Laboratoire d'Endocrinologie Moléculaire et Maladies Rares (V.T.-G., R.M., Y.M.), Centre de Biologie et de Pathologie Est, Hospices civils de Lyon, 69677 Bron, France; Département de Génétique (J.-M.C), Laboratoire Cerba, 95066 Cergy Pontoise, France; Département d'Endocrinologie, Diabétologie, et Métabolismes Pédiatriques (M.D.), Hôpital Mère-Enfant, HCL, 69677 Bron, France; Unité d'Endocrinologie pédiatrique (C.B.-M.), Centre Hospitalier de Bicêtre, 94275 Le Kremlin-Bicêtre, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France; Unité de Génétique Clinique (C.B.), Hôpital Robert Debré, AP-HP, 75019 Paris, France; Laboratoire d'Explorations Fonctionnelles (M.H.), Hôpital Trousseau, AP-HP, 75012 Paris, France; Unité d'Endocrinologie et Gynécologie Obstétrique (F.L.), Pôle Femme-Mère-Couple, Hôpital Paule de Viguier, 31059 Toulouse, France; Département de Génétique (N.P.), Hôpital Timone, Assistance Publique-Hôpitaux de Marseille, 13385 Marseille, France; Département de Génétique (S.O.), Hôpital Sud, 35203 Rennes, France; and Département de Génétique (A.G.), Centre Hospitalier UniversitaireAngers, 49033 Angers, France.
J Clin Endocrinol Metab. 2014 Apr;99(4):1180-8. doi: 10.1210/jc.2013-2895. Epub 2014 Jan 28.
Prenatal dexamethasone (DEX) treatment has been proposed since 1984 to prevent genital virilization in girls with congenital adrenal hyperplasia (CAH). DEX is effective in CAH females if initiated before the sixth week of gestation, but its safety in children treated in utero remains controversial regarding cognitive functions.
To avoid prenatal DEX in males and initiate DEX in due time in CAH females, we proposed in 2002 a protocol for fetal sex determination in the maternal serum (SRY test).
We conducted a retrospective study of the management of 258 fetuses in the period 2002 through 2011 in pregnancies managed in referent medical centers with an institutional practice.
A total of 258 fetuses at risk of CAH (134 males and 124 females) were included.
DEX was offered after informed consent to pregnant women.
The sensitivity of an early SRY test was evaluated after data collection.
The SRY test is sensitive from 4 weeks and 5 days of gestation. It avoided prenatal DEX in 68% of males, and this percentage increased over the years. DEX was maintained until prenatal diagnosis in non-CAH females. Virilization was prevented in 12 CAH girls treated at the latest at 6 weeks gestation and minimized in 3 girls treated between 6 and 7 weeks gestation. Maternal tolerance was correct. No fetal malformations were noted in the 154 children treated in utero.
The SRY test is reliable to avoid prenatal DEX in males, but its application must be improved. Prenatal DEX should be maintained to prevent virilization and traumatic surgery in CAH girls after informed consent and information provided to families about the benefit to risk ratio in limiting hyperandrogenism during fetal life. Our large multicentric French cohort has helped to better assess the risks previously reported.
自 1984 年以来,人们一直提议在患有先天性肾上腺皮质增生症(CAH)的女孩中使用产前地塞米松(DEX)治疗以防止生殖器男性化。如果在妊娠第六周之前开始,DEX 对 CAH 女性有效,但在子宫内治疗的儿童的认知功能方面,其安全性仍存在争议。
为了避免男性产前 DEX 并及时在 CAH 女性中开始 DEX,我们于 2002 年提出了一种在母体血清(SRY 测试)中确定胎儿性别的方案。
我们对 2002 年至 2011 年期间在参考医疗中心进行管理的 258 例妊娠中的胎儿管理进行了回顾性研究,这些妊娠均具有机构实践。
共有 258 例患有 CAH 风险的胎儿(134 名男性和 124 名女性)被纳入研究。
向孕妇提供知情同意后提供 DEX。
数据收集后评估早期 SRY 测试的敏感性。
SRY 测试从妊娠 4 周零 5 天开始具有敏感性。它避免了 68%的男性进行产前 DEX,并且这一比例随着时间的推移而增加。在非 CAH 女性中,DEX 一直维持到产前诊断。12 名最晚在 6 周龄时接受治疗的 CAH 女孩的性分化得到了预防,3 名在 6 至 7 周龄时接受治疗的女孩的性分化得到了最小化。母亲耐受性正确。在 154 名在子宫内接受治疗的儿童中未发现胎儿畸形。
SRY 测试可靠,可以避免男性的产前 DEX,但必须改进其应用。在获得知情同意并向家庭提供有关在胎儿期限制雄性激素过多的利弊比信息后,应继续进行产前 DEX 以防止 CAH 女孩的性分化和创伤性手术。我们的大型法国多中心队列有助于更好地评估以前报告的风险。