低氧诱导因子-1α、-2α和红细胞铁酮对慢性肾病3-5期及肾性贫血患者肝磷脂的影响

IF 0.6 4区 医学 Q4 IMMUNOLOGY European Journal of Inflammation Pub Date : 2022-01-01 DOI:10.1177/1721727X221103468
Jianghuai Hong, Jing-Yang Lai, Xiaoying Chen, Yan Yan, Yanyan Hong, Hailun Ke, Jing Zheng
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The serum levels of hepcidin, HIF-1α, HIF-2α, ERFE, and furin were measured using an avidin biotin peroxidase complex enzyme-linked immunosorbent assay to compare the differences between the groups in the related indicators. Results ① Serum HIF-2α, HIF-1α, ERFE, and furin levels increased gradually in the patients with CKD stages 3–5 (p < 0.05, p < 0.01). ②Simple correlation analysis:Serum hepcidin was positively correlated with HIF-2α, ERFE, and HIF-1α in the CKD patients (p < 0.01). ③Serum hepcidin was positively correlated with HIF-2α, HIF-1α, and ERFE in the CKD patients injected with erythropoietin (EPO) (p < 0.01), while serum hepcidin was positively correlated with HIF-2α and HIF-1α (p < 0.01) in the patients not injected with EPO. ④ Multivariate linear regression analysis showed that HIF-1α, (β = 4.36, p < 0.01), serum ferritin(SF) (β = 0.13, p < 0.01), and HIF-2α (β = 0.66, p < 0.01) were significantly correlated with hepcidin. 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引用次数: 1

摘要

目的探讨低氧诱导因子-1α (HIF-1α)、低氧诱导因子-2α (HIF-2α)和红细胞铁酮(ERFE)对慢性肾病(CKD) 3-5期及肾性贫血患者hepcidin的影响。方法选择福建省人民医院肾内科CKD 3 ~ 5期合并肾性贫血患者90例,按CKD分期分为3组,同期在该院体检的健康受试者30例为正常组。采用亲和素生物素过氧化物酶复合物酶联免疫吸附法测定血清hepcidin、HIF-1α、HIF-2α、ERFE和furin水平,比较各组间相关指标的差异。结果①CKD 3 ~ 5期患者血清HIF-2α、HIF-1α、ERFE、furin水平逐渐升高(p < 0.05, p < 0.01)。②简单相关分析:CKD患者血清hepcidin与HIF-2α、ERFE、HIF-1α呈正相关(p < 0.01)。③注射促红细胞生成素(EPO)的CKD患者血清hepcidin与HIF-2α、HIF-1α、ERFE呈正相关(p < 0.01),未注射EPO的CKD患者血清hepcidin与HIF-2α、HIF-1α呈正相关(p < 0.01)。④多元线性回归分析显示,HIF-1α (β = 4.36, p < 0.01)、血清铁蛋白(SF) (β = 0.13, p < 0.01)和HIF-2α (β = 0.66, p < 0.01)与hepcidin呈极显著相关。结论HIF-1α、HIF-2α和SF是影响CKD 3-5期肾性贫血患者hepcidin水平的因素。HIF-1α、HIF-2α和ERFE的升高似乎并没有抑制hepcidin的升高。
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The effects of hypoxia-inducible factors-1α and -2α and erythroferrone on hepcidin in patients with chronic kidney disease stages 3–5 and renal anemia
Objective This study aimed to investigate the effects of hypoxia-inducible factor-1α (HIF-1α), hypoxia-inducible factor-2α (HIF-2α), and erythroferrone (ERFE) on hepcidin in patients with chronic kidney disease (CKD) stages 3–5 and renal anemia. Methods A total of 90 patients with CKD stages 3–5 and renal anemia were selected for the study at the Nephrology Department of Fujian Provincial People’s Hospital and divided into three groups, according to CKD stage, while another 30 healthy subjects who underwent a physical examination at the hospital during the same period were selected as the normal group. The serum levels of hepcidin, HIF-1α, HIF-2α, ERFE, and furin were measured using an avidin biotin peroxidase complex enzyme-linked immunosorbent assay to compare the differences between the groups in the related indicators. Results ① Serum HIF-2α, HIF-1α, ERFE, and furin levels increased gradually in the patients with CKD stages 3–5 (p < 0.05, p < 0.01). ②Simple correlation analysis:Serum hepcidin was positively correlated with HIF-2α, ERFE, and HIF-1α in the CKD patients (p < 0.01). ③Serum hepcidin was positively correlated with HIF-2α, HIF-1α, and ERFE in the CKD patients injected with erythropoietin (EPO) (p < 0.01), while serum hepcidin was positively correlated with HIF-2α and HIF-1α (p < 0.01) in the patients not injected with EPO. ④ Multivariate linear regression analysis showed that HIF-1α, (β = 4.36, p < 0.01), serum ferritin(SF) (β = 0.13, p < 0.01), and HIF-2α (β = 0.66, p < 0.01) were significantly correlated with hepcidin. Conclusion HIF-1α, HIF-2α, and SF are factors which have an effect on hepcidin in patients with CKD stages 3–5 and renal anemia. The increase of HIF-1α, HIF-2α, and ERFE does not seem to inhibit the increase of hepcidin.
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来源期刊
CiteScore
0.90
自引率
0.00%
发文量
54
审稿时长
15 weeks
期刊介绍: European Journal of Inflammation is a multidisciplinary, peer-reviewed, open access journal covering a wide range of topics in inflammation, including immunology, pathology, pharmacology and related general experimental and clinical research.
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