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首页> 外文期刊>Current opinion in nephrology and hypertension >Erythropoiesis-stimulating agents, hypertension and left ventricular hypertrophy in the chronic kidney disease patient.
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Erythropoiesis-stimulating agents, hypertension and left ventricular hypertrophy in the chronic kidney disease patient.

机译:慢性肾脏病患者的促红细胞生成剂,高血压和左心室肥大。

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PURPOSE OF REVIEW: Left-ventricular hypertrophy (LVH) represents an important marker of cardiovascular morbidity and mortality. Numerous noninterventional studies in patients with chronic kidney disease (CKD) revealed a consistent relationship of LVH with modifiable risk factors attributable to failing renal function, particularly anemia and hypertension. RECENT FINDINGS: Given the clear role for anemia in initiating or accelerating LVH, it seems imperative to correct renal anemia with erythropoiesis-stimulating agents (ESAs). A few nonrandomized studies have described a regression of LVH with correction of anemia, but prospective randomized trials showed no evidence that ESA treatment is able to improve cardiac prognosis in the CKD patient. Current data alert physicians that normalization of hemoglobin in patients with advanced CKD is harmful. Recent studies are now trying to clarify the mechanisms for harm focussing on the influence of comorbidities, ESA doses, and hemoglobin variability. The pathogenesis of hypertension in CKD is multifactorial and only a small percentage of CKD patients have controlled their blood pressure, indicating poor medication adherence, insufficient control of volume overload and undertreatment. SUMMARY: This review provides an update of ESA treatment, hypertension and LVH in the CKD patient, indicating that pathogenesis of LVH in this population is currently not completely understood. In addition, the impact of pharmacological interventions targeted to prevent or reduce LVH in anemic or hypertensive CKD patients is not well defined. As adoption of the Framingham approach seems not feasible in the CKD patient, evidence from large-scale randomized clinical trials is mandatory to resolve this dilemma.
机译:审查目的:左心室肥大(LVH)代表心血管发病率和死亡率的重要标志。对慢性肾脏病(CKD)患者的大量非干预性研究表明,LVH与可归因于肾功能衰竭,尤其是贫血和高血压的可改变危险因素之间存在着一致的关系。最近的发现:鉴于贫血在发起或加速LVH中具有明显作用,因此似乎有必要用促红细胞生成素(ESA)纠正肾性贫血。少数非随机研究描述了贫血纠正后LVH的消退,但前瞻性随机试验没有证据表明ESA治疗能够改善CKD患者的心脏预后。当前数据提醒医生,晚期CKD患者的血红蛋白正常化是有害的。现在,最近的研究正试图阐明危害的机制,重点是合并症,ESA剂量和血红蛋白变异性的影响。 CKD高血压的发病机制是多因素的,只有一小部分CKD患者控制了血压,这表明药物依从性差,对容量超负荷的控制不足和治疗不足。摘要:这篇评论提供了CKD患者的ESA治疗,高血压和LVH的更新,表明该人群中LVH的发病机理目前尚不完全清楚。此外,针对贫血或高血压CKD患者预防或减少LVH的药物干预措施的影响尚不明确。由于在CKD患者中采用Framingham方法似乎不可行,因此必须使用大规模随机临床试验的证据来解决这一难题。

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