胆钙化醇-碳酸钙联合治疗对iib-iv期慢性肾病患者微量白蛋白尿和蛋白尿的多效作用

M. Polaina Rusillo , M. Ruiz González , M.M. Biechy Baldán , A. Liébana Cañada
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引用次数: 0

摘要

我们对99例iib-iv期慢性肾脏疾病(CKD)患者进行了一项描述性、回顾性研究,接受钙加维生素D治疗继发性甲状旁腺功能亢进(SHPT)。目的:本研究的主要目的是评估微蛋白尿和蛋白尿的减少作为治疗的多效性效果。第二个目的是分析肾功能、甲状旁腺激素值和钙x磷产品是否达到指南推荐值。结果纳入99例患者,平均年龄74.8±10岁(女性60%,男性40%)。最常见的CKD病因是肾硬化(35%),未知病因(25%),慢性间质性肾病(22%),糖尿病(15%)和先天性病因(2%)。50%的患者接受血管紧张素转换酶抑制剂治疗,59%的患者接受血管紧张素受体阻滞剂治疗,10%的患者直接接受肾素抑制剂治疗。糖尿病占34%,高血压占92%。平均治疗时间为430.85天。从基线值到研究结束时的平均变化如下:磷酸肌酸:从2.151到2.27 (P= 0.005);根据体表面积校正的24小时尿肌酐清除率:从33±17 ml/min/1.70 m到32 ml/min (NS):根据肾病患者饮食改变(MDRD)公式估计的肾小球滤过率:从7:28.7 ml/min到28.1 ml/min (NS);用Cockroft-Gault公式估计肌酐清除率:29 ~ 28 ml/min (NS);微量白蛋白尿:352.4 ~ 318.3 mg/天(NS);蛋白尿:0.63 ~ 0.62 (NS);白蛋白/肌酐比值:651±1.3 ~ 615±1.1 mg/g (NS)。在糖尿病患者中,数值如下:微量白蛋白尿:542 ~ 432 mg/天(P< 0.037);蛋白尿:1 ~ 0.8 g/24 h (P< 0.044);校正钙:从9.5到9.6 (P<.004);磷含量:从3.5±0.5到3.6±0.6 (NS);甲状旁腺激素水平:从187到143 pg/ml (P< 0.0001)。钙磷产物为33 34.5 mg2/dl2 (NS)。结论补充钙和维生素D在有效控制糖尿病患者SHPT的同时,可降低尿微量白蛋白和蛋白尿,独立于降压药物和血压控制的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efectos pleiotrópicos del tratamiento combinado con colecalciferol-carbonato cálcico sobre microalbuminuria y proteinuria en pacientes con enfermedad renal crónica estadio iiib-iv

Introduction

We performed a descriptive, retrospective study of 99 patients with stage iiib-iv chronic kidney disease (CKD) receiving calcium plus vitamin D for secondary hyperparathyroidism (SHPT).

Objectives

The main aim of this study was to evaluate reductions in microalbuminuria and proteinuria as a pleiotropic effect of treatment. A secondary aim was to analyze whether renal function, PTH values, and calcium x phosphorus product reached values recommended by guidelines.

Results

We included 99 patients with a mean age 74.8±10 years (60% women and 40% men). The most frequent cause of CKD was nephrosclerosis in 35% of the patients, unknown in 25%, chronic interstitial kidney disease in 22%, diabetes in 15%, and congenital causes in 2%. A total of 50% were receiving angiotensin converting-enzyme inhibitors, 59% were receiving angiotensin receptor blockers, and 10% direct renin inhibitors. Diabetes was present in 34% and hypertension in 92%.

The mean duration of treatment was 430.85 days. The mean changes from baseline values to those at the end of the study were as follows: creatine phosphate: from 2.151 to 2.27 (P=.005); 24-hour urinary creatinine clearance corrected for body surface area: from 33±17 ml/min/1.70 m to 32 ml/min (NS): estimated glomerular filtration rate based on the modification of diet in renal disease (MDRD) formula: from 7: 28.7 ml/min to 28.1 ml/min (NS); creatinine clearance estimated by the Cockroft-Gault formula: from 29 to 28 ml/min (NS); microalbuminuria: from 352.4 to 318.3 mg/day (NS); proteinuria: from 0.63 to 0.62 (NS); and albumin/creatinine ratio: from 651±1.3 to 615±1.1 mg/g (NS).

In diabetic patients, values were as follows: microalbuminuria: from 542 to 432 mg/day (P<.037); proteinuria: from 1 to 0,8 g/24 h (P<.044); corrected calcium: from 9.5 to 9.6 (P<.004); phosphorus levels: from 3.5±0.5 to 3.6±0.6 (NS); PTH levels: from 187 to 143 pg/ml (P<.0001). Calcium × phosphorus product was 33 34.5 mg2/dl2 (NS).

Conclusion

Calcium and vitamin D supplementation in patients with stage iiib-iv CKD in addition to effective control of SHPT in diabetic patients reduced microalbuminuria and proteinuria independently of the action of antihypertensive medication and blood pressure control.

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