Navarro J F, Mora C, Jiménez A, Torres A, Macía M, García J
Department of Nephrology and Research Unit, Hospital Nuestra Señora De Candelaria, Santa Cruz de Tenerife, Spain.
Am J Kidney Dis. 1999 Jul;34(1):43-8. doi: 10.1016/s0272-6386(99)70106-x.
Acute magnesium (Mg) infusion decreases patathyroid hormone (PTH) secretion. However, the effect of chronic hypermagnesemia on PTH levels in dialysis patients is not well established. We studied 110 hemodialysis patients (mean age, 55 +/- 14 years; time on dialysis, 35 +/- 28 months) not receiving vitamin D and undergoing dialysis with an Mg dialysate concentration of 1.2 mg/dL. The primary phosphate binder was calcium carbonate, and 43% of the patients also needed aluminum hydroxide. During a 6-month period, calcium (Ca), phosphorus (P), and total serum Mg were measured every 2 months; intact PTH and aluminum (Al) were measured every 6 months. The mean value of each parameter was computed. Hypermagnesemia (serum Mg > 2.47 mg/dL) was observed in 73% of the patients. Mg and Ca were inversely correlated with PTH levels (r = -0.48; P < 0.001 and r = -0.21; P < 0.05, respectively). After adjusting for Ca and P (partial correlation analysis), Mg and PTH were inversely correlated (r = -0.58; P < 0.001). A stepwise multiple regression analysis showed that PTH levels were predicted by Mg (P < 0.001), alkaline phosphatase (P < 0.01), and P levels (P< 0.05; multiple R = 0.57; P < 0.001), whereas Ca level, sex (dummy variable), diabetes (dummy variable), time on dialysis, and Al level were not predictive. Patients with inadequately low PTH levels (relative hypoparathyroidism, PTH < 120 pg/mL; n = 52) showed greater serum Mg concentrations than the rest (n = 58; 3.01 +/- 0.33 v 2.63 +/- 0.38 mg/dL; P < 0.001). In conclusion, serum Mg concentrations in dialysis patients are independently associated with PTH levels, suggesting that chronic hypermagnesemia may decrease PTH secretion and/or synthesis. In addition, chronic hypermagnesemia of dialysis patients may have a role in the pathogenesis of adynamic bone disease.
急性输注镁可降低甲状旁腺激素(PTH)的分泌。然而,慢性高镁血症对透析患者PTH水平的影响尚未完全明确。我们研究了110例未接受维生素D且透析液镁浓度为1.2mg/dL的血液透析患者(平均年龄55±14岁;透析时间35±28个月)。主要的磷结合剂是碳酸钙,43%的患者还需要氢氧化铝。在6个月的时间里,每2个月测量一次钙(Ca)、磷(P)和血清总镁;每6个月测量一次完整的PTH和铝(Al)。计算每个参数的平均值。73%的患者出现高镁血症(血清镁>2.47mg/dL)。镁和钙与PTH水平呈负相关(r=-0.48;P<0.001和r=-0.21;P<0.05)。在调整钙和磷后(偏相关分析),镁与PTH呈负相关(r=-0.58;P<0.001)。逐步多元回归分析显示,PTH水平可由镁(P<0.001)、碱性磷酸酶(P<0.01)和磷水平(P<0.05;复相关系数R=0.57;P<0.001)预测,而钙水平、性别(虚拟变量)、糖尿病(虚拟变量)及透析时间和铝水平无预测作用。PTH水平过低(相对性甲状旁腺功能减退,PTH<120pg/mL;n=52)的患者血清镁浓度高于其余患者(n=58;3.01±0.33对2.63±0.38mg/dL;P<0.001)。总之,透析患者的血清镁浓度与PTH水平独立相关,提示慢性高镁血症可能降低PTH的分泌和/或合成。此外,透析患者的慢性高镁血症可能在动力缺失性骨病的发病机制中起作用。