Literature DB >> 11155091

The testosterone:androstenedione ratio in male undermasculinization.

A Iqbal, I A Hughes.   

Abstract

OBJECTIVE: Recent reports suggest that low testosterone:androstenedione (T:A) ratio following hCG stimulation may be a useful method of diagnosing 17beta-hydroxysteroid dehydrogenase-3 (17 betaHSD3) deficiency. The aim of this study was to establish the range of T:A ratios in cases of undermasculinization with proven aetiologies other than 17 betaHSD3.
DESIGN: Register-based study of cases of male undermasculinization reported to a central database by clinicians.
SUBJECTS: Amongst the 421 cases of under-masculinization, 114 cases had testosterone and androstenedione levels before and after hCG stimulation. Of the 114, there were 18 cases of abnormal testes, 17 cases of complete androgen insensitivity syndrome (CAIS), 68 cases of partial AIS (PAIS). Of the 17 cases of CAIS, 13 had evidence of androgen receptor (AR) dysfunction; in the PAIS cohort, 26 cases had evidence of AR dysfunction. Analysis of T:A ratios in the above cohorts and comparison of these ratios to those in a group of previously described cases of 17 betaHSD3 deficiency with a mean ratio of 0.4 (SD: 0.2).
RESULTS: The median age (range) for the CAIS, PAIS and abnormal testes cohort was 1.25 years (0.06-16.5), 0.7 years (0.02-40.3) and 0.5 years (0.04-6.5), respectively. In CAIS, the median T:A rose from 0.4 (0.1 to 8.0) to 4.5 (0.5-16.7); in PAIS, median T:A rose from 0.7 (0.1 to 15) to 3.9 (0.3-20.5); in cases with abnormal testes, median T:A rose from 0.4 (0.1 to 5.6) to 0.6 (0.1-3.6). The median post-hCG T:A ratio was significantly lower in the abnormal testes cohort (P < 0.01). None of the cases of AIS with AR mutation had a low T:A ratio. Only four out of 84 cases diagnosed as AIS had a T:A ratio less than 0.8 (mean + 2SD in 17betaHSD3 deficiency). In one of the four cases, the T:A ratio rose to 3.5 following a prolonged hCG stimulation test.
CONCLUSION: Deficiency of 17betaHSD3 should be considered in 46XY undermasculinization if the post-hCG stimulation T:A ratio is less than 0.8. However, low T:A ratios may be encountered in conditions such as abnormal testes. Before embarking on mutational analysis, we would also recommend careful evaluation for testicular dysgenesis including a prolonged hCG stimulation test in cases with a low T:A ratio.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11155091     DOI: 10.1046/j.1365-2265.2000.01166.x

Source DB:  PubMed          Journal:  Clin Endocrinol (Oxf)        ISSN: 0300-0664            Impact factor:   3.478


  11 in total

1.  Serum Anti-Müllerian Hormone in the Prediction of Response to hCG Stimulation in Children With DSD.

Authors:  Angela K Lucas-Herald; Andreas Kyriakou; Malika Alimussina; Guilherme Guaragna-Filho; Louise A Diver; Ruth McGowan; Karen Smith; Jane D McNeilly; S Faisal Ahmed
Journal:  J Clin Endocrinol Metab       Date:  2020-05-01       Impact factor: 5.958

2.  "Spectrum of 46 XY Disorders of Sex Development": A Hospital-based Cross-sectional Study.

Authors:  Samiran Das; Uma K Saikia; Kandarpa K Saikia; Dipti Sarma; Bipul K Choudhury; Ashok K Bhuyan; Abhamoni Baro; Darvin V Das; Sonali Appaiah
Journal:  Indian J Endocrinol Metab       Date:  2020-08-27

3.  46,XY disorder of sex development due to 17-beta hydroxysteroid dehydrogenase type 3 deficiency: a plea for timely genetic testing.

Authors:  Chelsey Grimbly; Oana Caluseriu; Peter Metcalfe; Mary M Jetha; Elizabeth T Rosolowsky
Journal:  Int J Pediatr Endocrinol       Date:  2016-06-15

4.  Prevalence of endocrine and genetic abnormalities in boys evaluated systematically for a disorder of sex development.

Authors:  R Nixon; V Cerqueira; A Kyriakou; A Lucas-Herald; J McNeilly; M McMillan; A I Purvis; E S Tobias; R McGowan; S F Ahmed
Journal:  Hum Reprod       Date:  2017-10-01       Impact factor: 6.918

5.  Integrating clinical and genetic approaches in the diagnosis of 46,XY disorders of sex development.

Authors:  Zofia Kolesinska; James Acierno; S Faisal Ahmed; Cheng Xu; Karina Kapczuk; Anna Skorczyk-Werner; Hanna Mikos; Aleksandra Rojek; Andreas Massouras; Maciej R Krawczynski; Nelly Pitteloud; Marek Niedziela
Journal:  Endocr Connect       Date:  2018-12       Impact factor: 3.335

6.  46,XY Sex Development Defect due to a Novel Homozygous (Splice Site) c.673_1G>C Variation in the HSD17B3 Gene: Case Report

Authors:  Nurdan Çiftci; Leman Kayaş; Emine Çamtosun; Ayşehan Akıncı
Journal:  J Clin Res Pediatr Endocrinol       Date:  2021-01-04

7.  Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management".

Authors:  Antonio Balsamo; Federico Baronio; Marta Berra; Silvano Bertelloni; Franco D'Alberton; Giacinto Marrocco; Santiago Vallasciani
Journal:  Case Rep Obstet Gynecol       Date:  2014-05-12

8.  Clinical, hormonal and radiological profile of 46XY disorders of sexual development.

Authors:  Chauhan Vasundhera; Viveka P Jyotsna; Devasenathipathy Kandasamy; Nandita Gupta
Journal:  Indian J Endocrinol Metab       Date:  2016 May-Jun

9.  Severe Undervirilisation in a 46,XY Case Due to a Novel Mutation in HSD17B3 Gene.

Authors:  Ayfer Alikaşifoğlu; Doğuş Vurallı; Olaf Hiort; Nazlı Gönç; Alev Özön; Nurgün Kandemir
Journal:  J Clin Res Pediatr Endocrinol       Date:  2015-09

Review 10.  Dynamic Testing for Evaluation of Adrenal and Gonadal Function in Pediatric and Adult Endocrinology: An Overview.

Authors:  Alpesh Goyal; Suraj Kubihal; Yashdeep Gupta; Viveka P Jyotsna; Rajesh Khadgawat
Journal:  Indian J Endocrinol Metab       Date:  2019 Nov-Dec
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.