• Users Online: 250
  • Home
  • Print this page
  • Email this page
Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Contacts Login 


 
 Table of Contents  
SHORT REPORT
Year : 2018  |  Volume : 31  |  Issue : 5  |  Page : 274-278

Evaluation of sexual function and micro- testicular sperm extraction in men with mosaic Turner syndrome


1 Department of Urology, Novafertil IVF Center, Meram Yeni Yol No. 75, Meram, 42090 Konya, Turkey
2 Department of Medical Genetics, Necmettin Erbakan University, Meram, 42060 Konya, Turkey

Date of Web Publication24-Jun-2019

Correspondence Address:
Ahmet Salvarci
Department of Urology, Novafertil IVF Center, Meram Yeni Yol No. 75, Meram, 42090 Konya
Turkey
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0970-258X.261196

  Abstract 

Background. Men with mosaic Turner syndrome (TS) having karyotype 45,X/46,XY are infrequently seen. Their sexual function and fertility potential are not well documented. We describe the sexual function and outcomes of sperm extraction in 5 such men who were evaluated between 2008 and 2017.
Methods. Five phenotypic men diagnosed to have mosaic TS underwent detailed physical examination, semen analysis and evaluation of follicle-stimulating hormone, luteinizing hormone, prolactin and total testosterone. Blood, testis, oral mucosa and skin fluorescence in situ hybridization (FISH) analyses were done for evaluating the karyotype. Genomic DNA was extracted from peripheral blood for molecular analysis of azoospermic factor (AzF) deletions. Sexual function was assessed using the International Index of Erectile Function-5 (IIEF-5). One patient also underwent micro-testicular sperm extraction (micro-TESE) and intracytoplasmic sperm injection (ICSI).
Results. All 5 men had a mosaic 45,X/46,XY genotype and the sex-determining region (SRY) was positive in DYZ1- negative cells. None had a deletion in the AzF a, b or c regions. Sperm was detected in 3 patients through micro-TESE but ICSI could be done in only 1 patient. No embryo development was identified in time lapse (Embryoscope©) follow-up. It was observed that the rate of 46,XY was particularly high in gonadal tissues in the mosaic structure in patients detected to have sperms.
Conclusion. Patients with TS having 45,X/46,XY, SRY( + ), with no AzF deletions, and a high percentage of 46,XY in the peripheral blood, especially in gonadal tissues, could have a healthy sexual life and possibly father a child through in vitro fertilization or ICSI upon detection of sperms with micro-TESE.


How to cite this article:
Salvarci A, Zamani A. Evaluation of sexual function and micro- testicular sperm extraction in men with mosaic Turner syndrome. Natl Med J India 2018;31:274-8

How to cite this URL:
Salvarci A, Zamani A. Evaluation of sexual function and micro- testicular sperm extraction in men with mosaic Turner syndrome. Natl Med J India [serial online] 2018 [cited 2019 Sep 18];31:274-8. Available from: http://www.nmji.in/text.asp?2018/31/5/274/261196




  Introduction Top


Turner syndrome (TS) usually occurs in 45,X monosomic women and 45,X/46,XY mosaicism is a rare, and probably under-diagnosed, condition. Its reported incidence is 1.5 per 10 000 newborns.[1] 45,X/46,XY mosaicisms are believed to occur due to the loss of chromosome Y after normal disomic fertilization. The ratio of the 2 cell lines varies in different organs and tissues and the phenotype of such patients is also variable. This could include male phenotype with normal male genitalia and bilateral testis but TS stigmata, such as bilateral streak gonads with persistent Müllerian structures and mixed gonadal dysgenesis. Phenotypically normal men may present with infertility and azoospermia.[2],[3] Sex- determining region (SRY) may be positive in men with T S having 45, Xgenotype who may have a healthy Y chromo some with 4 5 ,X/46, XY mosaicism or a Y autosomal translocation.[4] It is known that the SRY on Yp induces testis development and is the transcription factor of the genes involved in the activation of the sex differentiation process[4],[5] Infertile Y mosaic men with karyotype 45,X/46,XY, SRY (+), who do not have Y chromosome deletions may be candidates for sperm retrieval for in vitro fertilization (IVF). We report the outcomes in such men who underwent microdissection testicular sperm extraction (micro-TESE) and intracytoplasmic sperm injection (ICSI) in our institution.


