Diabetes mellitus aggravates myocardial inflammation and oxidative stress in aortic stenosis: a mechanistic link to HFpEF features

• Type: Article in International Scientific Journal
• Date: 2025

Authors

Herwig, M (Author) Other; Sieme, M (Author) Other; Kovács, A (Author) Other; Khan, M (Author) Other; Mügge, A (Author) Other; Schmidt, WE (Author) Other; Elci, F (Author) Other; Sasidharan, S (Author) Other; Haldenwang, P (Author) Other; Wintrich, J (Author) Other; Sasko, B (Author) Other; Akin, I (Author) Other; Domokos, M (Author) Other; Paneni, F (Author) Other; El-Battrawy, I (Author) Other; Varga, ZV (Author) Other; Saraiva, F (Author) Other; Leite-Moreira AF (Author) FMUP; Ferdinandy, P (Author) Other; van Heerebeek, L (Author) Other; Falcao-Pires, I (Author) Other; Hamdani, N (Author) Other

Journal

Title: Cardiovascular Diabetology

ISSN: 1475-2840

Publisher: Springer Nature

Indexing

ISI Web of Knowledge - 0 Citations

Scopus - 6 Citations

Other information

Authenticus ID: P-018-YA4

DOI: 10.1186/s12933-025-02748-y

Abstract (EN): Background Patients diagnosed with both aortic stenosis (AS) and diabetes mellitus (DM) encounter a distinctive set of challenges due to the interplay between these two conditions. This study aimed to investigate the effects of DM on the left ventricle in AS patients, specifically focusing on the inflammatory response, oxidative stress, and their implications for cardiomyocyte function, titin phosphorylation, and the nitric oxide (NO)-soluble guanylyl cyclase (sGC)-cyclic guanosine monophosphate (cGMP)-protein kinase G (PKG) signaling pathway. Methods and results Left ventricular myocardial biopsies (in total: n = 28) were obtained from patients with diabetic AS (n = 11) and compared with those from non-diabetic AS patients (n = 17). Enzyme-linked immunosorbent assay (ELISA) demonstrated significantly elevated levels of pro-inflammatory mediators, including high mobility group box protein 1 (HMGB1) and calprotectin, as well as receptors associated with the inflammatory response, such as Toll-like receptor 2 (TLR2), 4 (TLR4), and receptor for advanced glycation endproducts (RAGE). These were correlated with an enhanced NOD-like receptor protein 3 (NLRP3) inflammasome and the release of interleukins (IL) 1, 6, and 18 in diabetic AS patients compared to their non-diabetic counterparts. Additionally, in the diabetic AS cohort, there was an increase in oxidative stress markers (hydrogen peroxide (H2O2), 3-nitrotyrosine, lipid peroxidation (LPO), oxidative glutathione (GSSG)/reduced glutathione (GSH) ratio) within the myocardium and mitochondria, accompanied by impaired NO-sGC-cGMP-PKG signaling, decreased titin phosphorylation, and increased passive stiffness (F-passive) of cardiomyocytes relative to non-diabetic AS patients. In vitro anti-inflammatory treatment with an IL-6 inhibitor and antioxidant treatment with GSH effectively normalized the elevated F-passive observed in AS patients with DM to levels comparable to the non-diabetic group. Furthermore, treatment with PKG and the sodium-glucose cotransporter 2 (SGLT2) inhibitor empagliflozin also resulted in a reduction of F-passive in cardiomyocytes from diabetic AS patients, although not to the levels observed in non-diabetic AS patients. Conclusion DM exacerbates inflammation and oxidative stress in AS patients, leading to impaired NO-sGC-cGMP-PKG signaling and increased cardiomyocyte F-passive. These conditions are reminiscent of the pathophysiology of heart failure with preserved ejection fraction (HFpEF). These alterations can be ameliorated through anti-inflammatory and antioxidant therapies, indicating potential therapeutic strategies for diabetic patients suffering from AS.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 20