Hirschberg Angelica Lindén, Gidlöf Sebastian, Falhammar Henrik, Frisén Louise, Almqvist Catarina, Nordenskjöld Agneta, Nordenström Anna
Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Department of Gynecology and Reproductive Medicine, Karolinska University Hospital, Stockholm, Sweden.
J Clin Endocrinol Metab. 2021 Jan 23;106(2):e957-e965. doi: 10.1210/clinem/dgaa801.
Reduced fertility has been reported for women with congenital adrenal hyperplasia (CAH), especially for those with the salt-losing form. However, data are sparse on reproductive and perinatal outcomes in these women.
To investigate reproductive and perinatal outcomes in women with CAH.
Population-based and nationwide study using the National CAH Register, the Total Population Register, and the Medical Birth Register of Sweden.
A total of 272 women with CAH due to 21-hydroxylase deficiency and 27 200 controls matched by sex, age, and place of birth. The median age was 31 years.
The proportion of CAH women that have given birth, and reproductive and perinatal outcomes.
Of the 272 women with CAH, 69 gave birth to at least 1 child (25.4%), which was a lower frequency than for the controls (45.8%) (P < .001). Furthermore, women with CAH had fewer children than controls and were slightly older at birth of their first child. More women with CAH were diagnosed with gestational diabetes than controls, 4.9% versus 1.4% (P < .05), and more women with CAH were delivered through cesarean section, 51.4% versus 12.3% (P < .05). There was no difference in Apgar score or frequency of small-for-gestational age between children born to mothers with CAH and controls.
This is, to our knowledge, the largest cohort designed to investigate reproductive and perinatal outcomes in women with CAH. We found the birth rate to be lower in women with CAH; gestational diabetes and cesarean section were more common, but perinatal outcomes were comparable with controls.
据报道,先天性肾上腺皮质增生症(CAH)女性的生育能力下降,尤其是失盐型患者。然而,关于这些女性的生殖和围产期结局的数据很少。
调查CAH女性的生殖和围产期结局。
基于瑞典全国CAH登记册、总人口登记册和医疗出生登记册的全国性人群研究。
共有272例因21-羟化酶缺乏导致CAH的女性以及27200名按性别、年龄和出生地匹配的对照者。中位年龄为31岁。
CAH女性的生育比例以及生殖和围产期结局。
在272例CAH女性中,69例至少生育了1个孩子(25.4%),这一频率低于对照者(45.8%)(P<0.001)。此外,CAH女性生育的子女数少于对照者,且她们生育第一个孩子时的年龄略大。与对照者相比,更多CAH女性被诊断为妊娠期糖尿病,分别为4.9%和1.4%(P<0.05);更多CAH女性通过剖宫产分娩,分别为51.4%和12.3%(P<0.05)。CAH母亲所生孩子与对照者所生孩子的阿氏评分或小于胎龄儿频率没有差异。
据我们所知,这是旨在调查CAH女性生殖和围产期结局的最大队列研究。我们发现CAH女性的出生率较低;妊娠期糖尿病和剖宫产更为常见,但围产期结局与对照者相当。