Del Vecchio Lucia, Pucci Bella Giulio, Locatelli Francesco
U.O. Nefrologia e Dialisi, ASST Lariana, Como.
U.O. Nefrologia e Dialisi, ASST Lecco, Lecco (Past Director).
G Ital Nefrol. 2024 Oct 9;41(Suppl 83):2024-S83.
Anaemia is a frequent complication of chronic kidney disease; if severe and untreated, it leads to a worsening of quality of life and an increased risk of resorting to haemotransfusions. Beginning with studies in physio-pathology that began in the late 19th century and continued into the 20th century, the first step was the identification of erythropoietin, then its purification, identification of the gene involved and finally the synthesis of recombinant human erythropoietin and its 'long-acting' analogues. Today, therapy with erythropoiesis-stimulating agents (ESAs), often in combination with martial therapy, is the standard of care for patients with chronic kidney disease and anaemia. Recently, ESAs have been joined by HIF-PHD inhibitors. Unfortunately, both categories of drugs, although effective and well-tolerated in most cases, may be associated with a possible increased cardiovascular and thrombotic risk, especially in particular categories of patients. For this reason, the choice of therapy with ESA and HIF-PHD must be customised in terms of haemoglobin target, molecule type and dosage to be used.
贫血是慢性肾脏病常见的并发症;如果严重且未得到治疗,会导致生活质量下降以及输血风险增加。从19世纪末开始并持续到20世纪的生理病理学研究,第一步是鉴定促红细胞生成素,接着是对其进行纯化、鉴定相关基因,最后合成重组人促红细胞生成素及其“长效”类似物。如今,促红细胞生成素刺激剂(ESA)治疗,通常联合铁剂治疗,是慢性肾脏病合并贫血患者的标准治疗方法。最近,缺氧诱导因子脯氨酰羟化酶(HIF-PHD)抑制剂也加入其中。不幸的是,这两类药物虽然在大多数情况下有效且耐受性良好,但可能会增加心血管和血栓形成风险,尤其是在特定类型的患者中。因此,ESA和HIF-PHD治疗的选择必须根据血红蛋白目标、所用分子类型和剂量进行个体化定制。