Yoshida Yukina, Takata Tomoaki, Taniguchi Sosuke, Kageyama Kana, Fujino Yudai, Hanada Hinako, Mae Yukari, Iyama Takuji, Hikita Katsuya, Isomoto Hajime
Division of Gastroenterology and Nephrology, Faculty of Medicine, Tottori University, Nishi-cho 36-1, Yonago 683-8504, Tottori, Japan.
Kidney Center, Tottori University Hospital, Nishi-cho 36-1, Yonago 683-8504, Tottori, Japan.
Biomedicines. 2024 Dec 23;12(12):2926. doi: 10.3390/biomedicines12122926.
BACKGROUND/OBJECTIVES: Renal anemia is one of the major complications associated with chronic kidney disease (CKD). Erythropoietin-stimulating agents (ESAs) are commonly used; however, some patients exhibit resistance. Hypoxia-inducible factor prolyl-hydroxylase inhibitors (HIF-PHIs) have emerged as a novel treatment for renal anemia, enhancing erythropoiesis and iron metabolism.
We retrospectively analyzed laboratory data related to erythropoiesis from 105 patients with CKD before and after treatment with HIF-PHI or ESA. The dialysis initiation and mortality rates were also assessed over a median follow-up of 614 days.
HIF-PHI and ESA significantly increased the hemoglobin levels within 6 months of treatment (9.5 ± 1.0 to 10.7 ± 1.1, < 0.01, and 9.9 ± 1.5 to 10.7 ± 1.2 g/dL, < 0.01, respectively). The HIF-PHI group demonstrated a significant decrease in red cell distribution width (14.5 ± 1.9% to 13.8 ± 1.4%, < 0.01), suggesting improved erythropoiesis, and exhibited a lower cumulative incidence of outcomes. The aged-adjusted multivariate analysis confirmed the independent association between HIF-PHI treatment and reduced risk of cumulative outcome ( = 0.042).
HIF-PHIs can serve as an alternative to ESA for managing renal anemia in CKD, improving both hematological parameters and long-term outcomes.
背景/目的:肾性贫血是慢性肾脏病(CKD)的主要并发症之一。促红细胞生成素刺激剂(ESAs)是常用药物;然而,一些患者会出现耐药性。缺氧诱导因子脯氨酰羟化酶抑制剂(HIF-PHIs)已成为治疗肾性贫血的一种新方法,可增强红细胞生成和铁代谢。
我们回顾性分析了105例CKD患者在接受HIF-PHI或ESA治疗前后与红细胞生成相关的实验室数据。在中位随访614天期间,还评估了透析起始率和死亡率。
HIF-PHI和ESA在治疗6个月内均显著提高了血红蛋白水平(分别从9.5±1.0升至10.7±1.1,<0.01;从9.9±1.5升至10.7±1.2 g/dL,<0.01)。HIF-PHI组红细胞分布宽度显著降低(从14.5±1.9%降至13.8±1.4%,<0.01),提示红细胞生成改善,且累积结局发生率较低。年龄调整后的多变量分析证实了HIF-PHI治疗与累积结局风险降低之间的独立关联(=0.042)。
HIF-PHIs可作为ESA的替代药物用于治疗CKD患者的肾性贫血,改善血液学参数和长期结局。