Division of Nephrology and Hypertension, Department of Medicine, University of Miami Miller School of Medicine, Miami, FL, USA.
Nephrol Dial Transplant. 2011 Apr;26(4):1258-65. doi: 10.1093/ndt/gfr026. Epub 2011 Mar 7.
Secondary hyperparathyroidism is a common complication of chronic kidney disease (CKD) that is associated with bone disease, cardiovascular disease and death. Pathophysiological factors that maintain secondary hyperparathyroidism in advanced CKD are well-known, but early mechanisms of the disease that can be targeted for its primary prevention are poorly understood. Diuretics are widely used to control volume status and blood pressure in CKD patients but are also known to have important effects on renal calcium handling, which we hypothesized could alter the risk of secondary hyperparathyroidism.
We examined the relationship of diuretic treatment with urinary calcium excretion, parathyroid hormone (PTH) levels and prevalence of secondary hyperparathyroidism (PTH ≥ 65 pg/mL) in a cross-sectional study of 3616 CKD patients in the Chronic Renal Insufficiency Cohort.
Compared with no diuretics, treatment with loop diuretics was independently associated with higher adjusted urinary calcium (55.0 versus 39.6 mg/day; P < 0.001), higher adjusted PTH [67.9, 95% confidence interval (CI) 65.2-70.7 pg/mL, versus 52.8, 95% CI 51.1-54.6 pg/mL, P < 0.001] and greater odds of secondary hyperparathyroidism (odds ratio 2.1; 95% CI 1.7-2.6). Thiazide monotherapy was associated with lower calciuria (25.5 versus 39.6 mg/day; P < 0.001) but only modestly lower PTH levels (50.0, 95% CI 47.8-52.3, versus 520.8, 95% CI 51.1-54.6 pg/mL, P = 0.04) compared with no diuretics. However, coadministration of thiazide and loop diuretics was associated with blunted urinary calcium (30.3 versus 55.0 mg/day; P <0.001) and odds of hyperparathyroidism (odds ratio 1.3 versus 2.1; P for interaction = 0.05) compared with loop diuretics alone.
Loop diuretic use was associated with greater calciuria, PTH levels and odds of secondary hyperparathyroidism compared to no treatment. These associations were attenuated in patients who were coadministered thiazides. Diuretic choice is a potentially modifiable determinant of secondary hyperparathyroidism in CKD.
继发性甲状旁腺功能亢进症是慢性肾脏病(CKD)的常见并发症,与骨病、心血管疾病和死亡有关。维持晚期 CKD 中继发性甲状旁腺功能亢进症的病理生理因素众所周知,但针对其一级预防的疾病早期机制知之甚少。利尿剂被广泛用于控制 CKD 患者的容量状态和血压,但也已知对肾脏钙处理有重要影响,我们假设这可能会改变继发性甲状旁腺功能亢进症的风险。
我们在慢性肾功能不全队列中对 3616 例 CKD 患者进行了横断面研究,检查了利尿剂治疗与尿钙排泄、甲状旁腺激素(PTH)水平和继发性甲状旁腺功能亢进症(PTH≥65pg/mL)患病率的关系。
与未使用利尿剂相比,使用袢利尿剂与更高的校正尿钙(55.0 与 39.6mg/天;P<0.001)、更高的校正 PTH[67.9,95%置信区间(CI)65.2-70.7pg/mL,与 52.8,95%CI51.1-54.6pg/mL,P<0.001]和继发性甲状旁腺功能亢进症的更高几率(比值比 2.1;95%CI1.7-2.6)相关。噻嗪类单药治疗与尿钙减少相关(25.5 与 39.6mg/天;P<0.001),但与未使用利尿剂相比,PTH 水平仅略有降低(50.0,95%CI47.8-52.3,与 520.8,95%CI51.1-54.6pg/mL,P=0.04)。然而,与单独使用袢利尿剂相比,噻嗪类和袢利尿剂联合使用与尿钙减少(30.3 与 55.0mg/天;P<0.001)和甲状旁腺功能亢进症的几率(比值比 1.3 与 2.1;P 交互=0.05)相关。
与不治疗相比,袢利尿剂的使用与更高的尿钙、PTH 水平和继发性甲状旁腺功能亢进症的几率相关。在联合使用噻嗪类药物的患者中,这些相关性减弱。利尿剂的选择是 CKD 中继发性甲状旁腺功能亢进症的一个潜在可改变的决定因素。