Serum Anti-Mullerian Hormone in the Prediction of Response to hCG Stimulation in Children With DSD

被引:16
作者
Lucas-Herald, Angela K. [1 ,2 ]
Kyriakou, Andreas [1 ]
Alimussina, Malika [1 ]
Guaragna-Filho, Guilherme [3 ]
Diver, Louise A. [4 ]
McGowan, Ruth [1 ,4 ]
Smith, Karen [5 ]
McNeilly, Jane D. [6 ]
Ahmed, S. Faisal [1 ]
机构
[1] Univ Glasgow, Dev Endocrinol Res Grp, Glasgow G51 4TF, Lanark, Scotland
[2] Univ Glasgow, British Heart Fdn, Ctr Res Excellence, Glasgow G12 8TD, Lanark, Scotland
[3] Univ Fed Rio Grande do Sul, Dept Pediat, BR-90040060 Porto Alegre, RS, Brazil
[4] Queen Elizabeth Univ Hosp, West Scotland Mol & Clin Genet Serv, Glasgow G51 4TF, Lanark, Scotland
[5] Glasgow Royal Infirm, Dept Biochem, Glasgow G4 0SF, Lanark, Scotland
[6] Queen Elizabeth Univ Hosp, Dept Biochem, Glasgow G51 4TF, Lanark, Scotland
关键词
AMH; androgen; DSD; testes; CHORIONIC-GONADOTROPIN STIMULATION; DIAGNOSIS; DESENSITIZATION; GENETICS; BOYS;
D O I
10.1210/clinem/dgaa052
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The relationship between serum anti-Mullerian hormone (AMH) and the testosterone response to human chorionic gonadotropin (hCG) stimulation test is unclear. Methods: Children who had hCG stimulation tests in one tertiary centre from 2001 to 2018 were included (n = 138). Serum testosterone was measured before (day 1 [D1]) and after 3 days (D4) of hCG stimulation. Sixty-one of these children also had prolonged hCG stimulation for 2 more weeks and serum testosterone measured after 21 days (D22). All children had a serum AMH measured on D1. Results: Of the 138 children, D4 testosterone was normal in 104 (75%). AMH was low in 24/138 (17%) children, and 16 (67%) of these had a low D4 testosterone. Median AMH in those who had a normal vs low D4 testosterone was 850 pmol/L (24, 2280) and 54 pmol/L (0.4, 1664), respectively (P < 0.0001). An AMH > 5th centile was associated with a low D4 testosterone in 18/118 (13%; P < 0.0001). Of the 61 children who had prolonged hCG stimulation, D22 testosterone was normal in 39 (64%). AMH was low in 10/61(16%) children and 9 (90%) of these had a low D22 testosterone. Median AMH in children who responded and did not respond by D22 was 639 pmol/L (107, 2280) and 261 pmol/L (15, 1034) (P < 0.0001). Conclusion: A normal AMH may provide valuable information on overall testicular function. However, a low AMH does not necessarily predict a suboptimal testosterone response to hCG stimulation.
引用
收藏
页数:9
相关论文
共 32 条
[1]   Adverse Effects Associated With Persistent Stimulation of Leydig Cells With hCG In Vitro [J].
Aggarwal, Archana ;
Misro, Man M. ;
Maheshwari, Ankur ;
Sehgal, Neeta ;
Nandan, Deoki .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 2009, 76 (11) :1076-1083
[2]   The concordance between serum anti-Mullerian hormone and testosterone concentrations depends on duration of hCG stimulation in boys undergoing investigation of gonadal function [J].
Ahmed, S. F. ;
Keir, L. ;
McNeilly, J. ;
Galloway, P. ;
O'Toole, S. ;
Wallace, A. M. .
CLINICAL ENDOCRINOLOGY, 2010, 72 (06) :814-819
[3]   Society for Endocrinology UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development (Revised 2015) [J].
