Risk factors for changes in carotid intima media thickness and plaque over 5 years in women with systemic lupus erythematosus

Author:

Lertratanakul Apinya,Sun JuliaORCID,Wu Peggy W,Lee Jungwha,Dyer Alan,Pearce William,McPherson David,Sutton-Tyrrell Kim,Thompson Trina,Barinas-Mitchell Emma,Ramsey-Goldman Rosalind

Abstract

ObjectiveTo investigate the occurrence of and risk factors for progression of carotid intima media thickness (IMT) and plaque in women with and without SLE.MethodsA cohort of 149 women with SLE and 126 controls participated in SOLVABLE (Study of Lupus Vascular and Bone Long-term Endpoints). Demographics, cardiovascular and SLE factors, and laboratory assessments were collected at baseline. Carotid IMT and plaque were measured using B-mode ultrasound at baseline and at 5-year follow-up. Regression models were used to identify predictors of progression in carotid IMT and plaque; multivariate models were adjusted for age, hypertension and total cholesterol to high-density lipoprotein ratio.ResultsThe mean±SD follow-up time was 5.35±0.60 years in cases and 5.62±0.66 years in controls. The mean IMT change per year was 0.008±0.015 mm in cases and 0.005±0.019 mm in controls (p=0.24). At follow-up, 31.5% of cases and 15% of controls had plaque progression, with a relative risk for plaque progression of 2.09 (95% CI 1.30 to 3.37). In SLE cases, higher fasting glucose and lower fibrinogen were associated with IMT progression after adjustment. Larger waist circumference and non-use of hydroxychloroquine were associated with plaque progression after adjustment.ConclusionPotential modifiable risk factors for carotid IMT and plaque progression in women with SLE were identified, suggesting that monitoring of glucose and waist circumference and use of hydroxychloroquine may be beneficial.

Funder

National Institute of Health

Nancy and Marvin Himmelstein through the Jack and Shirley DuBow Charitable Foundation

Pfizer Clinical Rheumatology Fellowship Award

Mary Kirkland Scholars Award

Solovy Arthritis Research Society

Publisher

BMJ

Subject

Immunology,General Medicine

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