Papazoglou Nikolaos, Sfikakis Petros P, Tektonidou Maria G
Rheumatology Unit, First Department of Propaedeutic Internal Medicine, Joint Academic Rheumatology Program, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
Arthritis Rheumatol. 2025 Jun;77(6):716-726. doi: 10.1002/art.43097. Epub 2025 Jan 24.
Cardiovascular disease (CVD) is a leading cause of death in individuals with systemic lupus erythematosus (SLE). We assessed atherosclerotic plaque progression and incident cardiovascular events in patients with SLE over a 10-year follow-up.
We prospectively analyzed 738 carotid ultrasound measurements (413 in patients with SLE and 325 in age/sex-matched healthy controls [HCs]) to assess new plaque development from baseline to 3-, 7-, and 10-year follow-up. Multivariate mixed-effects Poisson regression models examined potential predictors of plaque progression, including patient characteristics, Systemic Coronary Risk Evaluation, traditional cardiovascular risk factor (CVRF) target attainment, Definition of Remission in SLE (DORIS), medications, and persistent triple anti-phospholipid antibody (aPL) positivity during follow-up. Ten-year incident cardiovascular events were recorded, and univariate Cox regression analysis assessed potential associations.
Patients with SLE had a 2.3-fold higher risk of carotid plaque progression than HCs (incidence rate ratio [IRR] 2.26, P = 0.002). Plaque progression risk in patients with SLE was reduced by 32% (IRR 0.68, P = 0.004) per each sustainedly attained CVRF target during follow-up, including blood pressure, lipids, smoking, body weight, and physical activity. DORIS achievement ≥75% of follow-up was associated with a 43% decrease in atherosclerosis progression risk (IRR 0.57, P = 0.033). Ten-year risk of incident cardiovascular events was higher in individuals with SLE than HCs (eight versus one event, permutation-based log-rank P = 0.036) and was associated with persistent triple aPL positivity.
Patients with SLE experience a 2.3-fold higher 10-year atherosclerosis progression risk than HCs, mitigated by sustained CVRF control and prolonged clinical remission. Persistent triple aPL positivity is associated with increased incidence of CVD events.
心血管疾病(CVD)是系统性红斑狼疮(SLE)患者的主要死因。我们在一项为期10年的随访中评估了SLE患者动脉粥样硬化斑块进展情况及心血管事件的发生情况。
我们前瞻性分析了738次颈动脉超声测量结果(SLE患者413次,年龄/性别匹配的健康对照者[HCs] 325次),以评估从基线到3年、7年和10年随访期间新斑块的形成情况。多变量混合效应泊松回归模型研究了斑块进展的潜在预测因素,包括患者特征、系统性冠状动脉风险评估、传统心血管危险因素(CVRF)达标情况、SLE缓解定义(DORIS)、药物治疗以及随访期间持续的三联抗磷脂抗体(aPL)阳性。记录10年心血管事件的发生情况,单变量Cox回归分析评估潜在关联。
SLE患者颈动脉斑块进展风险比HCs高2.3倍(发病率比[IRR] 2.26,P = 0.002)。随访期间每持续达到一个CVRF目标(包括血压、血脂、吸烟、体重和体力活动),SLE患者的斑块进展风险降低32%(IRR 0.68,P = 0.004)。随访期间DORIS达标≥75%与动脉粥样硬化进展风险降低43%相关(IRR 0.57,P = 0.033)。SLE患者10年心血管事件发生风险高于HCs(分别为8例和1例事件,基于排列的对数秩检验P = 0.036),且与持续的三联aPL阳性相关。
SLE患者10年动脉粥样硬化进展风险比HCs高2.3倍,持续的CVRF控制和长期临床缓解可减轻该风险。持续的三联aPL阳性与CVD事件发生率增加相关。