  Methods Top


Five men who presented with infertility between 2008 and 2017 underwent a detailed physical examination including cardiovascular examination. Their partners had a normal ovulatory cycle, 46,XX karyotype, and a mean age of 25.6 years. They reported sexual intercourse at least twice a week and their International Index of Erectile Function-5 (IIEF-5) and Female Sexual Function Indexes (FSFIs) were recorded. Following a semen analysis, assessment of follicle-stimulating hormone (F SH), luteinizing hormone (LH), total testosterone, prolactin and oestradiol was done. Subsequently karyotype and Y chromosome microdeletion analysis was obtained. Three patients were diagnosed in 1996 in other clinics while in 2 patients the initial diagnosis was made in our clinic. The age of the subjects at the time of diagnosis ranged from 22 to 29 years. The karyotype analysis and fluorescence in situ hybridization (FISH) of all patients were done on cultured, phytohaemagglutinin-stimulated, peripheral blood lymphocytes, according to standard genetic procedures. FISH analysis was done by following the manufacturer’s instructions with a SRY-specific probe (SRY, Yp11.3, DYZ1, DXZ1; Cytocell). A second FISH analysis was done on skin fibroblast culture cells, and the testicular tissue of patients were assessed with the same probe. Two hundred cells were analysed from 3 different tissues. Genomic DNA was extracted from peripheral blood of the patient using QIAamp DNA blood kits according to the manufacturer’s instructions for molecular analysis of azoospermic factor (AzF) a, b, c regions. All patients also underwent scrotal ultrasonography and pelvic magnetic resonance imaging (MRI) to look for Müllerian structures. After discussion of the genetic diagnosis and obtaining consent, the men underwent micro-TESE with a 12.5x25 surgical microscope. Subsequently, 1 subject underwent ICSI with the retrieved sperms.


  Results Top


The mean age of the subj ects was 25.4 years [Table 1] and the mean duration of marriage was 6.6 years. All had normal masculinization with a reduction in body hair and mean height of 164.4 cm [Figure 1]. All patients had palpable testes, vas deferens and epididymis. One patient had previously undergone laparoscopic gonadectomy for a streak gonad. No cardiovascular pathology was observed but 2 patients had a short metatarsus. The mean semen volume was 3.24 ml and all men had azoospermia. The mean volume of the testes was 2.3 ml on scrotal ultrasound [Figure 1]. No internal genitalia that could be associated with T S were detected on pelvic MRI. The mean hormone levels were 30.96 mIU/ml for FSH (normal 1.7-12 mIU/ml), 12.3 mIU/ml for LH (normal 1.1-7 mIU/ml), 3.67 pg/ml for total testosterone (normal 3.5-8.6 pg/ ml), 50.44 pg/ml for oestradiol (normal <62 pg/ml) and 11.44 ng/ ml for prolactin (normal 1.5-19 ng/ml). The average IIEF-5 score was 26.8; the mean FSFI of the partners was 27.4.
Table 1: Characteristics of male patients with Turner syndrome having 45,X/46,XY

Click here to view
Figure 1: (a-c) Sample SRY (+) patients with 45,X/46,XY and no Y chromosome microdeletions and testes on scrotal ultrasound

Click here to view


Genetic results

Two hundred metaphases were scored and the 45,X/46,XY ratios of patients obtained from 3 different tissues are summarized in [Table 2]. Molecular analysis revealed that the SRY gene and the AzF a, b, c regions were present. It was observed that the SRY gene was translocated to the short arm of X in all the patients.
Table 2: Percentage of 45,X and 46,XY cell lines

