Evidence map›Paper›PMID 41843631›Full record

ArticlePloS one2026

A lightweight deep learning framework for reliable microscopy-based diagnosis of cutaneous leishmaniasis.

Nisreen Osman E Ahmed, Samuel Mwalili, Murtada K Elbashir

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Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Nisreen Osman E AhmedDepartment of Mathematics, Institute for Science, Technology and Innovation, Pan African University, Nairobi, Kenya.ORCID https://orcid.org/0009-0005-4550-5445
Samuel MwaliliDepartment of Statistics and Actuarial Sciences, Jomo Kenyatta University of Agriculture and Technology, Nairobi, Kenya.
Murtada K ElbashirCollege of Computer and Information Sciences, Jouf University, Sakaka, Saudi Arabia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cutaneous leishmaniasis (CL) is a neglected tropical and zoonotic disease affecting both human and animal health, for which microscopic examination of Giemsa-stained slides remains the diagnostic reference standard despite being time-consuming and operator-dependent. In this study, we developed a lightweight, calibration-aware deep learning framework for automated amastigote detection and slide-level diagnostic probability estimation from microscopy images. A U-Net architecture with a MobileNetV2 encoder was employed for pixel-level parasite segmentation using a weakly supervised pseudo-labeling strategy on a single-center dataset comprising 292 field-of-view images. Slide-level diagnostic probabilities were derived via probability pooling and subsequently refined using post-hoc calibration techniques, including isotonic regression, Platt scaling, and temperature scaling. Model performance was evaluated on an independent test set using segmentation metrics (Dice coefficient and Intersection-over-Union) and diagnostic reliability metrics (AUROC, Brier score, and Expected Calibration Error). The proposed framework achieved a Dice coefficient of 0.901 and an IoU of 0.820 for segmentation against pseudo-label references, with strong discriminative performance at the slide level (AUROC = 0.978). Isotonic regression markedly improved probability reliability, reducing the Brier score from 0.089 to 0.030 and the Expected Calibration Error from 0.120 to 0.023 without significantly affecting discrimination. Statistical analyses confirmed the robustness of the calibration improvements. Overall, the results demonstrate that isotonic calibration enhances the interpretability and reliability of deep-learning-based CL diagnostics. The proposed lightweight framework provides a robust foundation for microscopy-based screening and supports future validation across broader datasets and One Health-oriented diagnostic applications.

Indexed as

Deep LearningLeishmaniasis, CutaneousMicroscopyAnimalsCalibrationHumansImage Processing, Computer-AssistedReproducibility of Results

Identifiers

PMID41843631
PMCPMC12994852

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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.