Zhang Li, Zhu Yan-Lin, Li Meng-Tao, Gao Na, You Xin, Wu Qing-Jun, Su Jin-Mei, Shen Min, Zhao Li-Dan, Liu Jin-Jing, Zhang Feng-Chun, Zhao Yan, Zeng Xiao-Feng
Department of Rheumatology, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences; Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing 100032, China.
Chin Med J (Engl). 2015 Oct 5;128(19):2588-94. doi: 10.4103/0366-6999.166029.
Myocarditis is an uncommon but serious manifestation of systemic lupus erythematosus (SLE). This study aimed to investigate clinical characteristics and outcomes of lupus myocarditis (LM) and to determine risk factors of LM in hospitalized Chinese patients with SLE.
We conducted a retrospective case-control study. A total of 25 patients with LM from 2001 to 2012 were enrolled as the study group, and 100 patients with SLE but without LM were randomly pooled as the control group. Univariable analysis was performed using Chi-square tests for categorical variables, and the Student's t-test or Mann-Whitney U-test was performed for continuous variables according to the normality.
LM presented as the initial manifestation of SLE in 7 patients (28%) and occurred mostly at earlier stages compared to the controls (20.88 ± 35.73 vs. 44.08 ± 61.56 months, P = 0.008). Twenty-one patients (84%) experienced episodes of symptomatic heart failure. Echocardiography showed that 23 patients (92%) had decreased left ventricular ejection fraction (<50%) and all patients had wall motion abnormalities. A high SLE Disease Activity Index was the independent risk factor in the development of LM (odds ratio = 1.322, P < 0.001). With aggressive immunosuppressive therapies, most patients achieved satisfactory outcome. The in-hospital mortality was not significantly higher in the LM group than in the controls (4% vs. 2%,P = 0.491).
LM could result in cardiac dysfunction and even sudden death. High SLE disease activity might potentially predict the occurrence of LM at the early stage of SLE. Characteristic echocardiographic findings could confirm the diagnosis of LM. Early aggressive immunosuppressive therapy could improve the cardiac outcome of LM.
心肌炎是系统性红斑狼疮(SLE)一种不常见但严重的表现形式。本研究旨在调查狼疮性心肌炎(LM)的临床特征和结局,并确定中国住院SLE患者发生LM的危险因素。
我们进行了一项回顾性病例对照研究。2001年至2012年期间共纳入25例LM患者作为研究组,随机抽取100例无LM的SLE患者作为对照组。分类变量采用卡方检验进行单因素分析,连续变量根据正态性采用Student t检验或Mann-Whitney U检验。
7例患者(28%)的LM表现为SLE的首发症状,与对照组相比大多发生在疾病早期(20.88±35.73个月 vs. 44.08±61.56个月,P = 0.008)。21例患者(84%)发生有症状的心衰发作。超声心动图显示,23例患者(92%)左室射血分数降低(<50%),所有患者均有室壁运动异常。高SLE疾病活动指数是发生LM的独立危险因素(比值比 = 1.322,P < 0.001)。通过积极的免疫抑制治疗,大多数患者取得了满意的结局。LM组的院内死亡率并不显著高于对照组(4% vs. 2%,P = 0.491)。
LM可导致心脏功能障碍甚至猝死。高SLE疾病活动可能在SLE早期预测LM的发生。特征性的超声心动图表现可确诊LM。早期积极的免疫抑制治疗可改善LM的心脏结局。