From the Laboratory of Immunoallergy and Proteomics, Department of Immunology (M.M.-L., P.J.M., A.S.-H., G.A.-L.), IIS-Fundación Jiménez Díaz-UAM, Madrid, Spain.
Department of Vascular Physiopathology, Hospital Nacional de Parapléjicos SESCAM, Toledo, Spain (M.B.-M., M.G.B.).
Hypertension. 2019 Apr;73(4):794-802. doi: 10.1161/HYPERTENSIONAHA.118.12242.
Resistant hypertension prevalence is progressively increasing, and prolonged exposure to suboptimal blood pressure control results in higher cardiovascular risk and end-organ damage. Among various antihypertensive agents, spironolactone seems the most effective choice to treat resistant hypertension once triple therapy including a diuretic fails. However success in blood pressure control is not guaranteed, adverse effects are not negligible, and no clinical tools are available to predict patient's response. Complementary to our previous study of resistant hypertension metabolism, here we investigated urinary proteome changes with potential capacity to predict response to spironolactone. Twenty-nine resistant hypertensives were included. A prospective study was conducted and basal urine was collected before spironolactone administration. Patients were classified in responders or nonresponders in terms of blood pressure control. Protein quantitation was performed by liquid chromatography-mass spectrometry; ELISA and target mass spectrometry analysis were performed for confirmation. Among 3310 identified proteins, HP (haptoglobin) and HPR (haptoglobin-related protein) showed the most significant variations, with increased levels in nonresponders compared with responders before drug administration (variation rate, 5.98 and 7.83, respectively). Protein-coordinated responses were also evaluated by functional enrichment analysis, finding oxidative stress, chronic inflammatory response, blood coagulation, complement activation, and regulation of focal adhesions as physiopathological mechanisms in resistant hypertension. In conclusion, protein changes able to predict patients' response to spironolactone in basal urine were here identified for the first time. These data, once further confirmed, will support clinical decisions on patients' management while contributing to optimize the rate of control of resistant hypertensives with spironolactone.
抗药性高血压的患病率呈逐渐上升趋势,而长期血压控制不佳会导致更高的心血管风险和靶器官损害。在各种降压药物中,螺内酯似乎是治疗三联疗法(包括利尿剂)失败后抗药性高血压的最有效选择。然而,血压控制的成功率并不保证,不良反应不容忽视,而且目前还没有临床工具可以预测患者的反应。在我们之前对抗药性高血压代谢的研究基础上,我们在这里研究了尿蛋白质组的变化,以期找到潜在的预测螺内酯反应的能力。共纳入 29 例抗药性高血压患者。进行了一项前瞻性研究,并在螺内酯给药前收集基础尿液。根据血压控制情况,将患者分为应答者和无应答者。通过液相色谱-质谱法进行蛋白质定量;ELISA 和靶向质谱分析进行确认。在鉴定出的 3310 种蛋白质中,HP(触珠蛋白)和 HPR(触珠蛋白相关蛋白)的变化最为显著,与无应答者相比,给药前无应答者的水平升高(变化率分别为 5.98 和 7.83)。通过功能富集分析还评估了蛋白质的协调反应,发现氧化应激、慢性炎症反应、血液凝固、补体激活和焦点黏附的调节是抗药性高血压的生理病理机制。总之,首次在基础尿液中鉴定出能够预测患者对螺内酯反应的蛋白质变化。这些数据一旦得到进一步证实,将支持患者管理的临床决策,并有助于优化螺内酯治疗抗药性高血压的控制率。