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Identification of potential serum metabolic biomarkers for patient with keratoconus using untargeted metabolomics approach.
Daphne Teh, Ai Lin; Jayapalan, Jaime Jacqueline; Loke, Mun Fai; Wan Abdul Kadir, Azida Juana; Subrayan, Visvaraja.
Afiliación
  • Daphne Teh AL; Department of Ophthalmology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia. Electronic address: drdaphneteh@gmail.com.
  • Jayapalan JJ; Department of Molecular Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia. Electronic address: jaime_jacklyn@um.edu.my.
  • Loke MF; KK Women's and Children's Hospital, Singapore. Electronic address: lmunfai@gmail.com.
  • Wan Abdul Kadir AJ; Department of Ophthalmology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia. Electronic address: azidajuana@um.edu.my.
  • Subrayan V; Department of Ophthalmology, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia. Electronic address: dvisva@hotmail.com.
Exp Eye Res ; 211: 108734, 2021 10.
Article en En | MEDLINE | ID: mdl-34428458
ABSTRACT
This study aimed to investigate the metabolite differences between patients with keratoconus and control subjects and identify potential serum biomarkers for keratoconus using a non-targeted metabolomics approach. Venous blood samples were obtained from patients with keratoconus (n = 20) as well as from age-, gender- and race-matched control subjects (n = 20). Metabolites extracted from serum were separated and analyzed by liquid chromatography/quadrupole time-of-flight mass spectrometer. Processing of raw data and analysis of the data files was performed using Agilent Mass Hunter Qualitative software. The identified metabolites were subjected to a principal component and hierarchical cluster analysis. Appropriate statistical tests were used to analyze the metabolomic profiling data. Together, the analysis revealed that the dehydroepiandrosterone sulfate from the steroidal hormone synthesis pathway was significantly upregulated in patients with keratoconus (p < 0.05). Also, a combination of eicosanoids from the arachidonic acid pathway, mainly prostaglandin F2α, prostaglandin A2, 16,16-dimethyl prostaglandin E2, and 5-hydroxyeicosatetraenoic acid were collectively up-regulated as a group in keratoconus patients (p < 0.05). On the other hand, glycerophospholipid PS(172(9Z,12Z)/204(5Z,8Z,11Z,14Z)) was found to be significantly upregulated in the metabolomics profiles of control subjects (p < 0.05). The differently regulated metabolites provide insights into the pathophysiology of keratoconus and could potentially be used as biomarkers for keratoconus to aid in screening for individuals at risk hence, enabling early diagnosis and timely monitoring of disease.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Biomarcadores / Ácidos Hidroxieicosatetraenoicos / Metabolómica / Queratocono Tipo de estudio: Diagnostic_studies / Prognostic_studies / Qualitative_research / Screening_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Exp Eye Res Año: 2021 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Biomarcadores / Ácidos Hidroxieicosatetraenoicos / Metabolómica / Queratocono Tipo de estudio: Diagnostic_studies / Prognostic_studies / Qualitative_research / Screening_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Exp Eye Res Año: 2021 Tipo del documento: Article