Amelie Fassbender, Maria Debiec-Rychter, Rieta Van Bree, Joris Robert Vermeesch, Christel Meuleman, Carla Tomassetti, Karen Peeraer, Thomas D'Hooghe, Dan I Lebovic
Reproductive sciences (Thousand Oaks, Calif.) 2015 SepFetal microchimerism has been implicated in the etiology of autoimmune diseases. This study was done to test the hypothesis that male fetal microchimerism is present in eutopic and ectopic endometrium (EM) obtained from women with endometriosis but not in eutopic EM from women without endometriosis. A total of 31 patients were selected, including women with endometriosis (paired eutopic and ectopic EM; n = 19) and women without endometriosis (eutopic EM; n = 12). Tricolor interphase fluorescence in situ hybridization analysis was performed by cohybridization of CEP Y SpectrumAqua and CEP X SpectrumGreen (SG)/CEP Y SpectrumOrange probes. Ectopic EM from women with endometriosis had 75% XX chromosomes (double SG signals) and 25% X chromosomes (single SG signal). Y chromosomes were not observed in any of the eutopic/ectopic endometrial tissues from cases or controls. We were unable to confirm our hypothesis that male fetal microchimerism is present in eutopic and/or ectopic EM obtained from women with endometriosis. © The Author(s) 2015.
Amelie Fassbender, Maria Debiec-Rychter, Rieta Van Bree, Joris Robert Vermeesch, Christel Meuleman, Carla Tomassetti, Karen Peeraer, Thomas D'Hooghe, Dan I Lebovic. Lack of Evidence That Male Fetal Microchimerism is Present in Endometriosis. Reproductive sciences (Thousand Oaks, Calif.). 2015 Sep;22(9):1115-21
PMID: 25749809
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