Jiaqing Wu, Bei Wu, Weili Gao, Yan Wang, Li Zhu, Li Bai, Lixia Lu, Ji Feng, Yanyan Shao, Liangying Gan, Huiping Zhao, Chunfang Wang, Xinju Zhao, Li Zuo
{"title":"贫血透析患者红细胞寿命及相关影响因素分析。","authors":"Jiaqing Wu, Bei Wu, Weili Gao, Yan Wang, Li Zhu, Li Bai, Lixia Lu, Ji Feng, Yanyan Shao, Liangying Gan, Huiping Zhao, Chunfang Wang, Xinju Zhao, Li Zuo","doi":"10.1080/0886022X.2025.2529439","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Renal anemia is one of the most common complications in dialysis patients. The shortened red blood cell (RBC) lifespan is an important mechanism of renal anemia. This study aims to investigate the RBC lifespan and its influencing factors in anemic dialysis patients.</p><p><strong>Method: </strong>Prevalent patients on maintenance hemodialysis or peritoneal dialysis, treated with anti-anemia therapy including recombinant human erythropoietin (rHuEPO) or roxadustat for more than 4 months were enrolled. RBC lifespan was measured by the RBC lifespan analyzer RBCS-01A depended on Levitt's carbon monoxide (CO) breath test. Participants were primarily divided into low and high RBC lifespan groups by the average value.</p><p><strong>Result: </strong>A total of 187 patients were included in this study. The average RBC lifespan was 65.2 ± 28.55 days. The logistic regression analysis indicated treating with roxadustat rather than rHuEPO [OR 2.94, 95% CI (1.46, 5.95), <i>p</i> < 0.01], male [OR 2.15, 95% CI (1.08, 4.29), <i>p</i> = 0.03], higher body mass index (BMI) [OR 1.17, 95% CI (1.07, 1.27), <i>p</i> < 0.01], and higher total iron-binding capacity (TIBC) [OR 1.04, 95% CI (1.01, 1.06), <i>p</i> = 0.01] were independent risk factors for the shorten of RBC lifespan. While higher adjusted calcium [OR 0.14, 95% CI (0.03, 0.70), <i>p</i> = 0.02] and older age [OR 0.96, 95% CI (0.94, 0.99), <i>p</i> = 0.01] were independent protective factors.</p><p><strong>Conclusion: </strong>This study demonstrated that independent risk factors contributing to this reduction in RBC lifespan include male, elevated BMI, increased TIBC, and decreased adjusted calcium levels. 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The shortened red blood cell (RBC) lifespan is an important mechanism of renal anemia. This study aims to investigate the RBC lifespan and its influencing factors in anemic dialysis patients.</p><p><strong>Method: </strong>Prevalent patients on maintenance hemodialysis or peritoneal dialysis, treated with anti-anemia therapy including recombinant human erythropoietin (rHuEPO) or roxadustat for more than 4 months were enrolled. RBC lifespan was measured by the RBC lifespan analyzer RBCS-01A depended on Levitt's carbon monoxide (CO) breath test. Participants were primarily divided into low and high RBC lifespan groups by the average value.</p><p><strong>Result: </strong>A total of 187 patients were included in this study. The average RBC lifespan was 65.2 ± 28.55 days. The logistic regression analysis indicated treating with roxadustat rather than rHuEPO [OR 2.94, 95% CI (1.46, 5.95), <i>p</i> < 0.01], male [OR 2.15, 95% CI (1.08, 4.29), <i>p</i> = 0.03], higher body mass index (BMI) [OR 1.17, 95% CI (1.07, 1.27), <i>p</i> < 0.01], and higher total iron-binding capacity (TIBC) [OR 1.04, 95% CI (1.01, 1.06), <i>p</i> = 0.01] were independent risk factors for the shorten of RBC lifespan. While higher adjusted calcium [OR 0.14, 95% CI (0.03, 0.70), <i>p</i> = 0.02] and older age [OR 0.96, 95% CI (0.94, 0.99), <i>p</i> = 0.01] were independent protective factors.</p><p><strong>Conclusion: </strong>This study demonstrated that independent risk factors contributing to this reduction in RBC lifespan include male, elevated BMI, increased TIBC, and decreased adjusted calcium levels. 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引用次数: 0
