Literature DB >> 24193344

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

Deborah Lo Giacco1, Chiara Chianese2, Josvany Sánchez-Curbelo3, Lluis Bassas3, Patricia Ruiz4, Osvaldo Rajmil3, Joaquim Sarquella3, Alvaro Vives3, Eduard Ruiz-Castañé3, Rafael Oliva5, Elisabet Ars4, Csilla Krausz6.   

Abstract

AZF microdeletion screening is routinely performed in the diagnostic work-up for male infertility; however, some issues remain debated. In this study, we provide insights into the sperm concentration cutoff value for routine testing, the predictive value of AZFc deletion for testicular sperm retrieval and the Y-background contribution to the interpopulation variability of deletion frequencies. In the Spanish population, partial AZFc rearrangements have been poorly explored and no data exist on partial duplications. In our study, 27/806 (3.3%) patients carried complete AZF deletions. All were azoo/cryptozoospermic, except for one whose sperm concentration was 2 × 10(6)/ml. In AZFc-deleted men, we observed a lower sperm recovery rate upon conventional TESE (9.1%) compared with the literature (60-80% with microTESE). Haplogroup E was the most represented among non-Spanish and hgr P among Spanish AZF deletion carriers. The analysis of AZFc partial rearrangements included 330 idiopathic infertile patients and 385 controls of Spanish origin. Gr/gr deletion, but not AZFc partial duplications, was significantly associated with spermatogenic impairment. Our data integrated with the literature suggest that: (1) routine AZF microdeletion testing could eventually include only men with ≤2 × 10(6)/ml; (2) classical TESE is associated with low sperm recovery rate in azoospermic AZFc-deleted men, and therefore microTESE should be preferred; (3) Y background could partially explain the differences in deletion frequencies among populations. Finally, our data on gr/gr deletion further support the inclusion of this genetic test in the work-up of infertile men, whereas partial AZFc duplications do not represent a risk for spermatogenic failure in the Spanish population.

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Year:  2013        PMID: 24193344      PMCID: PMC4023226          DOI: 10.1038/ejhg.2013.253

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  40 in total

1.  The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.

Authors:  Helen Skaletsky; Tomoko Kuroda-Kawaguchi; Patrick J Minx; Holland S Cordum; LaDeana Hillier; Laura G Brown; Sjoerd Repping; Tatyana Pyntikova; Johar Ali; Tamberlyn Bieri; Asif Chinwalla; Andrew Delehaunty; Kim Delehaunty; Hui Du; Ginger Fewell; Lucinda Fulton; Robert Fulton; Tina Graves; Shun-Fang Hou; Philip Latrielle; Shawn Leonard; Elaine Mardis; Rachel Maupin; John McPherson; Tracie Miner; William Nash; Christine Nguyen; Philip Ozersky; Kymberlie Pepin; Susan Rock; Tracy Rohlfing; Kelsi Scott; Brian Schultz; Cindy Strong; Aye Tin-Wollam; Shiaw-Pyng Yang; Robert H Waterston; Richard K Wilson; Steve Rozen; David C Page
Journal:  Nature       Date:  2003-06-19       Impact factor: 49.962

2.  Screening for Y chromosome microdeletions in 226 Slovenian subfertile men.

Authors:  B Peterlin; T Kunej; J Sinkovec; N Gligorievska; B Zorn
Journal:  Hum Reprod       Date:  2002-01       Impact factor: 6.918

3.  AZFc deletions and spermatogenic failure: a population-based survey of 20,000 Y chromosomes.

Authors:  Steven G Rozen; Janet D Marszalek; Kathryn Irenze; Helen Skaletsky; Laura G Brown; Robert D Oates; Sherman J Silber; Kristin Ardlie; David C Page
Journal:  Am J Hum Genet       Date:  2012-10-25       Impact factor: 11.025

4.  Prevalence of Y chromosome microdeletions in infertile men who consulted a tertiary care medical centre: the Münster experience.

Authors:  B Maurer; J Gromoll; M Simoni; E Nieschlag
Journal:  Andrologia       Date:  2001-01       Impact factor: 2.775

5.  Clinical diagnostic testing for the cytogenetic and molecular causes of male infertility: the Mayo Clinic experience.

Authors:  Sean E Hofherr; Anne E Wiktor; Benjamin R Kipp; D Brian Dawson; Daniel L Van Dyke
Journal:  J Assist Reprod Genet       Date:  2011-09-13       Impact factor: 3.412

6.  Recombination between palindromes P5 and P1 on the human Y chromosome causes massive deletions and spermatogenic failure.

