Cohen Jordana B, Stephens-Shields Alisa J, Denburg Michelle R, Anderson Amanda H, Townsend Raymond R, Reese Peter P
Renal, Electrolyte and Hypertension Division, Department of Medicine, Hospital of the University of Pennsylvania, Philadelphia, Pa., USA.
Am J Nephrol. 2016;43(6):431-40. doi: 10.1159/000446862. Epub 2016 May 28.
Obesity substantially increases the risk of the development of chronic kidney disease. Adipose tissue expresses all of the components of the renin-angiotensin system (RAS), contributing to the high prevalence of hypertension in obese patients and driving renal hyperfiltration and subsequent glomerular injury.
We performed a retrospective cohort study using a United Kingdom primary care database, evaluating the effect of time-updated exposure to RAS blockade versus all other antihypertensive medications in obese, hypertensive, non-diabetic patients. We used Cox proportional hazards modeling with and without marginal structural modeling to assess the hazards of developing a primary outcome of 50% reduction in estimated glomerular filtration rate (eGFR) (across 2 consecutive values), end stage renal disease or death.
A total of 219,701 patients met inclusion criteria, with a median 7.2 years of follow-up. Median baseline eGFR was 72.6 ml/min/1.73 m2. Compared to other antihypertensive medications, patients treated with RAS blockade had a modestly elevated hazard of adverse renal outcomes using traditional Cox regression (hazard ratio (HR) 1.04, 95% CI 1.01-1.07) and no significantly increased hazard by marginal structural modeling (HR 1.02, 95% CI 0.97-1.08). Patients treated with RAS blockade had a significantly reduced hazard of incident diabetes, but no significant difference in mortality.
This study, conducted in a large real-world cohort, provides evidence that RAS blockade may not provide benefit with regard to longitudinal renal outcomes in obese, hypertensive patients. Further research is needed to elucidate the hemodynamic and renoprotective role of antihypertensive medications in obese patients.
肥胖显著增加慢性肾脏病发生风险。脂肪组织表达肾素 - 血管紧张素系统(RAS)的所有成分,这导致肥胖患者高血压患病率高,并促使肾脏高滤过及随后的肾小球损伤。
我们使用英国初级保健数据库进行了一项回顾性队列研究,评估肥胖、高血压、非糖尿病患者随时间更新暴露于RAS阻滞剂与所有其他抗高血压药物相比的效果。我们使用Cox比例风险模型,有或没有边际结构模型,以评估发生主要结局的风险,主要结局为估计肾小球滤过率(eGFR)降低50%(连续两个值)、终末期肾病或死亡。
共有219,701名患者符合纳入标准,中位随访时间为7.2年。基线eGFR中位数为72.6 ml/min/1.73 m²。与其他抗高血压药物相比,使用传统Cox回归分析,接受RAS阻滞剂治疗的患者出现不良肾脏结局的风险略有升高(风险比[HR] 1.04,95%可信区间[CI] 1.01 - 1.07),而边际结构模型分析显示风险没有显著增加(HR 1.02,95% CI 0.97 - 1.08)。接受RAS阻滞剂治疗的患者发生糖尿病的风险显著降低,但死亡率无显著差异。
这项在大型真实世界队列中进行的研究提供了证据,表明RAS阻滞剂对于肥胖、高血压患者的纵向肾脏结局可能并无益处。需要进一步研究以阐明抗高血压药物在肥胖患者中的血流动力学和肾脏保护作用。