Department of Nephrology, Second University of Naples, Naples, Italy.
Department of Medicine, Veterans Administration San Diego Healthcare System and University of California at San Diego Medical School, San Diego, California.
J Am Coll Cardiol. 2013 Jun 18;61(24):2461-2467. doi: 10.1016/j.jacc.2012.12.061. Epub 2013 Apr 23.
This study sought to evaluate in chronic kidney disease (CKD) prevalence and prognosis of true resistant hypertension (RH) (i.e., confirmed by ambulatory blood pressure [ABP] monitoring).
In CKD, uncontrolled hypertension is a major risk factor, but no study has properly investigated the role of RH.
We prospectively studied 436 hypertensive CKD patients under nephrology care. Four groups were constituted by combining 24-h ABP with diagnosis of RH (office blood pressure ≥130/80 mm Hg, despite adherence to ≥3 full-dose antihypertensive drugs including a diuretic agent or ≥4 drugs): control (ABP <125/75 mm Hg without RH); pseudoresistance (ABP <125/75 mm Hg with RH); sustained hypertension (ABP ≥125/75 mm Hg without RH); and true resistance (ABP ≥125/75 mm Hg with RH). Endpoints of survival analysis were renal (end-stage renal disease or death) and cardiovascular events (fatal and nonfatal cardiovascular event).
Age was 65 ± 14 years, men 58%, diabetes 36%, cardiovascular disease 30%, median proteinuria 0.24 (interquartile range 0.09 to 0.83) g/day, estimated glomerular filtration rate 43 ± 20 ml/min/1.73 m(2), office blood pressure 146 ± 19/82 ± 12 mm Hg, and 24-h ABP 129 ± 17/72 ± 10 mm Hg. True resistant patients were 22.9%, and pseudoresistant patients were 7.1%, whereas patients with sustained hypertension were 42.9%, and control subjects were 27.1%. Over 57 months of follow-up, 109 cardiovascular events and 165 renal events occurred. Cardiovascular risk (hazard ratio [95% confidence interval]) was 1.24 (0.55 to 2.78) in pseudoresistance, 1.11 (0.67 to 1.84) in sustained hypertension, and 1.98 (1.14 to 3.43) in true resistance, compared with control subjects. Corresponding hazards for renal events were 1.18 (0.45 to 3.13), 2.14 (1.35 to 3.40), and 2.66 (1.62 to 4.37).
In CKD, pseudoresistance is not associated with an increased cardio-renal risk, and sustained hypertension predicts only renal outcome. True resistance is prevalent and identifies patients carrying the highest cardiovascular risk.
本研究旨在评估慢性肾脏病(CKD)中真性难治性高血压(RH)(即通过动态血压监测[ABP]证实)的患病率和预后。
在 CKD 中,未控制的高血压是一个主要的危险因素,但尚无研究充分探讨 RH 的作用。
我们前瞻性研究了 436 名在肾病科接受治疗的高血压 CKD 患者。根据 24 小时 ABP 和 RH 诊断(诊室血压≥130/80mmHg,尽管使用了≥3 种全剂量降压药物,包括利尿剂或≥4 种药物),将患者分为 4 组:对照组(ABP<125/75mmHg 且无 RH);假性抵抗组(ABP<125/75mmHg 且有 RH);持续高血压组(ABP≥125/75mmHg 且无 RH);真性抵抗组(ABP≥125/75mmHg 且有 RH)。生存分析的终点是肾脏(终末期肾病或死亡)和心血管事件(致死性和非致死性心血管事件)。
患者年龄为 65±14 岁,男性占 58%,糖尿病占 36%,心血管疾病占 30%,中位蛋白尿 0.24(四分位间距 0.09 至 0.83)g/天,估算肾小球滤过率 43±20ml/min/1.73m²,诊室血压 146±19/82±12mmHg,24 小时 ABP 129±17/72±10mmHg。真性抵抗患者占 22.9%,假性抵抗患者占 7.1%,持续高血压患者占 42.9%,对照组占 27.1%。在 57 个月的随访期间,发生了 109 次心血管事件和 165 次肾脏事件。与对照组相比,心血管风险(危险比[95%置信区间])在假性抵抗组为 1.24(0.55 至 2.78),在持续高血压组为 1.11(0.67 至 1.84),在真性抵抗组为 1.98(1.14 至 3.43)。相应的肾脏事件风险在假性抵抗组为 1.18(0.45 至 3.13),在持续高血压组为 2.14(1.35 至 3.40),在真性抵抗组为 2.66(1.62 至 4.37)。
在 CKD 中,假性抵抗与增加的心血管-肾脏风险无关,而持续高血压仅预测肾脏结局。真性抵抗很常见,并确定了具有最高心血管风险的患者。