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首页> 外文期刊>Endocrine practice: official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists >Mechanistic and clinical aspects of renin-angiotensin-aldosterone system blockade in the prevention of diabetes mellitus and cardiovascular disease.
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Mechanistic and clinical aspects of renin-angiotensin-aldosterone system blockade in the prevention of diabetes mellitus and cardiovascular disease.

机译:肾素-血管紧张素-醛固酮系统阻滞的机制和临床方面可预防糖尿病和心血管疾病。

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OBJECTIVE: To review the rationale for the use of renin-angiotensin-aldosterone system (RAAS) inhibition to prevent type 2 diabetes mellitus and cardiovascular events and to discuss clinical data evaluating the relationship between RAAS blockade and diabetes prevention. METHODS: PubMed was searched to identify preclinical and clinical data addressing this aim. RESULTS: Potential mechanisms of angiotensin II-mediated insulin resistance and type 2 diabetes may include impaired blood flow and sympathetic activity, increased oxidative stress, alterations in insulin signaling, and effects on adipose tissue. Angiotensin-converting enzyme inhibitors and angiotensin receptor blockers have demonstrated reduced incidences of new-onset diabetes in patients with prediabetes or hypertension and in other cardiovascular populations; however, insight into the corresponding impact on cardiovascular-related morbidity and mortality has been lacking. A recent trial (NAVIGATOR) was designed to evaluate incident diabetes and cardiovascular outcomes as part of its primary endpoint. In this trial, valsartan-based therapy reduced the incidence of new-onset diabetes by 14% relative to placebo over the 5-year follow-up period (P<.001). Cardiovascular outcomes, however, were not significantly affected by active treatment, which may be attributed to a number of potential confounding factors including the low rate of cardiovascular disease at baseline, concurrent implementation of lifestyle modification in all patients, and the substantial use of other risk-reducing agents. CONCLUSIONS: Angiotensin II has been implicated in a number of pathophysiologic processes with the potential to indirectly or directly influence the pathogenesis of insulin resistance and type 2 diabetes. Most clinical trials show a reduced risk of new-onset diabetes with RAAS blockade; however, recent results of the NAVIGATOR trial show that the addition of valsartan to lifestyle modification reduces the risk of diabetes, but does not improve cardiovascular outcomes.
机译:目的:探讨抑制肾素-血管紧张素-醛固酮系统(RAAS)预防2型糖尿病和心血管事件的原理,并讨论评估RAAS阻断与糖尿病预防之间关系的临床数据。方法:对PubMed进行了搜索,以鉴定解决该目标的临床前和临床数据。结果:血管紧张素II介导的胰岛素抵抗和2型糖尿病的潜在机制可能包括血流量和交感障碍,氧化应激增加,胰岛素信号传导改变以及对脂肪组织的影响。血管紧张素转换酶抑制剂和血管紧张素受体阻滞剂已证明在糖尿病前期或高血压患者以及其他心血管疾病人群中降低了新发糖尿病的发病率;然而,缺乏对与心血管相关的发病率和死亡率的相应影响的见解。最近的一项试验(NAVIGATOR)旨在评估糖尿病和心血管事件的预后,作为其主要终点指标的一部分。在该试验中,基于缬沙坦的疗法在5年的随访期内相对于安慰剂使新发糖尿病的发生率降低了14%(P <.001)。但是,积极治疗并未显着影响心血管结局,这可能归因于许多潜在的混杂因素,包括基线时心血管疾病的发生率低,所有患者同时实施生活方式改变以及大量使用其他风险-还原剂。结论:血管紧张素II参与了许多病理生理过程,可能间接或直接影响胰岛素抵抗和2型糖尿病的发病机理。大多数临床试验表明,通过RAAS阻滞可降低新发糖尿病的风险。但是,NAVIGATOR试验的最新结果表明,在生活方式改善中添加缬沙坦可降低患糖尿病的风险,但不会改善心血管疾病的预后。

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