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Updated: Jan 20, 2026

Assessment of Vascular Function in Patients With Chronic Kidney Disease
Published on: June 16, 2014
Anemia in patients of diabetic kidney disease
Shang-Feng Tsai1,2,3, Der-Cherng Tarng4,5
1Division of Nephrology, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan, ROC.
Insights
Anemia in diabetic kidney disease (DKD) is complex, often severe, and linked to poor outcomes. Prompt anemia correction improves quality of life and cardiovascular health in DKD patients.
Area of Science:
- Nephrology
- Endocrinology
- Cardiology
Background:
- Anemia is a major complication of chronic kidney disease (CKD), impacting quality of life and cardiovascular health.
- Diabetic kidney disease (DKD) is the leading cause of CKD, with anemia developing earlier and being more severe than in non-DKD CKD.
- Mechanisms for DKD anemia include bleeding tendencies, impaired oxygen sensing, inflammation, urinary erythropoietin (EPO) loss, and poor EPO response.
Purpose of the Study:
- To review the complexities of anemia in DKD.
- To discuss current treatment recommendations and emerging therapies for DKD-related anemia.
- To explore the potential renal benefits of SGLT2 inhibitors in DKD patients.
Main Methods:
- Literature review and synthesis of existing research on DKD anemia.
- Analysis of mechanisms contributing to anemia severity in DKD.
- Evaluation of current and potential therapeutic strategies.
Main Results:
- DKD anemia presents unique challenges and requires prompt correction for improved cardiovascular outcomes and quality of life.
- Current guidelines suggest avoiding normalization of hemoglobin (Hb) levels in DKD anemia treatment.
- Sodium glucose cotransporter-2 inhibitors (SGLT2i) show promise for renal benefits, potentially linked to EPO production and improved Hb levels.
Conclusions:
- Anemia in DKD is multifactorial and impacts patient prognosis significantly.
- While EPO therapy has benefits, its renal protective effects in CKD/DKD are less clear.
- SGLT2 inhibitors may offer renal protection in DKD, possibly through mechanisms involving EPO, warranting further investigation.
Abstract:
Anemia is the major complication resulting from chronic kidney disease (CKD) and also a risk factor for cardiovascular events and a poor quality of life (QoL). Diabetic kidney disease (DKD) is the major cause of CKD. Initially, insulin resistance has been reported to increase erythropoiesis, but it might be a minor issue. DKD-related anemia developed earlier and was more severe than non-DKD-related anemia based on more complicated mechanisms, including greater bleeding tendency associated with antiplatelet effect, less O2 sensing due to autonomic neuropathy or renin-angiotensin-aldosterone system inhibitor use, inhibitory effect of inflammatory cytokines, urinary loss of erythropoietin (EPO), and poor response to EPO. In DKD patients, prompt correction of anemia allows for a better cardiovascular outcome and QoL, which are similar to the promising effect of anemia correction in CKD patients. However, current evidence recommended that the avoidance of a high or normalized hemoglobin (Hb) level has been suggested in the treatment of anemia in DKD patients. Despite that EPO has a pleotropic effect on renal protection from animal studies, the renal benefit was less evident in CKD and DKD patients. Recently, the antidiabetic agent, sodium glucose cotransporter-2 inhibitors (SGLT2i), has been reported to exhibit the renal benefits due to the tubulo-glomerular feedback in addition to sugar control. It may also be due to less renal ischemic through higher EPO levels, followed by higher Hb levels. More studies are needed to clarify the link between the renal benefit of SGLT2i and EPO production.
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