Methylation analysis of idiopathic recurrent spontaneous miscarriage cases reveals aberrant imprinting at H19 ICR in normozoospermic individuals
- PMID: 22959455
- DOI: 10.1016/j.fertnstert.2012.07.1143
Methylation analysis of idiopathic recurrent spontaneous miscarriage cases reveals aberrant imprinting at H19 ICR in normozoospermic individuals
Abstract
Objective: To study H19 ICR methylation levels in association with sperm parameters routinely analyzed in idiopathic recurrent spontaneous miscarriage cases.
Design: Case-control study.
Setting: Academic research setting.
Patient(s): Male partners of couples with a history of idiopathic recurrent spontaneous miscarriage (RSM group) and male partners of couples with proven fertility (control group).
Intervention(s): None.
Main outcome measure(s): Paternal age, sperm concentration, motility, chromatin compaction status, morphology, and H19 ICR methylation were assessed in control and idiopathic RSM group participants.
Result(s): Paternal age and basic semen parameters analyzed did not show any significant difference between the two groups; however H19 ICR methylation levels were reduced significantly in the idiopathic RSM group compared with the control group.
Conclusion(s): Significant reduction in the H19 ICR methylation without significant difference in the sperm parameters demonstrates aberrant imprinting to be associated with idiopathic RSM.
Copyright © 2012 American Society for Reproductive Medicine. Published by Elsevier Inc. All rights reserved.
Comment in
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Aberrant methylation of the H19 imprinting control region may increase the risk of spontaneous abortion.Epigenomics. 2013 Feb;5(1):23-4. Epigenomics. 2013. PMID: 23539767 No abstract available.
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