Evidence map›Paper›PMID 35884850›Full record

ArticleBiomedicines2022

Unique Deep Radiomic Signature Shows NMN Treatment Reverses Morphology of Oocytes from Aged Mice.

Abbas Habibalahi, Jared M Campbell, Michael J Bertoldo, Saabah B Mahbub, Dale M Goss, William L Ledger, Robert B Gilchrist, Lindsay E Wu, Ewa M Goldys

Abstract read
In one paragraph

Article in Biomedicines, 2022. 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.

  1. Article
  2. Review
  3. Ovarian aging: energy metabolism of oocytes.Journal of ovarian research · 2024
    Review
  4. Article
  5. 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

9 authors.

Abbas HabibalahiARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales Sydney, Sydney, NSW 2052, Australia.ORCID 0000-0001-7833-1705
Jared M CampbellARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales Sydney, Sydney, NSW 2052, Australia.
Michael J BertoldoFertility & Research Centre, School of Clinical Medicine, University of New South Wales Sydney, Sydney, NSW 2052, Australia.
Saabah B MahbubARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales Sydney, Sydney, NSW 2052, Australia.ORCID 0000-0002-3320-2499
Dale M GossSchool of Medical Sciences, University of New South Wales Sydney, Sydney, NSW 2052, Australia.
William L LedgerFertility & Research Centre, School of Clinical Medicine, University of New South Wales Sydney, Sydney, NSW 2052, Australia.
Robert B GilchristFertility & Research Centre, School of Clinical Medicine, University of New South Wales Sydney, Sydney, NSW 2052, Australia.
Lindsay E WuSchool of Medical Sciences, University of New South Wales Sydney, Sydney, NSW 2052, Australia.
Ewa M GoldysARC Centre of Excellence Centre for Nanoscale Biophotonics, University of New South Wales Sydney, Sydney, NSW 2052, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The purpose of this study is to develop a deep radiomic signature based on an artificial intelligence (AI) model. This radiomic signature identifies oocyte morphological changes corresponding to reproductive aging in bright field images captured by optical light microscopy. Oocytes were collected from three mice groups: young (4- to 5-week-old) C57BL/6J female mice, aged (12-month-old) mice, and aged mice treated with the NAD+ precursor nicotinamide mononucleotide (NMN), a treatment recently shown to rejuvenate aspects of fertility in aged mice. We applied deep learning, swarm intelligence, and discriminative analysis to images of mouse oocytes taken by bright field microscopy to identify a highly informative deep radiomic signature (DRS) of oocyte morphology. Predictive DRS accuracy was determined by evaluating sensitivity, specificity, and cross-validation, and was visualized using scatter plots of the data associated with three groups: Young, old and Old + NMN. DRS could successfully distinguish morphological changes in oocytes associated with maternal age with 92% accuracy (AUC~1), reflecting this decline in oocyte quality. We then employed the DRS to evaluate the impact of the treatment of reproductively aged mice with NMN. The DRS signature classified 60% of oocytes from NMN-treated aged mice as having a 'young' morphology. In conclusion, the DRS signature developed in this study was successfully able to detect aging-related oocyte morphological changes. The significance of our approach is that DRS applied to bright field oocyte images will allow us to distinguish and select oocytes originally affected by reproductive aging and whose quality has been successfully restored by the NMN therapy.

Indexed as

agingmachine learningmorphologyNMNoocyte

Identifiers

PMID35884850
PMCPMC9313081

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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.