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Clinical and molecular characterization of patients affected by Beckwith‐Wiedemann spectrum conceived through assisted reproduction techniques.

Authors :
Carli, Diana
Operti, Matteo
Russo, Silvia
Cocchi, Guido
Milani, Donatella
Leoni, Chiara
Prada, Elisabetta
Melis, Daniela
Falco, Mariateresa
Spina, Jennifer
Uliana, Vera
Sara, Osimani
Sirchia, Fabio
Tarani, Luigi
Macchiaiolo, Marina
Cerrato, Flavia
Sparago, Angela
Pignata, Laura
Tannorella, Pierpaola
Cardaropoli, Simona
Source :
Clinical Genetics. Oct2022, Vol. 102 Issue 4, p314-323. 10p.
Publication Year :
2022

Abstract

The prevalence of Beckwith–Wiedemann spectrum (BWSp) is tenfold increased in children conceived through assisted reproductive techniques (ART). More than 90% of ART‐BWSp patients reported so far display imprinting center 2 loss‐of‐methylations (IC2‐LoM), versus 50% of naturally conceived BWSp patients. We describe a cohort of 74 ART‐BWSp patients comparing their features with a cohort of naturally conceived BWSp patients, with the ART‐BWSp patients previously described in literature, and with the general population of children born from ART. We found that the distribution of UPD(11)pat was not significantly different in ART and naturally conceived patients. We observed 68.9% of IC2‐LoM and 16.2% of mosaic UPD(11)pat in our ART cohort, that strongly differ from the figure reported in other cohorts so far. Since UPD(11)pat likely results from post‐fertilization recombination events, our findings allows to hypothesize that more complex molecular mechanisms, besides methylation disturbances, may underlie BWSp increased risk in ART pregnancies. Moreover, comparing the clinical features of ART and non‐ART BWSp patients, we found that ART‐BWSp patients might have a milder phenotype. Finally, our data show a progressive increase in the prevalence of BWSp over time, paralleling that of ART usage in the last decades. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00099163
Volume :
102
Issue :
4
Database :
Academic Search Index
Journal :
Clinical Genetics
Publication Type :
Academic Journal
Accession number :
158963754
Full Text :
https://doi.org/10.1111/cge.14193