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Imaging Features of Systemic Sclerosis-Associated Interstitial Lung Disease
Published on: June 16, 2020
Silent cardiovascular involvement in patients with diffuse systemic sclerosis: a controlled cross-sectional study
Maurizio Turiel1, Luigi Gianturco, Cristian Ricci
1IRCCS Galeazzi Orthopedic Institute, University of Milan, Milan, Italy. maurizio.turiel@unimi.it
Insights
Systemic sclerosis patients show early signs of subclinical atherosclerosis, indicated by impaired coronary microcirculation and increased arterial stiffness. This pilot study highlights the need for cardiovascular risk assessment in SSc patients without clinical cardiovascular disease.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Vascular Biology
Background:
- Systemic autoimmune diseases like Systemic Sclerosis (SSc) are linked to increased cardiovascular morbidity and mortality due to atherosclerosis.
- SSc involves multisystem inflammation, endothelial damage, and vasculopathy, increasing atherosclerotic risk.
- Markers of endothelial dysfunction and atherosclerosis include asymmetric dimethylarginine (ADMA), arterial stiffness, carotid intima-media thickness (CIMT), and coronary flow reserve (CFR).
Purpose of the Study:
- To identify early cardiovascular involvement in Systemic Sclerosis patients using various endothelial and atherosclerosis markers.
- To assess subclinical atherosclerosis in SSc patients without overt cardiovascular disease symptoms.
Main Methods:
- A pilot study involving 20 diffuse SSc patients and 20 matched controls.
- Assessment included dipyridamole echocardiographic stress test for CFR, CIMT, arterial stiffness, and plasma ADMA levels.
- Patients had no clinical signs or symptoms of cardiovascular disease (CVD).
Main Results:
- SSc patients exhibited significantly elevated CIMT, pulse wave velocity, and stiffness index (β) compared to controls.
- Coronary flow reserve (CFR) was significantly lower in SSc patients.
- Plasma ADMA levels were significantly higher in SSc patients.
Conclusions:
- Systemic Sclerosis patients without clinical CVD show evidence of subclinical atherosclerosis.
- Early impairment of coronary microcirculation and macrovascular involvement are suggested by these findings.
- These markers may aid in early detection and management of cardiovascular risk in SSc.
Objective:
An association between systemic autoimmune diseases and atherosclerosis has been described in many connective tissue diseases, and this association is known to lead to increased cardiovascular morbidity and mortality. Systemic sclerosis (SSc) is characterized by multisystem organ inflammation, endothelial wall damage, and vasculopathy. There are many markers of endothelial dysfunction and/or atherosclerotic risk, such as asymmetric dimethylarginine (ADMA), arterial stiffness parameters, carotid intima-media thickness (CIMT), and coronary flow reserve (CFR) assessed by transthoracic echocardiography. The aim of this pilot study was to use various endothelial and atherosclerosis markers to identify early cardiovascular involvement in a group of SSc patients.
Methods:
The study involved 20 patients (2 men and 18 women with a mean ± SD age of 52.96 ± 12.51 years) with diffuse SSc who had no signs or symptoms of cardiovascular disease (CVD) and 20 age- and sex-matched controls. All subjects underwent a dipyridamole echocardiographic stress test that included a determination of CFR and an evaluation of CIMT, arterial stiffness, and plasma ADMA levels.
Results:
All of the arterial wall measurements of the patients with diffuse SSc were significantly different from those of the controls, and both right and left CIMT, pulse wave velocity, and stiffness index (β) were significantly elevated in the SSc patients compared to the healthy controls. Moreover, in patients with diffuse SSc, CFR was significantly lower (P = 0.0033) and plasma ADMA levels were higher (P < 0.0001) than in healthy controls.
Conclusion:
SSc patients without any clinical evidence of CVD seem to have had subclinical atherosclerosis, which was suggested by early impairment of coronary microcirculation and macrovascular involvement.
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