Evidence map›Paper›PMID 37104276›Full record

ArticlePLoS computational biology2023

Personalized prediction of the secondary oocytes number after ovarian stimulation: A machine learning model based on clinical and genetic data.

Krystian Zieliński, Sebastian Pukszta, Małgorzata Mickiewicz, Marta Kotlarz, Piotr Wygocki, Marcin Zieleń, Dominika Drzewiecka, Damian Drzyzga, Anna Kloska, Joanna Jakóbkiewicz-Banecka

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Observational
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. 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

10 authors at 3 institutions in 1 country.

Krystian ZielińskiINVICTA Research and Development Center, Sopot, Poland.
Sebastian PuksztaINVICTA Research and Development Center, Sopot, Poland.
Małgorzata MickiewiczINVICTA Research and Development Center, Sopot, Poland.
Marta KotlarzINVICTA Research and Development Center, Sopot, Poland.
Piotr WygockiInstitute of Computer Science, Faculty of Mathematics, Informatics, and Mechanics, University of Warsaw, Warsaw, Poland.
Marcin ZieleńMIM Solutions, Research and Development Center, Warsaw, Poland.
Dominika DrzewieckaINVICTA Research and Development Center, Sopot, Poland.
Damian DrzyzgaINVICTA Research and Development Center, Sopot, Poland.
Anna KloskaDepartment of Medical Biology and Genetics, Faculty of Biology, University of Gdańsk, Gdańsk, Poland.
Joanna Jakóbkiewicz-BaneckaINVICTA Research and Development Center, Sopot, Poland.ORCID 0000-0002-8846-5448
Gdańsk Medical University · PLGdańsk University of Technology · PLInstitute of Computer Science · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Controlled ovarian stimulation is tailored to the patient based on clinical parameters but estimating the number of retrieved metaphase II (MII) oocytes is a challenge. Here, we have developed a model that takes advantage of the patient's genetic and clinical characteristics simultaneously for predicting the stimulation outcome. Sequence variants in reproduction-related genes identified by next-generation sequencing were matched to groups of various MII oocyte counts using ranking, correspondence analysis, and self-organizing map methods. The gradient boosting machine technique was used to train models on a clinical dataset of 8,574 or a clinical-genetic dataset of 516 ovarian stimulations. The clinical-genetic model predicted the number of MII oocytes better than that based on clinical data. Anti-Müllerian hormone level and antral follicle count were the two most important predictors while a genetic feature consisting of sequence variants in the GDF9, LHCGR, FSHB, ESR1, and ESR2 genes was the third. The combined contribution of genetic features important for the prediction was over one-third of that revealed for anti-Müllerian hormone. Predictions of our clinical-genetic model accurately matched individuals' actual outcomes preventing over- or underestimation. The genetic data upgrades the personalized prediction of ovarian stimulation outcomes, thus improving the in vitro fertilization procedure.

Indexed as

Anti-Mullerian HormoneOvarian FollicleAnimalsFemaleFertilization in VitroOocytesOvulation InductionAnti-Mullerian Hormone

Identifiers

PMID37104276
PMCPMC10138216
OpenAlexW4367173981

What Socratic 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 Socratic graph.