Literature DB >> 19896650

A decade of experience emphasizes that testing for Y microdeletions is essential in American men with azoospermia and severe oligozoospermia.

Peter J Stahl1, Puneet Masson, Anna Mielnik, Michael B Marean, Peter N Schlegel, Darius A Paduch.   

Abstract

OBJECTIVE: To evaluate the benefit of Y microdeletion testing.
DESIGN: Retrospective analysis.
SETTING: University-based male fertility clinic and genetics laboratory. PATIENT(S): A total of 1,591 men with sperm concentrations less than 5 million sperm/mL. INTERVENTION(S): Semen analysis, Y microdeletion testing, microdissection testicular sperm extraction (TESE). MAIN OUTCOME MEASURE(S): Sperm concentration, incidence and nature of Y microdeletions, microdissection TESE outcome. RESULT(S): We identified 149 microdeletions (9.4%). 10.4% of azoospermic men and 10.1% of men with sperm concentrations >0-1 million sperm/mL harbored microdeletions. Two-thirds of microdeletions in azoospermic men were AZFa, AZFb, AZFb+c, or complete Yq deletions. Virtually all microdeletions in oligozoospermic patients were AZFc deletions. Seven hundred eighteen patients underwent microdissection TESE, including 41 with microdeletions. Microdissection TESE failed in all patients with AZFa, AZFb, AZFb+c, and complete Yq deletions. Sperm were retrieved in 15/21 AZFc deleted patients (71.4%). The presence of an AZFc deletion was associated with increased likelihood of sperm retrieval when compared with the 48.8% retrieval rate in 385 idiopathically azoospermic men who consecutively underwent microdissection TESE at our institution during the study period. Clinical pregnancy was achieved in 10/15 azoospermic AZFc deleted patients for whom sperm were successfully retrieved. CONCLUSION(S): Of azoospermic and severely oligozoospermic American men, 10% harbor Y microdeletions that alter prognosis for surgical sperm retrieval and are vertically transmissible. Y microdeletion testing is essential for genetic and preoperative counseling in these patients.
Copyright © 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Year:  2009        PMID: 19896650     DOI: 10.1016/j.fertnstert.2009.09.006

Source DB:  PubMed          Journal:  Fertil Steril        ISSN: 0015-0282            Impact factor:   7.329


  45 in total

Review 1.  Local signalling environments and human male infertility: what we can learn from mouse models.

Authors:  Roopa L Nalam; Martin M Matzuk
Journal:  Expert Rev Mol Med       Date:  2010-05-11       Impact factor: 5.600

2.  Single-nucleotide polymorphisms in HORMAD1 may be a risk factor for azoospermia caused by meiotic arrest in Japanese patients.

Authors:  Toshinobu Miyamoto; Akira Tsujimura; Yasushi Miyagawa; Eitetsu Koh; Mikio Namiki; Michiharu Horikawa; Yasuaki Saijo; Kazuo Sengoku
Journal:  Asian J Androl       Date:  2012-03-12       Impact factor: 3.285

Review 3.  Evaluation of the azoospermic male.

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

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.  Prevalent false positives of azoospermia factor a (AZFa) microdeletions caused by single-nucleotide polymorphism rs72609647 in the sY84 screening of male infertility.

Authors:  Qing Wu; Guo-Wu Chen; Tao-Fei Yan; Hui Wang; Yu-Ling Liu; Zheng Li; Shi-Wei Duan; Fei Sun; Yun Feng; Hui-Juan Shi
Journal:  Asian J Androl       Date:  2011-07-18       Impact factor: 3.285

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.  Chromosomal disorders and male infertility.

Authors:  Gary L Harton; Helen G Tempest
Journal:  Asian J Androl       Date:  2011-11-28       Impact factor: 3.285

8.  High prevalence of genetic abnormalities in Middle Eastern patients with idiopathic non-obstructive azoospermia.

Authors:  Marwan Alhalabi; Mazen Kenj; Fawza Monem; Zaina Mahayri; Ghalia Abou Alchamat; Ammar Madania
Journal:  J Assist Reprod Genet       Date:  2013-04-25       Impact factor: 3.412

9.  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

Review 10.  Genetics of Male Infertility.

Authors:  Filipe Tenorio Lira Neto; Phil Vu Bach; Bobby Baback Najari; Philip Shihua Li; Marc Goldstein
Journal:  Curr Urol Rep       Date:  2016-10       Impact factor: 3.092

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.