Methylation patterns of methylenetetrahydrofolate reductase gene promoter in infertile males.
Tuba KulacNeslihan HekimFatih KocamanogluCengiz BeyazSezgin GüneşRamazan AsciPublished in: Andrologia (2020)
Errors of folate/homocysteine pathways which are critical for transferring methyl groups have been suggested to affect male fertility. We aimed to evaluate the methylation patterns of the promoter of methylenetetrahydrofolate reductase (MTHFR) gene in infertile males and to investigate the association between MTHFR promoter methylation and success of sperm retrieval. Thirty-five nonobstructive azoospermic and 46 severe oligozoospermic patients constituted the study group and were compared with 49 fertile and/or normozoospermic men. The methylation status was analysed by methylation-specific polymerase chain reaction. MTHFR promoter methylation was detected in infertile men with NOA and SO in the ratio of 48.6% and 58.7%, respectively. Methylation was also observed in 51% of controls. MTHFR promoter was methylated in 65% of men with viable spermatozoon during TESE. No association was found regarding to the profile of MTHFR promoter methylation between both NOA and SO patients and controls (p = .621). There was no relation between the methylation status of MTHFR promoter and low motility and poor morphology (p = .682 and p = .413, respectively). No association was found between MTHFR promoter methylation and presence of viable spermatozoa (p = .382). Our data indicate that the promoter methylation of MTHFR gene may not be associated with male infertility.
Keyphrases
- dna methylation
- genome wide
- gene expression
- transcription factor
- copy number
- end stage renal disease
- ejection fraction
- newly diagnosed
- machine learning
- escherichia coli
- heart failure
- peritoneal dialysis
- emergency department
- adipose tissue
- type diabetes
- prognostic factors
- polycystic ovary syndrome
- left ventricular
- young adults
- pseudomonas aeruginosa
- electronic health record
- biofilm formation