Evidence map›Paper›PMID 34690927›Full record

Observational studyFrontiers in endocrinology2021

Could Cytochrome P450 2D6, 3A4 and 3A5 Polymorphisms Explain the Variability in Clinical Response to Clomiphene Citrate of Anovulatory PCOS Women?

Camille Robin, Benjamin Hennart, Franck Broly, Philippine Gruchala, Geoffroy Robin, Sophie Catteau-Jonard

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 33% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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

6 authors at 2 institutions in 1 country.

Camille RobinUniversity of Lille, Centre Hospitalier Universitaire (CHU) Lille, Department of Reproductive Medicine, Lille, France.
Benjamin HennartUniversity of Lille, CHU Lille, Service de Toxicologie et Génopathies, Pôle de Biochimie et Biologie Moléculaire, Centre de Biologie Pathologie, Lille, France.
Franck BrolyUniversity of Lille, CHU Lille, Service de Toxicologie et Génopathies, Pôle de Biochimie et Biologie Moléculaire, Centre de Biologie Pathologie, Lille, France.
Philippine GruchalaUniversity of Lille, Centre Hospitalier Universitaire (CHU) Lille, Department of Reproductive Medicine, Lille, France.
Geoffroy RobinUniversity of Lille, Centre Hospitalier Universitaire (CHU) Lille, Department of Reproductive Medicine, Lille, France.
Sophie Catteau-JonardUniversity of Lille, Centre Hospitalier Universitaire (CHU) Lille, Department of Reproductive Medicine, Lille, France.
Centre Hospitalier Universitaire de Lille · FRUniversité de Lille · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Cytochrome P450 2D6, 3A4 and 3A5 are involved in the metabolism of many drugs. These enzymes have a genetic polymorphism responsible for different metabolic phenotypes. They play a role in the metabolism of clomiphene citrate (CC), which is used to induce ovulation. Response to CC treatment is variable, and no predictive factors have thus far been identified. Objective: To study a possible link between the cytochrome P450 2D6, 3A4 and 3A5 polymorphisms and clinical response to CC. Study Design: Seventy-seven women with anovulatory Polycystic Ovarian Syndrome (PCOS) treated with CC were included which determined their cytochrome P450 2D6, 3A4 and 3A5 genotypes and used the results to predict ovarian response to this drug. Predicted responses based on the cytochrome genotypes were compared with the observed clinical responses using the calculation of a weighted Kappa coefficient. Main Outcome Measures: Number of dominant follicles assessed by ultrasound at the end of the follicular phase and confirmation of ovulation by blood progesterone assay in the luteal phase. Results: Concordance between the predicted and observed responses for the combination of the three cytochromes was 36.71%, with a negative Kappa coefficient (K = -0.0240), which corresponds to a major disagreement. Similarly, for predictions based on the cytochrome P450 2D6 genotype alone, only 39.24% of predictions were verified (coefficient K = -0.0609). Conclusion: The genetic polymorphism of cytochromes P450 2D6, 3A4 and 3A5 does not appear to influence clinical response to CC used to induce ovulation in anovulatory PCOS women.

Indexed as

AnovulationPolycystic Ovary SyndromeAdultClomipheneCytochrome P-450 CYP2D6Cytochrome P-450 CYP3AFemaleFertility Agents, FemaleFranceGenetic Association StudiesHumansInfertility, FemalePharmacogenomic VariantsPolymorphism, Single NucleotidePregnancyRetrospective StudiesClomipheneCytochrome P-450 CYP2D6Cytochrome P-450 CYP3AFertility Agents, Femaleanti-Müllerian hormone (AMH)clomiphene citratecytochrome P 450 2D6ovulation inductionpolycystic ovary syndrome (PCOS)

Identifiers

PMID34690927
PMCPMC8535872
OpenAlexW3203703015

What OpenQuestion holds

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LicenceCC BY
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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.