Semen quality and testicular adrenal rest tumour development in 46,XY congenital adrenal hyperplasia: the importance of optimal hormonal replacement.


Journal

European journal of endocrinology
ISSN: 1479-683X
Titre abrégé: Eur J Endocrinol
Pays: England
ID NLM: 9423848

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 12 10 2020
accepted: 28 01 2021
pubmed: 2 2 2021
medline: 19 3 2021
entrez: 1 2 2021
Statut: ppublish

Résumé

To study the impact of the quality of therapeutic control on fertility and on the prevalence of testicular adrenal rest tumours (TART) in young males with congenital adrenal hyperplasia (CAH). Combined cross-sectional and retrospective clinical study. Twenty-nine patients and age-matched controls underwent clinical investigation, including semen analysis, testicular and adrenal ultrasound imaging, and serum and hair steroid analysis. The quality of therapeutic control was categorized as 'poor', 'moderate' or 'medium'. Evaluation of current control was based on concentrations of 17-hydroxy-progesterone and androstenedione in serum and 3 cm hair; previous control was categorized based on serum 17-hydroxy-progesterone concentrations during childhood and puberty, anthropometric and puberty data, bone age data and adrenal sizes. Semen quality was similar in males with CAH and controls (P = 0.066), however patients with 'poor' past control and large TART, or with 'poor' current CAH control had low sperm counts. Follicle-stimulating hormone was decreased, if current CAH control was 'poor' (1.8 ± 0.9 U/L; 'good': 3.9 ± 2.2 U/L); P = 0.015); luteinizing hormone was decreased if it was 'poor' (1.8 ± 0.9 U/L; P = 0.041) or 'moderate' (1.9 ± 0.6 U/L; 'good': 3.0 ± 1.3 U/L; P = 0.025). None of the males with 'good' past CAH control, 50% of those with 'moderate' past control and 80% with 'poor past control had bilateral TART. The prevalence of TART in males with severe (class null or A) CYP21A2 mutations was 53% and 25% and 0% in those with milder class B and C mutations, respectively. TART development is favoured by inadequate long-term hormonal control in CAH. Reduced semen quality may be associated with large TART. Gonadotropin suppression by adrenal androgen excess during the latest spermatogenic cycle may contribute to impairment of spermatogenesis.

Identifiants

pubmed: 33524003
doi: 10.1530/EJE-20-1154
pii: EJE-20-1154
doi:
pii:

Substances chimiques

Adrenal Cortex Hormones 0
Androgens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

487-501

Auteurs

Julia Rohayem (J)

Department of Clinical and Surgical Andrology, Center of Reproductive Medicine and Andrology, University of Münster, Münster, Nordrhein-Westfalen, Germany.

Lena Maria Bäumer (LM)

Department of Clinical and Surgical Andrology, Center of Reproductive Medicine and Andrology, University of Münster, Münster, Nordrhein-Westfalen, Germany.

Michael Zitzmann (M)

Department of Clinical and Surgical Andrology, Center of Reproductive Medicine and Andrology, University of Münster, Münster, Nordrhein-Westfalen, Germany.

Susanne Fricke-Otto (S)

Department of Pediatric Endocrinology and Diabetes, Helios-Klinikum Krefeld, Krefeld, Nordrhein-Westfalen, Germany.

Klaus Mohnike (K)

Department of Pediatric Endocrinology and Diabetes, University of Magdeburg, Children's Hospital Magdeburg, Magdeburg, Sachsen-Anhalt, Germany.

Bettina Gohlke (B)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital Bonn, University of Bonn, Bonn, Nordrhein-Westfalen, Germany.

Felix Reschke (F)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital Dresden, University of Dresden, Dresden, Sachsen, Germany.

Claus Jourdan (C)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital Herford, Herford, Nordrhein-Westfalen, Germany.

Herman L Müller (HL)

Department of Pediatrics and Pediatric Hematology and Oncology, Children's Hospital Oldenburg, University of Oldenburg, Oldenburg, Niedersachsen, Germany.

Désirée Dunstheimer (D)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital Augsburg, University of Augsburg, Augsburg, Bayern, Germany.

Johannes Weigel (J)

Pediatric Endocrinology practice, Augsburg, Bayern, Germany.

Norbert Jorch (N)

Department of Pediatrics, Evangelisches Klinikum Bethel, Bielefeld, Nordrhein-Westfalen, Germany.

Elke Müller-Rossberg (E)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital, Esslingen, Baden-Württemberg, Germany.

Erwin Lankes (E)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital, Charity, University of Berlin, Berlin, Germany.

Imke Gätjen (I)

Pediatric Endocrinology practice, Bremen, Germany.

Annette Richter-Unruh (A)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital, University of Bochum, Bochum, Nordrhein-Westfalen, Germany.

Berthold P Hauffa (BP)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital, University of Essen, Essen, Nordrhein-Westfalen, Germany.

Sabine Kliesch (S)

Department of Clinical and Surgical Andrology, Center of Reproductive Medicine and Andrology, University of Münster, Münster, Nordrhein-Westfalen, Germany.

Aniko Krumbholz (A)

Institute for Doping Analytics and Sports Biochemistry, Dresden, Sachsen, Germany.

Jürgen Brämswig (J)

Department of Pediatric Endocrinology and Diabetes, Children's Hospital, University of Münster, Münster, Nordrhein-Westfalen, Germany.

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