Click here to view


Micro-testicular sperm extraction, IVF/ICSIand pathology results

Distinct tubular structures were observed under the microscope during micro-TESE in only 1 patient [Figure 2]. Sperms were stained with Spermac stain to ensure a clearer tracking of existing sperms. Immotile sperms with head and tail abnormalities, with extremely rare morphology, were identified in 2 patients. One immotile sperm was detected on centrifugation following the collagenase procedure on testicular tissue after micro-TESE in 1 patient. No sperm was observed in 2 other patients. IVF/ICSI was done following the detection of a sufficient amount of sperms in only 1 patient among patients identified to have sperm; however, no embryo development was observed following time-lapse (Embryoscope©) follow-up.
Figure 2: (a-c) Man with Turner syndrome with 45,X/46,XY during microscopic-testicular sperm extraction: Testis/epididymis and tubular view under 12.5x25 surgical enlargement microscope. Large-headed and multiple-tailed sperms x40, stained with Spermac of patient in whom sperm was detected

Click here to view


Masson trichromatic stain was applied in addition to the haematoxylin and eosin-stained sections of the testicular tissue, and basal membrane thickening was observed in 2 patients in whom no sperm was identified. The seminiferous tubules were generally surrounded by Sertoli cells in 3 patients in whom sperm was detected; few spermatocytes were observed in the germ line at the spermatogonium phase, while the Johnsen histopathological score was identified as 6, 6 and 7, respectively (a score of 6=absence of spermatozoa and <10 spermatids; a score of 7=a high number of spermatids and no spermatozoa). In patients in whom no sperm was detected, basal membrane thickening, absence of germ cells, predominance of Sertoli cells, Leydig cell proliferation and a Johnsen score of 1 and 2 was observed (a score of 1=no cells in the seminiferous tubular lumen; a score of 2=presence of only Sertoli cells and absence of germ cells).


  Discussion Top


Sexual differentiation is a complex process. Until the 6th week of gestation, the gonads of embryos of both sexes are indistinguishable. Testes develop in individuals with a 46,XY chromosome constitution, through the effect of the SRY gene. These are morphologically identifiable from week 7 to week 8 of gestation. In this process, the Sertoli cells are the first to become recognizable. These are organized as cells surrounding tubules and produce Müllerian-inhibiting factor, a hormone that, through local diffusion, leads to regression of the Müllerian duct derivatives (which give rise to the uterus, uterine tubes and proximal vagina).

Leydig cells produce an androgen, testosterone, which induces Wolffian ducts to differentiate into epididymis, vas deferens, seminal vesicles and ejaculatory duct.[2],[3],[6] The loss of the Y chromosome following normal disomic fertilization through nondisjunction leads to the development of the 45 ,X cell line. Ovarian development is observed in such individuals with TS in the absence of chromosome Y and the external genitalia becomes female.[7] If the loss of Y occurs during the early post-zygotic cell division period, greater number of cell groups and tissues are affected. This impacts the distribution of cells with 45 ,X karyotype, leading to phenotypic differences which are attributed to the non- disjunction in the Y chromosome. TS with 45,X/46,XY mosaic male phenotype has been rarely reported. Generally, men present with infertility and azoospermia similar to our series.[6],[8]

In patients with 45,X/46,XY complement, streak gonads and/ or abnormal testes may also be seen along with Müllerian components. While bilateral testis and reduced virilization are present along with Müllerian components in some 45,X/46,XY, some patients may have bilateral scrotal testis and normal male genitalia as in our patients.[6],[8] This phenotype is probably due to the high rate of 46,XY karyotype in the cells forming the gonads.[6] No internal organ association with TS was observed in our patients in the MRI assessment. The reason was thought to be the high rate of the 46,XY and SRY (+) in gonadal tissues. Clinical variations supporting this claim have also been observed in monozygotic twins.[9] Patients with mosaic TS having 45,X/46,XY karyotype had a normal height, with enhanced breast development rates and reduced somatic abnormality rate, as with our patients, compared to those with a 45,X karyotype.[8] In men who have a 45,X/46,XY mosaic TS and have undergone gonadectomy or have gonadal dysgenesis, sex steroid hormone therapies may be required to prevent loss of sexual characteristics and development of osteoporosis. However, none of our patients received sex steroid therapy and hormone values were normal in 45,X/46,XY despite hypergonadotropism.[6]

