Division of Rheumatology, Department of Medicine, NYU School of Medicine, New York, NY 10016, USA.
Circulation. 2011 Nov 1;124(18):1927-35. doi: 10.1161/CIRCULATIONAHA.111.033894. Epub 2011 Oct 3.
Cardiac manifestations of neonatal lupus include conduction disease and, rarely, an isolated cardiomyopathy. This study was initiated to determine the mortality and morbidity of cardiac neonatal lupus and associated risk factors in a multi-racial/ethnic US-based registry to provide insights into the pathogenesis of antibody-mediated injury and data for counseling.
Three hundred twenty-five offspring exposed to maternal anti-SSA/Ro antibodies with cardiac neonatal lupus met entry criteria. Maternal, fetal echocardiographic, and neonatal risk factors were assessed for association with mortality. Fifty-seven (17.5%) died, 30% in utero. The probability of in utero death was 6%. The cumulative probability of survival at 10 years for a child born alive was 86%. Fetal echocardiographic risk factors associated with increased mortality in a multivariable analysis of all cases included hydrops and endocardial fibroelastosis. Significant predictors of in utero death were hydrops and earlier diagnosis, and of postnatal death were hydrops, endocardial fibroelastosis, and lower ventricular rate. Isolated heart block was associated with a 7.8% case fatality rate, whereas the concomitant presence of dilated cardiomyopathy or endocardial fibroelastosis quadrupled the case fatality rate. There was a significantly higher case fatality rate in minorities compared with whites, who were at a lower risk of hydrops and endocardial fibroelastosis. Pacing was required in 70%; cardiac transplantation was required in 4 children.
Nearly one fifth of fetuses who develop cardiac neonatal lupus die of complications predicted by echocardiographic abnormalities consistent with antibody-associated disease beyond the atrioventricular node. The disparity in outcomes observed between minorities and whites warrants further investigation.
新生儿狼疮的心脏表现包括传导疾病,且很少见孤立性心肌病。本研究旨在确定多种族/族裔美国人群中存在心脏新生儿狼疮的死亡率和发病率以及相关风险因素,以便深入了解抗体介导损伤的发病机制,并为咨询提供数据。
符合条件的 325 名存在抗 SSA/Ro 抗体的母亲所生的子女患有心脏新生儿狼疮。评估了母亲、胎儿超声心动图和新生儿的风险因素与死亡率的关系。57 例(17.5%)死亡,30%在宫内。宫内死亡的概率为 6%。出生后存活 10 年的患儿累积生存率为 86%。多变量分析显示,所有病例中与死亡率增加相关的胎儿超声心动图危险因素包括水肿和心内膜心肌纤维化。在所有病例中,多变量分析显示,水肿和更早的诊断与宫内死亡相关,而水肿、心内膜心肌纤维化和更低的心室率与新生儿死亡相关。孤立性心脏传导阻滞的病死率为 7.8%,而扩张型心肌病或心内膜心肌纤维化的存在使病死率增加了四倍。与白人相比,少数族裔的病死率明显更高,而白人发生水肿和心内膜心肌纤维化的风险较低。需要起搏的比例为 70%;4 例患儿需要心脏移植。
近五分之一患有心脏新生儿狼疮的胎儿因心脏超声异常而出现并发症,这些异常与房室结以外的抗体相关疾病一致,导致胎儿死亡。少数族裔与白人之间观察到的结果差异需要进一步研究。