Predicting puberty in partial androgen insensitivity syndrome: Use of clinical and functional androgen receptor indicesResearch in context

• Published in: EBioMedicine Vol. 36; pp. 401 - 409
• Main Authors: Ngee Lek, Rieko Tadokoro-Cuccaro, Jonathan B. Whitchurch, Bismoy Mazumder, Harriet Miles, Philippa Prentice, Trevor Bunch, Karolina Zielińska, Veronika Metzler, Nigel P. Mongan, David M. Heery, Ieuan A. Hughes
• Format: Journal Article
• Language: English
• Published: Elsevier 01.10.2018
• ISSN: 2352-3964; 2352-3964

Background: PAIS exhibits a complex spectrum of phenotypes and pubertal outcomes. The paucity of reliable prognostic indicators can confound management decisions including sex-of-rearing. We assessed whether external masculinisation score (EMS) at birth or functional assays correlates with pubertal outcome in PAIS patients and whether the EMS is helpful in sex assignment. Methods: We collected pubertal outcome data for 27 male-assigned PAIS patients, all with confirmed androgen receptor (AR) mutations, including two previously uncharacterized variants (I899F; Y916C). Patients were grouped as follows; EMS at birth <5 and ≥ 5 (EMS in normal males is 12; median EMS in PAIS is 4·7) and pubertal outcomes compared. Findings: Only 6/9 patients (67%) with EMS <5 underwent spontaneous onset of puberty, versus all 18 patients with EMS ≥5 (p = .03). Only 1/6 patients (17%) with EMS <5 developed adult genitalia reaching Tanner stage 4 or 5, versus 11/13 (85%) with EMS ≥5 (p = 0·01). There was no significant difference between the two groups of patients in being prescribed androgen replacement, who reached adult testicular volume ≥ 15 ml, pubic hair Tanner stage 4 or 5, above average adult height, had gynaecomastia, and mastectomy. No correlation was observed between EMS and in vitro AR function. Interpretation: In PAIS with AR mutation, birth EMS is a simple predictor of spontaneous pubertal onset and satisfactory adult genitalia. This provides useful information when discussing the likely options for management at puberty. Fund: European Commission Framework 7 Programme, NIHR Cambridge Biomedical Research Centre, BBSRC DTP. Keywords: Androgen insensitivity, External masculinisation score, Puberty outcome, Sex assignment, Gynaecomastia, Androgen receptor, Mutation, Reporter assays, in silico modelling