Banigé Maïa, Estellat Candice, Biran Valerie, Desfrere Luc, Champion Valerie, Benachi Alexandra, Ville Yves, Dommergues Marc, Jarreau Pierre-Henri, Mokhtari Mostafa, Boithias Claire, Brioude Frederic, Mandelbrot Laurent, Ceccaldi Pierre-François, Mitanchez Delphine, Polak Michel, Luton Dominique
Department of Neonatology, Obstetrics and Gynecology, University Hospitals Paris Nord Val de Seine, Assistance Publique Hôpitaux de Paris, Beaujon Hospital, Clichy 92118, France.
Department of Epidemiology and Clinical Research, Assistance Publique Hôpitaux de Paris, Bichat Hospital, University Hospitals Paris Nord Val de Seine, UMR 1123 ECEVE/CIC-EC 1425, Inserm, Paris 75184, France.
J Endocr Soc. 2017 Jun;1(6):751-761. doi: 10.1210/js.2017-00189. Epub 2017 Apr 25.
Neonatal hyperthyroidism was first described in 1912 and in 1964 was shown to be linked to transplacental passage of maternal antibodies. Few multicenter studies have described the perinatal factors leading to fetal and neonatal dysthyroidism.
To show how fetal dysthyroidism (FD) and neonatal dysthyroidism (ND) can be predicted from perinatal variables, in particular, the levels of anti-thyrotropin receptor antibodies (TRAbs) circulating in the mother and child.
This was a retrospective multicenter study of data from the medical records of all patients monitored for pregnancy from 2007 to 2014.
Among 280,000 births, the medical records of 2288 women with thyroid dysfunction were selected and screened, and 417 women with Graves disease and positive for TRAbs during pregnancy were included.
Using the maternal TRAb levels, the cutoff value of 2.5 IU/L best predicted for FD, with a sensitivity of 100% and specificity of 64%. Using the newborn TRAb levels, the cutoff value of 6.8 IU/L best predicted for ND, with a sensitivity of 100% and a specificity of 94%. In our study, 65% of women with a history of Graves disease did not receive antithyroid drugs during pregnancy but still had infants at risk of ND.
In pregnant women with TRAb levels ≥2.5 IU/L, fetal ultrasound monitoring is essential until delivery. All newborns with TRAb levels ≥6.8 IU/L should be examined by a pediatrician with special attention for thyroid dysfunction and treated, if necessary.
新生儿甲状腺功能亢进症于1912年首次被描述,1964年被证明与母体抗体经胎盘传递有关。很少有多中心研究描述导致胎儿和新生儿甲状腺功能障碍的围产期因素。
展示如何根据围产期变量,特别是母婴体内循环的抗促甲状腺素受体抗体(TRAb)水平来预测胎儿甲状腺功能障碍(FD)和新生儿甲状腺功能障碍(ND)。
这是一项对2007年至2014年期间所有接受孕期监测患者的病历数据进行的回顾性多中心研究。
在280,000例分娩中,选择并筛查了2288例甲状腺功能障碍女性的病历,纳入了417例孕期患有格雷夫斯病且TRAb呈阳性的女性。
使用母体TRAb水平,2.5 IU/L的临界值对FD的预测效果最佳,敏感性为100%,特异性为64%。使用新生儿TRAb水平,6.8 IU/L的临界值对ND的预测效果最佳,敏感性为100%,特异性为94%。在我们的研究中,65%有格雷夫斯病病史的女性在孕期未接受抗甲状腺药物治疗,但仍有婴儿面临患ND的风险。
对于TRAb水平≥2.5 IU/L的孕妇,在分娩前进行胎儿超声监测至关重要。所有TRAb水平≥6.8 IU/L的新生儿应由儿科医生检查,特别关注甲状腺功能障碍情况,必要时进行治疗。