Evidence map›Paper›PMID 39126000›Full record

ArticleInternational journal of molecular sciences2024

Follicular Fluid Proteomic Analysis to Identify Predictive Markers of Normal Embryonic Development.

Janusz Przewocki, Dominik Kossiński, Adam Łukaszuk, Grzegorz Jakiel, Izabela Wocławek-Potocka, Stanisław Ołdziej, Krzysztof Łukaszuk

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

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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

7 authors.

Janusz PrzewockiInstitute of Mathematics, University of Gdansk, 80-308 Gdańsk, Poland.ORCID 0000-0003-4265-7353
Dominik KossińskiiYoni App-For Fertility Treatment, LifeBite, 10-763 Olsztyn, Poland.ORCID 0000-0003-2321-3677
Adam ŁukaszukEdinburgh Medical School, College of Medicine and Veterinary Medicine, The University of Edinburgh, 47 Little France Crescent, Edinburgh EH25 9RG, UK.ORCID 0009-0001-5522-3282
Grzegorz JakielInvicta Research and Development Center, 81-740 Sopot, Poland.ORCID 0000-0002-6094-2273
Izabela Wocławek-PotockaDepartment of Gamete and Embryo Biology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, 10-748 Olsztyn, Poland.ORCID 0000-0002-1270-3438
Stanisław OłdziejIntercollegiate Faculty of Biotechnology UG & MUG, University of Gdańsk, Abrahama 58, 80-307 Gdańsk, Poland.ORCID 0000-0002-4583-3941
Krzysztof ŁukaszukiYoni App-For Fertility Treatment, LifeBite, 10-763 Olsztyn, Poland.ORCID 0000-0001-5996-6991

Funding

Narodowe Centrum Nauki 2017/27/B/NZ5/02393
6 · The paper itself

Abstract

Ageing populations, mass "baby-free" policies and children born to mothers at the age at which they are biologically expected to become grandmothers are growing problems in most developed societies. Therefore, any opportunity to improve the quality of infertility treatments seems important for the survival of societies. The possibility of indirectly studying the quality of developing oocytes by examining their follicular fluids (hFFs) offers new opportunities for progress in our understanding the processes of final oocyte maturation and, consequently, for predicting the quality of the resulting embryos and personalising their culture. Using mass spectrometry, we studied follicular fluids collected individually during in vitro fertilisation and compared their composition with the quality of the resulting embryos. We analysed 110 follicular fluids from 50 oocyte donors, from which we obtained 44 high-quality, 39 medium-quality, and 27 low-quality embryos. We identified 2182 proteins by Sequential Window Acquisition of all Theoretical Mass Spectra (SWATH-MS) using a TripleTOF 5600+ hybrid mass spectrometer, of which 484 were suitable for quantification. We were able to identify several proteins whose concentrations varied between the follicular fluids of different oocytes from the same patient and between patients. Among them, the most important appear to be immunoglobulin heavy constant alpha 1 (IgA1hc) and dickkopf-related protein 3. The first one is found at higher concentrations in hFFs from which oocytes develop into poor-quality embryos, the other one exhibits the opposite pattern. None of these have, so far, had any specific links to fertility disorders. In light of these findings, these proteins should be considered a primary target for research aimed at developing a diagnostic tool for oocyte quality control and pre-fertilisation screening. This is particularly important in cases where the fertilisation of each egg is not an option for ethical or other reasons, or in countries where it is prohibited by law.

Indexed as

BiomarkersEmbryonic DevelopmentFollicular FluidOocytesProteomicsAdultFemaleFertilization in VitroHumansMass SpectrometryProteomeBiomarkersProteomedickkopf-related protein 3embryo qualityfollicular fluidheat shock cognate 71 kDa proteinimmunoglobulin heavy constant alpha 1keratin type II cytoskeletal 1 proteinmass spectrometryoocyte qualityproteomics

Identifiers

PMID39126000
PMCPMC11313438

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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.