Taylor A J, Wortham D C, Burge J R, Rogan K M
Cardiology Service, Walter Reed Army Medical Center, Washington, D.C.
Clin Cardiol. 1993 Nov;16(11):802-8. doi: 10.1002/clc.4960161110.
Although cardiac abnormalities have been reported in patients with idiopathic polymyositis-dermatomyositis (PM), the nature and extent of these abnormalities have varied. The purpose of this study was to determine the prevalence and to obtain a better description of the spectrum of cardiac abnormalities in a cohort of patients with PM by use of a thorough noninvasive cardiac evaluation. Accordingly, we studied 26 patients with a history of PM and clinically inactive myositis (22 polymyositis, 4 dermatomyositis) between June 1984 and June 1991. Examination included history, physical examination, 12-lead electrocardiography, 24-h ambulatory electrocardiographic monitoring, chest radiography, transthoracic echocardiography, and radionuclide ventriculography. Of the patients studied, 77% were taking corticosteroid medications at a mean dose of 39 +/- 27 mg at the time of their evaluation. All 26 patients were identified as having two or more cardiac abnormalities. Cardiac symptoms and signs were common (62 and 81%, respectively), but were generally nonspecific. Electrocardiographic findings were most common (in 85% of cases), followed by findings on ambulatory monitoring (77%), echocardiography (42%), and radionuclide ventriculography (15%). The prevalence of mitral valve prolapse (8%) and hyperkinetic left ventricular contraction (12%) was significantly lower than previously reported. A secondary aim of this study was to determine associations between demographic variables including age, disease duration, cardiovascular symptoms, immunosuppressive therapy, autoantibody status, and creatinine phosphokinase level, and the presence of cardiac abnormalities. Of these patient variables, only increasing patient age was associated with an increased likelihood of cardiac abnormalities on noninvasive testing.(ABSTRACT TRUNCATED AT 250 WORDS)
虽然特发性多肌炎-皮肌炎(PM)患者中已报告有心脏异常,但这些异常的性质和程度各不相同。本研究的目的是通过全面的非侵入性心脏评估,确定一组PM患者中心脏异常的患病率,并更好地描述心脏异常的范围。因此,我们研究了1984年6月至1991年6月期间26例有PM病史且临床无活动性肌炎的患者(22例多肌炎,4例皮肌炎)。检查包括病史、体格检查、12导联心电图、24小时动态心电图监测、胸部X线检查、经胸超声心动图和放射性核素心室造影。在接受研究的患者中,77%在评估时正在服用皮质类固醇药物,平均剂量为39±27毫克。所有26例患者均被确定有两种或更多种心脏异常。心脏症状和体征很常见(分别为62%和81%),但通常不具特异性。心电图检查结果最常见(85%的病例),其次是动态监测结果(77%)、超声心动图(42%)和放射性核素心室造影(15%)。二尖瓣脱垂(8%)和左心室收缩亢进(12%)的患病率明显低于先前报告。本研究的第二个目的是确定包括年龄、病程、心血管症状、免疫抑制治疗、自身抗体状态和肌酸磷酸激酶水平在内的人口统计学变量与心脏异常存在之间的关联。在这些患者变量中,只有患者年龄增加与非侵入性检测中出现心脏异常的可能性增加有关。(摘要截短于250字)