TY - JOUR
T1 - Anti-Mullerian hormone variability and its implications for the number of oocytes retrieved following individualized dosing with follitropin delta
AU - Nelson, Scott M.
AU - Larsson, Per
AU - Mannaerts, Bernadette M.J.L.
AU - Nyboe Andersen, Anders
AU - Fauser, Bart C.J.M.
N1 - Funding Information:
Writing support was provided by Christina Campbell (PAREXEL, London, UK) with funding from Ferring Pharmaceuticals Ltd. The study was funded by Ferring Pharmaceuticals Ltd.
Publisher Copyright:
© 2019 John Wiley & Sons Ltd
PY - 2019/5/1
Y1 - 2019/5/1
N2 - OBJECTIVE: The stability of anti-Müllerian hormone (AMH) across and between menstrual cycles has been the subject of debate. The objective of this analysis was to study the inter- and intracycle variability in repeated measurements and assess the impact on an individualized gonadotropin dosing algorithm and predicted oocyte yield.DESIGN: Retrospective analysis of repeat AMH measures from a randomized controlled trial.PATIENTS: A total of 1326 women aged 18-40 years.MEASUREMENTS: Serum AMH levels at screening and at cycle day 2-3 in up to three ovarian stimulation cycles. AMH variability and its impact on gonadotropin dose and the predicted number of oocytes.RESULTS: Repeat serum AMH measurements were strongly correlated within individual women (correlation coefficient 0.92). AMH exhibited limited within-subject variation (coefficient of variation 23%), a small time-related decline (mean 6% decrease/y), but no systematic variation across the menstrual cycle. Irrespective of whether the AMH screening value or the AMH at the initiation of ovarian stimulation was used, for women with an AMH level <15 pmol/L, 93% would receive the same gonadotropin dose and attain an identical number of oocytes in 97% of cases. For women with an AMH level ≥15 pmol/L, 80% would receive an individualized dose within ±1.5 μg and 90% would attain ±1 oocyte.CONCLUSION: AMH variability had limited impact on individualized gonadotropin dosing, with 95% of women predicted to obtain an oocyte yield that does not vary beyond 1 oocyte count, irrespective of whether a random or early follicular AMH measurement was used to determine the individualized gonadotropin dose.
AB - OBJECTIVE: The stability of anti-Müllerian hormone (AMH) across and between menstrual cycles has been the subject of debate. The objective of this analysis was to study the inter- and intracycle variability in repeated measurements and assess the impact on an individualized gonadotropin dosing algorithm and predicted oocyte yield.DESIGN: Retrospective analysis of repeat AMH measures from a randomized controlled trial.PATIENTS: A total of 1326 women aged 18-40 years.MEASUREMENTS: Serum AMH levels at screening and at cycle day 2-3 in up to three ovarian stimulation cycles. AMH variability and its impact on gonadotropin dose and the predicted number of oocytes.RESULTS: Repeat serum AMH measurements were strongly correlated within individual women (correlation coefficient 0.92). AMH exhibited limited within-subject variation (coefficient of variation 23%), a small time-related decline (mean 6% decrease/y), but no systematic variation across the menstrual cycle. Irrespective of whether the AMH screening value or the AMH at the initiation of ovarian stimulation was used, for women with an AMH level <15 pmol/L, 93% would receive the same gonadotropin dose and attain an identical number of oocytes in 97% of cases. For women with an AMH level ≥15 pmol/L, 80% would receive an individualized dose within ±1.5 μg and 90% would attain ±1 oocyte.CONCLUSION: AMH variability had limited impact on individualized gonadotropin dosing, with 95% of women predicted to obtain an oocyte yield that does not vary beyond 1 oocyte count, irrespective of whether a random or early follicular AMH measurement was used to determine the individualized gonadotropin dose.
KW - Adolescent
KW - Adult
KW - Anti-Mullerian Hormone/blood
KW - Female
KW - Fertilization in Vitro
KW - Follicle Stimulating Hormone, Human/administration & dosage
KW - Humans
KW - Infertility, Female/blood
KW - Menstrual Cycle/metabolism
KW - Oocytes/drug effects
KW - Ovulation Induction
KW - Recombinant Proteins/administration & dosage
KW - Retrospective Studies
KW - Young Adult
UR - http://www.scopus.com/inward/record.url?scp=85062981241&partnerID=8YFLogxK
U2 - 10.1111/cen.13956
DO - 10.1111/cen.13956
M3 - Article
C2 - 30801744
AN - SCOPUS:85062981241
SN - 0300-0664
VL - 90
SP - 719
EP - 726
JO - Clinical Endocrinology
JF - Clinical Endocrinology
IS - 5
ER -