Selected plasma oxysterols as a potential multi-marker biosignature panel for Behçet's Disease.

25- hydroxycholesterol 27- hydroxycholesterol 7-ketocholesterol Behçet’s Disease Oxysterols

Journal

The Journal of steroid biochemistry and molecular biology
ISSN: 1879-1220
Titre abrégé: J Steroid Biochem Mol Biol
Pays: England
ID NLM: 9015483

Informations de publication

Date de publication:
07 2022
Historique:
received: 11 02 2022
revised: 29 04 2022
accepted: 02 05 2022
pubmed: 20 5 2022
medline: 18 6 2022
entrez: 19 5 2022
Statut: ppublish

Résumé

Clinical, genetic, and medical evidence has shown the inflammatory vasculitis aspect of Behçet's Disease (BD). Whereas oxysterols are vital factors in inflammation and oxidative stress, it is still unknown whether they are involved in the pathophysiology of BD. The current study aims to explore the profile of oxysterols in plasma of BD patients. Thirty patients diagnosed with BD and forty healthy controls matched for age and gender were included. Results showed that the cholestane-3β,5α,6β-triol, 27-hydroxycholesterol (27-OHC) and cholestanol levels were higher in BD than controls. In addition, plasma levels of 7-ketocholesterol (7-KC) and 25-hydroxycholesterol (25-OHC) were lower in BD patient. However, levels of 24S-hydroxycholesterol (24-OHC) did not significantly differ. For BD patients, the plasma 7-KC level was negatively correlated with the BD activity index (BDAI) while 27-OHC was positively correlated with high-sensitivity C-reactive protein (hs-CRP) in patients with active course of the disease. According to ROC analysis, a remarkable increase in the area under the curve (AUC) with a higher sensitivity (Se) and specificity (Sp) for 7-KC, 25-OHC and 27-OHC combined markers was observed. The present study indicated that the identification of the predictive value of these three-selected biomarkers related to oxidative stress and inflammation in patients should lead to a better identification of the etiological mechanism of BD.

Identifiants

pubmed: 35588947
pii: S0960-0760(22)00073-5
doi: 10.1016/j.jsbmb.2022.106122
pii:
doi:

Substances chimiques

Biomarkers 0
Oxysterols 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

106122

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Auteurs

Meriam Messedi (M)

Research Laboratory "Molecular Basis of Human Diseases", LR19ES13, Sfax Medicine School, University of Sfax, Tunisia. Electronic address: meriammessedi@yahoo.fr.

Wassim Guidara (W)

Research Laboratory "Molecular Basis of Human Diseases", LR19ES13, Sfax Medicine School, University of Sfax, Tunisia.

Sahar Grayaa (S)

Research Laboratory "Molecular Basis of Human Diseases", LR19ES13, Sfax Medicine School, University of Sfax, Tunisia.

Walid Khrouf (W)

Service de Biochimie Métabolique, AP-HP.Sorbonne Université, Hôpitaux Universitaires Pitié-Salpêtrière-Charles Foix, DMU BioGeM, Paris F-75013, France.

Mouna Snoussi (M)

Internal medicine department, Hedi Chaker Hosptital, Sfax, Tunisia.

Zouhir Bahloul (Z)

Internal medicine department, Hedi Chaker Hosptital, Sfax, Tunisia.

Dominique Bonnefont-Rousselot (D)

Service de Biochimie Métabolique, AP-HP.Sorbonne Université, Hôpitaux Universitaires Pitié-Salpêtrière-Charles Foix, DMU BioGeM, Paris F-75013, France; Université de Paris, CNRS, Inserm, UTCBS, Paris F-75006, France.

Foudil Lamari (F)

Service de Biochimie Métabolique, AP-HP.Sorbonne Université, Hôpitaux Universitaires Pitié-Salpêtrière-Charles Foix, DMU BioGeM, Paris F-75013, France.

Fatma Ayadi (F)

Research Laboratory "Molecular Basis of Human Diseases", LR19ES13, Sfax Medicine School, University of Sfax, Tunisia.

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Classifications MeSH