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The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status

This study aimed to investigate whether female BRCA1- and BRCA2 mutation carriers have a reduced ovarian reserve status, based on serum anti-Mullerian hormone (AMH) levels, antral follicle count (AFC) and ovarian response to ovarian hyperstimulation. A prospective, multinational cohort study was per...

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Autores principales: C.E, Drechsel Katja, C., van Tilborg Theodora, J.C., Eijkemans Marinus, G.W.M., Lentjes Eef, Irene, Homminga, Mariette, Goddijn, J.T., van Golde Ron, Willem, Verpoest, D., Lichtenbelt Klaske, J.M., Broekmans Frank, M.E., Bos Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810575/
https://www.ncbi.nlm.nih.gov/pubmed/35705781
http://dx.doi.org/10.1007/s43032-022-00997-w
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author C.E, Drechsel Katja
C., van Tilborg Theodora
J.C., Eijkemans Marinus
G.W.M., Lentjes Eef
Irene, Homminga
Mariette, Goddijn
J.T., van Golde Ron
Willem, Verpoest
D., Lichtenbelt Klaske
J.M., Broekmans Frank
M.E., Bos Anna
author_facet C.E, Drechsel Katja
C., van Tilborg Theodora
J.C., Eijkemans Marinus
G.W.M., Lentjes Eef
Irene, Homminga
Mariette, Goddijn
J.T., van Golde Ron
Willem, Verpoest
D., Lichtenbelt Klaske
J.M., Broekmans Frank
M.E., Bos Anna
author_sort C.E, Drechsel Katja
collection PubMed
description This study aimed to investigate whether female BRCA1- and BRCA2 mutation carriers have a reduced ovarian reserve status, based on serum anti-Mullerian hormone (AMH) levels, antral follicle count (AFC) and ovarian response to ovarian hyperstimulation. A prospective, multinational cohort study was performed between October 2014 and December 2019. Normo-ovulatory women, aged 18–41 years old, applying for their first PGT-cycle for reason of a BRCA mutation (cases) or other genetic diseases unrelated to ovarian reserve (controls), were asked to participate. All participants underwent a ICSI-PGT cycle with a long-agonist protocol for controlled ovarian hyperstimulation. Linear and logistic regression models were used to compare AMH, AFC and ovarian response in cases and controls. Sensitivity analyses were conducted on BRCA1- and BRCA2 mutation carrier subgroups. Thirty-six BRCA mutation carriers (18 BRCA1- and 18 BRCA2 mutation carriers) and 126 controls, with mean female age 30.4 years, were included in the primary analysis. Unadjusted median AMH serum levels (IQR) were 2.40 (1.80–3.00) ng/ml in BRCA mutation carriers and 2.15 (1.30–3.40) ng/ml in controls (p = 0.45), median AFC (IQR) was 15.0 (10.8–20.3) and 14.5 (9.0–20.0), p = 0.54, respectively. Low response rate was 22.6% among BRCA mutation carriers and 9.3% among controls, p = 0.06. Median number of retrieved oocytes was 9 (6–14) in carriers and 10 (7–13) in controls, p = 0.36. No substantial differences were observed between BRCA1- and BRCA2 mutation carriers. Based on several biomarkers, no meaningful differences in ovarian reserve status were observed in female BRCA mutation carriers compared to controls in the context of ICSI-PGT treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43032-022-00997-w.
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spelling pubmed-98105752023-01-05 The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status C.E, Drechsel Katja C., van Tilborg Theodora J.C., Eijkemans Marinus G.W.M., Lentjes Eef Irene, Homminga Mariette, Goddijn J.T., van Golde Ron Willem, Verpoest D., Lichtenbelt Klaske J.M., Broekmans Frank M.E., Bos Anna Reprod Sci Reproductive Genetics: Original Article This study aimed to investigate whether female BRCA1- and BRCA2 mutation carriers have a reduced ovarian reserve status, based on serum anti-Mullerian hormone (AMH) levels, antral follicle count (AFC) and ovarian response to ovarian hyperstimulation. A prospective, multinational cohort study was performed between October 2014 and December 2019. Normo-ovulatory women, aged 18–41 years old, applying for their first PGT-cycle for reason of a BRCA mutation (cases) or other genetic diseases unrelated to ovarian reserve (controls), were asked to participate. All participants underwent a ICSI-PGT cycle with a long-agonist protocol for controlled ovarian hyperstimulation. Linear and logistic regression models were used to compare AMH, AFC and ovarian response in cases and controls. Sensitivity analyses were conducted on BRCA1- and BRCA2 mutation carrier subgroups. Thirty-six BRCA mutation carriers (18 BRCA1- and 18 BRCA2 mutation carriers) and 126 controls, with mean female age 30.4 years, were included in the primary analysis. Unadjusted median AMH serum levels (IQR) were 2.40 (1.80–3.00) ng/ml in BRCA mutation carriers and 2.15 (1.30–3.40) ng/ml in controls (p = 0.45), median AFC (IQR) was 15.0 (10.8–20.3) and 14.5 (9.0–20.0), p = 0.54, respectively. Low response rate was 22.6% among BRCA mutation carriers and 9.3% among controls, p = 0.06. Median number of retrieved oocytes was 9 (6–14) in carriers and 10 (7–13) in controls, p = 0.36. No substantial differences were observed between BRCA1- and BRCA2 mutation carriers. Based on several biomarkers, no meaningful differences in ovarian reserve status were observed in female BRCA mutation carriers compared to controls in the context of ICSI-PGT treatment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43032-022-00997-w. Springer International Publishing 2022-06-15 /pmc/articles/PMC9810575/ /pubmed/35705781 http://dx.doi.org/10.1007/s43032-022-00997-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Reproductive Genetics: Original Article
C.E, Drechsel Katja
C., van Tilborg Theodora
J.C., Eijkemans Marinus
G.W.M., Lentjes Eef
Irene, Homminga
Mariette, Goddijn
J.T., van Golde Ron
Willem, Verpoest
D., Lichtenbelt Klaske
J.M., Broekmans Frank
M.E., Bos Anna
The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status
title The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status
title_full The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status
title_fullStr The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status
title_full_unstemmed The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status
title_short The Impact of BRCA1- and BRCA2 Mutations on Ovarian Reserve Status
title_sort impact of brca1- and brca2 mutations on ovarian reserve status
topic Reproductive Genetics: Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9810575/
https://www.ncbi.nlm.nih.gov/pubmed/35705781
http://dx.doi.org/10.1007/s43032-022-00997-w
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