Children's Hospital of Michigan, Wayne State University, Detroit, MI, USA.
Pediatr Cardiol. 2012 Jan;33(1):122-8. doi: 10.1007/s00246-011-0101-y. Epub 2011 Sep 13.
Arterial wall stiffness is a recognized complication in children with chronic kidney disease (CKD). Vascular abnormalities in these patients are shown to predate cardiac abnormalities such as left ventricular hypertrophy and diastolic dysfunction. The etiology of vascular abnormalities in these patients currently is not clear. This study explored the relationship between various parameters of calcium-phosphorus metabolism including 25-hydroxy vitamin D and arterial wall stiffness in pediatric patients with CKD. This study investigated a cohort of 43 children with CKD who had no history of underlying congenital or structural cardiac disease. The Augmentation Index (AI), a measure of peripheral arterial reflective properties using radial artery tonometry, was used as an indirect measure of central aortic stiffness. Serum biochemical markers of calcium-phosphorus metabolism were simultaneously measured. Univariate testing showed that AI correlated with worsening kidney function. Serum 25-hydroxy vitamin D levels were low and correlated negatively with AI (r = -0.39; p < 0.05). Multiple regression analysis showed that 25-hydroxy vitamin D was the only significant independent predictor of increased central arterial stiffness in the subgroup of children receiving hemodialysis. No association was observed between AI and any other measured biochemical parameter of calcium-phosphorus metabolism. This is the first study to investigate pediatric patients with CKD that suggests an association between nutritional vitamin D deficiency and increased arterial stiffness in children with CKD. The pathophysiologic mechanisms of vitamin D that regulate increased arterial stiffness need to be integrated further in pediatric CKD patients.
动脉壁僵硬是慢性肾脏病(CKD)患儿公认的一种并发症。这些患者的血管异常被证明早于心脏异常,如左心室肥厚和舒张功能障碍。目前这些患者血管异常的病因尚不清楚。本研究探讨了包括25-羟维生素D在内的钙磷代谢的各种参数与CKD患儿动脉壁僵硬之间的关系。本研究调查了43名无先天性或结构性心脏病病史的CKD患儿队列。使用桡动脉压平测量法测量外周动脉反射特性的增强指数(AI),作为中心主动脉僵硬程度的间接指标。同时测量钙磷代谢的血清生化标志物。单变量测试显示AI与肾功能恶化相关。血清25-羟维生素D水平较低,且与AI呈负相关(r = -0.39;p < 0.05)。多元回归分析显示,在接受血液透析的儿童亚组中,25-羟维生素D是中心动脉僵硬增加的唯一显著独立预测因素。未观察到AI与钙磷代谢的任何其他测量生化参数之间存在关联。这是第一项调查CKD患儿的研究,提示营养性维生素D缺乏与CKD患儿动脉僵硬增加之间存在关联。调节动脉僵硬增加的维生素D的病理生理机制需要在儿童CKD患者中进一步整合。