Diabetes, anemia and CKD: Why TREAT?
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1Renal Division, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA. asingh@partners.org
Insights
Treating anemia in type 2 diabetes patients with chronic kidney disease (CKD) using darbepoetin did not improve mortality or cardiovascular outcomes. This anemia treatment increased stroke and cancer death risks, questioning its use in CKD patients.
Area of Science:
- Nephrology
- Endocrinology
- Cardiology
Background:
- Anemia is common in patients with diabetes mellitus and chronic kidney disease (CKD), increasing mortality and cardiovascular risks.
- Epoetin alfa revolutionized anemia treatment in CKD, but newer studies question risks associated with erythropoiesis-stimulating agents.
- The TREAT study investigated darbepoetin's efficacy and safety in anemic type 2 diabetic patients with CKD.
Purpose of the Study:
- To evaluate the effect of darbepoetin alfa on mortality and cardiovascular events in anemic type 2 diabetic patients with CKD.
- To assess the impact of darbepoetin alfa on renal events, stroke, thromboembolic complications, and cancer deaths.
- To determine the effect on health-related quality of life.
Main Methods:
- Randomized controlled trial (TREAT study) involving type 2 diabetic patients with CKD and anemia.
- Patients were randomized to receive darbepoetin alfa or placebo.
- Outcomes included mortality, cardiovascular events, renal events, stroke, thromboembolic complications, cancer deaths, and quality of life.
Main Results:
- Darbepoetin alfa treatment did not reduce mortality or cardiovascular/renal events.
- A twofold higher rate of stroke and thromboembolic complications was observed in the darbepoetin group.
- Cancer deaths were higher, and quality of life improvements were modest and inconsistent.
Conclusions:
- Anemia treatment with darbepoetin alfa in type 2 diabetic patients with CKD offers no mortality or cardiovascular benefit.
- The risks of stroke, thromboembolism, and cancer deaths outweigh potential benefits.
- Current evidence questions the routine use of erythropoiesis-stimulating agents for anemia in this high-risk population.
Abstract:
The triad of diabetes mellitus, anemia, and chronic kidney disease (CKD) define a group of patients at high risk for death and cardiovascular complications. The approval of epoetin alfa in 1989 transformed the treatment of anemia in patients with CKD. However, evidence has emerged from randomized controlled trials that correcting anemia with erythropoiesis-stimulating agents in CKD patients is associated with increased risk. Most recently, the TREAT (Trial to Reduce Cardiovascular Events With Aranesp Therapy) study of anemic type 2 diabetic patients with CKD reported that treatment with darbepoetin conferred no benefit in mortality or in attenuating cardiovascular or renal events. Instead, there was a twofold higher rate of stroke and thromboembolic complications and a higher rate of cancer deaths in patients randomized to treatment with darbepoetin. Furthermore, there was an inconsistent and modest improvement in health-related quality of life. TREAT raises questions about whether anemia in type 2 diabetic patients should be treated and under what circumstances.
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