心包炎,作为类风湿关节炎复发的第一征兆,通过心脏磁共振评估。

Sophie Mavrogeni, Konstantinos Bratis, Eliza Sfendouraki, Evangelia Papadopoulou, Genovefa Kolovou
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引用次数: 22

摘要

类风湿关节炎(RA)影响许多器官,包括心脏。心脏磁共振(CMR)可以评估RA患者的心脏病理生理。目的:利用CMR评估近期出现心脏症状的缓解期RA患者。患者和方法:20例RA缓解期(15F/5M),年龄60±5岁,近期出现心脏症状(RAH),采用CMR进行前瞻性评估。CMR包括左室射血分数(LVEF)、t2加权(T2-W)、早期(EGE)和晚期钆增强(LGE)图像评价。他们的结果与20例RA缓解期无心脏症状(RAC)和18例系统性红斑狼疮(SLE)伴临床明显心肌炎的患者进行了比较。结果:5/20 RAH心肌酶异常。CMR示下壁心肌梗死2/20 (1M, 1F),心肌炎13/20 (8M/5F)。与RAC相比,RAH和SLE患者心肌与骨骼肌的T2比(2.5±0.05和3.4±0.7 vs 1.8±0.5)均有所增加。结论:CMR在缓解期RA中诊断为非典型表现的心包炎可能先于RA复发。在1年的随访中,有心肌炎病史的RA患者疾病复发的频率更高,并可能发展为CHF。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myopericarditis, as the first sign of rheumatoid arthritis relapse, evaluated by cardiac magnetic resonance.

Introduction: Rheumatoid arthritis (RA) affects many organs, including the heart. Cardiac magnetic resonance (CMR) can assess heart pathophysiology in RA.

Aim: To evaluate, using CMR, RA patients under remission with recent onset of cardiac symptoms.

Patients and methods: Twenty RA under remission (15F/5M), aged 60±5 yrs, with recent onset of cardiac symptoms (RAH), were prospectively evaluated by CMR. The CMR included left ventricular ejection fraction (LVEF), T2-weighted (T2-W), early (EGE) and late gadolinium enhanced (LGE) images evaluation. Their results were compared with those of 20 RA under remission without cardiac symptoms (RAC) and 18 with systemic lupus erythematosus (SLE) with clinically overt myocarditis.

Results: Cardiac enzymes were abnormal in 5/20 RAH. CMR revealed inferior wall myocardial infarction in 2/20 (1M, 1F) and myocarditis in 13/20 (8M/5F) RAH. The T2 ratio of myocardium to skeletal muscle was increased in RAH and SLE compared to RAC (2.5 ± 0.05 and 3.4±0.7 vs 1.8 ± 0.5, p<0.001). EGE was increased in RAH and SLE compared to RAC (15 ± 3 and 12±4.7 vs 2.7±0.8, p<0.001). Epicardial LGEs were identified in 10/13 and pericarditis in 6/13 RAH. Coronary angiography, performed in 5 RAH with increased cardiac enzymes, proved a right coronary artery obstruction in 2/5. In 3/5 with CMR positive for myocarditis, coronary arteries were normal, but endomyocardial biopsy revealed inflammation with normal PCR. An RA relapse was observed after 7-40 days in 10/13 RAH with myopericarditis. The one year follow up showed that a) RAH with myocarditis had more disease relapses and b) CHF was developed in 4 RAH with myocarditis.

Conclusions: Myopericarditis with atypical presentation, diagnosed by CMR in RA under remission, may precede the development of RA relapse. In 1 year follow up, RA patients with history of myocarditis have a higher frequency of disease relapse and may develop CHF.

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