Abstract
Background: Type 2 diabetes (T2D) is a major risk factor for cardiovascular disease (CVD), but the relationships between myocardial function, microvascular function, and atherosclerotic burden remain underexplored in asymptomatic individuals. This study investigates the associations between left ventricular ejection fraction (LVEF)-reserve, myocardial flow reserve (MFR), perfusion defects, coronary artery calcium score (CACS), and global longitudinal strain (GLS) in individuals with T2D but without overt CVD. Methods: Cross-sectional analysis of 871 individuals with T2D without overt CVD, recruited between 2020 and 2023. All underwent cardiac 82-Rubidium PET/CT to assess LVEF-reserve, MFR, perfusion defects, and CACS. GLS was measured using echocardiography. Associations were examined using linear regression adjusted for cardiovascular risk factors and cardiometabolic therapies. Results: Mean (SD) age was 64.9 (± 9.0) years, diabetes duration was 13.9 (± 8.4) years, and 262 (30%) were women. Higher MFR was associated with higher LVEF-reserve (β = 1.63, 95% CI: 1.16 to 2.10, p < 0.001). Individuals with CACS > 300 had lower LVEF-reserve than those with CACS ≤ 300 (β = − 1.25, 95% CI: − 1.97 to − 0.53, p < 0.001). Presence of Perfusion defects were associated with lower LVEF-reserve (β = − 1.49, 95% CI: − 2.23 to − 0.75, p < 0.001). LVEF-reserve was not associated with GLS (p = 0.23). Sensitivity analysis excluding 248 participants with perfusion defects confirmed the association between MFR and LVEF-reserve (β = 1.45 (95% CI: 0.92, 1.97), p < 0.001). Conclusions: In individuals with T2D without overt CVD, lower MFR, presence of perfusion defects, and CACS > 300 were associated with lower LVEF-reserve. Underscoring a potential role of microvascular dysfunction in subclinical systolic impairment.
| Originalsprog | Engelsk |
|---|---|
| Artikelnummer | 352 |
| Tidsskrift | Cardiovascular Diabetology |
| Vol/bind | 24 |
| Antal sider | 10 |
| ISSN | 1475-2840 |
| DOI | |
| Status | Udgivet - sep. 2025 |
Bibliografisk note
Publisher Copyright:© The Author(s) 2025.
Finansiering
PR has received speaking fees and/or consultancy to Steno Diabetes Center Copenhagen from Eli Lilly, Novo Nordisk, Sanofi Aventis, Vifor, Boehringer Ingelheim, Astellas, Gilead, Bayer, AstraZeneca, Mundipharma, and MSD. PR has received research grants from Novo Nordisk AstraZeneca. AC, PR, TWH and RSR had shares in Novo Nordisk. AK and RSR has received consultancy fees from Novo Nordisk. EHZ is a full-time employee in Novo Nordisk and has shares in Novo Nordisk. IKR is a full-time employee at Novo Nordisk. ML: has received speaker and consultancy fees from AstraZeneca, Bayer, Boeringer Ingelheim, Novo Nordisk, GlaxoSmithKline, and is an investigator in clinical studies sponsored by Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Eli Lilly, Janssen, MSD and Novo Nordisk. JPG has served as consultant for Novo Nordisk on measurement of bioactive peptides. TBS has received research grants from Pfizer, Sanofi Pasteur, GSK, Novo Nordisk, AstraZeneca, Boston Scientific and GE Healthcare, consulting fees from Novo Nordisk, IQVIA, Parexel, Amgen, CSL Seqirus, GSK and Sanofi Pasteur, and lecture fees from Bayer, Novartis, Sanofi Pasteur, GE healthcare and GSK. The other authors declare that there is no duality of interest associated with this manuscript. This study was funded by Novo Nordisk Foundation (grant number NNF19OC0054674.).
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