Literature DB >> 20609027

Clinical experience with azoospermia: aetiology and chances for spermatozoa detection upon biopsy.

F Tüttelmann1, F Werny, T G Cooper, S Kliesch, M Simoni, E Nieschlag.   

Abstract

The clinical workup of the infertile male with azoospermia aims at determining the aetiology and estimating the chances of finding spermatozoa by testicular sperm extraction (TESE). To establish prognostic criteria, 1583 consecutive patients with azoospermia consulting the Centre of Reproductive Medicine and Andrology, Münster, a tertiary referral centre, between 1976 and 2009 comprising 9.8% of all patients providing a semen sample were included in this retrospective analysis. The frequencies of diagnoses were as follows: 21% genetic causes (14% Klinefelter syndrome, 1% other chromosomal aberrations, 2% Y-chromosomal microdeletions, 1% hypogonadotropic hypogonadism, 3% congenital bilateral absence of the vas deferens), 31% current or former maldescended testes, varicocele, urogenital infections, 15% malignancies, 11% obstructions, 7% endocrine or other chronic diseases and 12% idiopathic azoospermia. Receiver-operating characteristic curves for chances of finding spermatozoa by testicular biopsy were calculated for testicular volume, serum follicle-stimulating hormone (FSH) and the seminal markers α-glucosidase, fructose and zinc where these data were available (N=283). Histograms of the seminal markers comparing data from men with obstructive azoospermia and normozoospermia visualize their discriminating power. Evidence-based threshold values for high chances of positive testicular biopsy serving as surrogate marker for TESE were derived from the subgroup of men with obstructive azoospermia for testicular volume (≥21mL), FSH (≤10U/L) and seminal α-glucosidase (≤18mU/ejaculate). Fructose and zinc could not predict the chances of finding spermatozoa upon biopsy. Based on these three parameters, positive biopsy and presumably TESE success can be quickly and reliably estimated in everyday practice with the colour-coded figures constructed from these data. As a seminal α-glucosidase reference limit of 18mU/ejaculate can also be used to diagnose congenital bilateral absence of the vas deferens, α-glucosidase (rather than seminal fructose) should be determined as part of the clinical routine when counselling patients before testicular biopsy.
© 2010 The Authors. International Journal of Andrology © 2011 European Academy of Andrology.

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Year:  2010        PMID: 20609027     DOI: 10.1111/j.1365-2605.2010.01087.x

Source DB:  PubMed          Journal:  Int J Androl        ISSN: 0105-6263


  38 in total

1.  Mosaicism for an unbalanced Y;21 translocation in an infertile man: a case report.

Authors:  Albrecht Röpke; Yvonne Stratis; Dajana Dossow-Scheele; Peter Wieacker; Sabine Kliesch; Frank Tüttelmann
Journal:  J Assist Reprod Genet       Date:  2013-10-24       Impact factor: 3.412

2.  Prospective evaluation of scrotal ultrasound and intratesticular perfusion by color-coded duplex sonography (CCDS) in TESE patients with azoospermia.

Authors:  Bora Altinkilic; Adrian Pilatz; Thorsten Diemer; Julia Wolf; Martin Bergmann; Sarah Schönbrunn; Uwe Ligges; Hans-Christian Schuppe; Wolfgang Weidner
Journal:  World J Urol       Date:  2017-04-20       Impact factor: 4.226

3.  X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.

Authors:  Alexander N Yatsenko; Andrew P Georgiadis; Albrecht Röpke; Andrea J Berman; Thomas Jaffe; Marta Olszewska; Birgit Westernströer; Joseph Sanfilippo; Maciej Kurpisz; Aleksandar Rajkovic; Svetlana A Yatsenko; Sabine Kliesch; Stefan Schlatt; Frank Tüttelmann
Journal:  N Engl J Med       Date:  2015-05-13       Impact factor: 91.245

Review 4.  [Fertility in patients with Klinefelter syndrome (47,XXY)].

Authors:  S Kliesch; M Zitzmann; H M Behre
Journal:  Urologe A       Date:  2011-01       Impact factor: 0.639

Review 5.  Genetic intersection of male infertility and cancer.

Authors:  Liina Nagirnaja; Kenneth I Aston; Donald F Conrad
Journal:  Fertil Steril       Date:  2018-01       Impact factor: 7.329

6.  Comprehensive sequence analysis of the NR5A1 gene encoding steroidogenic factor 1 in a large group of infertile males.

Authors:  Albrecht Röpke; Ann-Christin Tewes; Jörg Gromoll; Sabine Kliesch; Peter Wieacker; Frank Tüttelmann
Journal:  Eur J Hum Genet       Date:  2013-01-09       Impact factor: 4.246

Review 7.  Monogenic causes of non-obstructive azoospermia: challenges, established knowledge, limitations and perspectives.

Authors:  Laura Kasak; Maris Laan
Journal:  Hum Genet       Date:  2020-01-18       Impact factor: 4.132

Review 8.  Evaluating genetic causes of azoospermia: What can we learn from a complex cellular structure and single-cell transcriptomics of the human testis?

Authors:  Samuele Soraggi; Meritxell Riera; Ewa Rajpert-De Meyts; Mikkel H Schierup; Kristian Almstrup
Journal:  Hum Genet       Date:  2020-01-16       Impact factor: 4.132

Review 9.  Biotechnological approaches to the treatment of aspermatogenic men.

Authors:  Pedro Manuel Aponte; Stefan Schlatt; Luiz Renato de Franca
Journal:  Clinics (Sao Paulo)       Date:  2013       Impact factor: 2.365

10.  Altered Gene Expression in the Testis of Infertile Patients with Nonobstructive Azoospermia.

Authors:  Zhiqiang Wang; Zhongjun Ding; Yan Guan; Chunhui Liu; Linjun Wang; Wensheng Shan; Jie Yang
Journal:  Comput Math Methods Med       Date:  2021-06-09       Impact factor: 2.238

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