Key result
Early eGFR decline >10% occurs in ~37% of HF patients starting SGLT2 inhibitors.
Why the study?
Early changes in eGFR after SGLT2 inhibitor initiation in heart failure are difficult to interpret in routine practice.
What are the clinical correlates of >10% early relative eGFR decline after SGLT2 inhibitor initiation in heart failure, and do eGFR levels return to pretreatment baseline at 12 months?
Cohort (n=295)
No
What are the clinical correlates of >10% early relative eGFR decline after SGLT2 inhibitor initiation in heart failure, and do eGFR levels return to pretreatment baseline at 12 months?
Following SGLT2 inhibitor initiation in heart failure, an early eGFR decline >10% is common and, while it partially recovers, it does not fully return to pretreatment levels at 12 months, emphasizing the need for clinical context during interpretation.
Answers are grounded in this paper and cite their sources.
Early eGFR decline after SGLT2i in HF may warrant closer monitoring; leaves open whether trajectories predict outcomes or guide therapy.
Background/Objectives: Early changes in estimated glomerular filtration rate (eGFR) after sodium–glucose cotransporter 2 (SGLT2) inhibitor initiation in heart failure (HF) are difficult to interpret in routine practice. We assessed the clinical correlates of >10% early relative eGFR decline and the subsequent trajectories relative to the pretreatment eGFR. Methods: This retrospective single-center study included 295 patients with HF who remained on SGLT2 inhibitor treatment at their first eligible creatinine assessment on days 10–45 (median 25 days [IQR 21–30]; range 10–42). Multivariable regression, mixed-effects modeling, and within-patient paired analyses were used. Results: Among the 333 initiation episodes, 33 (9.9%) were excluded after early treatment discontinuation, and five repeat episodes were removed. Early decline >10% occurred in 110/295 patients (37.3%). Age ≥ 80 years (adjusted OR 2.14, 95% CI 1.21–3.81), female sex (2.51, 1.42–4.44), higher baseline eGFR per 10 mL/min/1.73 m2 (1.43, 1.21–1.69), and loop-diuretic use (1.82, 1.03–3.23) were associated with decline; the loop-diuretic association attenuated in an expanded model. Twelve-month eGFR was available for 195/295 patients (66.1%). Among the 71 with >10% early decline and paired 12-month data, the mean eGFR increased by 4.70 mL/min/1.73 m2 from the early assessment but remained 6.99 mL/min/1.73 m2 below the pretreatment (both p < 0.001). Conclusions: In this selected cohort, a mean increase after early decline did not indicate a return to the pretreatment mean. The interpretation of an isolated early eGFR value requires clinical context and subsequent measurements.
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Suzuki et al. (2026) conducted a cohort in Heart Failure (n=295). SGLT2 inhibitor initiation was evaluated on >10% early relative eGFR decline. Following SGLT2 inhibitor initiation, an early eGFR decline >10% occurred in 37.3% of heart failure patients, and their 12-month mean eGFR remained 6.99 mL/min/1.73 m2 below pretreatment (P<0.001).
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