Assisted reproductive therapies and imprinting disorders - A preliminary British survey

A. G. Sutcliffe, C. J. Peters, S. Bowdin, K. Temple, W. Reardon, L. Wilson, J. Clayton-Smith, L. A. Brueton, W. Bannister, E. R. Maher

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Background: Recent reports have suggested a higher risk of Beckwith-Wiedemann syndrome (BWS) and Angelman syndrome (AS) after assisted reproductive technologies (ARTs), but it is unclear whether this might also apply to other disorders of genomic imprinting. Methods: We contacted families of children with BWS, AS, Prader-Willi syndrome (PWS) and transient neonatal diabetes mellitus (TNDM) to determine use of ART. Results: A statistically significant increased frequency of ART in children with BWS was confirmed [2.9%, 95% confidence interval (CI) 1.4-6.3% vs 0.8% expected] but there was no significant association with PWS or TNDM. Consideration of the molecular subgroup of BWS and AS suggested the feasibility of association with ART. Conclusions: These differences may relate to variations in (i) the molecular mechanisms for disordered imprinting in the different disorders and (ii) the susceptibility of specific imprinting control regions to ART-associated methylation alterations (epimutations). © 2006 Oxford University Press.
    Original languageEnglish
    Pages (from-to)1009-1011
    Number of pages2
    JournalHuman Reproduction
    Volume21
    Issue number4
    DOIs
    Publication statusPublished - Apr 2006

    Keywords

    • ART
    • BWS
    • Imprinting
    • IVF
    • PWS

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