摘要
肾性贫血是透析患者最常见的并发症之一。红细胞寿命缩短是肾性贫血的重要机制。本研究旨在探讨贫血透析患者红细胞寿命及其影响因素。方法:采用重组人促红细胞生成素(rHuEPO)或罗沙司他等抗贫血治疗4个月以上的维护性血液透析或腹膜透析患者为研究对象。红细胞寿命由红细胞寿命分析仪RBC - 01a测定,依赖于莱维特一氧化碳呼吸试验。参与者主要根据平均值分为低和高RBC寿命组。结果:本研究共纳入187例患者。红细胞平均寿命为65.2±28.55天。logistic回归分析显示,与rHuEPO相比,给予罗沙他特治疗[OR 2.94, 95% CI (1.46, 5.95), p p = 0.03]、较高的身体质量指数(BMI) [OR 1.17, 95% CI (1.07, 1.27), p p = 0.01]是缩短红细胞寿命的独立危险因素。而高校正钙[OR 0.14, 95% CI (0.03, 0.70), p = 0.02]和老年[OR 0.96, 95% CI (0.94, 0.99), p = 0.01]是独立的保护因素。结论:本研究表明,导致红细胞寿命缩短的独立危险因素包括男性、BMI升高、TIBC增加和调整后钙水平降低。此外,抗贫血治疗的类型似乎对红细胞寿命有影响。
Analysis of red blood cell lifespan and associated influencing factors in anemic dialysis patients.
Introduction: Renal anemia is one of the most common complications in dialysis patients. The shortened red blood cell (RBC) lifespan is an important mechanism of renal anemia. This study aims to investigate the RBC lifespan and its influencing factors in anemic dialysis patients.
Method: Prevalent patients on maintenance hemodialysis or peritoneal dialysis, treated with anti-anemia therapy including recombinant human erythropoietin (rHuEPO) or roxadustat for more than 4 months were enrolled. RBC lifespan was measured by the RBC lifespan analyzer RBCS-01A depended on Levitt's carbon monoxide (CO) breath test. Participants were primarily divided into low and high RBC lifespan groups by the average value.
Result: A total of 187 patients were included in this study. The average RBC lifespan was 65.2 ± 28.55 days. The logistic regression analysis indicated treating with roxadustat rather than rHuEPO [OR 2.94, 95% CI (1.46, 5.95), p < 0.01], male [OR 2.15, 95% CI (1.08, 4.29), p = 0.03], higher body mass index (BMI) [OR 1.17, 95% CI (1.07, 1.27), p < 0.01], and higher total iron-binding capacity (TIBC) [OR 1.04, 95% CI (1.01, 1.06), p = 0.01] were independent risk factors for the shorten of RBC lifespan. While higher adjusted calcium [OR 0.14, 95% CI (0.03, 0.70), p = 0.02] and older age [OR 0.96, 95% CI (0.94, 0.99), p = 0.01] were independent protective factors.
Conclusion: This study demonstrated that independent risk factors contributing to this reduction in RBC lifespan include male, elevated BMI, increased TIBC, and decreased adjusted calcium levels. Additionally, the type of anti-anemia therapy administered appears to have an impact on RBC lifespan.
期刊介绍:
Renal Failure primarily concentrates on acute renal injury and its consequence, but also addresses advances in the fields of chronic renal failure, hypertension, and renal transplantation. Bringing together both clinical and experimental aspects of renal failure, this publication presents timely, practical information on pathology and pathophysiology of acute renal failure; nephrotoxicity of drugs and other substances; prevention, treatment, and therapy of renal failure; renal failure in association with transplantation, hypertension, and diabetes mellitus.