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Diabetes mellitus and aortic stenosis head to head: toward personalized medicine in patients with both pathologies
Nerea Corbacho-Alonso1, Tamara Sastre-Oliva1, Luis F López-Almodovar2
1Department of Vascular Physiopathology, Hospital Nacional de Paraplejicos, Instituto de Investigación Sanitaria de Castilla-La Mancha (IDISCAM), Spain.
Insights
Diabetes mellitus (DM) accelerates aortic valve calcification by altering valve tissue proteins. This research clarifies the link between diabetes and heart valve disease, aiding personalized patient care.
Area of Science:
- Cardiology
- Endocrinology
- Proteomics
Background:
- Diabetes mellitus (DM) and calcific aortic stenosis (CAS) are prevalent in the elderly.
- DM is linked to increased CAS risk, but its precise influence on CAS progression is unclear.
Purpose of the Study:
- To investigate how DM affects aortic valve tissue and calcification processes.
- To identify potential therapeutic targets for managing CAS in diabetic patients.
Main Methods:
- Proteomic analysis using isobaric tags on calcified and noncalcified aortic valve tissues from patients with and without DM.
- Plasma protein concentrations were measured using three orthogonal methods.
- A separate cell model was utilized for validation.
Main Results:
- Proteomic analysis revealed differentially expressed proteins in aortic valves of patients with DM.
- These proteins are involved in endopeptidase activity, lipid metabolism, coagulation, and fibrinolysis.
- DM significantly alters the aortic valve proteome, influencing calcification.
Conclusions:
- Diabetes mellitus induces specific proteomic changes in aortic valves, contributing to calcification.
- Understanding these DM-driven alterations enhances knowledge of CAS pathogenesis.
- This research is crucial for developing personalized treatment strategies for patients with concurrent DM and CAS.
Abstract:
Diabetes mellitus (DM) and calcific aortic stenosis (CAS) are common morbidities in the elderly, which are both chronic, progressive and often concomitant diseases. Several studies revealed that DM increases the risk of developing severe CAS, yet clear information about the relationship between both these diseases and the influence of DM on the progression of CAS is currently lacking. To evaluate the effect of DM on aortic valves and on the process of calcification, and to achieve better patient management in daily clinical practice, we analysed calcified and noncalcified valve tissue from patients with severe CAS, with or without DM. A proteomic strategy using isobaric tags was adopted and the plasma concentrations of nine proteins were studied using 3 orthogonal methods and in a separate cell model. The differentially expressed proteins identified are implicated in biological processes like endopeptidase activity, lipid metabolism, coagulation, and fibrinolysis. The results obtained provide evidence that DM provokes changes in the proteome of aortic valves, affecting valve calcification. This finding may help enhance our understanding of the pathogenesis of CAS and how DM affects the evolution of this condition, an important step in identifying targets to personalize the treatment of these patients.
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