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Systemic lupus erythematosus is associated with an increased risk of cervical artery dissection
Robert J Trager1,2,3, Benjamin P Lynn4, Anthony N Baumann5,6
1Connor Whole Health, University Hospitals Cleveland Medical Center, 11100 Euclid Ave, Cleveland, 44106, OH, USA. Robert.Trager@UHhospitals.org.
Insights
Systemic lupus erythematosus (SLE) significantly increases the risk of cervical artery dissection (CeAD). This study found a 2.33 times higher risk in SLE patients, highlighting a crucial link between autoimmune disease and vascular events.
Area of Science:
- Rheumatology
- Vascular Neurology
- Epidemiology
Background:
- Autoimmune diseases may elevate cervical artery dissection (CeAD) risk.
- Systemic lupus erythematosus (SLE) is a prototypic autoimmune condition with potential systemic vascular implications.
Purpose of the Study:
- To investigate the association between SLE and the risk of CeAD.
- To compare CeAD incidence in SLE patients versus matched non-lupus controls.
Main Methods:
- Retrospective cohort study using de-identified electronic medical records (TriNetX).
- Inclusion of individuals aged 10+ from 2012-2020, excluding prior CeAD.
- Propensity score matching to control for confounders, followed by risk ratio calculation over four years.
Main Results:
- Matched cohorts of 77,008 patients (89% female) were analyzed.
- SLE patients exhibited a significantly higher incidence of CeAD (0.08% vs. 0.04%).
- The risk ratio for CeAD in SLE patients was 2.33 (95% CI [1.49;3.66], P < 0.0001).
Conclusions:
- Systemic lupus erythematosus is confirmed as a risk factor for cervical artery dissection.
- Further research is warranted to elucidate underlying mechanisms and explore associations with other autoimmune conditions.
Abstract:
Limited evidence suggests that autoimmune diseases are associated with an increased risk of cervical artery dissection (CeAD). We hypothesized individuals with systemic lupus erythematosus (SLE) would have an increased risk of CeAD following SLE diagnosis compared to matched non-lupus controls. We queried a de-identified United States electronic medical records network (TriNetX, Inc.) for individuals aged 10 and older from 2012 to 2020, for two cohorts: (1) SLE and (2) non-lupus controls, excluding those with prior CeAD. We used propensity matching to control for confounding variables and calculated the risk ratio (RR) for CeAD occurring over four years' follow-up, secondarily exploring cumulative incidence. After matching, both cohorts contained 77,008 patients, who were mostly female (89%). The incidence and risk of CeAD was significantly greater among those with SLE compared to matched non-lupus controls [95% CI] (0.08% vs. 0.04%; RR = 2.33 [1.49;3.66]; P < 0.0001). These findings support the hypothesis that SLE is a risk factor for CeAD. Additional research is needed to identify the mechanisms that may underly the SLE-CeAD association and examine the potential association between other autoimmune diseases and CeAD.
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