Revising the Diagnosis of Idiopathic Uveitis by Peripheral Blood Transcriptomics.


Journal

American journal of ophthalmology
ISSN: 1879-1891
Titre abrégé: Am J Ophthalmol
Pays: United States
ID NLM: 0370500

Informations de publication

Date de publication:
02 2021
Historique:
received: 09 06 2020
revised: 03 09 2020
accepted: 04 09 2020
pubmed: 18 9 2020
medline: 17 3 2021
entrez: 17 9 2020
Statut: ppublish

Résumé

To test the hypothesis that idiopathic uveitis can be categorized into subtypes based on gene expression from blood. Case control study. We applied RNA-Seq to peripheral blood from patients with uveitis associated with 1 of 4 systemic diseases, including axial spondyloarthritis (n = 17), sarcoidosis (n = 13), inflammatory bowel disease (n = 12), tubulo-interstitial nephritis with uveitis (n = 10), or idiopathic uveitis (n = 38) as well as 18 healthy control subjects evaluated predominantly at Oregon Health and Science University. A high-dimensional negative binomial regression model implemented in the edgeR R package compared each disease group with the control subjects. The 20 most distinctive genes for each diagnosis were extracted. Of 80 genes, there were 75 unique genes. A classification algorithm was developed by fitting a gradient boosting tree with 5-fold cross-validation. Messenger RNA from subjects with idiopathic uveitis were analyzed to see if any fit clinically and by gene expression pattern with one of the diagnosable entities. For uveitis associated with a diagnosable systemic disease, gene expression profiling achieved an overall accuracy of 85% (balanced average of sensitivity plus specificity, P < .001). Although most patients with idiopathic uveitis presumably have none of these 4 associated systemic diseases, gene expression profiles helped to reclassify 11 of 38 subjects. Peripheral blood gene expression profiling is a potential adjunct in accurate differential diagnosis of the cause of uveitis. Validation of these results and characterization of the gene expression profile from additional discrete diagnoses could enhance the value of these observations.

Identifiants

pubmed: 32941857
pii: S0002-9394(20)30505-5
doi: 10.1016/j.ajo.2020.09.012
pmc: PMC7935743
mid: NIHMS1628940
pii:
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

15-23

Subventions

Organisme : NIAMS NIH HHS
ID : P30 AR073752
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY010572
Pays : United States
Organisme : NIH HHS
ID : P51 OD011092
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY026572
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

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Auteurs

James T Rosenbaum (JT)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA; Department of Medicine, Oregon Health and Science University, Portland, Oregon, USA; Department of Cell Biology, Oregon Health and Science University, Portland, Oregon, USA; Legacy Devers Eye Institute, Portland, Oregon, USA. Electronic address: rosenbaj@ohsu.edu.

Christina A Harrington (CA)

Integrated Genomics Laboratory, Oregon Health and Science University, Portland, Oregon, USA; Department of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon, USA.

Robert P Searles (RP)

Integrated Genomics Laboratory, Oregon Health and Science University, Portland, Oregon, USA.

Suzanne S Fei (SS)

Bioinformatics and Biostatistics Core, Oregon National Primate Research Center, Oregon Health and Science University, Beaverton, Oregon, USA.

Amr Zaki (A)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA.

Sruthi Arepalli (S)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA.

Michael A Paley (MA)

Division of Rheumatology, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, USA.

Lynn M Hassman (LM)

Department of Ophthalmology, Washington University, St Louis, Missouri, USA.

Albert T Vitale (AT)

Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, Utah, USA.

Christopher D Conrady (CD)

Department of Ophthalmology and Visual Sciences, John A. Moran Eye Center, University of Utah, Salt Lake City, Utah, USA.

Puthyda Keath (P)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA.

Claire Mitchell (C)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA.

Lindsey Watson (L)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA.

Stephen R Planck (SR)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA.

Tammy M Martin (TM)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA; Department of Molecular Microbiology and Immunology, Oregon Health and Science University, Portland, Oregon, USA.

Dongseok Choi (D)

Department of Ophthalmology/Casey Eye Institute, Oregon Health and Science University, Portland, Oregon, USA; Department of Medicine, Oregon Health and Science University, Portland, Oregon, USA; Oregon Health and Science University-Portland State University School of Public Health, Oregon Health and Science University, Portland, Oregon, USA; Graduate School of Dentistry, Kyung Hee University, Seoul, Korea.

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