Key result
Add-on SGLT2 inhibitors linked to ~7.7-fold higher odds of 1-year functional improvement in CHF.
Why the study?
Anemia and iron deficiency are common in elderly patients with chronic heart failure and are associated with reduced functional capacity and worse prognosis. This study evaluated whether adding SGLT2i therapy to intravenous ferric carboxymaltose is associated with improved functional abilities in elderly HFrEF/HFmrEF patients with iron deficiency anemia.
Does add-on SGLT2 inhibitor therapy improve functional abilities (SPPB >8 points) at 1 year in elderly patients with HFrEF/HFmrEF and iron deficiency anemia receiving intravenous ferric carboxymaltose?
Cohort (n=222)
Does add-on SGLT2 inhibitor therapy improve functional abilities (SPPB >8 points) at 1 year in elderly patients with HFrEF/HFmrEF and iron deficiency anemia receiving intravenous ferric carboxymaltose?
Concomitant SGLT2 inhibitor therapy is strongly associated with greater 1-year physical function improvement in elderly HFrEF/HFmrEF patients with iron deficiency anemia treated with intravenous ferric carboxymaltose.
Answers are grounded in this paper and cite their sources.
Supports hypothesis of benefit from SGLT2i add-on to iron in anemic elderly HF; needs RCTs before practice change.
Anemia and iron deficiency (ID) are extremely common comorbidities in elderly patients with chronic heart failure (CHF), and are associated with reduced functional capacity and worse prognosis. The objective of this study was to evaluate the association of one-year therapy with SGLT2i as add-on to intravenous infusion of ferric carboxymaltose (FCM) with improvement in functional abilities, in a cohort of elderly patients with HFrEF/HFmrEF with ID anemia. This study enrolled outpatients with CHF with ID anemia receiving intravenous administration of FCM and stratified into two groups according to SGLT2i use. The study endpoint was an achievement of Short physical performance battery (SPPB)>8pt at one year of follow-up. 222 patients, with a mean age of 75.5±6.0 years were enrolled and 53 received SGLT2i while 169 not. After 1 year of follow-up, a significant improvement in the main clinical, laboratory, echocardiographic and CGA parameters were observed in both groups; however, these improvements were statistically greater in those patients receiving also SGLT2i. The mean dose of FCM administered to the entire population at baseline was 734.2 ± 331.7 mg, with no significant differences between the two groups (p=0.475). Add on therapy with SGLT2i was associated with a greater improvement in functional abilities (OR 7.66; CI 95% 3.70–15.9, p<0.0001), while the presence of obesity was associated with a reduced probability of functional abilities improvement of 68% (OR 0.32; CI 95% 0.14–0.71, p=0.005). In patients with CHF and ID anemia, improvements in clinical symptoms and physical function were observed at one-year follow-up, as reflected by changes in SPPB scores. These improvements were greater among patients receiving concomitant SGLT2i therapy.
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Armentaro et al. (2026) conducted a cohort in Chronic heart failure (HFrEF/HFmrEF) with iron deficiency anemia (n=222). SGLT2 inhibitor as add-on to intravenous ferric carboxymaltose vs. Intravenous ferric carboxymaltose without SGLT2 inhibitor was evaluated on Achievement of Short Physical Performance Battery (SPPB) >8 points at 1 year (OR 7.66, 95% CI 3.70-15.9, p=<0.0001). Add-on SGLT2 inhibitor therapy to ferric carboxymaltose was associated with greater functional improvement (SPPB >8) at 1 year in elderly CHF patients with anemia (OR 7.66; 95% CI 3.70-15.9; p<0.0001).
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