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Updated: May 12, 2026

Intradermal Microdialysis: An Approach to Investigating Novel Mechanisms of Microvascular Dysfunction in Humans
Published on: July 21, 2023
Micro- and macrovascular treatment targets in scleroderma heart disease
Theodoros Dimitroulas, George Giannakoulas, Haralambos Karvounis
1Department of Rheumatology, Dudley Group NHS FT, Russells Hall Hospital, Dudley, DY1 2HQ, UK. dimitroul@hotmail.com.
Insights
Systemic sclerosis (SSc) often involves the heart, causing myocardial fibrosis and heart failure. Early detection and vasodilators can improve cardiac function and prevent disease progression in SSc patients.
Area of Science:
- Cardiology
- Rheumatology
- Internal Medicine
Background:
- Cardiac involvement is a frequent and prognostically significant complication of systemic sclerosis (SSc).
- Myocardial fibrosis, leading to arrhythmias and heart failure, is the hallmark.
- Subclinical cardiac disease is common, with overt symptoms indicating a poor prognosis.
Purpose of the Study:
- To review the pathophysiology, diagnosis, and management of cardiac involvement in SSc.
- To clarify the role of microvascular dysfunction versus atherosclerotic coronary artery disease in SSc.
- To discuss current and future therapeutic strategies for SSc-related heart disease.
Main Methods:
- Review of existing literature on cardiac manifestations in SSc.
- Analysis of pathophysiological mechanisms, including myocardial fibrosis and coronary abnormalities.
- Evaluation of diagnostic techniques and therapeutic interventions.
Main Results:
- Myocardial fibrosis and microvascular dysfunction are primary mechanisms, though atherosclerotic disease prevalence is debated.
- Vasodilators show potential in improving myocardial function and perfusion.
- Clinically apparent cardiac disease in SSc is associated with adverse outcomes.
Conclusions:
- Cardiac involvement significantly impacts SSc prognosis, primarily through myocardial fibrosis and microvascular dysfunction.
- Further research is needed to elucidate the role of coronary artery disease and develop targeted therapies.
- Early detection and management, potentially with vasodilators, are crucial for improving outcomes in SSc patients with cardiac complications.
Abstract:
Cardiac involvement in systemic sclerosis (SSc) is a frequent visceral complication that considerably affects the prognosis of the disease. The pathophysiologic hallmark is myocardial fibrosis which can progress leading to arrhythmia, right and/or left heart dysfunction and failure. Symptoms range from unusual to prominent and from mild to dramatic, but clinically overt disease is a poor prognostic factor. Primary myocardial involvement is related to focal ischemia due to transient coronary spasm, and the available data support that microvascular functional and structural abnormalities rather than macrovascular coronary involvement represent the main underlying mechanism of the disease. However, the existence and prevalence of atherosclerotic coronary artery disease in SSc remain to be determined, as several studies have generated conflicting reports. Despite the lack of effective targeted therapy for SSc itself, sensitive and quantitative techniques have demonstrated the ability of vasodilators to improve myocardial function and perfusion and to prevent the evolution of subclinical heart involvement to decompensated heart failure. Further research will provide a better understanding of the disease by detecting the potent contribution of coronary artery involvement, explaining differences in accelerated atherosclerosis between SSc and other autoimmune disorders, and opening directions for the development of novel treatment strategies for this life-threatening complication of SSc.
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