Ovarian reserve and fertility parameters in post-pubertal females with congenital adrenal hyperplasia: a case-control study.

IF 1.3 4区 医学 Q4 ENDOCRINOLOGY & METABOLISM Journal of Pediatric Endocrinology & Metabolism Pub Date : 2024-03-11 Print Date: 2024-04-25 DOI:10.1515/jpem-2023-0462
Marwa Nawar, Marwa Sayed Mohammad, Asmaa Shabaan, Heba Elsedfy
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Abstract

Objectives: Congenital adrenal hyperplasia (CAH) is an autosomal recessive disorder characterized by impaired activity of the enzyme required for cortisol and aldosterone production, resulting in increased adrenal androgen synthesis. Factors affecting fertility in CAH patients include ambiguous genitalia and their complications, excessive androgen secretion, adrenal progesterone hypersecretion, and various psychosocial factors. Serum anti-Müllerian hormone (AMH) level is used to assess ovarian reserve in women. A few data on serum AMH levels in CAH patients are available in the literature. The aim of the study was to evaluate ovarian reserve in a group of post-menarche females diagnosed with CAH by measuring serum AMH level and assessing the number of antral follicles sonographically.

Methods: A case-control study was conducted on 17 post-pubertal CAH females and 17 age-matched healthy female controls; the mean age of the patient group was 15.09 ± 3.55 years ranging from 11 to 24 years, while the mean age of the control group was 16.04 ± 3.72 years ranging from 12 to 25 years, the mean post-menarchal age of the patients group was 3.29 ± 1.37 years ranging from 1 to 6 years while the mean post-menarchal age of the control group was 4.13 ± 1.62 years ranging from 1 to 9 years. The degree of hirsutism was compared between the two groups according to the modified Ferriman-Gallwey score, clitoral length was assessed using a digital caliber. Serum levels of adrenal androgens in addition to basal levels of serum follicle-stimulating hormone (FSH), luteinizing hormone (LH), estradiol, progesterone, and serum AMH were measured in both groups.

Results: Patients had smaller uterine volumes, and smaller ovarian volumes but a comparable number of antral follicles and comparable serum AMH levels relative to controls.

Conclusions: Good compliance with treatment in patients with CAH results in good hormonal control, low risk of PCOS, good fertility parameters, and a good ovarian reserve.

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患有先天性肾上腺皮质增生症的青春期后女性的卵巢储备和生育参数:一项病例对照研究。
背景:先天性肾上腺增生症(CAH)是一种常染色体隐性遗传疾病,其特点是皮质醇和醛固酮生成所需酶的活性受损,导致肾上腺雄激素合成增加。影响 CAH 患者生育能力的因素包括生殖器发育不全及其并发症、雄激素分泌过多、肾上腺孕酮分泌过多以及各种社会心理因素。血清抗缪勒氏管激素(AMH)水平用于评估女性的卵巢储备功能。有关 CAH 患者血清 AMH 水平的文献资料很少:通过测量血清 AMH 水平和声像图评估前卵泡数量,评估一组经诊断患有 CAH 的初潮后女性的卵巢储备功能:对17名青春期后CAH女性和17名年龄匹配的健康女性对照组进行了病例对照研究;患者组的平均年龄为(15.09 ± 3.55)岁,从11岁到24岁不等;对照组的平均年龄为(16.患者组的平均年龄为(15.09±3.55)岁,介于 11-24 岁之间;对照组的平均年龄为(16.04±3.72)岁,介于 12-25 岁之间;患者组的平均绝经后年龄为(3.29±1.37)岁,介于 1-6 岁之间;对照组的平均绝经后年龄为(4.13±1.62)岁,介于 1-9 岁之间。两组的多毛症程度根据改良的费里曼-高尔维评分进行比较,阴蒂长度用数字口径进行评估。除了血清卵泡刺激素(FSH)、黄体生成素(LH)、雌二醇、孕酮和血清抗缪勒氏管激素(AMH)的基础水平外,还测量了两组患者的血清肾上腺雄激素水平。对子宫体积、卵巢体积和前卵泡数量进行超声评估:结果:与对照组相比,患者的子宫体积较小,卵巢体积也较小,但前区卵泡数量和血清 AMH 水平相当:结论:CAH 患者对治疗的依从性良好,可获得良好的激素控制、较低的多囊卵巢综合征风险、良好的生育参数和卵巢储备功能。
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来源期刊
CiteScore
2.70
自引率
7.10%
发文量
176
审稿时长
3-6 weeks
期刊介绍: The aim of the Journal of Pediatric Endocrinology and Metabolism (JPEM) is to diffuse speedily new medical information by publishing clinical investigations in pediatric endocrinology and basic research from all over the world. JPEM is the only international journal dedicated exclusively to endocrinology in the neonatal, pediatric and adolescent age groups. JPEM is a high-quality journal dedicated to pediatric endocrinology in its broadest sense, which is needed at this time of rapid expansion of the field of endocrinology. JPEM publishes Reviews, Original Research, Case Reports, Short Communications and Letters to the Editor (including comments on published papers),. JPEM publishes supplements of proceedings and abstracts of pediatric endocrinology and diabetes society meetings.
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