Department of Medicine, Division of Nephrology, Medical University of South Carolina, Charleston, SC 29425, USA.
J Hum Hypertens. 2012 Aug;26(8):502-6. doi: 10.1038/jhh.2011.60. Epub 2011 Jun 16.
Hypertension is a major risk factor for the development and progression of chronic kidney disease (CKD). Mineralocorticoid receptor antagonists (MRAs) are effective in the management of resistant hypertension but are not widely used in CKD because of the risk of hyperkalemia. We retrospectively evaluated the long-term effects and safety of MRAs added to a pre-existing antihypertensive regimen in subjects with resistant hypertension associated with stage 3 CKD. In all, 32 patients were treated with spironolactone and 4 with eplerenone for a median follow-up of 312 days. MRAs induced a significant decrease in systolic blood pressure from 162±22 to 138±14 mm Hg (P<0.0001) and in diastolic blood pressure from 87±17 to 74±12 mm Hg (P<0.0001). Serum potassium increased from 4.0±0.5 to 4.4±0.5 mEq l(-1) (P=0.0001), with the highest value being 5.8 mEq l(-1). The serum creatinine increased from 1.5±0.3 to 1.8±0.5 mg dl(-1) (P=0.0004) and the estimated glomerular filtration rate decreased from 48.6±8.7 to 41.2±11.5 ml min(-1) per 1.73 m(2) (P=0.0002). One case of acute renal failure and three cases of significant hyperkalemia occurred. MRAs significantly reduced blood pressure in subjects with resistant hypertension associated with stage 3 CKD, although close biochemical monitoring is recommended because of an increased risk of hyperkalemia and worsening of renal function.
高血压是慢性肾脏病(CKD)发展和进展的主要危险因素。醛固酮受体拮抗剂(MRA)在治疗耐药性高血压方面有效,但由于高钾血症的风险,在 CKD 中并未广泛使用。我们回顾性评估了将 MRA 加入到与 3 期 CKD 相关的耐药性高血压患者的现有降压方案中后的长期疗效和安全性。共有 32 例患者接受螺内酯治疗,4 例患者接受依普利酮治疗,中位随访 312 天。MRA 可显著降低收缩压(从 162±22mmHg 降至 138±14mmHg,P<0.0001)和舒张压(从 87±17mmHg 降至 74±12mmHg,P<0.0001)。血清钾从 4.0±0.5mEq/L 增加至 4.4±0.5mEq/L(P=0.0001),最高值为 5.8mEq/L。血清肌酐从 1.5±0.3mg/dL 增加至 1.8±0.5mg/dL(P=0.0004),估算肾小球滤过率从 48.6±8.7ml/min/1.73m²降低至 41.2±11.5ml/min/1.73m²(P=0.0002)。发生了 1 例急性肾衰竭和 3 例严重高钾血症。MRA 可显著降低与 3 期 CKD 相关的耐药性高血压患者的血压,但由于高钾血症和肾功能恶化的风险增加,建议进行密切的生化监测。