Publication: Unsupervised machine learning identifies biomarkers of disease progression in post-kala-azar dermal leishmaniasis in Sudan
| dc.contributor.author | Torres Garcia, Ana Maria | |
| dc.contributor.author | Younis, Brima Musa | |
| dc.contributor.author | Tesema, Samuel | |
| dc.contributor.author | Solana, Jose Carlos | |
| dc.contributor.author | Moreno, Javier | |
| dc.contributor.author | Martin-Galiano, Antonio Javier | |
| dc.contributor.author | Musa, Ahmed Mudawi | |
| dc.contributor.author | Alves, Fabiana | |
| dc.contributor.author | Carrillo, Eugenia | |
| dc.contributor.funder | Instituto de Salud Carlos III | |
| dc.contributor.funder | Centro de Investigación Biomédica en Red - CIBERINFEC (Enfermedades Infecciosas) | |
| dc.date.accessioned | 2025-05-13T09:50:59Z | |
| dc.date.available | 2025-05-13T09:50:59Z | |
| dc.date.issued | 2025-03 | |
| dc.description.abstract | Background: Post-kala-azar dermal leishmaniasis (PKDL) appears as a rash in some individuals who have recovered from visceral leishmaniasis caused by Leishmania donovani. Today, basic knowledge of this neglected disease and how to predict its progression remain largely unknown. Methods and findings: This study addresses the use of several biochemical, haematological and immunological variables, independently or through unsupervised machine learning (ML), to predict PKDL progression risk. In 110 patients from Sudan, 31 such factors were assessed in relation to PKDL disease state at the time of diagnosis: progressive (worsening) versus stable. To identify key factors associated with PKDL worsening, we used both a conventional statistical approach and multivariate analysis through unsupervised ML. The independent use of these variables had limited power to predict skin lesion severity in a baseline examination. In contrast, the unsupervised ML approach identified a set of 10 non-redundant variables that was linked to a 3.1 times higher risk of developing progressive PKDL. Three of these clustering factors (low albumin level, low haematocrit and low IFN-γ production in PBMCs after Leishmania antigen stimulation) were remarkable in patients with progressive disease. Dimensionality re-establishment identified 11 further significantly modified factors that are also important to understand the worsening phenotype. Our results indicate that the combination of anaemia and a weak Th1 immunological response is likely the main physiological mechanism that leads to progressive PKDL. Conclusions: A combination of 14 biochemical variables identified by unsupervised ML was able to detect a worsening PKDL state in Sudanese patients. This approach could prove instrumental to train future supervised algorithms based on larger patient cohorts both for a more precise diagnosis and to gain insight into fundamental aspects of this complication of visceral leishmaniasis. | |
| dc.description.peerreviewed | Sí | |
| dc.description.sponsorship | This work was funded by DNDi via agreement MVP322/19 with ISCIII (to E.C.) and by the Instituto de Salud Carlos III through the ISCIII-AES project (PI22/00009 to E.C.). J.C. was supported by a contract awarded by CIBERINFEC (CB21/13/00018). The funders had no role in the study design, data collection and analysis, decision to publish, or prepara tion of the manuscript. | |
| dc.format.number | 3 | |
| dc.format.page | e0012924 | |
| dc.format.volume | 19 | |
| dc.identifier.citation | Torres A, Younis BM, Tesema S, Solana JC, Moreno J, Martín-Galiano AJ, Musa AM, Alves F, Carrillo E. Unsupervised machine learning identifies biomarkers of disease progression in post-kala-azar dermal leishmaniasis in Sudan. PLoS Negl Trop Dis. 2025 Mar 11;19(3):e0012924. | |
| dc.identifier.doi | 10.1371/journal.pntd.0012924 | |
| dc.identifier.e-issn | 1935-2735 | |
| dc.identifier.issn | 1935-2727 | |
| dc.identifier.journal | PLoS neglected tropical diseases | |
| dc.identifier.pubmedID | 40067811 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12105/26655 | |
| dc.language.iso | eng | |
| dc.publisher | Public Library of Science (PLOS) | |
| dc.relation.projectID | info:eu-repo/grantAgreement/ESMVP322/19 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/ESPI22/00009 | |
| dc.relation.projectID | info:eu-repo/grantAgreement/ESCB21/13/00018 | |
| dc.relation.publisherversion | https://doi.org/10.1371/journal.pntd.0012924 | |
| dc.repisalud.centro | ISCIII::Centro Nacional de Microbiología (CNM) | |
| dc.repisalud.centro | ISCIII::Unidades Centrales Científico-Técnicas (UCCTs) | |
| dc.repisalud.institucion | ISCIII | |
| dc.rights.accessRights | open access | |
| dc.rights.license | Attribution 4.0 International | |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
| dc.subject.mesh | Adolescent | |
| dc.subject.mesh | Adult | |
| dc.subject.mesh | Biomarkers | |
| dc.subject.mesh | Child | |
| dc.subject.mesh | Disease Progression | |
| dc.subject.mesh | Female | |
| dc.subject.mesh | Humans | |
| dc.subject.mesh | Leishmania donovani | |
| dc.subject.mesh | Leishmaniasis, Cutaneous | |
| dc.subject.mesh | Leishmaniasis, Visceral | |
| dc.subject.mesh | Machine Learning | |
| dc.subject.mesh | Male | |
| dc.subject.mesh | Middle Aged | |
| dc.subject.mesh | Sudan | |
| dc.subject.mesh | Young Adult | |
| dc.title | Unsupervised machine learning identifies biomarkers of disease progression in post-kala-azar dermal leishmaniasis in Sudan | |
| dc.type | research article | |
| dc.type.hasVersion | VoR | |
| dspace.entity.type | Publication | |
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