Carotid intima-media thickness and arterial stiffness in pediatric systemic lupus erythematosus

Author:

Su-angka N1,Khositseth A1,Vilaiyuk S1,Tangnararatchakit K1,Prangwatanagul W1

Affiliation:

1. Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Thailand

Abstract

Objectives The carotid intima-media thickness (CIMT) and carotid arterial stiffness index (CASI) act as the surrogate markers of atherosclerosis. We aim to assess CIMT and CASI in pediatric systemic lupus erythematosus (SLE). Methods Patients ≤ 20 years old fulfilling diagnostic criteria for SLE were enrolled. Patients with active smoking, coronary heart disease, cerebrovascular disease, arterial thrombosis, family history of hypercholesterolemia, chronic liver disease, or other chronic severe diseases were excluded. The patients were categorized into four groups: active SLE, age- and sex-matched control (control A), inactive SLE, and age- and sex-matched control (control I), according to the Systemic Lupus Erythematosus Disease Activity Index (SLEDAI). All subjects underwent ultrasound of carotid arteries to evaluate CIMT and CASI. Results One hundred and two SLE patients (26 active and 76 inactive) and one hundred and three healthy controls (26 control A and 77 control I) were enrolled. The median CIMT in all groups were not significantly different (0.43, 0.41–0.44; 0.43, 0.41–0.44; 0.42, 0.41–0.43; and 0.42, 0.41–0.43 mm, respectively).The CASI in active SLE (13.5, 11.4–17.3) was significantly higher than in control A (8.2, 7.2–9.2) ( p < 0.0001), whereas CASI in inactive SLE (12.7, 10.9–15.7) was significantly higher than in control I (8.9, 7.6–9.8). However, the CASI in active and inactive SLE was not significantly different. Conclusions The higher CASI in active and inactive pediatric SLE, implying functional change of carotid arteries, may be early evidence of increased atherosclerosis in pediatric SLE. This functional dysfunction has been found both in inactive and active SLE.

Publisher

SAGE Publications

Subject

Rheumatology

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