Key result
Empagliflozin and dapagliflozin improve cardio-renal and metabolic markers in diabetic kidney disease.
Why the study?
SGLT2 inhibitors provide cardiorenal benefits beyond glucose lowering, yet longitudinal changes across renal, glycemic, metabolic, hematological, and inflammatory laboratory domains in patients with diabetic kidney disease remained incompletely characterized.
Does treatment with empagliflozin or dapagliflozin improve renal, glycemic, metabolic, hematological, and inflammatory laboratory parameters over 12 months in patients with type 2 diabetes mellitus and diabetic kidney disease?
Cohort (n=452)
No
Does treatment with empagliflozin or dapagliflozin improve renal, glycemic, metabolic, hematological, and inflammatory laboratory parameters over 12 months in patients with type 2 diabetes mellitus and diabetic kidney disease?
In a 12-month real-world cohort of patients with diabetic kidney disease, empagliflozin and dapagliflozin were associated with favorable changes across glycemic, renal (eGFR), metabolic (HDL-C, TyG index), and hematological parameters, though most inflammatory markers remained unchanged.
Answers are grounded in this paper and cite their sources.
Sex and age associated with TyG and eGFR changes on SGLT2i in DKD; hypothesis-generating and should not yet change practice.
Background/ Objectives: Sodium–glucose cotransporter-2 inhibitors (SGLT2i) provide cardiorenal benefits beyond glucose lowering, yet longitudinal changes across multiple laboratory domains in patients with diabetic kidney disease (DKD) remain incompletely characterized. This study aimed to evaluate 12-month changes in renal, glycemic, metabolic, hematological, and inflammatory parameters in patients with DKD treated with empagliflozin or dapagliflozin. Methods: This retrospective, single-center cohort study included 452 patients with type 2 diabetes mellitus and DKD who received empagliflozin or dapagliflozin. Laboratory parameters were assessed at baseline and after 12 months. Longitudinal changes, between-group differences, correlations, and exploratory path analyses were evaluated. Results: Over 12 months, glycated hemoglobin and fasting glucose levels decreased, whereas estimated glomerular filtration rate (eGFR), vitamin D, hematocrit, mean corpuscular volume, and high-density lipoprotein cholesterol (HDL-C) increased. Ferritin, the triglyceride–glucose (TyG) index, bicarbonate, and plateletcrit decreased. Most other measured hematological and inflammatory parameters did not change significantly. The overall patterns of change were broadly similar between treatment groups, although selected differences were observed in individual parameters. In exploratory path analyses, age was negatively associated with change in eGFR (β = −0.269, p < 0.001), whereas KDIGO category was positively associated with change in eGFR (β = 0.200, p < 0.001). Sex was associated with change in the TyG index (β = −0.261, p = 0.013), and treatment group was associated with change in the platelet-to-lymphocyte ratio (β = −0.194, p = 0.010). The models explained a modest proportion of the variance. Conclusions: This real-world cohort provides a multidomain assessment of laboratory changes observed over 12 months in patients with DKD receiving empagliflozin or dapagliflozin. Changes extended beyond glycemic measures to selected renal, metabolic, and hematological parameters, while most conventional and composite inflammatory markers remained unchanged. The observational design and absence of a non-SGLT2i control group preclude causal conclusions or claims of long-term renoprotection. Prospective controlled studies are warranted to clarify the clinical significance and comparative effects of these changes.
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Esen et al. (2026) conducted a cohort in Type 2 diabetes mellitus and diabetic kidney disease (n=452). Empagliflozin or dapagliflozin vs. Empagliflozin vs. dapagliflozin (no non-SGLT2i control group) was evaluated on 12-month changes in renal, glycemic, metabolic, hematological, and inflammatory parameters. Empagliflozin and dapagliflozin improved glycemic, renal, and metabolic markers over 12 months in DKD, with treatment group associated with platelet-to-lymphocyte ratio change.
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