Evidence map›Paper›PMID 38928171›Full record

ArticleInternational journal of molecular sciences2024

Imaging Flow Cytometry and Convolutional Neural Network-Based Classification Enable Discrimination of Hematopoietic and Leukemic Stem Cells in Acute Myeloid Leukemia.

Trine Engelbrecht Hybel, Sofie Hesselberg Jensen, Matthew A Rodrigues, Thomas Engelbrecht Hybel, Maya Nautrup Pedersen, Signe Håkansson Qvick, Marie Hairing Enemark, Marie Bill, Carina Agerbo Rosenberg, Maja Ludvigsen

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 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

10 authors.

Trine Engelbrecht HybelDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0003-0166-8558
Sofie Hesselberg JensenDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Matthew A RodriguesAmnis Flow Cytometry, Cytek Biosciences, Seattle, WA 98119, USA.ORCID 0000-0003-0989-8403
Thomas Engelbrecht HybelDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Maya Nautrup PedersenDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Signe Håkansson QvickDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Marie Hairing EnemarkDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Marie BillDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.
Carina Agerbo RosenbergDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0002-9609-8991
Maja LudvigsenDepartment of Hematology, Aarhus University Hospital, 8200 Aarhus N, Denmark.ORCID 0000-0001-5089-3271

Funding

Aase og Ejnar Danielsens Fond NADagmar Marshalls Fond NADanish Cancer Society NADepartment of Clinical Medicine, Aarhus University NAEva and Henry Frænkel's Memorial Foundation NAFamilien Hede Nielsens Fond NAMax Wørzner and wife Inger Wørzner's Foundation NAPoul and Ellen Hertz's Foundation NAThe Toyota Foundation NA
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a heterogenous blood cancer with a dismal prognosis. It emanates from leukemic stem cells (LSCs) arising from the genetic transformation of hematopoietic stem cells (HSCs). LSCs hold prognostic value, but their molecular and immunophenotypic heterogeneity poses challenges: there is no single marker for identifying all LSCs across AML samples. We hypothesized that imaging flow cytometry (IFC) paired with artificial intelligence-driven image analysis could visually distinguish LSCs from HSCs based solely on morphology. Initially, a seven-color IFC panel was employed to immunophenotypically identify LSCs and HSCs in bone marrow samples from five AML patients and ten healthy donors, respectively. Next, we developed convolutional neural network (CNN) models for HSC-LSC discrimination using brightfield (BF), side scatter (SSC), and DNA images. Classification using only BF images achieved 86.96% accuracy, indicating significant morphological differences. Accuracy increased to 93.42% when combining BF with DNA images, highlighting differences in nuclear morphology, although DNA images alone were inadequate for accurate HSC-LSC discrimination. Model development using SSC images revealed minor granularity differences. Performance metrics varied substantially between AML patients, indicating considerable morphologic variations among LSCs. Overall, we demonstrate proof-of-concept results for accurate CNN-based HSC-LSC differentiation, instigating the development of a novel technique within AML monitoring.

Indexed as

Flow CytometryHematopoietic Stem CellsLeukemia, Myeloid, AcuteNeoplastic Stem CellsNeural Networks, ComputerFemaleHumansImage Processing, Computer-AssistedImmunophenotypingMaleMiddle Agedacute myeloid leukemiaartificial intelligenceconvolutional neural networkdeep learninghematopoietic stem cellsimaging flow cytometryleukemic stem cells

Identifiers

PMID38928171
PMCPMC11203419

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Registered trials

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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.