Harold Simmons Center for Chronic Disease Research and Epidemiology, University of California Irvine Medical Center, Irvine, CA, USA.
Nephrol Dial Transplant. 2013 Jun;28(6):1516-25. doi: 10.1093/ndt/gfs598. Epub 2013 Jan 24.
BACKGROUND: The implications of chemical hyperparathyroidism on bone and mineral metabolism measures in maintenance hemodialysis (MHD) are not well known. We hypothesized that a higher serum intact parathyroid hormone (iPTH) level is associated with the higher likelihood of hyperphosphatemia, hyperphosphatasemia [high serum alkaline phosphatase (ALP) levels] and hypercalcemia. METHODS: Over an 8-year period (July 2001-June 2009), we identified 106 760 MHD patients with iPTH and calcium (Ca), phosphorous (P) and ALP data from a large dialysis clinic. Logistic regression models were examined to assess the association between serum iPTH increments and the likelihood of hyperphosphatemia (P ≥5.5 mg/dL), hypercalcemia (Ca ≥10.2 mg/dL) and hyperphosphatasemia (ALP ≥120 U/L). RESULTS: Patients were 61 ± 16 years old and included 45% women, 59% diabetics and 33% Blacks. Compared with an iPTH level of 100 to <200 pg/mL, patients with an iPTH level of 600-700, 700 to <800 and ≥800 pg/mL had 122% (OR: 2.22, 95% CI: 2.04-2.41), 153% (OR: 2.53, 95% CI: 2.29-2.80) and 243% (OR: 3.43, 95% CI: 3.22-3.66) higher risk of hyperphosphatemia, respectively, and had 109% (OR: 2.09, 95% CI: 1.93-2.26), 130% (OR: 2.30, 95% CI: 2.10-2.52) and 376% (OR: 4.76, 95% CI: 4.50-5.04) higher risk of hyperphosphatasemia, respectively. Compared with an iPTH level of 100 to <200 pg/mL, both the low iPTH (<100 pg/mL, OR: 2.45, 95% CI: 2.27-2.64) and the high iPTH (≥800 pg/mL: OR: 2.13, 95% CI: 1.95-2.33) levels were associated with hypercalcemia. CONCLUSIONS: Higher levels of iPTH are incremental correlates of hyperphosphatemia and hyperphosphatasemia, whereas both very low and high PTH levels are linked to hypercalcemia. If these associations are causal, correction of hyperparathyroidism may have overarching implications on bone and mineral disorders in MHD patients.
背景:甲状旁腺激素(iPTH)化学性亢进对维持性血液透析(MHD)患者的骨和矿物质代谢指标的影响尚不清楚。我们假设较高的血清 iPTH 水平与高磷血症、高磷血症[高血清碱性磷酸酶(ALP)水平]和高钙血症的可能性更高有关。
方法:在 8 年期间(2001 年 7 月至 2009 年 6 月),我们从一个大型透析诊所中确定了 106760 名 MHD 患者,这些患者具有 iPTH 和钙(Ca)、磷(P)和 ALP 数据。使用逻辑回归模型评估血清 iPTH 增量与高磷血症(P≥5.5mg/dL)、高钙血症(Ca≥10.2mg/dL)和高磷血症(ALP≥120U/L)的可能性之间的关联。
结果:患者年龄为 61±16 岁,包括 45%的女性、59%的糖尿病患者和 33%的黑人。与 iPTH 水平为 100-<200pg/mL 相比,iPTH 水平为 600-700、700-<800 和≥800pg/mL 的患者发生高磷血症的风险分别增加 122%(OR:2.22,95%CI:2.04-2.41)、153%(OR:2.53,95%CI:2.29-2.80)和 243%(OR:3.43,95%CI:3.22-3.66),发生高磷血症的风险分别增加 109%(OR:2.09,95%CI:1.93-2.26)、130%(OR:2.30,95%CI:2.10-2.52)和 376%(OR:4.76,95%CI:4.50-5.04)。与 iPTH 水平为 100-<200pg/mL 相比,iPTH 水平较低(<100pg/mL,OR:2.45,95%CI:2.27-2.64)和较高(≥800pg/mL,OR:2.13,95%CI:1.95-2.33)均与高钙血症有关。
结论:较高的 iPTH 水平与高磷血症和高磷血症呈递增相关,而 iPTH 水平非常低和非常高都与高钙血症有关。如果这些关联是因果关系的,那么甲状旁腺功能亢进的纠正可能对 MHD 患者的骨骼和矿物质紊乱产生全面影响。
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