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Endothelial dysfunction: a unifying hypothesis for the burden of cardiovascular diseases in sub-Saharan Africa
Uchechukwu K A Sampson1, Michael M Engelgau2, Emmanuel K Peprah2
1Center for Translation Research and Implementation Science, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA. uchechukwu.sampson@nih.gov.
Insights
Cardiovascular diseases (CVD) share common roots in endothelial dysfunction, specifically endothelial nitric oxide synthase (eNOS) uncoupling. Understanding this mechanism is key to preventing global CVD burden.
Area of Science:
- Cardiovascular Science
- Molecular Biology
- Public Health
Background:
- Cardiovascular diseases (CVD), including ischaemic heart disease, are leading global causes of death and disability.
- CVD often coexists with other vascular conditions, suggesting a common underlying pathobiology.
- Metabolic, behavioral, and social factors converge to drive CVD development, implicating a shared molecular platform.
Purpose of the Study:
- To explore the unifying role of endothelial dysfunction in the development of cardiovascular diseases.
- To investigate the mechanism of endothelial nitric oxide synthase (eNOS) uncoupling as a central pathophysiological event.
- To highlight the relevance of endothelial health in clinical practice and public health strategies for CVD prevention.
Main Methods:
- Review of established knowledge on cardiovascular disease etiology and risk factors.
- Analysis of the role of endothelial activation and endothelial nitric oxide synthase (eNOS) function.
- Exploration of the interplay between risk factors, genomic, epigenetic, and environmental influences on eNOS uncoupling.
Main Results:
- Endothelial dysfunction, characterized by eNOS uncoupling and predominant reactive oxygen signaling, is central to CVD development.
- This dysfunction can be triggered by cardiovascular disease risk factors or innate immune system activation.
- Individual responses to CVD drivers are influenced by genetic, epigenetic, and environmental factors impacting eNOS uncoupling.
Conclusions:
- Endothelial dysfunction offers a unifying hypothesis for the global burden of CVD, particularly in regions like sub-Saharan Africa.
- Further research into the genetic and molecular mechanisms of eNOS uncoupling is crucial.
- Elucidating these mechanisms can inform targeted strategies for CVD prevention and management worldwide.
Abstract:
It is well established that the leading causes of death and disability worldwide are cardiovascular diseases (CVD), chief among which is ischaemic heart disease. However, it is also recognised that ischaemic heart disease frequently coexists with other vascular conditions, such as cerebrovascular, renovascular and peripheral vascular disease, thus raising the notion of a common underlying pathobiology, albeit with differing manifestations, dictated by the implicated vascular bed. The understanding that common metabolic and behavioural risk factors as well as social determinants and drivers are convergent in the development of CVD evokes the idea that the dysfunction of a common bio-molecular platform is central to the occurrence of these diseases. The state of endothelial activation, otherwise known as endothelial dysfunction, occurs when reactive oxygen signalling predominates due to an uncoupled state of endothelial nitric oxide synthase (eNOS). This can be a physiological response to stimulation of the innate immune system or a pathophysiological response triggered by cardiovascular disease risk factors. The conventional wisdom is that the endothelium plays an important role in the initiation, progression and development of CVD and other non-communicable diseases. Consequently, the endothelium has remarkable relevance in clinical and public health practice as well as in health education, health promotion, and disease- and risk-factor prevention strategies. It also presents a plausible unifying hypothesis for the burden of CVD seen globally and in sub-Saharan Africa. Importantly, the heterogeneity in individual responses to metabolic, behavioural, and social drivers of CVD may stem from a complex interplay of these drivers with genomic, epigenetic and environmental factors that underpin eNOS uncoupling. Therefore, further biomedical research into the underlying genetic and other mechanisms of eNOS uncoupling may enlighten and shape strategies for addressing the burden of CVD in sub-Saharan Africa and other regions of the world.
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