Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine Baltimore, 1830 East Monument Street Suite 7500, Baltimore, MD 21205, USA.
Rheumatology (Oxford). 2011 Nov;50(11):2071-9. doi: 10.1093/rheumatology/ker285. Epub 2011 Aug 28.
Cardiovascular disease remains the major cause of death in SLE. We assessed the degree to which cardiovascular risk factors (CVRFs) and disease activity were associated with 2-year changes in measures of subclinical atherosclerosis.
One hundred and eighty-seven SLE patients participating in a placebo-controlled trial of atorvastatin underwent multi-detector CT [for coronary artery calcium (CAC)] and carotid duplex [for carotid intima-media thickness (IMT) and carotid plaque] twice, 2 years apart. During the 2 years, patients were assessed every 3 months for CVRF. Both groups were combined for analysis, as atorvastatin did not differ from placebo in preventing progression of coronary calcium. We examined the correlation between these clinical measures and progression of CAC, IMT and plaque during the follow-up period.
In an analysis adjusting for age, gender and ethnicity, CAC progression was positively associated with total serum cholesterol measured over the 2-year period (P = 0.04) and smoking (P = 0.003). Carotid IMT progression was associated with systolic BP (P = 0.003), high-sensitivity CRP (hsCRP) (P = 0.013) and white blood cell (WBC) count (P = 0.029). Carotid plaque progression, defined as patients without carotid plaque at baseline with subsequent development of plaque at follow-up, was associated with systolic BP (P = 0.003), WBC count (P = 0.02), physician's global assessment (P = 0.05), blood lymphocyte count (P = 0.048), urine protein (P = 0.017) and duration of SLE (P = 0.019).
Our data did not provide evidence of an association between measures of SLE disease activity (SLEDAI, anti-dsDNA, anti-phospholipid and treatment) and progression of subclinical atherosclerosis. Age and hypertension were associated with the progression of carotid IMT and plaque. Age, smoking and cholesterol were associated with progression of CAC.
心血管疾病仍然是系统性红斑狼疮(SLE)患者的主要死亡原因。我们评估了心血管危险因素(CVRFs)和疾病活动度与亚临床动脉粥样硬化 2 年变化之间的关联程度。
187 名参与阿托伐他汀安慰剂对照试验的 SLE 患者进行了多探测器 CT[用于冠状动脉钙(CAC)]和颈动脉双功能超声[用于颈动脉内膜中层厚度(IMT)和颈动脉斑块]两次检查,两次检查相隔 2 年。在这 2 年内,患者每 3 个月评估一次 CVRF。由于阿托伐他汀在预防冠状动脉钙进展方面与安慰剂无差异,因此将两组合并进行分析。我们检查了这些临床测量指标与随访期间 CAC、IMT 和斑块进展之间的相关性。
在调整年龄、性别和种族后进行的分析中,CAC 进展与 2 年内总血清胆固醇(P=0.04)和吸烟(P=0.003)呈正相关。颈动脉 IMT 进展与收缩压(P=0.003)、高敏 C 反应蛋白(hsCRP)(P=0.013)和白细胞(WBC)计数(P=0.029)相关。颈动脉斑块进展定义为基线时无颈动脉斑块但随访时出现斑块的患者,与收缩压(P=0.003)、WBC 计数(P=0.02)、医生整体评估(P=0.05)、血淋巴细胞计数(P=0.048)、尿蛋白(P=0.017)和 SLE 持续时间(P=0.019)相关。
我们的数据并未提供 SLE 疾病活动度(SLEDAI、抗 dsDNA、抗磷脂和治疗)与亚临床动脉粥样硬化进展之间存在关联的证据。年龄和高血压与颈动脉 IMT 和斑块的进展有关。年龄、吸烟和胆固醇与 CAC 进展有关。