Shinohara K, Miyagawa S, Fujita T, Aono T, Kidoguchi K
Department of Obstetrics and Gynecology, University of Tokushima School of Medicine, Japan.
Obstet Gynecol. 1999 Jun;93(6):952-7. doi: 10.1016/s0029-7844(99)00006-x.
To assess the possibility of preventing cardiac or cutaneous manifestations of neonatal lupus erythematosus or treating the fetus with congenital heart block by administering corticosteroid therapy to the mother.
Eighty-seven offspring of 40 anti-Ro/SSA-positive mothers, followed up from 1979 to 1996, were evaluated. Autoantibodies against Ro/SSA and La/SSB antigens were detected by immunodiffusion and enzyme-linked immunosorbent assay.
None of 26 neonates whose mothers received corticosteroid maintenance therapy initiated before 16 weeks' gestation demonstrated congenital heart block, whereas 15 of 61 neonates whose mothers received no corticosteroids during pregnancy or began receiving steroid therapy after 16 weeks' gestation had congenital heart block. Complete congenital heart block, once developed, did not respond to corticosteroid treatment in utero. Four infants whose mothers received steroid treatment before 16 weeks' gestation had skin lesions of neonatal lupus erythematosus.
Once established, complete congenital heart block was irreversible and maternal corticosteroid therapy did not effectively prevent cutaneous lupus erythematosus. However, prenatal maintenance therapy with prednisolone or betamethasone given to the mother starting early in pregnancy (before 16 weeks' gestation) might reduce the risk of developing antibody-mediated congenital heart block in the offspring.
评估通过对母亲进行皮质类固醇治疗来预防新生儿红斑狼疮的心脏或皮肤表现或治疗患有先天性心脏传导阻滞胎儿的可能性。
对1979年至1996年随访的40名抗Ro/SSA阳性母亲的87名后代进行了评估。通过免疫扩散和酶联免疫吸附测定法检测针对Ro/SSA和La/SSB抗原的自身抗体。
在妊娠16周前开始接受皮质类固醇维持治疗的母亲所生的26名新生儿中,无一例出现先天性心脏传导阻滞,而在妊娠期间未接受皮质类固醇治疗或在妊娠16周后开始接受类固醇治疗的母亲所生的61名新生儿中,有15例患有先天性心脏传导阻滞。一旦出现完全性先天性心脏传导阻滞,宫内皮质类固醇治疗无效。4名母亲在妊娠16周前接受类固醇治疗的婴儿出现了新生儿红斑狼疮的皮肤病变。
一旦确立,完全性先天性心脏传导阻滞是不可逆的,母亲的皮质类固醇治疗不能有效预防皮肤红斑狼疮。然而,在妊娠早期(妊娠16周前)开始对母亲进行泼尼松龙或倍他米松的产前维持治疗可能会降低后代发生抗体介导的先天性心脏传导阻滞的风险。