缺铁和促红细胞生成剂对CKD进展中贫血的影响。

IF 1.4 Q3 UROLOGY & NEPHROLOGY
International Journal of Nephrology Pub Date : 2025-09-24 eCollection Date: 2025-01-01 DOI:10.1155/ijne/2567637
Collince Odiwuor Ogolla, Lucy W Karani, Stanslaus Musyoki, Phidelis Maruti
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引用次数: 0

摘要

背景:贫血是慢性肾脏疾病(CKD)患者常见的并发症,发病率在3-5期上升。缺铁和红细胞功能障碍是主要原因。然而,铁的状态和esa的刺激能力在CKD进展中的作用几乎没有得到评估。目的:评价缺铁和ESA治疗在3-5期CKD患者贫血矫正和肾功能保护方面的作用。方法:对2023年1月至2024年12月在某高等院校肾内科就诊的120例CKD患者进行随访观察性研究。将患者分为三组:1组和3组分别为缺铁,不进行ESA和ESA治疗;2组为非缺铁,不进行ESA治疗。测试的参数是基线和治疗后6个月时的血红蛋白水平、血清铁蛋白、转铁蛋白饱和度(TSAT)和肾小球滤过率(eGFR)。欧空局治疗包括依生成素α或达贝生成素α,并根据缺铁情况补充铁。结果:1组基线血红蛋白水平显著降低(9.5±1.2 g/dL),与2组和3组相比,这些受试者的eGFR每年下降速度更快(eGFR年下降速度:3.5±2.3 mL/min/1.73 m2) (p < 0.01)。esa处理组(3组)血红蛋白水平改善最大(12.3±1.5 g/dL),肾功能下降最慢(1.7±1.2 mL/min/1.73 m2)。补铁对铁蛋白和TSAT的影响更大。结论:缺铁是贫血和CKD进展的重要可改变驱动因素。ESA治疗可以改善贫血和延缓肾脏恶化,特别是在补充铁的情况下。早期发现和纠正贫血可能在追求优化的CKD结果中值得相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Iron Deficiency and Erythropoiesis-Stimulating Agents on Anemia in CKD Progression.

Background: Anemia is a frequent complication in patients with chronic kidney disease (CKD), with the incidence rising in stages 3-5. Iron deficiency and defective erythropoiesis are the major causes. Still, the role of iron status and the stimulating capability of ESAs on the progression of CKD have hardly been evaluated. Objective: To assess the effect of iron deficiency and ESA therapy with respect to the correction of anemia and preservation of kidney function in patients with CKD stages 3-5. Methods: A follow-up observational study was carried out in 120 CKD patients at nephrology department in a tertiary institution, from January 2023 to December 2024. The patients were classified into three groups: Group 1 and Group 3 considered iron-deficient, with no ESA and ESA therapy, respectively, while Group 2 was non-iron-deficient with no ESA. The parameters tested were hemoglobin levels, serum ferritin, transferrin saturation (TSAT), and estimated glomerular filtration rate (eGFR) at baseline and at 6 months after treatment. The ESA treatment given consisted of epoetin alfa or darbepoetin alfa, with iron supplementation given according to iron-deficiency status. Results: Baseline hemoglobin levels were significantly lower in Group 1 (9.5 ± 1.2 g/dL), and these subjects were associated with a faster decline of eGFR by value per year (annual decline in eGFR: 3.5 ± 2.3 mL/min/1.73 m2) compared to Groups 2 and 3 (p < 0.01). The ESA-treated group (Group 3) exhibited relatively the greatest improvement in hemoglobin level (to 12.3 ± 1.5 g/dL) and the slowest decline in kidney function (1.7 ± 1.2 mL/min/1.73 m2). Iron supplementation produced greater changes in ferritin and TSAT. Conclusion: Iron deficiency is a paramount modifiable driver of anemia and CKD progression. ESA treatment improves anemia and retards renal deterioration, especially when coupled with iron supplementation. Early detection and correction of anemia might merit interplay in pursuit of optimized CKD outcomes.

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来源期刊
International Journal of Nephrology
International Journal of Nephrology UROLOGY & NEPHROLOGY-
CiteScore
3.40
自引率
4.80%
发文量
44
审稿时长
17 weeks
期刊介绍: International Journal of Nephrology is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies focusing on the prevention, diagnosis, and management of kidney diseases and associated disorders. The journal welcomes submissions related to cell biology, developmental biology, genetics, immunology, pathology, pathophysiology of renal disease and progression, clinical nephrology, dialysis, and transplantation.
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