Literature DB >> 18284889

Clinical consequences of microdeletions of the Y chromosome: the extended Münster experience.

Manuela Simoni1, Frank Tüttelmann, Jörg Gromoll, Eberhard Nieschlag.   

Abstract

A total of 3179 patients were screened for Y-chromosome microdeletions and 821 patients for partial AZFc deletions. Thirty-nine Y-chromosomal microdeletions were found (2.4% of men with <1 x 10(6)/ml spermatozoa): two AZFa, two AZFb, one AZFbc, one partial AZFb, one partial AZFb+c and 32 AZFc (b2/b4). Partial AZFc deletions were found in 45 patients (5.5%), mostly gr/gr deletions (n = 28). In patients with AZFc deletion, azoospermia was found in 53.1% and sperm concentrations of mostly <0.1 x 10(6)/ml were found in 46.9%. Semen analyses and FSH measurements showed no trend over time. Elongated spermatids were seen in 6/15 AZFc patients and bilateral Sertoli cell-only was found in 4/15. Testicular sperm extraction (TESE) was attempted in 10 patients and spermatozoa were found in six. Compared with infertile men matched by sperm concentration, no differences in hormonal and seminal parameters could be found in patients with AZFc or gr/gr deletions. It is concluded that: (i) frequency of AZF deletions in Germany is much lower than in other countries; (ii) AZFc deletions are associated with severe disturbances of spermatogenesis and TESE is not possible in half of these patients; (iii) AZFc and gr/ gr deletions are not associated with any clinical diagnostic parameter; (iv) and no trend is apparent over time.

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Year:  2008        PMID: 18284889     DOI: 10.1016/s1472-6483(10)60588-3

Source DB:  PubMed          Journal:  Reprod Biomed Online        ISSN: 1472-6483            Impact factor:   3.828


  47 in total

Review 1.  Evaluation of the azoospermic male.

Authors:  Robert Oates
Journal:  Asian J Androl       Date:  2011-12-19       Impact factor: 3.285

2.  The frequencies of Y chromosome microdeletions in infertile males.

Authors:  Emre Can Akınsal; Numan Baydilli; Munis Dündar; Oğuz Ekmekçioğlu
Journal:  Turk J Urol       Date:  2018-01-04

3.  Male reproductive disorders, diseases, and costs of exposure to endocrine-disrupting chemicals in the European Union.

Authors:  Russ Hauser; Niels E Skakkebaek; Ulla Hass; Jorma Toppari; Anders Juul; Anna Maria Andersson; Andreas Kortenkamp; Jerrold J Heindel; Leonardo Trasande
Journal:  J Clin Endocrinol Metab       Date:  2015-03-05       Impact factor: 5.958

4.  Y chromosome microdeletions in infertile men: prevalence, phenotypes and screening markers for the Indian population.

Authors:  S Sen; A R Pasi; R Dada; M B Shamsi; D Modi
Journal:  J Assist Reprod Genet       Date:  2013-01-24       Impact factor: 3.412

5.  Distinctive pattern of expression of spermatogenic molecular markers in testes of azoospermic men with non-mosaic Klinefelter syndrome.

Authors:  Sandra E Kleiman; Leah Yogev; Ofer Lehavi; Haim Yavetz; Ron Hauser
Journal:  J Assist Reprod Genet       Date:  2016-03-19       Impact factor: 3.412

6.  Deletion or underexpression of the Y-chromosome genes CDY2 and HSFY is associated with maturation arrest in American men with nonobstructive azoospermia.

Authors:  Peter J Stahl; Anna N Mielnik; Christopher E Barbieri; Peter N Schlegel; Darius A Paduch
Journal:  Asian J Androl       Date:  2012-07-23       Impact factor: 3.285

Review 7.  Management of non-obstructive azoospermia.

Authors:  Koji Chiba; Noritoshi Enatsu; Masato Fujisawa
Journal:  Reprod Med Biol       Date:  2016-01-18

Review 8.  [Genetics of male infertility].

Authors:  F Tüttelmann; J Gromoll; S Kliesch
Journal:  Urologe A       Date:  2008-12       Impact factor: 0.639

9.  A biopsy sample reduction approach to identify significant alterations of the testicular transcriptome in the presence of Y-chromosomal microdeletions that are independent of germ cell composition.

Authors:  Heike Cappallo-Obermann; Kathrein von Kopylow; Wolfgang Schulze; Andrej-Nikolai Spiess
Journal:  Hum Genet       Date:  2010-07-29       Impact factor: 4.132

10.  Clinical relevance of Y-linked CNV screening in male infertility: new insights based on the 8-year experience of a diagnostic genetic laboratory.

Authors:  Deborah Lo Giacco; Chiara Chianese; Josvany Sánchez-Curbelo; Lluis Bassas; Patricia Ruiz; Osvaldo Rajmil; Joaquim Sarquella; Alvaro Vives; Eduard Ruiz-Castañé; Rafael Oliva; Elisabet Ars; Csilla Krausz
Journal:  Eur J Hum Genet       Date:  2013-11-06       Impact factor: 4.246

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