首页> 外文期刊>Seminars in Arthritis and Rheumatism >Immune-mediated congenital heart block (CHB): identifying and counseling patients at risk for having children with CHB.
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Immune-mediated congenital heart block (CHB): identifying and counseling patients at risk for having children with CHB.

机译:免疫介导的先天性心脏传导阻滞(CHB):识别和咨询有患CHB患儿风险的患者。

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摘要

OBJECTIVE: To identify patterns of maternal antibodies associated with an increased risk of having a child with congenital heart block (CHB) and to provide a basis for counseling women with a previously affected child. METHODS: This retrospective clinical study of the obstetric histories of 46 Finnish women with a CHB child compared the strength and specificity of the immune response to SS-A/Ro and SS-B/La, as determined by immunoblot and ELISA, in 44 affected women with 85 women with systemic lupus erythematosus (SLE) and 32 women with primary Sjogren's syndrome (SS) with healthy children. RESULTS: High levels of anti-SS-A/Ro and anti-SS-B/La by practically all assays were associated with a significantly increased risk of having a CHB child. The best single test to identify high-risk mothers was anti-52 kd SS-A/Ro by immunoblot (OR 18.9), and it was the only assay to detect mothers at increased risk of CHB as compared with controls with primary SS. Low risk of CHB was indicated by undetectable or low levels of antibodies in the ELISA assays and no reactivity on immunoblot. Mothers with a previous child with CHB had a history of fetal loss (mostly spontaneous abortions) or a history of recurrent fetal losses (> or = 3) slightly more often than controls. Late-trimester obstetric complications in non-CHB pregnancies were insignificant. The relative risk for a female child compared with a male child to have CHB was 1.9 (1.2-2.9, P = .009), and the risk of the mother having another child with CHB was 12% (4 of 34). CONCLUSION: Although there is no unique antibody profile specific for CHB, mothers with a high or low risk of having a child with CHB can be identified. Female children appear to have an increased risk of CHB, but the risk of the mother having another child with CHB is low.
机译:目的:确定与先天性心脏传导阻滞(CHB)患儿风险增加相关的母源抗体类型,并为咨询先前患病儿童的妇女提供基础。方法:这项回顾性临床研究对46例有CHB患儿的芬兰妇女的产科历史进行了比较,比较了44例受感染的人对SS-A / Ro和SS-B / La免疫应答的强度和特异性,方法是通过免疫印迹和ELISA确定妇女中有85名患有系统性红斑狼疮(SLE)的妇女和32名患有原发性干燥综合征(SS)的健康儿童。结果:几乎所有检测方法均发现高水平的抗SS-A / Ro和抗SS-B / La与患CHB患儿的风险显着增加有关。识别高危母亲的最佳单一检测方法是通过免疫印迹检测抗52 kd SS-A / Ro(OR 18.9),这是唯一检测出与原发性SS对照相比母亲CHB风险增加的母亲的检测方法。在ELISA分析中检测不到或抗体水平低,并且在免疫印迹上无反应性,表明CHB风险低。有CHB前胎的母亲比对照组有更多的胎儿丢失史(多为自然流产)或复发性胎儿丢失史(>或= 3)。非CHB妊娠的妊娠晚期产科并发症微不足道。与男婴相比,女婴患CHB的相对风险为1.9(1.2-2.9,P = .009),而母亲又有CHB患儿的风险为12%(34之4)。结论:尽管没有针对CHB的独特抗体谱,但可以确定有CHB患儿风险的母亲高低。女童患CHB的风险似乎增加,但是母亲生另一个CHB患儿的风险较低。

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