Healthy birth after testicular extraction of sperm and ICSI from an azoospermic man with mild androgen insensitivity syndrome caused by an androgen receptor partial loss-of-function mutation

被引:21
作者
Massin, Nathalie [1 ]
Bry, Helene [1 ]
Vija, Lavinia [2 ,3 ]
Maione, Luigi [2 ,3 ]
Constancis, Elizabeth [4 ]
Haddad, Bassam [5 ]
Morel, Yves [6 ]
Claessens, Frank [7 ]
Young, Jacques [2 ,3 ]
机构
[1] Univ Paris 12, Ctr Assistance Med Procreat, Ctr Hosp Intercommunal, Creteil, France
[2] Univ Paris Sud, Hop Bicetre, Assistance Publ Hop Paris, Serv Endocrinol Reprod, F-94274 Le Kremlin Bicetre, France
[3] INSERM, U693, F-94275 Le Kremlin Bicetre, France
[4] Ctr Hosp Intercommunal, Serv Anatomopathol, Creteil, France
[5] Univ Paris 12, Serv Gynecol Obstet, Ctr Hosp Intercommunal, Creteil, France
[6] Biol & Pathol E Ctr, Bron, France
[7] Katholieke Univ Leuven, Mol Endocrinol Lab, Dept Mol Cell Biol, Louvain, Belgium
关键词
ANTI-MULLERIAN HORMONE; CONGENITAL HYPOGONADOTROPIC HYPOGONADISM; MALE-INFERTILITY; GENE-MUTATIONS; NONOBSTRUCTIVE AZOOSPERMIA; MALE-FERTILITY; SERTOLI-CELLS; MEN; TRANSACTIVATION; EXPRESSION;
D O I
10.1111/j.1365-2265.2012.04402.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context The androgen receptor (AR) is essential for the development and maintenance of the male phenotype, and for spermatogenesis. Mutations in the AR gene cause a wide variety of androgen insensitivity syndromes (AIS), ranging from complete feminization to phenotypic males with infertility. Objective We report the first birth achieved after intracytoplasmic sperm injection (ICSI) with sperm from an azoospermic man with an AR mutation associated with mild AIS (MAIS). Patients and methods A couple with primary infertility was referred to our centre. The man had azoospermia with testicular hypotrophy and an undervirilized phenotype despite a normal plasma testosterone level. His androgen sensitivity index and serum anti-mullerian hormone (AMH) levels were elevated, pointing to AIS. Molecular analysis of the AR gene revealed a point mutation resulting in an F754S substitution (renumbered F755S in the 2012 McGill University AR gene database), in the ligand-binding domain of the protein, and further analysis indicated impaired receptor function. Results After genetic counselling of the couple, oocytes were retrieved after controlled ovarian hyperstimulation, and sperm were obtained simultaneously by testicular extraction for ICSI. Nine embryos were obtained. Two were transferred and two were suitable for cryopreservation. A pregnancy was obtained and a healthy girl, carrying the F754S AR mutation, was born at 37 similar to weeks of gestation. AR and AMH were detected by immunohistochemistry in the patient's testicular specimens. AMH immuno-staining was intense in tubules without spermatogenesis and weak in those with ongoing spermatogenesis. Conclusion A healthy child can be obtained by testicular extraction and ICSI despite azoospermia in MAIS. The parents must be informed of the X-linked transmission of the mutation to their descendants. The relationship between AR signalling, testicular AMH expression and spermatogenesis in this patient is discussed.
引用
收藏
页码:593 / 598
页数:6
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