Literature DB >> 32061499

A different look at genetic factors in individuals with non-obstructive azoospermia or oligospermia in our research study: To whom, which threshold, when, in what way?

Evren Gumus1, Bulent Kati2, Eyyup Sabri Pelit2, Eser Ordek2, Halil Ciftci2.   

Abstract

INTRODUCTION: In our study, we sought answers to many questions about male infertility from a different perspective. The first step in male infertility is anamnesis, physical examination and sperm count. The European Academy of Andrology recommends examination of genetic causes in individuals with fewer than 5million/ml semen counts. The American Urological Association and American Society for Reproductive Medicine have guidelines recommending performing karyotype and AZF subgroup deletion testing in azoospermia and fewer than 5 million sperm total count. Klinefelter syndrome and Y chromosome microdeletions are still very important in male infertility. Based on patients with Klinefelter syndrome or Y microdeletion, we sought answers to many questions in male infertility.
MATERIALS AND METHODS: In the presented study 327 male patients with having fewer than 15millionsperm/ml detected in at least two consecutive sperm analysis were examined. Patients were divided into sub-groups according to the presence of semen count, chromosomal anomaly and Y microdeletion. In addition, FSH, LH and testosterone levels were analyzed.
RESULTS: Numerical chromosomal anomalies were observed in 34 (10.4%) of 327 patients, and all of these anomalies were found as 47, XXY. Individuals with no AZF microdeletion constituted 95.1% (n=311) of the study group. The overall frequency of AZF microdeletions was 4.9% (16/327). No AZF microdeletions were detected for the patients who have sperm counts above 2million/ml. FSH, LH and testosterone levels were found significantly different between the groups. DISCUSSION: The results of our study provide another layer of evidence to demonstrate the controversial threshold value of the EAA. In light of our data and current literature, we recommend to set the threshold value at 2million/ml for semen analysis. Further studies conducted in different ethnic groups and larger patient groups would contribute to clarify what exact value should be used to apply genetic tests.
Copyright © 2019 Asociación Española de Andrología, Medicina Sexual y Reproductiva. Publicado por Elsevier España, S.L.U. All rights reserved.

Entities:  

Keywords:  AZF; Azoospermia; FSH; Infertilidad masculina; Klinefelter syndrome; Male infertility; Micro-deleciones del cromosoma Y; Síndrome de Klinefelter; Y microdeletions

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Substances:

Year:  2020        PMID: 32061499     DOI: 10.1016/j.androl.2019.08.001

Source DB:  PubMed          Journal:  Rev Int Androl        ISSN: 1698-031X            Impact factor:   1.063


  2 in total

1.  Bi-allelic SHOC1 loss-of-function mutations cause meiotic arrest and non-obstructive azoospermia.

Authors:  Chencheng Yao; Chao Yang; Liangyu Zhao; Peng Li; Ruhui Tian; Huixing Chen; Ying Guo; Yuhua Huang; Erlei Zhi; Jing Zhai; Hongfang Sun; Jianxiong Zhang; Yan Hong; Li Zhang; Zhiyong Ji; Feng Zhang; Zhi Zhou; Zheng Li
Journal:  J Med Genet       Date:  2020-09-08       Impact factor: 6.318

Review 2.  The Role of Genetics and Oxidative Stress in the Etiology of Male Infertility-A Unifying Hypothesis?

Authors:  Robert John Aitken; Mark A Baker
Journal:  Front Endocrinol (Lausanne)       Date:  2020-09-30       Impact factor: 5.555

  2 in total

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