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非经典型21-羟化酶缺乏症不孕女性孕前及围产期的临床特征与治疗

Clinical characteristics and treatment during preconception and perinatal period of infertile women with non-classical 21-hydroxylase deficiency.

作者信息

Cui Xuejiao, Li Ping

机构信息

Department of Endocrinology, Shengjing Hospital of China Medical University, Tiexi District, 39 Huaxiang Road, Shenyang, 110022, Liaoning, China.

出版信息

Reprod Health. 2024 Oct 1;21(1):139. doi: 10.1186/s12978-024-01874-2.

DOI:10.1186/s12978-024-01874-2
PMID:39354633
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11443925/
Abstract

OBJECTIVE

A single-center observational study to determine the clinical characteristics and therapeutic dose adjustments in women of reproductive age with infertility and non-classical 21-hydroxylase deficiency (NC-21OHD).

DESIGN

A retrospective analysis of 20 women of reproductive age who were diagnosed with NC-21OHD during an infertility evaluation at Shengjing Hospital of China Medical University from January 2013 to May 2024 was performed. The clinical manifestations, auxiliary examinations, adjustment of glucocorticoid (GC) treatment during preconception and perinatal period, and pregnancy outcomes were analyzed.

RESULTS

14 of 16 patients (87.5%) had inappropriately elevated progesterone levels during the follicular phase. The average levels of 17α-hydroxyprogesterone, testosterone, androstenedione, and dehydroepiandrosterone sulfate in the follicular phase were also significantly increased. All 20 infertile patients received GC treatment before preparing for pregnancy. During the follow-up, six of 20 patients had seven conceptions. three patients had spontaneous abortions in the first trimester and four patients delivered babies (4/20). Three patients had a GC dose that was maintained throughout pregnancy and one had an increase in the GC dose starting in the second trimester. Of the remaining 16 patients, seven are still trying to conceive and nine had discontinued treatment.

CONCLUSIONS

An abnormal increase in the follicular phase progesterone level is the most common serologic marker for NC-21OHD among infertile women. Ovulation can be restored after GC treatment, but the proportion of successful conceptions remains low. The dose of GCs in most pregnant women remained unchanged throughout pregnancy.

摘要

目的

一项单中心观察性研究,以确定患有不孕症和非经典21-羟化酶缺乏症(NC-21OHD)的育龄女性的临床特征和治疗剂量调整。

设计

对2013年1月至2024年5月在中国医科大学附属盛京医院进行不孕症评估时被诊断为NC-21OHD的20名育龄女性进行回顾性分析。分析临床表现、辅助检查、孕前和围产期糖皮质激素(GC)治疗的调整以及妊娠结局。

结果

16例患者中有14例(87.5%)在卵泡期孕酮水平异常升高。卵泡期17α-羟孕酮、睾酮、雄烯二酮和硫酸脱氢表雄酮的平均水平也显著升高。所有20例不孕患者在备孕前均接受了GC治疗。随访期间,20例患者中有6例怀孕7次。3例患者在孕早期自然流产,4例患者分娩(4/20)。3例患者在整个孕期维持GC剂量不变,1例患者从孕中期开始增加GC剂量。其余16例患者中,7例仍在尝试受孕,9例已停止治疗。

结论

卵泡期孕酮水平异常升高是不孕女性中NC-21OHD最常见的血清学标志物。GC治疗后排卵可恢复,但成功受孕的比例仍然较低。大多数孕妇在整个孕期GC剂量保持不变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78bb/11443925/3efbbe0318a6/12978_2024_1874_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78bb/11443925/3efbbe0318a6/12978_2024_1874_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78bb/11443925/3efbbe0318a6/12978_2024_1874_Fig1_HTML.jpg

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[Expert Consensus on Obesity Prevention and Treatment in China].《中国肥胖防治专家共识》
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Efficacy and safety of prenatal dexamethasone treatment in offspring at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: A systematic review and meta-analysis.
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Clin Endocrinol (Oxf). 2020 Feb;92(2):109-123. doi: 10.1111/cen.14126. Epub 2019 Dec 2.
4
Assisted Reproduction in Congenital Adrenal Hyperplasia.先天性肾上腺皮质增生症中的辅助生殖
Front Endocrinol (Lausanne). 2019 Oct 23;10:723. doi: 10.3389/fendo.2019.00723. eCollection 2019.
5
Pregnancy in Congenital Adrenal Hyperplasia.先天性肾上腺皮质增生症患者的妊娠问题。
Endocrinol Metab Clin North Am. 2019 Sep;48(3):619-641. doi: 10.1016/j.ecl.2019.05.011.
6
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7
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