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Eosinophilic granulomatosis with polyangiitis (Churg-Strauss): clinical characteristics and long-term followup of the 383 patients enrolled in the French Vasculitis Study Group cohort.嗜酸性肉芽肿性多血管炎(Churg-Strauss综合征):法国血管炎研究组队列中383例患者的临床特征及长期随访
Arthritis Rheum. 2013 Jan;65(1):270-81. doi: 10.1002/art.37721.
2
The diagnostic role of cardiac magnetic resonance imaging in detecting myocardial inflammation in systemic lupus erythematosus. Differentiation from viral myocarditis.心脏磁共振成像在系统性红斑狼疮心肌炎症检测中的诊断作用。与病毒性心肌炎的鉴别。
Lupus. 2013 Jan;22(1):34-43. doi: 10.1177/0961203312462265. Epub 2012 Oct 3.
3
A contemporary case series of lupus myocarditis.狼疮性心肌炎的当代病例系列。
Lupus. 2012 Nov;21(13):1378-84. doi: 10.1177/0961203312456752. Epub 2012 Aug 14.
4
Morbidity and mortality in adult polymyositis and dermatomyositis.成人多发性肌炎和皮肌炎的发病率和死亡率。
Curr Rheumatol Rep. 2012 Jun;14(3):275-85. doi: 10.1007/s11926-012-0249-3.
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Update on myocarditis.心肌炎最新进展。
J Am Coll Cardiol. 2012 Feb 28;59(9):779-92. doi: 10.1016/j.jacc.2011.09.074.
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Acute lupus myocarditis: Clinical features and outcome.急性狼疮性心肌炎:临床特征和结局。
Lupus. 2011 Aug;20(9):981-8. doi: 10.1177/0961203310395800. Epub 2011 Apr 8.
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Rituximab in childhood lupus myocarditis.利妥昔单抗治疗儿童狼疮性心肌炎。
Rheumatol Int. 2012 Jun;32(6):1843-4. doi: 10.1007/s00296-011-1881-3. Epub 2011 Apr 6.
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Cardiac complications of systemic sclerosis: recent progress in diagnosis.系统性硬化症的心脏并发症:诊断方面的最新进展。
Curr Opin Rheumatol. 2010 Nov;22(6):696-703. doi: 10.1097/BOR.0b013e32833dfbd8.
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Causes and risk factors for death in systemic sclerosis: a study from the EULAR Scleroderma Trials and Research (EUSTAR) database.系统性硬化症死亡的原因和危险因素:来自 EULAR 硬皮病试验和研究 (EUSTAR) 数据库的研究。
Ann Rheum Dis. 2010 Oct;69(10):1809-15. doi: 10.1136/ard.2009.114264. Epub 2010 Jun 15.
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Anti-CD20 therapy in patients with refractory systemic lupus erythematosus: a longitudinal analysis of 52 Hispanic patients.抗 CD20 治疗难治性系统性红斑狼疮患者:52 例西班牙裔患者的纵向分析。
Lupus. 2010 Feb;19(2):213-9. doi: 10.1177/0961203309351541. Epub 2009 Dec 4.

狼疮性心肌炎:一项来自中国的病例对照研究。

Lupus Myocarditis: A Case-Control Study from China.

作者信息

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

机构信息

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.

出版信息

Chin Med J (Engl). 2015 Oct 5;128(19):2588-94. doi: 10.4103/0366-6999.166029.

DOI:10.4103/0366-6999.166029
PMID:26415795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4736867/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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).

CONCLUSIONS

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.

摘要

背景

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。

方法

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。

结果

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)。

结论

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。