Evidence map›Paper›PMID 30610662›Full record

ArticleJournal of assisted reproduction and genetics2019

Successful in vitro maturation of oocytes in a woman with gonadotropin-resistant ovary syndrome associated with a novel combination of FSH receptor gene variants: a case report.

C Flageole, C Toufaily, D J Bernard, S Ates, V Blais, S Chénier, M Benkhalifa, P Miron

Open access · bronzeAbstract readCase Reports
In one paragraph

Article in Journal of assisted reproduction and genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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  11. Utilization of in vitro maturation in cases with a FSH receptor mutation.Journal of assisted reproduction and genetics · 2021
    Article
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  14. Exploring the Potential ofAvicenna journal of medical biotechnology
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

C FlageoleCentre d'aide médicale à la procréation FERTILYS, Laval, Québec, Canada.
C ToufailyDepartment of Pharmacology and Therapeutics, McGill University, Montréal, Québec, Canada.
D J BernardDepartment of Pharmacology and Therapeutics, McGill University, Montréal, Québec, Canada.
S AtesCentre d'aide médicale à la procréation FERTILYS, Laval, Québec, Canada.
V BlaisCentre d'aide médicale à la procréation FERTILYS, Laval, Québec, Canada.
S ChénierDepartment of Pediatrics, Division of Medical Genetics, Centre hospitalier universitaire de Sherbrooke, Université de Sherbrooke, Sherbrooke, Québec, Canada.
M BenkhalifaCentre d'aide médicale à la procréation FERTILYS, Laval, Québec, Canada.
P MironCentre d'aide médicale à la procréation FERTILYS, Laval, Québec, Canada. pierre.miron@fertilys.org.
McGill University · CACentre Hospitalier Universitaire de Sherbrooke · CAInstitut National de la Recherche Scientifique · CAUniversité de Picardie Jules Verne · FR

Funding

Canadian Institutes of Health Research MOP-133557 and -123447Natural Sciences and Engineering Research Council of Canada 2015-05178
6 · The paper itself

Abstract

Infertility due to Gonadotropin-Resistant Ovary Syndrome (GROS) is a rare type of hypergonadotropic hypogonadism. Here, we report an original case of GROS, associated with compound heterozygous follicle-stimulating hormone receptor (FSHR) variants, in a woman who achieved a live birth by in vitro maturation (IVM) of her oocytes. This 31-year-old woman consulted our assisted reproduction center for a second opinion after having been advised, because of pervasive high serum follicle-stimulating hormone (FSH) levels, to pursue in vitro fertilization (IVF) with donor oocytes. She presented with primary infertility and progressively prolonged menstrual cycles. Her serum FSH levels were indeed found to be high, but in discordance with a normal anti-Müllerian hormone (AMH) level and antral follicle count. Genetic investigation found the patient to be compound heterozygous for two FSHR variants: I160T, a known pathologic variant, and N558H, which has never been previously reported. As there was no ovarian response to high daily doses of exogenous gonadotropins, IVM was proposed to the patient with success and she finally delivered at term a healthy boy. Effects of the receptor variants were analyzed in heterologous cells. Whereas the I160T mutation blocked FSHR membrane trafficking and FSH-stimulated cAMP-dependent signaling in transfected CHO cells, the novel variant, N558H, functioned equivalently to wild-type FSHR in the assays employed. In conclusion, IVM should always be offered as a first-line therapy to infertile women presenting with GROS. The N558H variant discovered in FSHR is novel, but its functional significance, if any, is unresolved and merits further investigation as it may be associated with a recessive FSHR-related disorder.

Indexed as

In Vitro Oocyte Maturation TechniquesAdultAnimalsAnti-Mullerian HormoneCHO CellsCricetulusFemaleFollicle Stimulating HormoneHumansLive BirthOocytesPrimary Ovarian InsufficiencyReceptors, FSHSignal TransductionAnti-Mullerian HormoneFollicle Stimulating HormoneReceptors, FSHFollicle-stimulating hormone (FSH)FSH receptorGonadotropinsIn vitro maturation (IVM)Ovarian resistance

Identifiers

PMID30610662
PMCPMC6439039
OpenAlexW2907168776

What OpenQuestion holds

Textmetadata
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.