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Peer-reviewedCC BYMedical sciences (Basel, Switzerland)

AI-Guided Histopathological and Molecular Phenotyping of Salivary Glands in Sjögren's Disease: Subtyping, Mechanistic Insights, and Translational Implications-A Systematic Review and Structured Functional Synthesis.

  1. 1Department of Periodontics, Saveetha Dental College, and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai 600077, India.
  2. 2Biomedical Stomatology Research Group, Basic Sciences Department, Faculty of Dentistry, Universidad de Antioquia U de A, Medellín 050010, Colombia.
  3. 3Faculty of Dentistry, Institución Universitaria Visión de las Américas, Medellín 050040, Colombia.

Abstract

Background/objectives

Salivary-gland biopsy is central to Sjögren's disease (SjD) assessment, but conventional measures incompletely capture glandular heterogeneity. This systematic review evaluated artificial intelligence (AI)/machine learning (ML) applications to SjD salivary-gland histopathology and molecular profiling, including biological and translational validation.Methods

PubMed, Scopus, and Embase were searched. Eligible studies used salivary-gland tissue as the primary analytical substrate or provided substantive glandular validation of systemic AI/ML findings. Evidence was synthesized functionally because of methodological heterogeneity.Results

Twenty-five studies were included. AI/ML identified histopathological and molecular phenotypes spanning immune/interferon activation, tissue architecture and immune-cell organization, epithelial stress and metabolic/cell-death remodeling, and translational response. Only a limited subset progressed beyond computational or tissue-level confirmation to functional perturbation, pharmacological testing, in vivo validation, or human treatment-response assessment. Recurrent public-dataset reuse, small cohorts, heterogeneous pipelines, and limited independent validation constrained reproducibility.Conclusions

AI/ML supports multidimensional SjD glandular phenotyping and shows emerging translational potential, but demonstrated clinical or therapeutic utility remains unestablished. Prospective multicenter validation is required before AI-derived glandular phenotypes can inform routine patient stratification or therapeutic decision-making.

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BibTeX
@article{ardila2026aiguided,
  title = {{AI-Guided Histopathological and Molecular Phenotyping of Salivary Glands in Sjögren's Disease: Subtyping, Mechanistic Insights, and Translational Implications-A Systematic Review and Structured Functional Synthesis.}},
  author = {Carlos M Ardila and Eliana Pineda-Vélez and Anny M Vivares-Builes},
  journal = {Medical sciences (Basel, Switzerland)},
  year = {2026},
  month = oct,
  doi = {10.3390/medsci14060677},
  url = {https://europepmc.org/article/MED/42930596},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - AI-Guided Histopathological and Molecular Phenotyping of Salivary Glands in Sjögren's Disease: Subtyping, Mechanistic Insights, and Translational Implications-A Systematic Review and Structured Functional Synthesis.
AU  - Carlos M Ardila
AU  - Eliana Pineda-Vélez
AU  - Anny M Vivares-Builes
PY  - 2026
DA  - 2026/10/15
JO  - Medical sciences (Basel, Switzerland)
DO  - 10.3390/medsci14060677
UR  - https://europepmc.org/article/MED/42930596
AB  - Background/objectives  Salivary-gland biopsy is central to Sjögren's disease (SjD) assessment, but conventional measures incompletely capture glandular heterogeneity. This systematic review evaluated artificial intelligence (AI)/machine learning (ML) applications to SjD salivary-gland histopathology and molecular profiling, including biological and translational validation.Methods  PubMed, Scopus, and Embase were searched. Eligible studies used salivary-gland tissue as the primary analytical substrate or provided substantive glandular validation of systemic AI/ML findings. Evidence was synthesized functionally because of methodological heterogeneity.Results  Twenty-five studies were included. AI/ML identified histopathological and molecular phenotypes spanning immune/interferon activation, tissue architecture and immune-cell organization, epithelial stress and metabolic/cell-death remodeling, and translational response. Only a limited subset progressed beyond computational or tissue-level confirmation to functional perturbation, pharmacological testing, in vivo validation, or human treatment-response assessment. Recurrent public-dataset reuse, small cohorts, heterogeneous pipelines, and limited independent validation constrained reproducibility.Conclusions  AI/ML supports multidimensional SjD glandular phenotyping and shows emerging translational potential, but demonstrated clinical or therapeutic utility remains unestablished. Prospective multicenter validation is required before AI-derived glandular phenotypes can inform routine patient stratification or therapeutic decision-making.
SN  - 2076-3271
ER  -