Discovery of Dynamic Models for AML Disease Progression from Longitudinal Multi-Modal Clinical Data Using Explainable Machine Learning
| dc.contributor.author | Mousavi, Reza Jafarabad | |
| dc.contributor.author | Ali, Moaath K. Mustafa | |
| dc.contributor.author | Lobo, Daniel | |
| dc.date.accessioned | 2026-02-03T18:14:42Z | |
| dc.date.issued | 2025-04-15 | |
| dc.description.abstract | Acute Myeloid Leukemia (AML) is a complex and heterogeneous disease identified by severe clinical progression, fast cellular proliferation, and often high mortality rates. Incorporating diverse longitudinal information on patients’ medical histories is essential for developing effective disease predictive models applicable to both research and clinical settings. Here, we present a robust methodology for discovering dynamic predictive models to elucidate AML disease progression dynamics from a novel longitudinal multimodal clinical dataset of patients diagnosed with AML. The clinical dataset was analyzed to reveal the main clinical, genetic, and treatment features modulating disease progression. To discover mathematical models—including interactions, parameters, and nodes—predictive of AML progression, we present an explainable machine learning algorithm based on high-performance evolutionary computation. The results demonstrate that the predictive methodology could accurately estimate the clinical dynamics of AML progression in terms of blast percentages for both training and novel patients. This study demonstrates that the developed explainable machine learning approach can successfully predict AML progression by leveraging the heterogeneous and longitudinal dynamics of patients’ clinical data. More importantly, this methodology shows significant potential for application in modeling the progression dynamics of other acute diseases, providing a flexible and adaptable framework for advancing clinical and translational research. | |
| dc.description.sponsorship | We thank the members of the Lobo Lab for helpful discussions. This work was supported by the National Institute of General Medical Sciences of the National Institutes of Health under award number R35GM137953. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. Computations used the UMBC High Performance Computing Facility (HPCF) supported by the NSF MRI program grants CNS-1920079 and OAC-1726023. | |
| dc.description.uri | https://www.medrxiv.org/content/10.1101/2025.04.07.25325267v2 | |
| dc.format.extent | 37 pages | |
| dc.genre | journal articles | |
| dc.genre | preprints | |
| dc.identifier | doi:10.13016/m2aor6-vb9k | |
| dc.identifier.uri | https://doi.org/10.1101/2025.04.07.25325267 | |
| dc.identifier.uri | http://hdl.handle.net/11603/41655 | |
| dc.language.iso | en | |
| dc.relation.isAvailableAt | The University of Maryland, Baltimore County (UMBC) | |
| dc.relation.ispartof | UMBC Faculty Collection | |
| dc.relation.ispartof | UMBC Biological Sciences Department | |
| dc.rights | Attribution-NonCommercial 4.0 International | |
| dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.en | |
| dc.title | Discovery of Dynamic Models for AML Disease Progression from Longitudinal Multi-Modal Clinical Data Using Explainable Machine Learning | |
| dc.type | Text | |
| dcterms.creator | https://orcid.org/0009-0000-4225-2669 | |
| dcterms.creator | https://orcid.org/0000-0003-4666-6118 |
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