Literature DB >> 16789634

Fertility in patients with congenital adrenal hyperplasia.

H L Claahsen-van der Grinten1, N M M L Stikkelbroeck, C G J Sweep, A R M M Hermus, B J Otten.   

Abstract

Congenital adrenal hyperplasia (CAH) is generally regarded as a paediatric endocrine disease, but nowadays nearly all patients reach adulthood as a result of improved diagnosis and treatment. It is now increasingly recognised that treatment goals shift during life: one of the major treatment goals in childhood and puberty, i.e. normal growth and development, is no longer relevant after childhood, whereas other aspects, such as fertility and side effects of long-term glucocorticoid treatment, become more important in adulthood. This paper focuses on fertility in male and female adult patients with CAH. In males with CAH the fertility rate is reduced compared with the normal population, the most frequent cause being testicular adrenal rest tumours. Development and growth of these tumours is assumed to be ACTH dependent and undertreatment may play an important role. If intensifying glucocorticoid treatment does not lead to tumour decrease, surgical intervention may be considered, but the effect on fertility is not yet known. In females with CAH the degree of fertility depends on the phenotype of the CAH. Most fertility problems are seen in the classic salt-wasting type. Age of menarche and regularity of the menstrual cycle depends on the degree of adrenal suppression. Not only adrenal androgens have to be normalised but also the levels of adrenal progestins (progesterone and 17-OH-progesterone) that interfere with normal ovulatory cycles. The regularity of menstrual cycles can be considered as an important measure of therapeutic control in adolescent females with CAH and therefore as a therapeutic goal from (peri)pubertal years on. Other factors that contribute to impaired fertility in females with CAH are ovarian hyperandrogenism (polycystic ovary syndrome), ovarian adrenal rest tumours, genital surgery and psychological factors. Subfertility in CAH can have its origin already in the peripubertal years and is therefore of interest to the paediatric endocrinologist.

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Year:  2006        PMID: 16789634     DOI: 10.1515/jpem.2006.19.5.677

Source DB:  PubMed          Journal:  J Pediatr Endocrinol Metab        ISSN: 0334-018X            Impact factor:   1.634


  11 in total

1.  Development of a biomarker database toward performing disease classification and finding disease interrelations.

Authors:  Shaikh Farhad Hossain; Ming Huang; Naoaki Ono; Aki Morita; Shigehiko Kanaya; Md Altaf-Ul-Amin
Journal:  Database (Oxford)       Date:  2021-03-11       Impact factor: 3.451

2.  Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency: an Endocrine Society clinical practice guideline.

Authors:  Phyllis W Speiser; Ricardo Azziz; Laurence S Baskin; Lucia Ghizzoni; Terry W Hensle; Deborah P Merke; Heino F L Meyer-Bahlburg; Walter L Miller; Victor M Montori; Sharon E Oberfield; Martin Ritzen; Perrin C White
Journal:  J Clin Endocrinol Metab       Date:  2010-09       Impact factor: 5.958

3.  Growth and reproductive outcomes in congenital adrenal hyperplasia.

Authors:  Todd D Nebesio; Erica A Eugster
Journal:  Int J Pediatr Endocrinol       Date:  2010-02-01

4.  Approach to the adult with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.

Authors:  Deborah P Merke
Journal:  J Clin Endocrinol Metab       Date:  2008-03       Impact factor: 5.958

5.  Testicular adrenal rest tumors in patients with congenital adrenal hyperplasia.

Authors:  Esra Deniz Papatya Çakir; Fatma Sentürk Mutlu; Erdal Eren; Aliye Ozlem Paşa; Halil Sağlam; Omer Tarim
Journal:  J Clin Res Pediatr Endocrinol       Date:  2012-06

6.  Clinical manifestations of testicular adrenal rest tumor in males with congenital adrenal hyperplasia.

Authors:  Min Kyung Yu; Mo Kyung Jung; Ki Eun Kim; Ah Reum Kwon; Hyun Wook Chae; Duk Hee Kim; Ho-Seong Kim
Journal:  Ann Pediatr Endocrinol Metab       Date:  2015-09-30

Review 7.  Management issues of congenital adrenal hyperplasia during the transition from pediatric to adult care.

Authors:  Jin-Ho Choi; Han-Wook Yoo
Journal:  Korean J Pediatr       Date:  2017-02-27

8.  Testicular adrenal rest tumours in congenital adrenal hyperplasia.

Authors:  H L Claahsen-van der Grinten; A R M M Hermus; B J Otten
Journal:  Int J Pediatr Endocrinol       Date:  2009-02-26

Review 9.  Reproductive outcomes of female patients with congenital adrenal hyperplasia due to 21-hydroxylase defi ciency.

Authors:  Mouna Feki Mnif; Mahdi Kamoun; Faten Hadj Kacem; Fatma Mnif; Nadia Charfi; Basma Ben Naceur; Nabila Rekik; Mohamed Abid
Journal:  Indian J Endocrinol Metab       Date:  2013-09

10.  Positive fertility outcomes in a female with classic congenital adrenal hyperplasia following bilateral adrenalectomy.

Authors:  Urania Dagalakis; Ashwini Mallappa; Meredith Elman; Martha Quezado; Deborah P Merke
Journal:  Int J Pediatr Endocrinol       Date:  2016-05-20
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