Key result
Prevalent diabetes mellitus was significantly associated with impaired ventricular-arterial coupling, as reflected by an increased PWV/GLS ratio (Beta = 0.28) compared to normoglycemia.
Why the study?
Diabetes mellitus is a known risk factor for heart disease and vascular damage, but whether changes in ventricular-arterial coupling occur before clinically evident cardiovascular disease in the general population was unknown.
Does diabetes or prediabetes impair ventricular-arterial coupling in a general population without established cardiovascular disease?
Cross-Sectional (n=2,884)
Yes
Does diabetes or prediabetes impair ventricular-arterial coupling in a general population without established cardiovascular disease?
In a general population without established cardiovascular disease, type 2 diabetes is independently associated with impaired ventricular-arterial coupling, driven by both increased arterial stiffness and reduced myocardial strain.
Answers are grounded in this paper and cite their sources.
Should not yet change practice; hypothesis-generating for longitudinal studies on ventricular-arterial coupling in diabetes.
BACKGROUND/AIMS: Ventricular-arterial coupling (VAC) plays a crucial role in cardiovascular physiology, affecting cardiac function and arterial properties for optimal organ perfusion. Considering that diabetes mellitus (DM) is a known risk factor for incident heart disease and vascular damage, this study aims to investigate whether changes in VAC due to DM occur earlier, even before the onset of clinically evident cardiovascular disease in the general population. METHODS: This retrospective study included 2,884 participants (mean age 57 years, 48% male) of the Swedish CArdioPulmonary BioImage Study (SCAPIS), where data on echocardiography and Pulse wave velocity (PWV) were available. Of these, 162 individuals (6%) had prevalent type 2 diabetes (DM), and 334 (12%) had prediabetes. VAC was quantified as the ratio of PWV to Global longitudinal strain (GLS). Linear regression models were used to assess associations between glycemic status (DM, prediabetes), HbA1c, fasting plasma glucose (fP-glucose), and VAC, adjusting for relevant covariates. RESULTS: I the fully adjusted model, prevalent DM and the combination of DM and prediabetes were significantly associated with increased values of PWV/GLS (Beta = 0.28, p < 0.001 and Beta = 0.14, p < 0.001 respectively), while no significant association was found between prediabetes and PWV/GLS. Increasing values of HbA1c and fP-glucose were significantly associated with higher values of PWV/GLS (Beta = 0.01,p < 0.001 and Beta = 0.07,p < 0.001, respectively) signaling worse VAC. In participants without prevalent DM, higher HbA1c levels were linked to increased PWV/GLS in the age- and sex-adjusted model; however, this association was attenuated after further adjustment for additional confounders. Conversely, fP-glucose remained significantly associated with elevated PWV/GLS across all adjusted models. CONCLUSIONS: This study demonstrates a significant association between DM and impaired VAC, as reflected by elevated PWV/GLS, while no such link was observed in prediabetes. The transition from prediabetes to DM appears critical for VAC deterioration. Additionally, higher HbA1c and fP-glucose levels, even in non-diabetic individuals, were associated with worsened VAC, highlighting the impact of glycemic control on vascular function.
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Holm et al. (2025) conducted a cross-sectional in Diabetes and prediabetes in the general population (n=2,884). Diabetes mellitus vs. Normoglycemia was evaluated on Ventricular-arterial coupling (VAC) measured as the ratio of pulse wave velocity (PWV) to global longitudinal strain (GLS) (Beta 0.28, 95% CI 0.17-0.39, p=<0.001). Prevalent diabetes mellitus was significantly associated with impaired ventricular-arterial coupling, as reflected by an increased PWV/GLS ratio (Beta = 0.28) compared to normoglycemia.
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