2016
Dysfunctional protection against advanced glycation due to thiamine metabolism abnormalities in gestational diabetes
BARTÁKOVÁ, Vendula, Anna PLESKAČOVÁ, Katarína KURICOVÁ, Lukáš PÁCAL, Veronika DVOŘÁKOVÁ et. al.Základní údaje
Originální název
Dysfunctional protection against advanced glycation due to thiamine metabolism abnormalities in gestational diabetes
Autoři
BARTÁKOVÁ, Vendula (203 Česká republika, garant, domácí), Anna PLESKAČOVÁ (203 Česká republika, domácí), Katarína KURICOVÁ (703 Slovensko, domácí), Lukáš PÁCAL (203 Česká republika, domácí), Veronika DVOŘÁKOVÁ (203 Česká republika, domácí), Jana BĚLOBRÁDKOVÁ (203 Česká republika), Marie TOMANDLOVÁ (203 Česká republika, domácí), Josef TOMANDL (203 Česká republika, domácí) a Kateřina KAŇKOVÁ (203 Česká republika, domácí)
Vydání
Glycoconjugate Journal, Dordrecht, Springer, 2016, 0282-0080
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30202 Endocrinology and metabolism
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.186
Kód RIV
RIV/00216224:14110/16:00088860
Organizační jednotka
Lékařská fakulta
UT WoS
000381157600011
Klíčová slova česky
tiamin, gestační diabetes, těhotenství, pokročilé produkty glykace
Klíčová slova anglicky
thiamine; gestational diabetes mellitus; pregnancy; advanced glycation end porducts
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 17. 12. 2019 11:32, Mgr. Marie Šípková, DiS.
Anotace
V originále
While the pathogenic role of dicarbonyl stress and accelerated formation of advanced glycation end products (AGEs) to glucose intolerance and to the development of diabetic complications is well established, little is known about these processes in gestational diabetes mellitus (GDM), a condition pathogenically quite similar to type 2 diabetes. The aims of the present study were (i) to determine plasma thiamine and erythrocyte thiamine diphosphate (TDP) and transketolase (TKT) activity in pregnant women with and without GDM, (ii) to assess relationships between thiamine metabolism parameters and selected clinical, biochemical and anthropometric characteristics and, finally, (iii) to analyse relationship between variability in the genes involved in the regulation of transmembrane thiamine transport (i.e. SLC19A2 and SLC19A3) and relevant parameters of thiamine metabolism. We found significantly lower plasma BMI adjusted thiamine in women with GDM (P = 0.002, Mann-Whitney) while levels of erythrocyte TDP (an active TKT cofactor) in mid-trimester were significantly higher in GDM compared to controls (P = 0.04, Mann-Whitney). However, mid-gestational TKT activity - reflecting pentose phosphate pathway activity - did not differ between the two groups (P > 0.05, Mann-Whitney). Furthermore, we ascertained significant associations of postpartum TKT activity with SNPs SLC19A2 rs6656822 and SLC19A3 rs7567984 (P = 0.03 and P = 0.007, resp., Kruskal-Wallis). Our findings of increased thiamine delivery to the cells without concomitant increase of TKT activity in women with GDM therefore indicate possible pathogenic role of thiamine mishandling in GDM. Further studies are needed to determine its contribution to maternal and/or neonatal morbidity.
Návaznosti
NT13198, projekt VaV |
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