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
Affiliations
- Fatima Zulqarnain
- University of Virginia, Charlottesville, VA, USA
- Xueheng Zhao
- Cincinnati Children’s Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, USA
- Kenneth D.R. Setchell
- Cincinnati Children’s Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, USA
- Yash Sharma
- University of Virginia, Charlottesville, VA, USA
- Phillip Fernandes
- University of Virginia, Charlottesville, VA, USA
- Sanjana Srivastava
- University of Virginia, Charlottesville, VA, USA
- Aman Shrivastava
- University of Virginia, Charlottesville, VA, USA
- Lubaina Ehsan
- University of Virginia, Charlottesville, VA, USA
- Varun Jain
- University of Virginia, Charlottesville, VA, USA
- Shyam Raghavan
- University of Virginia, Charlottesville, VA, USA
- Christopher Moskaluk
- University of Virginia, Charlottesville, VA, USA
- Yael Haberman
- Cincinnati Children’s Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, USA
- Lee A. Denson
- Cincinnati Children’s Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, USA
- Khyati Mehta
- Cincinnati Children’s Hospital Medical Center, University of Cincinnati School of Medicine, Cincinnati, OH, USA
- Najeeha T. Iqbal
- Aga Khan University, Karachi, Pakistan
- Najeeb Rahman
- Aga Khan University, Karachi, Pakistan
- Kamran Sadiq
- Aga Khan University, Karachi, Pakistan
- Zubair Ahmad
- Aga Khan University, Karachi, Pakistan
- Romana Idress
- Aga Khan University, Karachi, Pakistan
- Junaid Iqbal
- Aga Khan University, Karachi, Pakistan
- Sheraz Ahmed
- Aga Khan University, Karachi, Pakistan
- Aneeta Hotwani
- Aga Khan University, Karachi, Pakistan
- Fayyaz Umrani
- Aga Khan University, Karachi, Pakistan
- Beatrice Amadi
- University Teaching Hospital, Lusaka, Zambia
- Paul Kelly
- University Teaching Hospital, Lusaka, Zambia; Queen Mary University of London, London, UK
- Donald E. Brown
- University of Virginia, Charlottesville, VA, USA
- Sean R. Moore
- University of Virginia, Charlottesville, VA, USA
- Syed Asad Ali
- Aga Khan University, Karachi, Pakistan
- Sana Syed
- University of Virginia, Charlottesville, VA, USA; Aga Khan University, Karachi, Pakistan; Corresponding author
- Journal volume & issue
-
Vol. 27,
no. 6
p. 110013
Abstract
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.