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Prevalence of the Antiphospholipid Syndrome and Its Effect on Survival in 679 Chinese Patients With Systemic Lupus Erythematosus: A Cohort Study

机译:679例中国系统性红斑狼疮患者抗磷脂综合征的患病率及其对生存率的影响:一项队列研究

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Abstract: In this work we evaluate the prevalence of the antiphospholipid syndrome (APS) and its impact on survival in Chinese patients with systemic lupus erythematosus (SLE). We studied a prospective cohort of southern Chinese patients who fulfilled ≥4 American College of Rheumatology criteria for SLE. The cumulative rate of survival over time was calculated by the Kaplan-Meier method. APS was defined by the 2006 updated consensus criteria. We evaluated the prevalence and manifestations of APS, and compared the survival of patients with and without APS. We followed 679 patients with SLE (92% women; age of onset, 32.5 ± 14 yr) for 9.7 ± 7.3 years. Sixty-eight (10%) patients died and 33 (4.9%) patients were lost to follow-up. Forty-four (6.5%) patients met the criteria for APS, manifested by the following: ischemic stroke (55%), deep venous thrombosis (32%), obstetric morbidity (14%), cardiovascular events (9%), and peripheral vascular disease (9%). Nine (9/44 [20%]) APS patients died, which was more frequent than the non-APS patients (59/635 [9%]; p = 0.02). The cumulative mortality of patients with APS was 4.6% at 5 years, 7.8% at 10 years, and 22.2% at 15 years, which was not significantly higher than that of non-APS patients (5.4% at 5 years, 9.2% at 10 years, and 11.3% at 15 years; p = 0.14). However, if we considered only patients with APS caused by arterial thrombosis, the presence of APS was significantly associated with mortality (hazard ratio, 2.29; 95% confidence interval, 1.13–4.64; p = 0.02). We conclude that the presence of APS increases the mortality risk of Chinese patients with SLE, which is mainly contributed by arterial thrombotic events. Clinical significance: 1) APS is infrequent in southern Chinese patients with SLE compared to white patients. 2) Arterial thrombosis is a more common manifestation of APS than venous thrombosis in Chinese SLE patients. 3) APS related to arterial thrombosis is associated with increased mortality in Chinese patients with SLE.
机译:摘要:在这项工作中,我们评估了抗磷脂综合征(APS)的患病率及其对中国系统性红斑狼疮(SLE)患者生存的影响。我们研究了符合≥4个美国风湿病学会SLE标准的中国南方患者的前瞻性队列。通过Kaplan-Meier方法计算随时间的累积存活率。 APS由2006年更新的共识标准定义。我们评估了APS的患病率和表现,并比较了有和没有APS的患者的生存率。我们对679例SLE患者(92%为女性;发病年龄32.5±14岁)进行了9.7±7.3年的随访。六十八(10%)名患者死亡,33名(4.9%)患者失去随访。四十四名(6.5%)患者符合APS标准,表现为:缺血性中风(55%),深静脉血栓形成(32%),产科发病率(14%),心血管事件(9%)和外周血血管疾病(9%)。 9例(9/44 [20%])APS患者死亡,这比非APS患者更为常见(59/635 [9%]; p = 0.02)。 APS患者的累积死亡率在5年时为4.6%,在10年时为7.8%,在15年时为22.2%,但与非APS患者相比(5年时为5.4%,10岁时为9.2%)没有显着较高。年,在15年时为11.3%; p = 0.14)。但是,如果仅考虑由动脉血栓形成引起的APS患者,则APS的存在与死亡率显着相关(危险比2.29; 95%置信区间1.13-4.64; p = 0.02)。我们得出的结论是,APS的存在增加了中国SLE患者的死亡风险,这主要是由动脉血栓事件引起的。临床意义:1)与白人患者相比,中国南方患有SLE的患者很少发生APS。 2)在中国SLE患者中,动脉血栓形成是APS比静脉血栓形成更常见的表现。 3)中国SLE患者与动脉血栓形成相关的APS与死亡率增加相关。

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