Rheumatology Unit, First Department of Propaedeutic Internal Medicine, Joint Academic Rheumatology Program.
First Department of Propaedeutic Internal Medicine.
Rheumatology (Oxford). 2022 Aug 3;61(8):3408-3413. doi: 10.1093/rheumatology/keab882.
Antiphospholipid syndrome (APS) is an autoimmune thrombophilia leading to life-threatening cardiovascular events. Cross-sectional data support that APS is associated with accelerated atherosclerosis, but this has not been confirmed in prospective studies. We aimed to compare the rate of atherosclerosis progression over a 3 year period between patients with APS, diabetes mellitus (DM) and healthy controls (HCs).
Eighty-six patients with APS [43 with primary APS (PAPS), 43 with SLE-related APS (SLE-APS)] and an equal number of age- and sex-matched patients with DM and HCs who underwent a baseline US of the carotid and femoral arteries were invited for a 3 year follow-up evaluation for atherosclerotic plaque progression. Multivariate analysis was performed for the assessment of determinants of plaque progression after adjustment for disease-related and traditional cardiovascular risk factors.
Seventy-four APS patients (74.3% female, 38 with PAPS), 58 DM patients and 73 HCs were included. APS patients exhibited a 3.3-fold higher risk of new atherosclerotic plaque formation compared with HCs (P = 0.031), similar to that in DM [odds ratio (OR) 3.45, P = 0.028]. In APS patients, plaque development risk was higher in SLE-APS vs PAPS (OR 7.75, P = 0.038) and was independently associated with the presence of traditional cardiovascular risk factors as expressed by the Systematic Coronary Risk Evaluation risk (OR 2.31, P = 0.008).
APS is characterized by accelerated rates of subclinical atherosclerosis to a degree comparable to DM, which is more pronounced in SLE-APS patients. Traditional cardiovascular risk factors are major determinants of this risk, warranting aggressive management as in other disorders with high cardiovascular risk.
抗磷脂综合征(APS)是一种自身免疫性血栓形成倾向,可导致危及生命的心血管事件。横断面数据支持 APS 与动脉粥样硬化加速有关,但这尚未在前瞻性研究中得到证实。我们旨在比较 APS、糖尿病(DM)和健康对照组(HC)患者在 3 年内动脉粥样硬化进展的速度。
我们邀请了 86 名 APS 患者(43 名原发性 APS [PAPS],43 名与 SLE 相关的 APS [SLE-APS])和年龄、性别匹配的 DM 患者和 HCs 患者,他们在基线时接受了颈动脉和股动脉的超声检查,并在 3 年内进行了随访评估,以评估动脉粥样硬化斑块的进展情况。进行多变量分析,以评估疾病相关和传统心血管危险因素调整后的斑块进展决定因素。
共纳入 74 名 APS 患者(74.3%为女性,38 名为 PAPS)、58 名 DM 患者和 73 名 HCs。与 HCs 相比,APS 患者新发动脉粥样硬化斑块形成的风险高 3.3 倍(P=0.031),与 DM 相似[比值比(OR)3.45,P=0.028]。在 APS 患者中,SLE-APS 比 PAPS 发生斑块进展的风险更高(OR 7.75,P=0.038),并且与传统心血管危险因素的存在独立相关,这由系统性冠状动脉风险评估风险(OR 2.31,P=0.008)来表示。
APS 表现为亚临床动脉粥样硬化的加速进展程度与 DM 相当,在 SLE-APS 患者中更为明显。传统心血管危险因素是这种风险的主要决定因素,需要积极管理,就像其他心血管风险高的疾病一样。