Background: Systemic sclerosis (SSc), a chronic autoimmune disease characterized by progressive fibrosis and vascular abnormalities, poses significant cardiovascular risks for affected individuals. Among these, subclinical atherosclerosis has gained increasing attention as a critical contributor to morbidity and mortality in SSc. Intima-media thickness (IMT) of the carotid arteries, measured through non-invasive imaging techniques, serves as a reliable surrogate marker for early atherosclerotic changes and a predictor of cardiovascular events. In recent years, a growing body of evidence has sought to elucidate the extent and clinical significance of increased IMT in patients with SSc compared to healthy controls.
Objectives: This study aims to evaluate carotid intima-media thickness (IMT) in patients with systemic sclerosis (SSc) through an updated meta-analysis. By synthesizing data from existing literature, the objective is to determine the extent of subclinical atherosclerosis in SSc, identify influencing factors, and assess its clinical significance in cardiovascular risk stratification.
Methods: A systematic review of PubMed, Scopus and Cochrane of studies comparing CIMT in SSc patients and controls was conducted. Effect sizes were pooled using a random-effects model, and heterogeneity was assessed via I² and Tau² statistics. A funnel plot evaluated publication bias.
Results: Data from 18 studies encompassing 1,864 participants (Figure 1) revealed a statistically significant increase in CIMT in SSc patients (Cohen’s d = 1.13, 95% CI 0.18–2.08, p = 0.02). Heterogeneity was substantial (I² = 98%, p < 0.01), highlighting variability in study populations and methodologies. The funnel plot showed several studies outside the pseudo confidence intervals.
Conclusion: This updated meta-analysis confirms significantly increased CIMT in SSc patients, advocating for intensified cardiovascular monitoring and preventative strategies in SSc management.
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Acknowledgements: NIL.
Disclosure of Interests: None declared.
© The Authors 2025. This abstract is an open access article published in Annals of Rheumatic Diseases under the CC BY-NC-ND license (