Machine learning assisted real-time deformability cytometry of CD34+ cells allows to identify patients with myelodysplastic syndromes.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
18 01 2022
18 01 2022
Historique:
received:
08
09
2021
accepted:
03
01
2022
entrez:
19
1
2022
pubmed:
20
1
2022
medline:
25
2
2022
Statut:
epublish
Résumé
Diagnosis of myelodysplastic syndrome (MDS) mainly relies on a manual assessment of the peripheral blood and bone marrow cell morphology. The WHO guidelines suggest a visual screening of 200 to 500 cells which inevitably turns the assessor blind to rare cell populations and leads to low reproducibility. Moreover, the human eye is not suited to detect shifts of cellular properties of entire populations. Hence, quantitative image analysis could improve the accuracy and reproducibility of MDS diagnosis. We used real-time deformability cytometry (RT-DC) to measure bone marrow biopsy samples of MDS patients and age-matched healthy individuals. RT-DC is a high-throughput (1000 cells/s) imaging flow cytometer capable of recording morphological and mechanical properties of single cells. Properties of single cells were quantified using automated image analysis, and machine learning was employed to discover morpho-mechanical patterns in thousands of individual cells that allow to distinguish healthy vs. MDS samples. We found that distribution properties of cell sizes differ between healthy and MDS, with MDS showing a narrower distribution of cell sizes. Furthermore, we found a strong correlation between the mechanical properties of cells and the number of disease-determining mutations, inaccessible with current diagnostic approaches. Hence, machine-learning assisted RT-DC could be a promising tool to automate sample analysis to assist experts during diagnosis or provide a scalable solution for MDS diagnosis to regions lacking sufficient medical experts.
Identifiants
pubmed: 35042906
doi: 10.1038/s41598-022-04939-z
pii: 10.1038/s41598-022-04939-z
pmc: PMC8766444
doi:
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
870Subventions
Organisme : Deutsche Forschungsgemeinschaft
ID : 399422891
Organisme : Deutsche Forschungsgemeinschaft
ID : SF1243
Organisme : DKMS Mechthild Harf Research Grant
ID : DKMS-SLS-MHG-2016-02
Organisme : Bundesministerium für Bildung und Forschung
ID : 03Z22CN11
Organisme : German Jose Carreras Leukämiestiftung
ID : DJCLS R14/18
Organisme : Collaborative Research Center 655
ID : SFB 655
Informations de copyright
© 2022. The Author(s).
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