III Medizinische Klinik, Universitätsklinikum Hamburg Eppendorf, Hamburg, Germany.
Semin Nephrol. 2013 Jan;33(1):66-74. doi: 10.1016/j.semnephrol.2012.12.009.
Obesity is an increasingly observed pathologic entity in the industrialized world and causally linked to the development of hypertension. Consequently, not only the prevalence of obesity but also the prevalence of obesity hypertension is increasing worldwide. In the context of antihypertensive treatment, data from clinical trials indicate that all first-line antihypertensive drugs possess a similar efficacy in reducing systemic blood pressure and hypertension-related end-organ damage in obese hypertensive subjects. Nevertheless, some antihypertensive agents, such as β-blockers or thiazide diuretics, may have unwanted side effects on the metabolic and hemodynamic abnormalities that occur in both obesity and hypertension. However, current guidelines still do not include recommendations for state-of-the-art treatment of obese patients with hypertension. Hence, the aim of this article is to provide recommendations for the appropriate use of antihypertensive agents in obese patients mostly based on personal expertise and pathophysiologic assumptions. For instance, thiazide diuretics and β-blockers are reported to reduce insulin sensitivity and (at least transiently) increase triglyceride and low-density lipoprotein cholesterol levels, whereas calcium channel blockers are metabolically neutral and angiotensin-converting enzyme inhibitors, angiotensin-receptor blockers, and renin inhibition may increase insulin sensitivity. The renin-angiotensin-aldosterone system in the adipose tissue has been implicated in the development of arterial hypertension and sodium retention plays a central role in the development of obesity-related hypertension. Therefore, treatment with a blocker of the renin-angiotensin-aldosterone-system and a thiazide diuretic should be considered as first-line antihypertensive drug therapy in obesity hypertension.
肥胖症是工业化世界中越来越常见的病理实体,与高血压的发生有因果关系。因此,不仅肥胖症的患病率在增加,肥胖相关性高血压的患病率也在全球范围内增加。在抗高血压治疗方面,临床试验数据表明,所有一线抗高血压药物在降低肥胖高血压患者的系统性血压和与高血压相关的终末器官损伤方面均具有相似的疗效。然而,一些抗高血压药物,如β受体阻滞剂或噻嗪类利尿剂,可能会对肥胖和高血压中发生的代谢和血液动力学异常产生不良的副作用。然而,目前的指南仍然没有包括对肥胖高血压患者的最新治疗建议。因此,本文的目的是根据个人专业知识和病理生理假设,为肥胖患者的抗高血压药物的合理使用提供建议。例如,噻嗪类利尿剂和β受体阻滞剂被报道会降低胰岛素敏感性,并(至少暂时)增加甘油三酯和低密度脂蛋白胆固醇水平,而钙通道阻滞剂在代谢上是中性的,血管紧张素转换酶抑制剂、血管紧张素受体阻滞剂和肾素抑制可能会增加胰岛素敏感性。脂肪组织中的肾素-血管紧张素-醛固酮系统与动脉高血压的发生有关,而钠潴留在肥胖相关性高血压的发生中起着核心作用。因此,对于肥胖相关性高血压患者,应考虑使用肾素-血管紧张素-醛固酮系统阻滞剂和噻嗪类利尿剂作为一线抗高血压药物治疗。