Sarda L, Assayag P, Palazzo E, Vilain D, Guillevin L, Faraggi M, Meyer O, Le Guludec D
Department of Nuclear Medicine, Hôpital Avicenne, Bobigny, France.
Ann Rheum Dis. 1999 Feb;58(2):90-5. doi: 10.1136/ard.58.2.90.
The diagnosis of primary myocardial involvement in systemic diseases is clinically relevant but difficult in the absence of specific criteria. Whatever the underlying disease, myocytes degeneration is observed during the active phase of myocardial damage. The aim of this study was to assess the diagnostic value of scintigraphic imaging with 111Indium antimyosin antibody (AM), a specific marker of the damaged myocyte, for ongoing myocardial damage related to systemic diseases.
40 patients with histologically confirmed systemic diseases were studied. They were classified into two groups according to the presence (group 1, n = 30), or the absence (group 2, n = 10) of clinical, electrocardiographic (ECG) or echocardiographic signs suggestive of myocardial involvement. Planar and tomographic acquisitions were obtained 48 hours after injection of AM (90 MBq). Rest 201thallium (T1) scintigraphy was also performed to assess myocardial perfusion and scarring. Clinical, ECG, and echocardiographic +/- scintigraphic evaluations were repeated during follow up (17 +/- 19 months) in 36 of 40 patients.
In group 1, 13 of 30 patients (43%) showed diffuse significant AM uptake throughout the left ventricle (LV), and no or mild T1 abnormality. Two of these were asymptomatic, four had normal ECG, and two had no clinical or echographic LV dysfunction. All patients in group 2 had negative AMA scintigraphy and normal T1 scintigraphy. During follow up of 12 AM positive patients, cardiac status improved after immunosuppressive treatment was intensified in nine cases, worsened in two cases, and remained stable in one. During follow up of 24 AM negative patients, cardiac status remained stable in 23 cases despite treatment not being increased in 20, including two patients with sequellary myocardial involvement. The last patient developed mild LV dysfunction after 36 months.
AM scintigraphy allows detection of active myocardial damage related to systemic diseases, with increased specificity compared with conventional methods, and increased sensitivity in some cases. Further studies are needed to assess the potential value of AM scintigraphy as a therapeutic guide.
在缺乏特定标准的情况下,诊断系统性疾病中的原发性心肌受累在临床上具有重要意义,但却很困难。无论潜在疾病是什么,在心肌损伤的活跃期均会观察到心肌细胞变性。本研究的目的是评估使用111铟抗肌凝蛋白抗体(AM)进行闪烁显像的诊断价值,AM是受损心肌细胞的一种特异性标志物,用于诊断与系统性疾病相关的持续性心肌损伤。
对40例经组织学确诊为系统性疾病的患者进行研究。根据是否存在提示心肌受累的临床、心电图(ECG)或超声心动图征象,将他们分为两组(第1组,n = 30;第2组,n = 10)。注射AM(90 MBq)48小时后进行平面和断层显像采集。还进行了静息201铊(T1)闪烁显像以评估心肌灌注和瘢痕形成。40例患者中的36例在随访期间(17±19个月)重复进行了临床、ECG和超声心动图及/或闪烁显像评估。
在第1组中,30例患者中有13例(43%)显示整个左心室(LV)弥漫性显著摄取AM,且T1无异常或仅有轻度异常。其中2例无症状,4例ECG正常,2例无临床或超声心动图显示的LV功能障碍。第2组所有患者的AMA闪烁显像均为阴性,T1闪烁显像正常。在对12例AM阳性患者的随访中,9例患者在强化免疫抑制治疗后心脏状况改善,2例恶化,1例保持稳定。在对24例AM阴性患者的随访中,23例患者的心脏状况保持稳定,尽管20例患者未增加治疗,其中包括2例有继发性心肌受累的患者。最后1例患者在36个月后出现轻度LV功能障碍。
AM闪烁显像能够检测与系统性疾病相关的活动性心肌损伤,与传统方法相比特异性更高,在某些情况下敏感性也更高。需要进一步研究以评估AM闪烁显像作为治疗指导的潜在价值。