In a series of 14 subjects with 45,X/46,XY karyotype, there were 5 male and 9 female phenotypes.[6] Four of 5 men in this series had ambiguous genitalia while normal male genitalia were reported in 1 man.[6] SRY (+) was detected in all our patients; no abnormalities such as ambiguous genitalia, scrotal fusion, micro-penis and perineal urethral meatus were observed in our patients. It was presumed that this was due to the presence of the SRY gene translocated to the X chromosome through a post-zygotic translocation in the 45,X cell line and the high rate of karyotype 46,X Y in the cells forming the gonads. An interesting finding was a SRY (+), TS man with 45,X. No Y chromosome was detected, the SRY gene was translocated to X and no spermatogenetic activity was observed due to the absence of chromosome Y in the individual followed up until the age of12 years.[6] Mosaic karyotype was observed in all patients in our series. Although there was a mosaic structure in only 1 of our patients, it was observed that SRY was translocated to Xp. Moreover, the karyotyping performed in the testicular tissue retrieved from our patients was also 45,X/ 46,XY. It was observed in patients no. 2, 3 and 5 that the rate of 45,X/46,XY was high in favour of 46,XY in the gonads of those where sperm was detected at micro-TESE [Table 1] and [Table 2].

Structural alterations of the Y chromosome in the 46,XY cell line of the mosaic patients comprising AzF region have previously been described.[10] Interestingly, deletion of one or more loci in these regions can affect the development of the testes and cause impaired spermatogenesis.[6] We assessed the AzF a, b, c regions in our patients and observed no deletions. Although we could obtain an amount of sperm sufficient to perform IVF/ICSI in only 1 patient, we obtained sperm in 3 patients at micro-TESE. Although mature seminiferous tubules were detected in the pathological assessment of the testes, it was determined that they were disorganized, hyalinized and atrophic tubules.[11],[12] We also observed basal membrane thickening and atrophic tubules in the trichromatic staining performed in patients in whom we could not detect any sperm. Contrary to the patients in whom we detected spermato- genetic activity or sperm [Table 2]; patients 1-4), the mosaic rate was in favour of 45,X, most notably in gonadal tissues.

It was reported that no pregnancy was achieved in the follow- up of 45,X/46,XY in a multicentre study.[13] It was also reported that a healthy, oligospermic adult male phenotype with karyotype 45, X/46, X, r(Y) could father a child with karyotype 47,XX, r(Y)/ 46, XX. Sperm was detected in this patient following m-TESE, but pregnancy could not be achieved in 2 ICSI cycles.[11],[12]

Patients with male external genitalia can present with hypospadias and/or cryptorchidism.[14] Dysgenetic testes, gonadal streaks and contralateral dysgenetic testes are frequently observed.[13] One of our patients had previously undergone orchiopexy for undescended testis along with removal of a streak gonad. No sperm was detected at micro-TESE in this patient.

Individuals with 45,X/46,XY mosaicism having male external genitalia may also have short stature.[15] The mean height of our patients was 164.4 cm. The slower growth in these patients appears to be related to deficiencies of both their hypothalamic- gonadal axis and primary gonadal function.[7]

Some major abnormalities, such as cardiovascular and renal abnormalities, and dysmorphia, such as low implantation of hair, shortening of metacarpal and metatarsal bones and a short and webbed neck, which are observed in individuals with TS, may also be observed among patients with 45,X/46,XY mosaicism.[16] Our patients had abnormalities in hair, weight, height and epicanthus folds. The rate of 45,X in the mosaic structure was observed to be higher in these patients compared with those devoid of these stigmata [Table 3].
Table 3: Stigmas identified in patients with 45,X/46,XY, sex-determining region (+) and no Y chromosome microdeletions

Click here to view


Mosaic patients with 45,X/46,XY are also at a higher risk for development of malignancies. Tumour frequency varies between 10% and 15%, especially for gonadoblastoma and dy sgerminoma for mosaic patients. Tumours are observed mostly in the second decade of life. Therefore, it is necessary to monitor these patients.[17]

