Pio-Abreu Andrea, de Castro Isac, da Silva Giovanio Vieira, Ortega Katia Coelho, Mion Decio
Hypertension Unit, Renal Division of Hospital das Clínicas, University of São Paulo Medical School, São Paulo, SP, Brazil.
Renal Division of Hospital das Clínicas, University of São Paulo Medical School, São Paulo, SP, Brazil.
Int J Hypertens. 2018 Nov 15;2018:7437858. doi: 10.1155/2018/7437858. eCollection 2018.
Salt sensitivity is associated with an increased cardiovascular risk, but the gold standard method (diet cycles) requires 24-h urine samples and has poor patient compliance.
Test the hypothesis that oral fludrocortisone (0.4 mg per day for 7 days) is a good alternative in identifying salt-sensitive patients.
We conducted a randomized crossover study with 30 hypertensive individuals comprising the following steps: (1) washout; (2) phase A (low- and high-sodium diet cycles); (3) washout 2; (4) phase B (fludrocortisone test). Phase A and B steps were performed in a random way. Consistent with the literature, we found that 53.3% were salt-sensitive according to the reference test. Using the ROC curve, the fludrocortisone test defined salt sensitivity by a median blood pressure increase of ≥3 mmHg. A good accuracy of fludrocortisone in detecting salt sensitivity was observed (AUC: 0.732±0.065; p<0.001), with 80% sensitivity and 53% specificity.
The fludrocortisone test is a good option for screening salt sensitivity in hypertensive patients. However, the low specificity prevents this test from being an ideal substitute to the labor-intensive diet cycles exam in the definition of salt sensitivity. This clinical trial is registered with NCT01453959.
盐敏感性与心血管疾病风险增加相关,但金标准方法(饮食周期法)需要采集24小时尿液样本,且患者依从性较差。
验证口服氟氢可的松(每日0.4毫克,共7天)是识别盐敏感患者的良好替代方法这一假设。
我们对30名高血压患者进行了一项随机交叉研究,包括以下步骤:(1)洗脱期;(2)A阶段(低钠和高钠饮食周期);(3)洗脱期2;(4)B阶段(氟氢可的松试验)。A阶段和B阶段的步骤以随机方式进行。与文献一致,根据参考试验,我们发现53.3%的患者为盐敏感型。使用ROC曲线,氟氢可的松试验将盐敏感性定义为平均血压升高≥3 mmHg。观察到氟氢可的松检测盐敏感性的准确性良好(AUC:0.732±0.065;p<0.001),敏感性为80%,特异性为53%。
氟氢可的松试验是筛查高血压患者盐敏感性的良好选择。然而,低特异性使得该试验在定义盐敏感性时无法成为劳动强度大的饮食周期检查的理想替代方法。该临床试验已在NCT01453959注册。