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Use of Hematopoietic Stem Cell Transplantation to Assess the Origin of Myelodysplastic Syndrome
Published on: October 3, 2018
A Case Series of SGLT2i Improving Hemoglobin in Adults with Myelodysplastic Syndrome
Patricia Olar1, Stephanie Lee2, Michael Fralick3,4
1Department of Medicine, University of Toronto, Toronto, Ontario, Canada.
Introduction:
The objective of our case series was to assess the change in hemoglobin for adults with myelodysplastic syndrome (MDS) started on a sodium glucose cotransporter 2 inhibitor (SGLT2i) for their diabetes, heart failure, or chronic kidney disease.
Case Presentation:
Four patients with bone marrow biopsy confirmed low- or intermediate-risk MDS were referred for consideration of SGLT2i between July 2024 and December 2024. The patients were followed prospectively and had a repeat complete blood count at least 3 months after starting empagliflozin at 10 mg daily. The patients provided written consent for their results to be published. Median age was 78 years (range 76-82 years), 3 of the 4 patients were men, and the median baseline hemoglobin was 11.6 g/dL (IQR 9.3-12.8). Over a median duration of 4 months of taking empagliflozin, the median repeat hemoglobin was 12.8 g/dL (IQR 10.3-13.7).
Conclusions:
In our case series of 4 patients with MDS started on empagliflozin, we observed an increase in hemoglobin for all 4 patients. Larger studies are needed to assess whether the increase in hemoglobin is sufficiently robust and sustained to reduce a person's need for future red blood cell transfusion or other treatments for MDS.
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