Intercellular Adhesion Molecule-1 Lys469Glu Polymorphism, Systemic Redox Homeostasis and Gestational Diabetes Mellitus in Pregnant Women.
Lys469Glu polymorphism
antioxidants
antioxydants
diabète sucré gestationnel
gestational diabetes mellitus
homéostasie redox
intercellular adhesion molecule-1
lipid peroxidation
molécule d'adhérence intercellulaire 1
peroxydation des lipides
polymorphisme Lys469Glu
redox homeostasis
Journal
Canadian journal of diabetes
ISSN: 2352-3840
Titre abrégé: Can J Diabetes
Pays: Canada
ID NLM: 101148810
Informations de publication
Date de publication:
Apr 2019
Apr 2019
Historique:
received:
04
04
2018
revised:
27
07
2018
accepted:
27
07
2018
pubmed:
10
10
2018
medline:
28
7
2019
entrez:
10
10
2018
Statut:
ppublish
Résumé
Intercellular adhesion molecule-1 (ICAM-1) plays an important role in endothelial function. Hyperglycemia-induced impaired redox status is 1 of the well-known pathophysiologic characteristics of gestational diabetes mellitus (GDM), and it plays a crucial role in the causes of disease. Our aim was to clarify any possible relationship between the ICAM-1 Lys469Glu polymorphism and systemic redox status in women with and without GDM. Also, we investigated whether this polymorphism could be associated with a change for better or worse as evidenced by clinical and redox biomarkers. The ICAM-1 polymorphism statuses of 89 pregnant women without GDM and 53 pregnant women with GDM were found. Stratifying patients based on GDM and polymorphism status, we investigated various redox homeostasis markers. The independent t test was used. Significantly higher systemic oxidative damage and diminished antioxidant defense were found in pregnant women with GDM. Also, results showed that whether pregnant women were carrying the Lys469Glu polymorphism or not did not seem to be associated with significant differences, as evidenced by comparable systemic oxidative damage. Although no significant difference was observed between genotypes, the oxidative damage observed in patients with GDM warrants earlier screening and management in the light of new evidence.
Identifiants
pubmed: 30297297
pii: S1499-2671(18)30184-9
doi: 10.1016/j.jcjd.2018.07.003
pii:
doi:
Substances chimiques
Intercellular Adhesion Molecule-1
126547-89-5
Types de publication
Journal Article
Langues
eng
Pagination
173-178.e1Informations de copyright
Copyright © 2018 Diabetes Canada. Published by Elsevier Inc. All rights reserved.