Understanding anaemia of CKD
Anaemia is a common feature of chronic kidney disease,1 and one of the hallmarks of advanced CKD.
The prevalence of anaemia increases as CKD progresses, from 42.5% at stage 3b CKD to 83.7% in people with stage 5 CKD.
Anaemia of CKD was previously attributed primarily to decreased production of erythropoietin (EPO).
It is now known to be caused by a number of factors, including:
Reduced oxygen sensing in the kidney
Reduced erythropoietin production
Chronic inflammation resulting in increased hepcidin levels
Iron deficiency
As CKD progresses:
- EPO production decreases, leading to a reduction in red blood cells and haemoglobin
- Hepcidin levels are elevated due to inflammation and decreased renal excretion
- Elevated hepcidin leads to a reduction in absorption, recycling and mobilisation of iron
CKD, chronic kidney disease; EPO, erythropoietin.
Treatment Challanges
A specialist's view
Management of anaemia of CKD can often be sub-optimal.
Current treatment of anaemia of CKD is mainly based on iron supplements and ESAs (erythropoiesis-stimulating agents).
These treatments target individual factors and not the underlying pathology of anaemia of CKD.
When ESA treatment commences, a state of “functional” iron deficiency may develop as a result of elevated hepcidin levels and increased iron demand, blunting the therapeutic response to ESA.
CKD, chronic kidney disease; ESA, erythropoiesis-stimulating agent.
The need for an alternate treatment option
The limitations of current therapies have highlighted the need for alternative treatment options.
Advances in the study of CKD-associated anaemia have focused on the pathophysiology of anaemia with the hope of discovering more targeted and physiological therapies.
The discovery of hypoxia-inducible factors (HIFs) has led to the development of an alternate category of drugs that stimulate erythropoiesis by activating the HIF pathway.
CKD, chronic kidney disease; HIF, hypoxia-inducible factor.
EVZ_2022_0252_UK / August 2022
Reporting Adverse Events
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. Adverse events should also be reported to SKF Pharma Ltd. on 0800 783 5018