Authors:  Sjoerd Repping; Helen Skaletsky; Julian Lange; Sherman Silber; Fulco Van Der Veen; Robert D Oates; David C Page; Steve Rozen
Journal:  Am J Hum Genet       Date:  2002-09-20       Impact factor: 11.025

7.  Screening for AZF deletion in a large series of severely impaired spermatogenesis patients.

Authors:  M C Martínez; M J Bernabé; E Gómez; A Ballesteros; J Landeras; G Glover; M Gíl-Salom; J Remohí; A Pellicer
Journal:  J Androl       Date:  2000 Sep-Oct

8.  Detection of sperm in men with Y chromosome microdeletions of the AZFa, AZFb and AZFc regions.

Authors:  C V Hopps; A Mielnik; M Goldstein; G D Palermo; Z Rosenwaks; P N Schlegel
Journal:  Hum Reprod       Date:  2003-08       Impact factor: 6.918

9.  Screening for microdeletions in human Y chromosome--AZF candidate genes and male infertility.

Authors:  Florina Raicu; L Popa; Pompilia Apostol; D Cimponeriu; Letitia Dan; Elena Ilinca; Laura Luana Dracea; B Marinescu; L Gavrila
Journal:  J Cell Mol Med       Date:  2003 Jan-Mar       Impact factor: 5.310

10.  Association of spermatogenic failure with the b2/b3 partial AZFc deletion.

Authors:  Abdelmajid Eloualid; Houria Rhaissi; Ahmed Reguig; Safaa Bounaceur; Brahim El Houate; Omar Abidi; Majida Charif; Noureddine Louanjli; Elbakkay Chadli; Abdelhamid Barakat; Anu Bashamboo; Ken McElreavey; Hassan Rouba
Journal:  PLoS One       Date:  2012-04-13       Impact factor: 3.240

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  19 in total

1.  Copy-number variations in Y-chromosomal azoospermia factor regions identified by multiplex ligation-dependent probe amplification.

Authors:  Kazuki Saito; Mami Miyado; Yoshitomo Kobori; Yoko Tanaka; Hiromichi Ishikawa; Atsumi Yoshida; Momori Katsumi; Hidekazu Saito; Toshiro Kubota; Hiroshi Okada; Tsutomu Ogata; Maki Fukami
Journal:  J Hum Genet       Date:  2015-01-08       Impact factor: 3.172

2.  Susceptibility of gr/gr rearrangements to azoospermia or oligozoospermia is dependent on DAZ and CDY1 gene copy deletions.

Authors:  S Sen; P Ambulkar; I Hinduja; K Zaveri; J Gokral; A Pal; D Modi
Journal:  J Assist Reprod Genet       Date:  2015-07-07       Impact factor: 3.412

Review 3.  Consequences of Y chromosome microdeletions beyond male infertility.

Authors:  Stacy Colaco; Deepak Modi
Journal:  J Assist Reprod Genet       Date:  2019-06-18       Impact factor: 3.412

Review 4.  Spermatogenic failure and the Y chromosome.

Authors:  C Krausz; E Casamonti
Journal:  Hum Genet       Date:  2017-04-29       Impact factor: 4.132

Review 5.  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 6.  Male Reproductive Disorders and Fertility Trends: Influences of Environment and Genetic Susceptibility.

Authors:  Niels E Skakkebaek; Ewa Rajpert-De Meyts; Germaine M Buck Louis; Jorma Toppari; Anna-Maria Andersson; Michael L Eisenberg; Tina Kold Jensen; Niels Jørgensen; Shanna H Swan; Katherine J Sapra; Søren Ziebe; Lærke Priskorn; Anders Juul
Journal:  Physiol Rev       Date:  2016-01       Impact factor: 37.312

7.  Common AZFc structure may possess the optimal spermatogenesis efficiency relative to the rearranged structures mediated by non-allele homologous recombination.

Authors:  Bo Yang; Yong-yi Ma; Yun-qiang Liu; Lei Li; Dong Yang; Wen-ling Tu; Ying Shen; Qiang Dong; Yuan Yang
Journal:  Sci Rep       Date:  2015-05-22       Impact factor: 4.379

Review 8.  Individualized medicine enabled by genomics in Saudi Arabia.

Authors:  Muhammad Abu-Elmagd; Mourad Assidi; Hans-Juergen Schulten; Ashraf Dallol; Peter Pushparaj; Farid Ahmed; Stephen W Scherer; Mohammed Al-Qahtani
Journal:  BMC Med Genomics       Date:  2015-01-15       Impact factor: 3.063

Review 9.  EAA/EMQN best practice guidelines for molecular diagnosis of Y-chromosomal microdeletions: state-of-the-art 2013.

Authors:  C Krausz; L Hoefsloot; M Simoni; F Tüttelmann
Journal:  Andrology       Date:  2014-01       Impact factor: 3.842

10.  Novel Y-chromosomal microdeletions associated with non-obstructive azoospermia uncovered by high throughput sequencing of sequence-tagged sites (STSs).

Authors:  Xiao Liu; Zesong Li; Zheng Su; Junjie Zhang; Honggang Li; Jun Xie; Hanshi Xu; Tao Jiang; Liya Luo; Ruifang Zhang; Xiaojing Zeng; Huaiqian Xu; Yi Huang; Lisha Mou; Jingchu Hu; Weiping Qian; Yong Zeng; Xiuqing Zhang; Chengliang Xiong; Huanming Yang; Karsten Kristiansen; Zhiming Cai; Jun Wang; Yaoting Gui
Journal:  Sci Rep       Date:  2016-02-24       Impact factor: 4.379

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