Genome and Epigenome Disorders and Male Infertility: Feedback from 15 Years of Clinical and Research Experience.
Debbie MontjeanMarion BeaumontAbdelhafid NatiqNoureddine LouanjliAndre HazoutPierre MironThomas LiehrRosalie CabryIlham RatbiMoncef BenkhalifaPublished in: Genes (2024)
Infertility affects around 20% of couples of reproductive age; however, in some societies, as many as one-third of couples are unable to conceive. Different factors contribute to the decline of male fertility, such us environmental and professional exposure to endocrine disruptors, oxidative stress, and life habits with the risk of de novo epigenetics dysregulation. Since the fantastic development of new "omes and omics" technologies, the contribution of inherited or de novo genomes and epigenome disorders to male infertility have been further elucidated. Many other techniques have become available to andrology laboratories for the investigation of genome and epigenome integrity and the maturation and the competency of spermatozoa. All these new methods of assessment are highlighting the importance of genetics and epigenetics investigation for assisted reproduction pathology and for supporting professionals in counselling patients and proposing different management strategies for male infertility. This aims to improve clinical outcomes while minimizing the risk of genetics or health problems at birth.
Keyphrases
- dna methylation
- oxidative stress
- end stage renal disease
- mental health
- polycystic ovary syndrome
- genome wide
- healthcare
- ejection fraction
- public health
- chronic kidney disease
- gene expression
- metabolic syndrome
- peritoneal dialysis
- adipose tissue
- risk assessment
- human health
- diabetic rats
- human immunodeficiency virus
- antiretroviral therapy
- induced apoptosis
- endoplasmic reticulum stress
- hiv infected
- pregnant women
- patient reported