Anemia of chronic diseases in the early stages of chronic kidney disease as a risk factor for cardiovascular complications in patients with glomerulonephritis

Pub Date : 2024-07-07 DOI:10.26442/00403660.2024.06.202729
Marina V. Markina, L. Milovanova, Lidia V. Lysenko, S. Milovanova, A. V. Volkov, V. Beketov, Marina V. Lebedeva, Kirill S. Nezhdanov, S. V. Moiseev
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Abstract

Aim. To determine biomarkers of anemia of chronic disease (ACD) in patients with glomerulonephritis (GN) in the early stages of CKD, to assess their role as risk factors for cardiovascular complications (CVС). Materials and methods. Seventy nine patients with GN were studied, among them: 40 with primary сhronic GN (CGN), 39 with secondary forms:19 – GN with ANCA-associated systemic vasculitis, 20 – GN with systemic lupus erythematosus (SLE) at early (all I–II) CKD stages. In all patients, the level of serum C-reactive protein (CRP), hepcidin, interferon γ, and the circulating form of protein Klotho (s-Klotho) were determined. When a relative iron deficiency was detected [transferrin iron saturation coefficient (TSAT) 20%], patients were administered parenterally iron [III] sucrose hydroxide complex (Venofer). Results. The frequency of anemia among patients with systemic diseases is 3.2 times higher than among patients with primary CGN. Patients with anemia (group I; n=43) had higher rates of daily proteinuria (p0.001), systolic blood pressure (p0.05), serum levels of interferon γ (p0.001) and hepcidin (p0.001) and lower values of eGFR (p0.05) than patients without anemia (group II; n=36). A strong inverse correlation was noted between the level of hepcidin and the content of iron in serum (r=-0.856; p0.001), between the level of hemoglobin and the level of interferon γ (r=-0.447; p0.05), hepcidin (r=-0.459; p0.05) and CRP (r=-0.453; p0.05). A significant inverse correlation was found between the level of hemoglobin and CVC risk factors – the value of systolic blood pressure (r=-0.512; p0.05) and the mass index of the left ventricular myocardium (r=-0.619; p0.01). At the same time, the contribution of 2 from 6 analyzed factors, hepcidin and eGFR, to the development of ACD was 92.5%, of which 86.6% accounted for hepcidin. A strong direct correlation was also found between a decrease in hemoglobin level and a decrease in the level of s-Klotho protein (r=0.645; p0.001), a decrease in the level of s-Klotho and an increase in the level of serum hepcidin (r=-0.541; p0.05). The leading value of anemia (beta -0,29; p=0,04) and depression of the s-Klotho level (beta -0,44; p=0,02) as independent cardiovascular risk factors in this group of patients was confirmed by multivariate analysis. In patients with identified deficiency of iron (n=40), after 3–4 weeks of intravenous administration of venofer, the target level of hemoglobin (Нb120 g/l) and transferrin saturation with iron (TSAT20%) were achieved. Conclusion. Among the biomarkers of ACD in patients with immunoinflammatory diseases of the kidneys (primary and secondary СGN), the increase in the serum level of hepcidin is greatest importance. The concomitant to anemia decrease in s-Klotho is a leading risk factor for CVС in CKD. Early correction of ACD with iron supplements makes it possible to achieve target levels of Hb and TSAT and have subsequently a positive effect on the production of s-Klotho and the severity of left ventricular hypertrophia.
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慢性肾脏病早期的慢性病贫血是肾小球肾炎患者出现心血管并发症的风险因素
目的确定慢性病早期肾小球肾炎(GN)患者慢性病贫血(ACD)的生物标志物,评估其作为心血管并发症(CVС)风险因素的作用。材料和方法研究对象为 79 名 GN 患者,其中其中 40 人患有原发性 сhronic GN (CGN),39 人患有继发性 GN:19 人患有 ANCA 相关性系统性血管炎,20 人患有系统性红斑狼疮 (SLE)。所有患者的血清 C 反应蛋白 (CRP)、血钙素、γ 干扰素和 Klotho 蛋白(s-Klotho)循环形式的水平均已测定。当检测到相对缺铁[转铁蛋白铁饱和系数(TSAT)20%]时,给患者服用肠外铁[III]蔗糖氢氧化物复合物(Venofer)。结果全身性疾病患者贫血的频率是原发性 CGN 患者的 3.2 倍。与无贫血患者(II 组;n=36)相比,贫血患者(I 组;n=43)每日蛋白尿(p0.001)、收缩压(p0.05)、血清干扰素 γ (p0.001)和血红蛋白(p0.001)水平较高,而 eGFR 值(p0.05)较低。血红蛋白水平与血清中铁的含量(r=-0.856;p0.001)、血红蛋白水平与干扰素γ(r=-0.447;p0.05)、血红蛋白(r=-0.459;p0.05)和 CRP(r=-0.453;p0.05)之间呈强逆相关。血红蛋白水平与 CVC 风险因素--收缩压值(r=-0.512;p0.05)和左心室心肌质量指数(r=-0.619;p0.01)之间存在明显的反相关性。同时,6个分析因素中有2个因素(血红细胞生成素和肾小球滤过率)对ACD发病的贡献率为92.5%,其中血红细胞生成素占86.6%。血红蛋白水平下降与 s-Klotho 蛋白水平下降(r=0.645;p0.001)、s-Klotho 水平下降与血清血红素水平上升(r=-0.541;p0.05)之间也存在很强的直接相关性。多变量分析证实,贫血(贝塔值-0.29;p=0.04)和 s-Klotho 水平下降(贝塔值-0.44;p=0.02)是该组患者的独立心血管风险因素。在确定缺铁的患者(40 人)中,经过 3-4 周的静脉注射 venofer 后,血红蛋白(Нb120 克/升)和铁转铁蛋白饱和度(TSAT20%)均达到了目标水平。结论在肾脏免疫炎症性疾病(原发性和继发性СGN)患者 ACD 的生物标志物中,血红素血清水平的升高最为重要。在贫血的同时,s-Klotho 的下降是慢性肾脏病患者心血管疾病的主要危险因素。通过补充铁剂及早纠正 ACD 可使血红蛋白和 TSAT 达到目标水平,从而对 s-Klotho 的生成和左心室肥厚的严重程度产生积极影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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