Markers of Fertility in Adolescents With Chronic Endocrinopathies at Transition From Paediatric to Adult Care

被引:0
|
作者
Choukair, Daniela [1 ]
Mittnacht, Janna [1 ]
Bettendorf, Markus [1 ]
机构
[1] Univ Hosp Heidelberg, Dept Paediat, Div Paediat Endocrinol & Diabet, Heidelberg, Germany
关键词
adolescents with chronic endocrinopathies; fertility markers; transition; ANTI-MULLERIAN HORMONE; TURNER SYNDROME; KLINEFELTER SYNDROME; INHIBIN-B; BOYS; HYPOGONADISM; DEFICIENCY; DIAGNOSIS; PITUITARY; PUBERTY;
D O I
10.1002/edm2.493
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: During the process of transition from paediatric to adult health care, counselling concerning fertility is an important issue and is based mainly on serum markers of gonadal function. Here, we analysed these markers in adolescents with various underlying endocrine diseases at the time of transition. Methods: After reaching near adult height and late puberty (girls: bone age [BA] >= 14 years, and boys: BA >= 16 years), we assessed stages of puberty according to Tanner and measured testes or ovarian volumes and serum markers of gonadal function (anti-Mullerian hormone [AMH], inhibin B, 17 beta-estradiol, testosterone). Results: One hundred and ten patients (56 females and 54 males) were included from May 2010 to March 2016 with multiple pituitary hormone deficiency (MPHD; n = 17), growth hormone deficiency (GHD; n = 35), Turner syndrome (TS; n = 27), short stature after being born small for gestational age (SGA; n = 20) and Klinefelter syndrome (KS; n = 11). Female and male adolescents exhibited mature secondary sexual characteristics. The levels of serum inhibin B and AMH were lower in TS and female MPHD than in GHD and SGA, each independently (p < 0.05). The levels of serum AMH were higher whereas serum inhibin B were lower in male MPHD and KS (p < 0.05). Ovary volumes were significantly smaller in patients with TS, and testicular volumes were smaller in patients with KS. Conclusions: After current established treatments with sex steroids, the development of secondary sexual characteristics was mature. However, impaired markers of fertility have been identified in patients with TS, KS and MPHD, reflecting gonadal dysgenesis in TS and KS, but gonadal immaturity in MPHD as gonadal gonadotropin stimulation is lacking throughout development. Consequently, in patients with MPHD, these markers cannot reliably predict individual fertility, which warrants consideration and incorporation in future treatment concepts.
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页数:8
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