Another major issue in these patients is the gender of rearing the child. Although several factors are involved in this process, the degree of virilization of the external genitalia and the presence of gonads with testicular features in the labioscrotal folds are the most important.[18],[19] In our patients, the external genitalia were male due to the presence of SRY and a high rate of 46,XY karyotype in the mosaic structure, especially in the gonads and they were all raised as male [Figure 1]. However, there is no consensus on what would be the best way of determining the gender of rearing.[20] Cools et al.[21] stated that the masculinization score for the external genitalia that was suggested by Ahmed et al.[22] could reflect both gonadal differentiation and the risk of tumours in patients with 45,X/46,XY mosaicism (malignancy risk seems to be inversely related with this score).[6] Our approach to managing male patients with mosaic TS having 45,X/46,XY, SRY(+) genotype with no AzF deletions of the Y chromosome is summarized in [Figure 3].
Figure 3: Treatment diagram proposed for male patients with mosaic Turner syndrome having 45,X/46,XY, sex-determining region (+) and no Y chromosome micro deletions
IIEF-5 International Index of Erectile Function-5 FSFI Female Sexual Function Index micro-TESE microscopic-testicular sperm extraction SRY sex-determining region AzF azoospermic factor IVF in vitro fertilization ICSI intracytoplasmic sperm injection


Click here to view


Conclusions

Patients with mosaic TS having 45,X/46,XY present with variable phenotypes, have a complex genetic structure and need a thorough multidisciplinary evaluation. Among these patients, those who are positive for SRY, have no AzF deletions and a higher percentage of 46,XY in the peripheral blood, especially in gonadal tissues may have a healthy sexual life and sperm detectable in micro-TESE.

Conflicts of interest. None declared



 
  References Top

1.
Stochholm K, Juul S, Juel K, Naeraa RW, Gravholt CH. Prevalence, incidence, diagnostic delay, and mortality in Turner syndrome. J Clin Endocrinol Metab 2006;91:3897-902.  Back to cited text no. 1
    
2.
Hamerton JL, Canning N, Ray M, Smith S. A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities. Clin Genet 1975;8:223^3.  Back to cited text no. 2
    
3.
Lee PA, Houk CP, Ahmed SF, Hughes IA; International Consensus Conference on Intersex organized by the Lawson Wilkins Pediatric Endocrine Society and the European Society for Paediatric Endocrinology. Consensus statement on management of intersex disorders. International Consensus Conference on Intersex. Pediatrics 2006;118:e488-500.  Back to cited text no. 3
    
4.
Peng D, Zhang YS, Zhang XY, Hu C, Liu MH, Liu RZ. An infertile 45,X male with a SRY-bearing chromosome 13 : A clinical case report and literature review. J Assist Reprod Genet 2015;32:107-9.  Back to cited text no. 4
    
5.
Salvarci A, Yurdakul H. Normogonadotropik, SRY (+), 46 XX Erkek (Normogonadotropic, SRY (+), 46 xx Men). Türk Klin 2014;5:73-6.  Back to cited text no. 5
    
6.
Rosa RF, D’Ecclesiis WF, Dibbi RP, Rosa RC, Trevisan P, Graziadio C, et al. 45,X/ 46,XY mosaicism: Report on 14 patients from a Brazilian hospital. A retrospective study. Sao Paulo Med J 2014; 132:332-8.  Back to cited text no. 6
    
7.
Tosson H, Rose SR, Gartner LA. Description of children with 45,X/46,XY karyotype. Eur J Pediatr 2012;171:521-9.  Back to cited text no. 7
    
8.
Morgan T. Turner syndrome: Diagnosis and management. Am Fam Physician 2007;76:405-10.  Back to cited text no. 8
    
9.
Tho SP, Jackson R, Kulharya AS, Reindollar RH, Layman LC, McDonough PG. Long-term follow-up and analysis of monozygotic twins concordant for 45,X/46,XY peripheral blood karyotype but discordant for phenotypic sex. Am J Med Genet A 2007; 143A: 2616-22.  Back to cited text no. 9
    
