significantly associated with older maternal age (R¼-0.27, p<0.01), fewer 2PNs, higher aneuploidy rate, and fewer usable embryos for transfer. (Table 1)However, when controlling for maternal age using multivariate regression analysis, AMH was not an independent predictor of the rate of aneuploid embryos (p¼0.11) CONCLUSIONS: AMH is an established marker of ovarian reserve and is predictive of the number of embryos available for biopsy, however our results suggest that it is not an independent predictor of blastocyst euploidy rates. This is important information for both obstetrician/gynecologists and reproductive endocrinologists when counseling patients with diminished ovarian reserve prior to undergoing IVF.
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