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Low-grade albuminuria and cardiovascular risk

机译:低度白蛋白尿和心血管风险

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摘要

Microalbuminuria (MA), conventionally defined as a urinary albumin excretion (UAE) of 30–300 mg/day, is recognised as a marker of endothelial dysfunction. Furthermore, it represents an established risk factor for cardiovascular morbidity and mortality and for end-stage renal disease in individuals with an adverse cardiovascular risk profile. It is common in the general population, particularly in patients with diabetes mellitus or arterial hypertension. There is growing evidence from prospective observational trials that UAE levels well below the current MA threshold (“lowgrade MA”) are also associated with an increased risk of incident cardiovascular disease and allcause mortality. Even in apparently healthy individuals (without diabetes or hypertension), such an association has been shown. As albuminuria screening assays that are reliable even in the lower ranges are commercially available, there may be an important clinical role for MA in disease screening, comparable to the role of blood pressure and lipid screening. MA is modifiable, and the inhibition of the renin-angiotensin system by ACE inhibitors and AT1 receptor antagonists has been shown to result in a lower incidence of cardiovascular events.
机译:微量白蛋白尿(MA)通常定义为30-300 mg /天的尿白蛋白排泄(UAE),被认为是内皮功能障碍的标志。此外,它代表心血管疾病风险状况不良的个体的心血管疾病发病率和死亡率以及终末期肾脏疾病的既定危险因素。它在普通人群中很常见,尤其是在患有糖尿病或高血压的患者中。越来越多的前瞻性观察性试验证据表明,阿联酋的水平远低于当前的MA阈值(“低级MA”)也与发生心血管疾病和全因死亡率的风险增加有关。即使在看起来健康的个体(没有糖尿病或高血压)中,也显示出这种关联。由于即使在较低范围内也可靠的白蛋白尿筛查测定法可商购,因此与血压和脂质筛查的作用相比,MA在疾病筛查中可能具有重要的临床作用。 MA是可改变的,并且已经显示ACE抑制剂和AT1受体拮抗剂对肾素-血管紧张素系统的抑制导致较低的心血管事件发生率。

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