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Understanding the association between endothelial dysfunction and left ventricle diastolic dysfunction in development
Livija Sušić1, Lana Maričić2, Josip Vincelj3
1Department of Internal Medicine, Osijek-Baranja County Health Center, Osijek, Croatia and Josip Juraj Strossmayer University of Osijek, Faculty of Medicine, Osijek, Croatia. livija.susic@gmail.com.
Insights
Cardiovascular diseases are a leading cause of death. New research highlights endothelial dysfunction as a key factor in conditions like INOCA and HFpEF, especially in younger populations and women, necessitating improved risk assessment methods.
Area of Science:
- Cardiology
- Biomarker Research
Background:
- Cardiovascular diseases (CVDs) remain the leading global cause of mortality.
- Historically, CVDs primarily affected middle-aged men via obstructive coronary artery disease (CAD).
- Recent trends show increased incidence of ischemia with non-obstructive coronary arteries (INOCA) and heart failure with preserved ejection fraction (HFpEF), particularly in women and young adults.
Purpose of the Study:
- To address the limitations of conventional risk assessment in emerging CVD patient groups.
- To explore the role of endothelial dysfunction (ED) in INOCA and HFpEF.
- To investigate the potential of plasma biomarkers for early detection and risk stratification.
Main Methods:
- Review of current literature on INOCA and HFpEF pathophysiology.
- Analysis of the role of endothelial dysfunction (ED) and left ventricular diastolic dysfunction (LVDD).
- Exploration of plasma biomarkers, including endothelial dysfunction markers and natriuretic peptides (NPs).
Main Results:
- Endothelial dysfunction (ED) is identified as a common underlying factor in INOCA and HFpEF.
- Conventional risk assessment tools are insufficient for newer patient demographics experiencing these conditions.
- Plasma biomarkers show promise for improved cardiovascular risk assessment.
Conclusions:
- Endothelial dysfunction (ED) is a critical pathophysiological link between INOCA and HFpEF.
- There is a need for novel diagnostic and risk assessment strategies for these conditions.
- Investigated plasma biomarkers may offer future potential for early detection and management of cardiovascular risk.
Abstract:
Cardiovascular diseases (CVDs) have been the most common cause of death worldwide for decades. Until recently the most affected patients were middle-aged and elderly, predominantly men, with more frequent ST elevation myocardial infarction (STEMI) caused by obstructive coronary artery disease (CAD). However, in the last two decades we have noticed an increased incidence of ischemia with non-obstructive coronary arteries (INOCA), which includes myocardial infarction with non-obstructive coronary arteries (MINOCA) and non-myocardial infarction syndromes, such as microvascular and vasospastic angina, conditions that have been particularly pronounced in women and young adults - the population we considered low-risky till than. Therefore, it has become apparent that for this group of patients conventional methods of assessing the risk of future cardiovascular (CV) events are no longer specific and sensitive enough. Heart failure with preserved ejection fraction (HFpEF) is another disease, the incidence of which has been rising rapidly during last two decades, and predominantly affects elderly population. Although the etiology and pathophysiology of INOCA and HFpEF are complex and not fully understood, there is no doubt that the underlying cause of both conditions is endothelial dysfunction (ED) which further promotes the development of left ventricular diastolic dysfunction (LVDD). Plasma biomarkers of ED, as well as natriuretic peptides (NPs), have been intensively investigated recently, and some of them have great potential for early detection and better assessment of CV risk in the future.
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