Evidence map›Paper›PMID 35705781›Full record

ArticleReproductive sciences (Thousand Oaks, Calif.)2023

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

Drechsel Katja C E, van Tilborg Theodora C, Eijkemans Marinus J C, Lentjes Eef G W M, Homminga Irene, Goddijn Mariette, van Golde Ron J T, Verpoest Willem, Lichtenbelt Klaske D, Broekmans Frank J M and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Reproductive sciences (Thousand Oaks, Calif.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  7. Article
  8. BRCA Mutations and Fertility Preservation.International journal of molecular sciences · 2023
    Review
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 6 institutions in 2 countries.

Drechsel Katja C EDepartment of Reproductive Medicine, University Medical Centre Utrecht, Utrecht University, Heidelberglaan 100, PO Box 85500, 3508 GA, Utrecht, The Netherlands. K.C.E.Drechsel-2@umcutrecht.nl.
van Tilborg Theodora CDepartment of Reproductive Medicine, University Medical Centre Utrecht, Utrecht University, Heidelberglaan 100, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Eijkemans Marinus J CJulius Centre for Health Sciences and Primary Care, University Medical Centre Utrecht, Utrecht University, Heidelberglaan 100, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Lentjes Eef G W MCentral Diagnostic Laboratory (CDL), University Medical Centre Utrecht, Utrecht University, Heidelberglaan 100, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Homminga IreneDepartment of Obstetrics and Gynaecology, Section Reproductive Medicine, University of Groningen, University Medical Centre Groningen, Hanzeplein 1, 9700 RB, Groningen, The Netherlands.
Goddijn MarietteDepartment of Obstetrics and Gynaecology, Centre for Reproductive Medicine Amsterdam UMC, University of Amsterdam, Meibergdreef 9, AZ, 1105, Amsterdam, The Netherlands.
van Golde Ron J TDepartment of Obstetrics and Gynaecology, Maastricht University Medical Centre, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands.
Verpoest WillemCentre for Reproductive Medicine, Universitair Ziekenhuis Brussel, Laarbeeklaan 101, 1090, Brussels, Belgium.
Lichtenbelt Klaske DDepartment of Genetics, University Medical Centre Utrecht, Heidelberglaan 100, 3508 GA, Utrecht, The Netherlands.
Broekmans Frank J MDepartment of Reproductive Medicine, University Medical Centre Utrecht, Utrecht University, Heidelberglaan 100, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
Bos Anna M EDepartment of Reproductive Medicine, University Medical Centre Utrecht, Utrecht University, Heidelberglaan 100, PO Box 85500, 3508 GA, Utrecht, The Netherlands.
University Medical Center Utrecht · NLUtrecht University · NLAmsterdam University Medical Centers · NLMaastricht University Medical Centre · NLUniversitair Ziekenhuis Brussel · BEUniversity Medical Center Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

Ovarian ReserveAnimalsAnti-Mullerian HormoneBRCA2 ProteinCohort StudiesFemaleMutationProspective StudiesAnti-Mullerian HormoneBRCA2 ProteinAnti-Müllerian hormoneBRCA1BRCA2BRCA gene mutationsOvarian reserveOvarian response

Identifiers

PMID35705781
PMCPMC9810575
OpenAlexW4282935493

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.