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Updated: Aug 24, 2025

Comparative Proteomic Analysis of Whole Kidney, Medulla, and Cortical Tubules in Diabetic Pathogenesis of Kidney Injury in Mice
Published on: May 2, 2025
The Vascular Disease of Diabetic Kidney Disease
Paolo Lentini1, Luca Zanoli2, Claudio Ronco3,4,5
1Nephrology and dialysis, "San Bassiano Hospital", Bassano del Grappa, Italy.
Insights
Diabetic kidney disease (DKD) increases cardiovascular disease (CVD) risk. Arterial stiffening links diabetes to heart dysfunction, and sodium-glucose cotransporter type-2 inhibitors offer protection.
Area of Science:
- Nephrology
- Cardiology
- Endocrinology
Background:
- Diabetic kidney disease (DKD) is associated with a higher incidence of cardiovascular disease (CVD).
- The global prevalence of diabetes and DKD is increasing.
- Factors like insulin resistance, hyperglycemia, and hypertension contribute to CVD pathogenesis in type-2 diabetes.
Purpose of the Study:
- To explore arterial stiffening as a mediator between diabetes and cardiac dysfunction.
- To discuss the cardiovascular and kidney protective effects of sodium-glucose cotransporter type-2 inhibitors.
Main Methods:
- This study is a narrative review.
- Analysis of existing literature on arterial stiffening, diabetes, and cardiovascular outcomes.
- Review of evidence on sodium-glucose cotransporter type-2 inhibitors' effects.
Main Results:
- Arterial stiffening is identified as a key vascular mechanism linking diabetes to cardiac dysfunction.
- Sodium-glucose cotransporter type-2 inhibitors demonstrate significant cardiovascular and nephroprotective benefits.
Conclusions:
- Arterial stiffening plays a crucial role in the development of cardiac dysfunction in diabetic patients.
- Sodium-glucose cotransporter type-2 inhibitors represent a promising therapeutic strategy for managing cardiovascular and renal complications in DKD.
Background:
The incidence of cardiovascular disease (CVD) is increased in patients with diabetic kidney disease (DKD).
Summary:
Aortic stiffness is a well-accepted biomarker for cardiovascular (CV) events in all stages of CKD. The worldwide prevalence of diabetes continues to grow, as does the prevalence of DKD. Insulin resistance, hyperglycaemia, hypertension, and the metabolic abnormalities of type-2 diabetes are all involved in the pathogenesis of CVD. The effect of these toxins on cardiac and vascular function is amplified by the worsening of renal function and the parallel rise of uraemic toxins.
Key Messages:
In this narrative review, we analysed why arterial stiffening can be considered a vascular mediator between diabetes and cardiac dysfunction, and we discussed the strong CV and nephroprotective effects of sodium-glucose cotransporter type-2 inhibitors.
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