Ahmed, S. Faisal ;
Achermann, John C. ;
Arlt, Wiebke ;
Balen, Adam ;
Conway, Gerry ;
Edwards, Zoe ;
Elford, Sue ;
Hughes, Ieuan A. ;
Izatt, Louise ;
Krone, Nils ;
Miles, Harriet ;
O'Toole, Stuart ;
Perry, Les ;
Sanders, Caroline ;
Simmonds, Margaret ;
Watt, Andrew ;
Willis, Debbie .
CLINICAL ENDOCRINOLOGY, 2016, 84 (05) :771-788
[4]   UK guidance on the initial evaluation of an infant or an adolescent with a suspected disorder of sex development [J].
Ahmed, S. Faisal ;
Achermann, John C. ;
Arl, Wiebke ;
Balen, Adam H. ;
Conway, Gerry ;
Edwards, Zoe L. ;
Elford, Sue ;
Hughes, Ieuan A. ;
Izatt, Louise ;
Krone, Nils ;
Miles, Harriet L. ;
O'Toole, Stuart ;
Perry, Les ;
Sanders, Caroline ;
Simmonds, Margaret ;
Wallace, A. Michael ;
Watt, Andrew ;
Willis, Debbie .
CLINICAL ENDOCRINOLOGY, 2011, 75 (01) :12-26
[5]   Changes in Anti-Mullerian Hormone (AMH) throughout the Life Span: A Population-Based Study of 1027 Healthy Males from Birth (Cord Blood) to the Age of 69 Years [J].
Aksglaede, L. ;
Sorensen, K. ;
Boas, M. ;
Mouritsen, A. ;
Hagen, C. P. ;
Jensen, R. B. ;
Petersen, J. H. ;
Linneberg, A. ;
Andersson, A. -M. ;
Main, K. M. ;
Skakkebaek, N. E. ;
Juul, A. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2010, 95 (12) :5357-5364
[6]   The current state of diagnostic genetics for conditions affecting sex development [J].
Alhomaidah, D. ;
McGowan, R. ;
Ahmed, S. F. .
CLINICAL GENETICS, 2017, 91 (02) :157-162
[7]   The Role of International Databases in Understanding the Aetiology and Consequences of Differences/Disorders of Sex Development [J].
Ali, Salma Rashid ;
Lucas-Herald, Angela ;
Bryce, Jillian ;
Ahmed, Syed Faisal .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (18)
[8]   GENETICS IN ENDOCRINOLOGY Approaches to molecular genetic diagnosis in the management of differences/disorders of sex development (DSD): position paper of EU COST Action BM 1303 'DSDnet' [J].
Audi, L. ;
Ahmed, S. F. ;
Krone, N. ;
Cools, M. ;
McElreavey, K. ;
Holterhus, P. M. ;
Greenfield, A. ;
Bashamboo, A. ;
Hiort, O. ;
Wudy, S. A. ;
McGowan, R. .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2018, 179 (04) :R197-R206
[9]   Biochemical selection of prepubertal patients with androgen insensitivity syndrome by sex hormone-binding globulin response to the human chorionic gonadotropin test [J].
Bertelloni, S ;
Federico, G ;
Baroncelli, GI ;
Cavallo, L ;
Corsello, G ;
Liotta, A ;
Rigon, F ;
Saggese, G .
PEDIATRIC RESEARCH, 1997, 41 (02) :266-271
[10]   5α-Reductase-2 Deficiency: Clinical Findings, Endocrine Pitfalls, and Genetic Features in a Large Italian Cohort [J].
Bertelloni, Silvano ;
Baldinotti, Fulvia ;
Russo, Gianni ;
Ghirri, Paolo ;
Dati, Eleonora ;
Michelucci, Angela ;
Moscuzza, Francesca ;
Meroni, Silvia ;
Colombo, Ilaria ;
Sessa, Maria R. ;
Baroncelli, Giampiero I. .
SEXUAL DEVELOPMENT, 2016, 10 (01) :28-36