Evidence map›Paper›PMID 42539975›Full record

ArticleSkin health and disease2026

ALADIN (Acne Lesion And Density INdex): a novel tool for automatic acne severity assessment.

Alfonso Medela, Alberto Sabater, Ignacio Hernández Montilla, Taig Mac Carthy, Andy Aguilar, Gerardo Fernández, Antonio Martorell, Sofia Vera Carretero, Constanza Balboni, Javier Martín Alcalde and 4 more

Abstract read
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Article in Skin health and disease, 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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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Alfonso MedelaDepartment of Medical Data Science, Legit.Health, Bilbao, Spain.
Alberto SabaterDepartment of Medical Data Science, Legit.Health, Bilbao, Spain.
Ignacio Hernández MontillaDepartment of Medical Data Science, Legit.Health, Bilbao, Spain.
Taig Mac CarthyDepartment of Clinical Endpoint Innovation, Legit.Health, Bilbao, Spain.
Andy AguilarDepartment of Clinical Endpoint Innovation, Legit.Health, Bilbao, Spain.
Gerardo FernándezDepartment of Medical Data Science, Legit.Health, Bilbao, Spain.
Antonio MartorellDepartment of Clinical Endpoint Innovation, Legit.Health, Bilbao, Spain.
Sofia Vera CarreteroDepartment of Medical Data Science, Legit.Health, Bilbao, Spain.
Constanza BalboniDepartment of Dermatology, DermoMedic Center, Hospital Universitario Fundación de Alcorcón, Madrid, Spain.
Javier Martín AlcaldeDepartment of Dermatology, DermoMedic Center, Hospital Universitario Fundación de Alcorcón, Madrid, Spain.
Jose Luis Ramírez BellverDermatology Department, Instituto Médico Ricart, Madrid, Spain.
Alejandro Martin-GorgojoSTI/Dermatology Department, Madrid City Council, Madrid, Spain.
Pedro Rodriguez JiménezDepartment of Dermatology, Hospital Universitario de la Princesa, Hospital Ruber Internacional, Madrid, Spain.
Jose Luis López EstebaranzDepartment of Dermatology, DermoMedic Center, Hospital Universitario Fundación de Alcorcón, Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Acne affects approximately 80% of adolescents worldwide, regardless of age, sex or ethnicity. Effective treatment depends on timely and accurate severity assessment. However, the lack of methodological standardization results in high inter- and intraobserver variability. A standardized and explainable grading tool is needed to support consistent acne severity evaluation. Objectives: To develop an artificial intelligence-driven tool that quantifies inflammatory lesion count and density from facial images to calculate scores aligned with the Investigator Global Assessment (IGA) scale. Methods: ALADIN (Acne Lesion And Density INdex) is designed as a simple mathematical model able to deliver reproducible and interpretable acne severity scores. We validated ALADIN retrospectively using two datasets: (i) a public dataset with predominantly severe cases of acne and (ii) a private dataset of mild-to-moderate cases. Validation results evaluated ALADIN against IGA and Global Acne Grading System (GAGS) scores, annotated by expert dermatologists. Results: Lesion detection with ALADIN was evaluated using precision, recall, mean average precision and mean absolute error (MAE). Acne grading performance was assessed via Pearson/Spearman correlations, MAE and Cohen's kappa. ALADIN's performance aligned well with the interobserver correlation of dermatologists, achieving Pearson correlations of 0.58 vs. 0.56 and 0.65 vs. 0.65 (private and public datasets, respectively) for IGA scores, and 0.32 vs. 0.44 and 0.43 vs. 0.44 for GAGS scores. Conclusions: ALADIN demonstrates consistent performance and excellent interpretability. Compared with manual scoring systems, it provides a streamlined, data-driven alternative capable of minimizing observer bias. When integrated into a medical device software, it can further aid in standardizing acne severity assessment and enhance patient monitoring. However, in this study, analyses were predominately carried out with White and Asian patients. Future work will validate and ensure robustness with darker skin tones.

Identifiers

PMID42539975
PMCPMC13425072

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