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Single-cell Analysis of Immunophenotype and Cytokine Production in Peripheral Whole Blood via Mass Cytometry
Published on: June 26, 2018
[Chronic inflammation and endothelial dysfunction: analysis of a cohort of patients with SLE and UCTD]
1UO Reumatologia, Dipartimento di Medicina Interna, Università di Pisa, Italia.
Insights
Patients with systemic autoimmune diseases show impaired endothelial function, a key factor in atherosclerosis. Anti-inflammatory therapy may help prevent cardiovascular complications in these patients.
Area of Science:
- Cardiovascular research
- Rheumatology
- Vascular biology
Background:
- Cardiovascular complications, primarily accelerated atherosclerosis, are a major cause of mortality in systemic autoimmune diseases.
- Endothelial dysfunction is an early, reversible indicator of atherogenesis.
Purpose of the Study:
- To investigate endothelial function in patients with systemic lupus erythematosus (SLE) and undifferentiated connective tissue diseases (UCTD).
- To correlate endothelial function with clinical and laboratory variables in these patient groups.
Main Methods:
- Endothelial function assessed using the perfused forearm technique, measuring endothelium-dependent and -independent vasodilation.
- Evaluations were performed in patients with SLE or UCTD and compared to healthy controls.
- Vascular reactivity was re-evaluated after corticosteroid administration in two patients.
Main Results:
- Patients with SLE and UCTD exhibited significantly reduced endothelium-dependent and -independent vasodilation compared to controls.
- UCTD patients showed a notable decrease in nitric oxide pathway function compared to controls and SLE patients.
- Corticosteroid administration led to improved vascular reactivity.
Conclusions:
- Findings suggest that anti-inflammatory and immunosuppressive therapy may play a role in preventing premature atherosclerosis in patients with systemic autoimmune diseases.
- Despite known side effects, these therapies warrant consideration for cardiovascular risk management.
Objective:
Cardiovascular complications, mainly caused by an accelerated atherosclerosis, are one of the leading causes of death and disability in patients with systemic autoimmune diseases. Endothelial dysfunction is considered the earliest and reversible step of atherogenesis. Aim of the present study is to investigate endothelial function (EF) in patients with systemic lupus erythematosus (SLE), undifferentiated connective tissue diseases (UCTD) and correlate the results with clinical and laboratory variables.
Methods:
EF was assessed on the peripheral microcirculation by the perfused forearm technique that can estimate both endothelium- dependent and endothelium- independent vasodilatation. The same evaluation has been repeated in two patients after the administration of 20 mg of 6-metilprednisolone.
Results:
Twenty-three female patients with SLE or UCTD, with a follow up of at least 1 year have been studied and compared with 8 healthy controls matched for epidemiological variables and traditional risk factors for cardiovascular disease. A significant reduction both in endothelium dependent than endothelium independent vasodilatation was observed in both patients groups compared with controls. In addition, UCTD patients demonstrated a significant reduction in the nitric oxide pathway compared with controls and SLE patients. Finally, steroid administration induced an improvement of vascular reactivity.
Conclusions:
Despite the well documented side effects of chronic corticosteroid therapy, our data might suggest a role for antinflammatory and immunosuppressive therapy in the prevention of premature atherosclerosis in patients with systemic autoimmune diseases.
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