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Updated: Feb 25, 2026

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
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Heterogeneous Kidney Patterns in Diabetic Patients Following SGLT2 Inhibitor Use.

Sohyun Bae1, Donghwan Yun1,2, Jeeyoung Kim1

  • 1Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Korea.

Journal of Korean Medical Science
|February 24, 2026
PubMed
Summary
This summary is machine-generated.

Sodium-glucose cotransporter 2 inhibitors (SGLT2is) show varied kidney function responses in diabetic patients. Identifying those at risk for rapid decline is key to optimizing treatment and preventing adverse outcomes.

Keywords:
Diabetes ComplicationsDiabetes MellitusDiabetic NephropathiesEstimated Glomerular Filtration Rate (eGFR)Sodium-Glucose Transporter 2 Inhibitors

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Area of Science:

  • Nephrology
  • Endocrinology
  • Diabetology

Background:

  • Sodium-glucose cotransporter 2 inhibitors (SGLT2is) are known to slow kidney disease progression in diabetic patients.
  • However, patient responses to SGLT2is can be heterogeneous, with some experiencing rapid kidney function decline.
  • This study investigates these varied responses and identifies contributing factors.

Purpose of the Study:

  • To analyze kidney function trajectories in type 2 diabetes patients treated with SGLT2is.
  • To identify distinct patterns of estimated glomerular filtration rate (eGFR) changes.
  • To determine factors associated with rapid eGFR decline.

Main Methods:

  • Retrospective cohort study of 66,375 type 2 diabetes patients, with 5,209 on SGLT2is.
  • Latent class linear mixed model analysis of eGFR trajectories in 4,185 patients over a median of 29.7 months.
  • Multinomial logistic regression to identify factors associated with eGFR patterns.

Main Results:

  • Four distinct eGFR trajectory patterns were identified: stable high, stable low, rapidly declining high, and rapidly declining low.
  • Rapid eGFR decline was observed in 2.6% of patients, more common in younger individuals with albuminuria and hypoalbuminemia.
  • Patients with rapidly declining eGFR faced higher risks of hospitalization and death.

Conclusions:

  • Significant heterogeneity exists in eGFR trajectories among diabetic patients treated with SGLT2is.
  • Early identification of patients at risk for rapid eGFR decline is crucial.
  • Optimizing treatment strategies and providing timely warnings can improve patient outcomes.