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完全性房室传导阻滞的迟发性发病可能与免疫介导和先天性有关。

Late development of complete atrioventricular block may be immune mediated and congenital in origin.

机构信息

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

出版信息

Acta Paediatr. 2014 Mar;103(3):275-81. doi: 10.1111/apa.12483. Epub 2013 Dec 30.

Abstract

AIM

To investigate the correlation between maternal autoantibodies and age at diagnosis of isolated complete atrioventricular (AV) block (CAVB) and to study signs of late progression of foetal immune-mediated insults in cases of postnatally diagnosed CAVB.

METHODS

Patients with CAVB (n = 190) identified in a population-based manner were included. Maternal autoantibody profile was correlated with age at CAVB diagnosis. A structured review of medical records was performed if a late CAVB diagnosis (>27 days post-partum) was associated with a sero-positive mother.

RESULTS

Maternal Ro/La autoantibodies were observed in 88% of cases with a congenital diagnosis. Thirteen cases with a sero-positive mother and late CAVB diagnosis were found (age-range: 4 months-43 years). In two cases, CAVB was diagnosed in conjunction with infections, one case had a family history of cardiomyopathy and two cases had nontypical clinical presentations, indicating alternative pathogenetic mechanisms. In the remaining eight cases, no likely factors inducing CAVB, other than maternal autoantibodies, could be identified.

CONCLUSION

Our observations support the hypothesis that late progression to CAVB can be the result of an immune-mediated pathogenetic mechanism during foetal life. An autoantibody-associated diagnosis after the neonatal period is therefore possible, and testing of maternal serology at the time of diagnosis is recommended.

摘要

目的

探讨母体自身抗体与孤立性完全性房室(AV)阻滞(CAVB)诊断年龄之间的相关性,并研究新生儿期后诊断的 CAVB 病例中胎儿免疫介导损伤的晚期进展迹象。

方法

以人群为基础的方式纳入了 190 例 CAVB 患者。将母体自身抗体谱与 CAVB 的诊断年龄相关联。如果晚期 CAVB 诊断(>27 天产后)与血清阳性母亲相关,则对病历进行结构化审查。

结果

88%的先天性诊断病例中观察到母体 Ro/La 自身抗体。发现 13 例血清阳性母亲和晚期 CAVB 诊断病例(年龄范围:4 个月-43 岁)。在 2 例中,CAVB 与感染同时诊断,1 例有心肌病家族史,2 例有非典型临床表现,表明存在其他发病机制。在其余 8 例中,除了母体自身抗体之外,无法确定其他可能导致 CAVB 的因素。

结论

我们的观察结果支持这样一种假设,即晚期进展为 CAVB 可能是胎儿期免疫介导发病机制的结果。因此,在新生儿期后出现与自身抗体相关的诊断是可能的,建议在诊断时检测母体血清学。

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