AI Article Synopsis

  • Recent research highlights how toxic endocrine disrupting chemicals (EDCs) can affect the epigenetic information in sperm, potentially impacting reproductive health and outcomes.
  • While studies typically focus on female reproductive issues, the male's role in reproduction, especially regarding sperm epigenetics and health, has been largely overlooked in diagnostics.
  • Given that environmental pollutants are common and can disrupt endocrine functions, it's crucial to include sperm epigenetics in reproductive health research and diagnostics to improve understanding and outcomes in reproductive disorders.

Article Abstract

Endocrine control of reproduction is very well known and has been echoed by many research groups. However, recent developments point to the ability of toxic endocrine disrupting chemicals (EDC) to alter epigenetic information of the gametes which gets transferred to the developing embryo and affects the immediate reproductive outcome or even persists transgenerationally. These epigenetic aberrations contribute to the ensuing pathophysiology of reproductive disorders. Investigations of the female in cases of poor reproductive outcome have been the main strategy towards diagnosis. However, despite the male partner contributing half of his genome to the progeny, thorough investigations in the male have been ignored. Environmental pollutants are all pervading and are encountered in our day-to-day life. Many of these pollutants have potential to disrupt the endocrine system. Here, we discuss how the male gametes (spermatozoa) are susceptible to a myriad of epigenetic insults inflicted by exposure to endocrine disruptors and how important is the contribution of the epigenetic marks of the spermatozoa in healthy reproduction. We advocate that sperm epigenetics should be considered as a significant contributor to reproductive health and should be researched further and be subsequently included in routine diagnostic workup in cases of poor reproductive outcome.

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Source
http://dx.doi.org/10.1515/hmbci-2016-0007DOI Listing

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