Macrovascular disease and atherosclerosis in SSc
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Updated: Jul 6, 2026

Quantitative Analysis and Characterization of Atherosclerotic Lesions in the Murine Aortic Sinus
Published on: December 7, 2013
M E Hettema1, H Bootsma, C G M Kallenberg
1Division of Rheumatology and Clinical Immunology, University Medical Center Groningen, PO Box 30001, 9700 RB Groningen, The Netherlands. m.e.hettema@int.umcg.nl
Insights
Systemic sclerosis (SSc) is linked to accelerated atherosclerosis, particularly peripheral artery disease in digits. While coronary and cerebrovascular disease prevalence isn't increased, non-traditional risk factors are present, warranting further research into early atherosclerosis.
Area of Science:
- Cardiovascular Medicine
- Rheumatology
- Immunology
Background:
- Atherosclerosis is a chronic inflammatory disorder.
- Autoimmune rheumatic diseases, including Systemic Sclerosis (SSc), exhibit premature and accelerated atherosclerosis.
- SSc involves vasculopathy, with common microvascular and reported macrovascular involvement.
Purpose of the Study:
- To review the literature on coronary artery disease (CAD), cerebrovascular disease (CeVD), and peripheral arterial disease (PAD) in SSc.
- To investigate the prevalence and risk factors of atherosclerosis in SSc patients.
- To determine if generalized premature atherosclerosis is present in SSc.
Main Methods:
- Literature review of studies on atherosclerosis in SSc.
- Analysis of prevalence data for CAD, CeVD, and PAD in SSc.
- Examination of traditional and non-traditional risk factors for atherosclerosis in SSc.
Main Results:
- Increased prevalence of distal PAD in the digits of SSc patients.
- No increased prevalence of CAD or CeVD in SSc, though carotid intima-media thickness studies show mixed results.
- Non-traditional risk factors like lipoprotein(a), oxidized LDL, inflammation, vasospasm, and endothelial dysfunction are prevalent in SSc.
Conclusions:
- SSc is associated with specific macrovascular complications, notably PAD in the digits.
- Generalized premature atherosclerosis is not definitively detected in SSc, despite the presence of risk factors.
- Further research is needed to fully understand subclinical and clinical early atherosclerosis in SSc.
Abstract:
Atherosclerosis is considered to be a chronic inflammatory disorder. Several autoimmune rheumatic diseases are characterized by premature and accelerated atherosclerosis in which both classical and non-classical risk factors contribute to atherogenesis. SSc is characterized by vasculopathy, and microvascular involvement is common. Macrovascular involvement is considered rare, although increased prevalence of macrovascular disease has been reported as well. Here, we review the literature regarding coronary artery disease, cerebrovascular disease and peripheral arterial disease in SSc. An increased prevalence of distal peripheral artery disease in the digits has been found. The prevalence of coronary artery disease and cerebrovascular disease is not increased, although studies using intima-media thickness of the carotid artery as a marker of early atherosclerosis showed discrepant results. Besides traditional risk factors, as present in the general population, non-traditional risk factors are present in SSc as well, such as increased lipoprotein(a), oxidized LDL, inflammation, vasospasm and endothelial dysfunction. Moreover, markers of vascular damage in atherosclerosis, like antibodies to oxidized LDL, and increased levels of soluble vascular adhesion molecules, have been described in association with vascular damage in SSc. Nevertheless, generalized premature atherosclerosis has not been detected in SSc. Therefore, further research is necessary to assess the prevalence of clinically manifest or subclinical early atherosclerosis in SSc.
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