Guidelines on sperm DNA fragmentation testing
Commentary

Guidelines on sperm DNA fragmentation testing

Frank Vandekerckhove

Centre for Reproductive Medicine, University Hospital, Gent, Belgium

Correspondence to: Frank Vandekerckhove. Centre for Reproductive Medicine, University Hospital, Gent, Belgium. Email: vandekerckhove@gmail.com.

Comment on: Agarwal A, Majzoub A, Esteves SC, et al. Clinical utility of sperm DNA fragmentation testing: practice recommendations based on clinical scenarios. Transl Androl Urol 2016;5:935-50.


Submitted Jan 27, 2017. Accepted for publication Feb 04, 2017.

doi: 10.21037/tau.2017.03.49


Male factor subfertility is present in more than 50% of the couples treated with assisted reproductive techniques. Routine semen analysis provides information on semen volume as well as sperm concentration, motility, and morphology. Standardized methods have been published by the World Health Organization (WHO) (1). Nevertheless the investigation of male factor involvement should always include a complete medical history and physical examination. Endocrine evaluation, ultrasonography, specialized tests on semen and sperm, and genetic screening are additional tests to be used if required.

The etiology of sperm DNA fragmentation is multifactorial and it should not be forgotten that it affects both nuclear as well as mitochondrial DNA (2). Sperm DNA fragmentation (SDF) tests evaluate sperm DNA integrity and have been added to the diagnostic arsenal recently. They are mentioned in recent guidelines (3) and time has come to prepare a review about the tests available.

The authors (4) have summarized the various tests which are used and have evaluated in a very comprehensive way the advantages and disadvantages of each of them. They have marked the terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL), sperm chromatin structure assay (SCSA) and Halo test as the most popular ones. The availability of the technique and the costs and needs for expensive instrumentation are also important issues to compare. Each center has to decide which test to use and also to evaluate its results and define its cut off levels individually. The same authors (5,6) sometimes changed their values between one study and another. In a small study about the predictive value of the sperm chromatin dispersion test in cases of unexplained infertility treated with intra-uterine insemination in our centre (7), we found that DNA fragmentation >20% resulted in a lower pregnancy outcome. Mostly a threshold value of 27% to 30% is mentioned in literature (8). Although SDF is performed on the whole sperm, some authors suggested to analyze only motile sperm (9,10) or morphologically normal sperm cells (11). Most authors agreed that dead sperm cells in a sample may influence the results from most assays (10). Further fine tuning of the tests used is still recommended.

Which patients should be tested by means of SDF and what are the treatment strategies in various clinical situations? New techniques often come and go and in the beginning overconsumption looks around the corner. The authors tackled it in a very pragmatic way. They collected cases from daily practice and reviewed the literature for four groups:

  • Clinical varicocele;
  • Unexplained infertility/recurrent pregnancy loss/intrauterine insemination failure;
  • IVF and/or ICSI failure;
  • Borderline abnormal (or normal) sperm analysis with risk factors.

They formulated recommendations and graded them to quality of evidence. That’s how guidelines should be used: an objective analysis followed by ready to use information for treatment.

Some challenges for the future may be formulated. Damaged spermatozoa can fertilize an oocyte and a conceptus with a suboptimal paternal integrity may develop. So further research for technology methods to select individual DNA-intact sperm cells must continue.


Acknowledgements

None.


Footnote

Conflicts of Interest: The author has no conflicts of interest to declare.


References

  1. Cooper TG, Noonan E, von Eckardstein S, et al. World Health Organization reference values for human semen characteristics. Hum Reprod Update 2010;16:231-45. [Crossref] [PubMed]
  2. Sakkas D, Alvarez JG. Sperm DNA fragmentation: mechanisms of origin, impact on reproductive outcome, and analysis. Fertil Steril 2010;93:1027-36. [Crossref] [PubMed]
  3. Practice Committee of the American Society for Reproductive Medicine. Diagnostic evaluation of the infertile male: a committee opinion. Fertil Steril 2015;103:e18-25. [Crossref] [PubMed]
  4. Agarwal A, Majzoub A, Esteves SC, et al. Clinical utility of sperm DNA fragmentation testing: practice recommendations based on clinical scenarios. Transl Androl Urol 2016;5:935-50. [Crossref] [PubMed]
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  7. Vandekerckhove FW, De Croo I, Gerris J, et al. Sperm Chromatin Dispersion Test before Sperm Preparation Is Predictive of Clinical Pregnancy in Cases of Unexplained Infertility Treated with Intrauterine Insemination and Induction with Clomiphene Citrate. Front Med (Lausanne) 2016;3:63. [Crossref] [PubMed]
  8. Boe-Hansen GB, Fedder J, Ersbøll AK, et al. The sperm chromatin structure assay as a diagnostic tool in the human fertility clinic. Hum Reprod 2006;21:1576-82. [Crossref] [PubMed]
  9. Liu DY, Liu ML. Clinical value of sperm DNA damage should be assessed in motile sperm fraction rather than whole ejaculated sperm. Fertil Steril 2013;99:367-71. [Crossref] [PubMed]
  10. Palermo GD, Neri QV, Cozzubbo T, et al. Perspectives on the assessment of human sperm chromatin integrity. Fertil Steril 2014;102:1508-17. [Crossref] [PubMed]
  11. Avendaño C, Oehninger S. DNA fragmentation in morphologically normal spermatozoa: how much should we be concerned in the ICSI era? J Androl 2011;32:356-63. [Crossref] [PubMed]
Cite this article as: Vandekerckhove F. Guidelines on sperm DNA fragmentation testing. Transl Androl Urol 2017;6(Suppl 4):S586-S587. doi: 10.21037/tau.2017.03.49