慢性肾病患者缺铁与重大事件风险之间的关系

Gabriel Choukroun, Yasmine Baghdadi, Pascaline Rabiéga, Elise Cazaubon, Serge Maillet, Luc Frimat, Bénédicte Stengel
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引用次数: 0

摘要

简介:铁缺乏症(ID)在慢性肾脏病(CKD)患者中很常见,但诊断率仍然很低,而且在没有贫血的情况下,铁缺乏症的预后也很少被记录。本研究旨在评估缺铁与 CKD 患者主要不良预后风险之间的关系:利用法国慢性肾脏病-肾脏流行病学和信息网络(CKD-REIN)队列的数据,我们估算了ID(定义为铁蛋白水平<100 mg/L和/或转铁蛋白饱和度<20%)的患病率,以及接受替代治疗后肾衰竭、肾衰竭(定义为eGFR<15 mL/min per 1.73 m2 或开始肾脏替代疗法的肾衰竭、全因死亡率以及因心力衰竭死亡或住院:队列中 ID 的基线患病率为 50%(66% 为男性;平均年龄为 67 ± 13 岁)(48-52)。平均血红蛋白为 13 ± 1.7 g/dL,只有 31% 的 ID 患者血红蛋白低于 12 g/dL。在 2,803 名基线期为 2-4 期 CKD 的患者中,ID 与肾衰竭风险显著增加以及肾衰竭替代疗法相关,根据混杂因素和血红蛋白水平调整后的 HR 分别为 1.22 (1.03-1.45) 和 1.57 (1.27-1.94)。全因死亡率和因心力衰竭住院或死亡的调整HR分别为1.31(1.04-1.66)和1.38(1.07-1.80):本研究表明,ID与肾衰竭、全因死亡率和心力衰竭的风险显著相关,与贫血的存在无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association between iron deficiency and risk of major events in chronic kidney disease

Introduction: Iron deficiency (ID) is common in patients with chronic kidney disease (CKD) but remains under-diagnosed and its prognosis poorly documented in the absence of anemia. The aim of the study was to assess the relationship between ID and the risk of major adverse outcomes in patients with CKD.

Methods: Using data from the French Chronic Kidney Disease - Renal Epidemiology and Information Network (CKD-REIN) cohort which included and followed over five years, 3,033 patients with CKD stages 2 to 5 CKD, we estimated the prevalence of ID, defined by a ferritin level < 100 μg/L and/or a transferrin saturation < 20%, and associated hazard ratios (HR) of kidney failure with replacement therapy, kidney failure defined by an eGFR < 15 mL/min per 1.73 m2 or initiation of kidney replacement therapy, all-cause mortality, and death or hospitalization for heart failure.

Results: Baseline prevalence of ID in the cohort (66% men; mean age 67 ± 13 years) was 50% (48-52). Mean hemoglobin was 13 ± 1.7 g/dL, and only 31% of patients with ID also had a hemoglobin < 12 g/dL. In 2,803 patients with CKD stages 2-4 at baseline, ID was associated with significant increased risk of kidney failure, and of kidney failure with replacement therapy, with HRs adjusted for confounders and hemoglobin level of 1.22 (1.03-1.45) and 1.57 (1.27-1.94), respectively. Adjusted HRs for all-cause mortality and hospitalization or death for heart failure, were 1.31 (1.04-1.66) and 1.38 (1.07-1.80), respectively.

Conclusion: This study shows that ID is significantly associated with the risk for kidney failure, all-cause mortality, and heart failure, independent of the presence of anemia.

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