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Anaemia of Chronic Kidney Disease: What We Know Now

机译:慢性肾脏病贫血:我们现在所知道的

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Our understanding of the pathophysiology of the anaemia of chronic kidney disease (CKD) has improved considerably in the last decade with the discovery of the iron regulatory peptide hepcidin. Reduced clearance of hepcidin and the presence of a chronic inflammatory state contribute to elevated hepcidin levels in kidney disease. The recent discovery of the various factors and signalling pathways regulating hepcidin has opened up an exciting avenue for research into the development of newer agents that could treat anaemia of CKD. This review highlights our current understanding of iron metabolism in health, the regulators of hepcidin, issues associated with the current available therapies for the treatment of anaemia in CKD and potential novel therapies that could be available in the near future targeting the various factors that regulate hepcidin.
机译:随着铁调节肽铁调素的发现,我们对慢性肾脏病(CKD)贫血的病理生理学的了解已大大提高。 Hepcidin清除率的降低和慢性炎症状态的存在导致肾脏疾病中hepcidin水平升高。调节铁调素的各种因素和信号通路的最新发现为研究可以治疗CKD贫血的新型药物的研究开辟了令人兴奋的途径。这篇综述强调了我们对健康中铁代谢的了解,铁调素的调节剂,与当前可用于治疗CKD贫血的现有疗法有关的问题以及可能在不久的将来针对调节铁调素的各种因素的潜在新疗法。

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