Metabolomic Signature Discriminates Normal Human Cornea from Keratoconus—A Pilot GC/MS Study

Bibliographic Details
Title: Metabolomic Signature Discriminates Normal Human Cornea from Keratoconus—A Pilot GC/MS Study
Authors: Anna Wojakowska, Monika Pietrowska, Piotr Widlak, Dariusz Dobrowolski, Edward Wylęgała, Dorota Tarnawska
Source: Molecules, Vol 25, Iss 12, p 2933 (2020)
Publisher Information: MDPI AG, 2020.
Publication Year: 2020
Collection: LCC:Organic chemistry
Subject Terms: keratoconus, cornea, ocular metabolomics, GC/MS profiling, Organic chemistry, QD241-441
More Details: The molecular etiology of keratoconus (KC), a pathological condition of the human cornea, remains unclear. The aim of this work was to perform profiling of metabolites and identification of features discriminating this pathology from the normal cornea. The combination of gas chromatography and mass spectrometry (GC/MS) techniques has been applied for profiling and identification of metabolites in corneal buttons from 6 healthy controls and 7 KC patients. An untargeted GC/MS-based approach allowed the detection of 377 compounds, including 46 identified unique metabolites, whose levels enabled the separation of compared groups of samples in unsupervised hierarchical cluster analysis. There were 13 identified metabolites whose levels differentiated between groups of samples. Downregulation of several carboxylic acids, fatty acids, and steroids was observed in KC when compared to the normal cornea. Metabolic pathways associated with compounds that discriminated both groups were involved in energy production, lipid metabolism, and amino acid metabolism. An observed signature may reflect cellular processes involved in the development of KC pathology, including oxidative stress and inflammation.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1420-3049
Relation: https://www.mdpi.com/1420-3049/25/12/2933; https://doaj.org/toc/1420-3049
DOI: 10.3390/molecules25122933
Access URL: https://doaj.org/article/6af98b027b3841a4b05382a2164a2c96
Accession Number: edsdoj.6af98b027b3841a4b05382a2164a2c96
Database: Directory of Open Access Journals
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More Details
ISSN:14203049
DOI:10.3390/molecules25122933
Published in:Molecules
Language:English