Cargando…
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...
Autores principales: | , , , , , , , , , , |
---|---|
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 |
_version_ | 1784863336724168704 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9810575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT cedrechselkatja theimpactofbrca1andbrca2mutationsonovarianreservestatus AT cvantilborgtheodora theimpactofbrca1andbrca2mutationsonovarianreservestatus AT jceijkemansmarinus theimpactofbrca1andbrca2mutationsonovarianreservestatus AT gwmlentjeseef theimpactofbrca1andbrca2mutationsonovarianreservestatus AT irenehomminga theimpactofbrca1andbrca2mutationsonovarianreservestatus AT mariettegoddijn theimpactofbrca1andbrca2mutationsonovarianreservestatus AT jtvangolderon theimpactofbrca1andbrca2mutationsonovarianreservestatus AT willemverpoest theimpactofbrca1andbrca2mutationsonovarianreservestatus AT dlichtenbeltklaske theimpactofbrca1andbrca2mutationsonovarianreservestatus AT jmbroekmansfrank theimpactofbrca1andbrca2mutationsonovarianreservestatus AT mebosanna theimpactofbrca1andbrca2mutationsonovarianreservestatus AT cedrechselkatja impactofbrca1andbrca2mutationsonovarianreservestatus AT cvantilborgtheodora impactofbrca1andbrca2mutationsonovarianreservestatus AT jceijkemansmarinus impactofbrca1andbrca2mutationsonovarianreservestatus AT gwmlentjeseef impactofbrca1andbrca2mutationsonovarianreservestatus AT irenehomminga impactofbrca1andbrca2mutationsonovarianreservestatus AT mariettegoddijn impactofbrca1andbrca2mutationsonovarianreservestatus AT jtvangolderon impactofbrca1andbrca2mutationsonovarianreservestatus AT willemverpoest impactofbrca1andbrca2mutationsonovarianreservestatus AT dlichtenbeltklaske impactofbrca1andbrca2mutationsonovarianreservestatus AT jmbroekmansfrank impactofbrca1andbrca2mutationsonovarianreservestatus AT mebosanna impactofbrca1andbrca2mutationsonovarianreservestatus |