10.
Alvarez-Nava F, Puerta H. Y-chromosome microdeletions in 45,X/46,XY patients. Am J Med Genet A 2006;140:1128-30.  Back to cited text no. 10
    
11.
Flannigan RK, Chow V, Ma S, Yuzpe A. 45,X/46,XY mixed gonadal dysgenesis: A case of successful sperm extraction. Can Urol Assoc J 2014;8:E108-10.  Back to cited text no. 11
    
12.
Miura C, Shimizu Y, Uehara M, Ozaki Y, Young G, Miura T. Gh is produced by the testis of Japanese eel and stimulates proliferation of spermatogonia. Reproduction 2011;142:869-77.  Back to cited text no. 12
    
13.
Gassó-Matoses M, Picó-Alfonso A, Fernández-García J, Lobato-Encinas J, Mira- Llinares A. 45,X/46,XY gonadal dysgenesis in an infertile adult male. Urol Int 1992;48:239-41.  Back to cited text no. 13
    
14.
Aarskog D. Intersex conditions masquerading as simple hypospadias. Birth Defects Orig Artic Ser 1971;7:122-30.  Back to cited text no. 14
    
15.
Lindhardt Johansen M, Hagen CP, Rajpert-De Meyts E, Kjœrgaard S, Petersen BL, Skakkebœk NE, et al. 45,X/46,XY mosaicism: Phenotypic characteristics, growth, and reproductive function-- A retrospective longitudinal study. J Clin Endocrinol Metab 2012;97:E1540-9.  Back to cited text no. 15
    
16.
Méndez JP, Ulloa-Aguirre A, Kofman-Alfaro S, Mutchinick O, Fernández-del- Castillo C, Reyes E, et al. Mixed gonadal dysgenesis: Clinical, cytogenetic, endocrinological, and histopathological findings in 16 patients. Am J Med Genet 1993;46:263-7.  Back to cited text no. 16
    
17.
Verp MS, Simpson JL. Abnormal sexual differentiation and neoplasia. Cancer Genet Cytogenet 1987;25:191-218.  Back to cited text no. 17
    
18.
Knudtzon J, Aarskog D. 45,X/46,XY mosaicism. A clinical review and report of ten cases. Eur J Pediatr 1987;146:266-71.  Back to cited text no. 18
    
19.
Maciel-Guerra AT, Júnior G (eds). Menino ou menina?Distúrbios daDiferenciaçao do Sexo. 2nd ed. Rio de Janeiro:Editora Rubio; 2010.  Back to cited text no. 19
    
20.
Chang HJ, Clark RD, Bachman H. The phenotype of 45,X/46,XY mosaicism: An analysis of 92 prenatally diagnosed cases. Am J Hum Genet 1990;46:156-67.  Back to cited text no. 20
    
21.
Cools M, Pleskacova J, Stoop H, Hoebeke P, Van Laecke E, Drop SL, et al. Gonadal pathology and tumor risk in relation to clinical characteristics in patients with 45,X/ 46,XY mosaicism. J Clin EndocrinolMetab 2011;96:E1171-80.  Back to cited text no. 21
    
22.
Ahmed SF, Khwaja O, Hughes IA. The role of a clinical score in the assessment of ambiguous genitalia. BJUInt 2000;85:120-4.  Back to cited text no. 22
    


    Figures

  [Figure 1], [Figure 2], [Figure 3]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]



 

Top
 
 
  Search
 
Similar in PUBMED
   Search Pubmed for
   Search in Google Scholar for
Access Statistics
Email Alert *
Add to My List *
* Registration required (free)

 
  In this article
Abstract
Introduction
Methods
Results
Discussion
References
Article Figures
Article Tables

 Article Access Statistics
    Viewed240    
    Printed6    
    Emailed0    
    PDF Downloaded211    
    Comments [Add]    

Recommend this journal


[TAG2]
[TAG3]
[TAG4]