Owen Jonathan G, Reisin Efrain
Section of Nephrology and Hypertension, Louisiana State University Health Sciences Center, 1542 Tulane Avenue, Room 330, Box T4M-2, New Orleans, LA, 70112, USA,
Curr Hypertens Rep. 2015 Jun;17(6):558. doi: 10.1007/s11906-015-0558-9.
Epidemiological studies have shown an increasing prevalence of obesity and the metabolic syndrome worldwide. Lifestyle modifications that include dietary changes, weight reduction, and exercise are the cornerstones in the treatment of this pathology. However, adherence to this approach often meets with failure in clinical practice; therefore, drug therapy should not be delayed. The ideal pharmacological antihypertensive regimen should target the underlying mechanisms involved in this syndrome, including sympathetic activation, increased renal tubular sodium reabsorption, and overexpression of the renin-angiotensin-aldosterone system by the adipocyte. Few prospective trials have been conducted in the search of the ideal antihypertensive regimen in patients with obesity and the metabolic syndrome. We summarize previously published ad hoc studies, prospective studies, and guideline publications regarding the treatment of hypertension in patients with obesity and the metabolic syndrome. We conclude that the optimal antihypertensive drug therapy in these patients has not been defined. Though caution exists regarding the use of thiazide diuretics due to potential metabolic derangements, there is insufficient data to show worsened cardiovascular or renal outcomes in patients treated with these drugs. In regard to beta blockers, the risk of accelerating conversion to diabetes and worsening of inflammatory mediators described in patients treated with traditional beta blockers appears much less pronounced or absent when using the vasodilating beta blockers. Renin-angiotensin-aldosterone system (RAAS) inhibition with an ACE or an ARB and treatment with calcium channel blockers appears safe and well tolerated in obesity-related hypertension and in patients with metabolic syndrome. Future prospective pharmacological studies in this population are needed.
流行病学研究表明,全球肥胖症和代谢综合征的患病率正在上升。包括饮食改变、减重和运动在内的生活方式调整是治疗这种病症的基石。然而,在临床实践中,坚持这种方法往往会失败;因此,药物治疗不应延迟。理想的药理学降压方案应针对该综合征所涉及的潜在机制,包括交感神经激活、肾小管钠重吸收增加以及脂肪细胞中肾素 - 血管紧张素 - 醛固酮系统的过度表达。在肥胖症和代谢综合征患者中寻找理想降压方案的前瞻性试验很少。我们总结了先前发表的关于肥胖症和代谢综合征患者高血压治疗的专项研究、前瞻性研究和指南出版物。我们得出结论,这些患者的最佳降压药物治疗方案尚未确定。尽管由于潜在的代谢紊乱,使用噻嗪类利尿剂存在谨慎之处,但尚无足够数据表明使用这些药物治疗的患者心血管或肾脏结局会恶化。关于β受体阻滞剂,与使用血管舒张性β受体阻滞剂相比,传统β受体阻滞剂治疗的患者中所述的加速转化为糖尿病和炎症介质恶化的风险似乎不太明显或不存在。在肥胖相关高血压和代谢综合征患者中,使用ACE或ARB抑制肾素 - 血管紧张素 - 醛固酮系统(RAAS)以及使用钙通道阻滞剂进行治疗似乎是安全且耐受性良好的。需要对该人群进行未来的前瞻性药理学研究。