Serum adipokines as non-invasive biomarkers in Crohn's disease.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
22 10 2020
22 10 2020
Historique:
received:
01
07
2020
accepted:
23
09
2020
entrez:
23
10
2020
pubmed:
24
10
2020
medline:
19
3
2021
Statut:
epublish
Résumé
Adipose tissue secretes molecules that can promote activity in Crohn's disease. We aimed to evaluate the role of serum adipokines as possible biomarkers in Crohn's disease. Serum samples were obtained from 40 patients with endoscopically active or quiescent Crohn's disease and 36 healthy controls. Serum leptin, ghrelin, resistin and adiponectin levels were analysed by Multiplex in a Luminex 200 system technology. Receiver Operating Characteristic curves were performed to evaluate the adipokines discriminatory capacity. A logistic regression adjusted by possible confounders (i.e. gender, age, BMI) was performed for those adipokines that showed an area under the curve > 0.7. No differences were found in age, gender or BMI among groups. Distribution for serum resistin was different among the three groups of study, and only this adipokine showed an area under the curve of 0.75 comparing actives patients and healthy control groups. Resistin median concentration was selected as a cut-off for a logistic regression analysis; odds ratio along its 95% confidence interval adjusted by gender, age, and BMI yielded a value of 5.46 (1.34-22.14) comparing actives patients and healthy controls. High concentration of serum resistin is probably associated to activity, being this association independent of gender, age or BMI.
Identifiants
pubmed: 33093517
doi: 10.1038/s41598-020-74999-6
pii: 10.1038/s41598-020-74999-6
pmc: PMC7582883
doi:
Substances chimiques
ADIPOQ protein, human
0
Adipokines
0
Adiponectin
0
Biomarkers
0
Ghrelin
0
LEP protein, human
0
Leptin
0
RETN protein, human
0
Resistin
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
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