iScience (Jun 2024)

Machine-learning-based integrative –‘omics analyses reveal immunologic and metabolic dysregulation in environmental enteric dysfunction

  • Fatima Zulqarnain,
  • Xueheng Zhao,
  • Kenneth D.R. Setchell,
  • Yash Sharma,
  • Phillip Fernandes,
  • Sanjana Srivastava,
  • Aman Shrivastava,
  • Lubaina Ehsan,
  • Varun Jain,
  • Shyam Raghavan,
  • Christopher Moskaluk,
  • Yael Haberman,
  • Lee A. Denson,
  • Khyati Mehta,
  • Najeeha T. Iqbal,
  • Najeeb Rahman,
  • Kamran Sadiq,
  • Zubair Ahmad,
  • Romana Idress,
  • Junaid Iqbal,
  • Sheraz Ahmed,
  • Aneeta Hotwani,
  • Fayyaz Umrani,
  • Beatrice Amadi,
  • Paul Kelly,
  • Donald E. Brown,
  • Sean R. Moore,
  • Syed Asad Ali,
  • Sana Syed

Journal volume & issue
Vol. 27, no. 6
p. 110013

Abstract

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Summary: Environmental enteric dysfunction (EED) is a subclinical enteropathy challenging to diagnose due to an overlap of tissue features with other inflammatory enteropathies. EED subjects (n = 52) from Pakistan, controls (n = 25), and a validation EED cohort (n = 30) from Zambia were used to develop a machine-learning-based image analysis classification model. We extracted histologic feature representations from the Pakistan EED model and correlated them to transcriptomics and clinical biomarkers. In-silico metabolic network modeling was used to characterize alterations in metabolic flux between EED and controls and validated using untargeted lipidomics. Genes encoding beta-ureidopropionase, CYP4F3, and epoxide hydrolase 1 correlated to numerous tissue feature representations. Fatty acid and glycerophospholipid metabolism-related reactions showed altered flux. Increased phosphatidylcholine, lysophosphatidylcholine (LPC), and ether-linked LPCs, and decreased ester-linked LPCs were observed in the duodenal lipidome of Pakistan EED subjects, while plasma levels of glycine-conjugated bile acids were significantly increased. Together, these findings elucidate a multi-omic signature of EED.

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