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Managing a fateful alliance: anaemia and cardiovascular outcomes
1Department of Nephrology and Hypertension, University of Erlangen-Nurember, Germany. med4@rzmail.uni-erlangen.de
Insights
Early anemia correction in chronic kidney disease (CKD) may reduce cardiovascular risk. Recombinant human erythropoietin (rhEPO) treatment shows potential for improving cardiac outcomes, but timing and target hemoglobin levels are crucial.
Area of Science:
- Nephrology
- Cardiology
- Hematology
Background:
- Cardiovascular disease (CVD) is a leading cause of mortality in chronic kidney disease (CKD) patients.
- Anemia is independently associated with increased CVD risk and adverse cardiac remodeling, including left ventricular (LV) growth.
Purpose of the Study:
- To investigate the impact of early anemia correction on cardiovascular risk in CKD patients.
- To evaluate the efficacy of recombinant human erythropoietin (rhEPO) in mitigating cardiac complications associated with anemia.
Main Methods:
- The CREATE study is examining whether early anemia treatment with epoetin beta reduces cardiovascular risk.
- Observational data suggests partial or complete anemia correction can lead to regression of LV hypertrophy and prevent dilatation.
Main Results:
- Partial anemia correction partially reverses LV hypertrophy; complete correction may prevent LV dilatation in hemodialysis patients.
- Pilot studies in non-dialysis patients with CVD showed improved cardiac function and reduced hospitalizations with increased hemoglobin.
- Pre-dialysis epoetin treatment is linked to reduced cardiac disease risk in CKD patients.
Conclusions:
- Early anemia correction in CKD appears crucial for improving cardiovascular prognosis.
- The optimal strategy for anemia management in CKD requires careful consideration of timing and target hemoglobin levels to avoid increased mortality risk in advanced cardiac disease.
Abstract:
Cardiovascular disease (CVD) is a significant complication in chronic kidney disease (CKD) and a major cause of death in dialysis patients. Clinical studies have shown that anaemia is associated with reduced survival in patients with renal disease, heart failure or both. There is also evidence that, even in otherwise healthy individuals, anaemia is independently associated with an increased risk of CVD. The body adapts to anaemia by increasing cardiac output, which may result in cardiac remodelling and progression of left ventricular (LV) growth. Indeed, low haemoglobin (Hb) has been identified as an independent risk factor for LV growth in CKD patients, suggesting that there is a direct link between anaemia and adverse cardiac outcomes. This suggests that correction of anaemia with recombinant human erythropoietin (rhEPO; epoetin) may improve prognosis. Partial correction of anaemia produces partial regression of LV hypertrophy, while complete correction of anaemia can help to prevent LV dilatation in haemodialysis patients with normal LV volumes. Moreover, in non-dialysis patients with advanced CVD, pilot studies showed that a moderate increase in Hb improved cardiac function and reduced hospitalization rates. In addition, consistent epoetin treatment before the start of dialysis was associated with a reduced risk of developing cardiac disease in CKD patients. In contrast, in dialysis patients with advanced cardiac disease, Hb normalization increased mortality risk. Therefore, early correction of anaemia appears important. The Cardiovascular risk Reduction by Early Anaemia Treatment with Epoetin beta (CREATE) study is investigating whether this approach is associated with a measurable reduction in cardiovascular risk.
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