Streja Elani, Lau Wei Ling, Goldstein Leanne, Sim John J, Molnar Miklos Z, Nissenson Allen R, Kovesdy Csaba P, Kalantar-Zadeh Kamyar
Harold Simmons Center for Kidney Disease Research and Epidemiology, Division of Nephrology and Hypertension, University of California, Irvine School of Medicine , Orange, California, USA.
Kaiser Permanente , Los Angeles, California, USA.
Kidney Int Suppl (2011). 2013 Dec;3(5):462-468. doi: 10.1038/kisup.2013.96.
Elevated serum phosphorus is associated with higher death risk in hemodialysis patients. Previous studies have suggested that both higher serum parathyroid hormone (PTH) level and higher dietary protein intake may contribute to higher serum phosphorus levels. However, it is not well known how these two factors simultaneously contribute to the combined risk of hyperphosphatemia in real patient-care scenarios. We hypothesized that the likelihood of hyperphosphatemia increases across higher serum PTH and higher normalized protein catabolic rate (nPCR) levels, a surrogate of protein intake. Over an 8-year period (July 2001-June 2009), we identified 69,355 maintenance hemodialysis patients with PTH, nPCR, and phosphorus data in a large dialysis provider. Logistic regression models were examined to assess the association between likelihood of hyperphosphatemia (serum phosphorus >5.5 mg/dl) and serum PTH and nPCR increments. Patients were 61±15 years old and included 46% women, 33% blacks, and 57% diabetics. Both higher serum PTH level and higher protein intake were associated with higher risk of hyperphosphatemia in dialysis patients. Compared with patients with PTH level 150-<300 pg/ml and nPCR level 1.0-<1.2 g/kg/day, patients with iPTH>600 pg/ml and nPCR>1.2 g/kg/day had a threefold higher risk of hyperphosphatemia (OR: 3.17, 95% CI: 2.69-3.75). Hyperphosphatemia is associated with both higher dietary protein intake and higher serum PTH level in maintenance hemodialysis patients. Worsening or resistant hyperphosphatemia may be an under-appreciated consequence of secondary hyperparathyroidism independent of dietary phosphorus load. Management of hyperphosphatemia should include diligent correction of hyper-parathyroidism while maintaining adequate intake of high protein foods with low phosphorus content.
血清磷升高与血液透析患者较高的死亡风险相关。先前的研究表明,较高的血清甲状旁腺激素(PTH)水平和较高的膳食蛋白质摄入量都可能导致较高的血清磷水平。然而,在实际的患者护理场景中,这两个因素如何同时导致高磷血症的综合风险,目前尚不清楚。我们假设,随着血清PTH水平升高和蛋白质摄入量替代指标——标准化蛋白质分解代谢率(nPCR)水平升高,高磷血症的可能性会增加。在8年期间(2001年7月至2009年6月),我们在一家大型透析服务提供商中确定了69355例有PTH、nPCR和磷数据的维持性血液透析患者。采用逻辑回归模型评估高磷血症(血清磷>5.5mg/dl)的可能性与血清PTH和nPCR升高之间的关联。患者年龄为61±15岁,其中女性占46%,黑人占33%,糖尿病患者占57%。较高的血清PTH水平和较高的蛋白质摄入量均与透析患者高磷血症风险较高相关。与PTH水平为150-<300pg/ml且nPCR水平为1.0-<1.2g/kg/天的患者相比,iPTH>600pg/ml且nPCR>1.2g/kg/天的患者发生高磷血症的风险高三倍(OR:3.17,95%CI:2.69-3.75)。在维持性血液透析患者中,高磷血症与较高的膳食蛋白质摄入量和较高的血清PTH水平均相关。继发性甲状旁腺功能亢进导致的高磷血症恶化或难治可能是一个未得到充分认识的后果,与膳食磷负荷无关。高磷血症的管理应包括在维持低磷含量的高蛋白食物充足摄入的同时,积极纠正甲状旁腺功能亢进。