• Je něco špatně v tomto záznamu ?

Dysfunctional protection against advanced glycation due to thiamine metabolism abnormalities in gestational diabetes

V. Bartáková, A. Pleskačová, K. Kuricová, L. Pácal, V. Dvořáková, J. Bělobrádková, M. Tomandlová, J. Tomandl, K. Kaňková,

. 2016 ; 33 (4) : 591-598. [pub] 20160610

Jazyk angličtina Země Spojené státy americké

Typ dokumentu klinické zkoušky, časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/bmc18017213

Grantová podpora
NT13198 MZ0 CEP - Centrální evidence projektů

E-zdroje Online Plný text

NLK ProQuest Central od 1997-01-01 do Před 1 rokem
Medline Complete (EBSCOhost) od 2011-01-01 do Před 1 rokem
Health & Medicine (ProQuest) od 1997-01-01 do Před 1 rokem

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.

Citace poskytuje Crossref.org

000      
00000naa a2200000 a 4500
001      
bmc18017213
003      
CZ-PrNML
005      
20191002081521.0
007      
ta
008      
180515s2016 xxu f 000 0|eng||
009      
AR
024    7_
$a 10.1007/s10719-016-9688-9 $2 doi
035    __
$a (PubMed)27287225
040    __
$a ABA008 $b cze $d ABA008 $e AACR2
041    0_
$a eng
044    __
$a xxu
100    1_
$a Bartáková, Vendula $u Department of Pathophysiology, Faculty of Medicine, Masaryk University Brno, UKB Kamenice 5/A18, 625 00, Brno, Czech Republic. $7 xx0240193
245    10
$a Dysfunctional protection against advanced glycation due to thiamine metabolism abnormalities in gestational diabetes / $c V. Bartáková, A. Pleskačová, K. Kuricová, L. Pácal, V. Dvořáková, J. Bělobrádková, M. Tomandlová, J. Tomandl, K. Kaňková,
520    9_
$a 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.
650    _2
$a dospělí $7 D000328
650    _2
$a gestační diabetes $x krev $7 D016640
650    _2
$a erytrocyty $x metabolismus $7 D004912
650    _2
$a ženské pohlaví $7 D005260
650    _2
$a následné studie $7 D005500
650    _2
$a produkty pokročilé glykace $x krev $7 D017127
650    _2
$a lidé $7 D006801
650    _2
$a membránové transportní proteiny $x krev $7 D026901
650    _2
$a těhotenství $7 D011247
650    _2
$a thiaminpyrofosfát $x krev $7 D013835
650    _2
$a transketolasa $x krev $7 D014174
655    _2
$a klinické zkoušky $7 D016430
655    _2
$a časopisecké články $7 D016428
700    1_
$a Pleskačová, Anna $u Department of Pathophysiology, Faculty of Medicine, Masaryk University Brno, UKB Kamenice 5/A18, 625 00, Brno, Czech Republic. Department of Biochemistry, Faculty of Medicine, Masaryk University Brno, Kamenice 5, 625 00, Brno, Czech Republic.
700    1_
$a Chalásová, Katarína, $d 1986- $7 mub2017949800 $u Department of Pathophysiology, Faculty of Medicine, Masaryk University Brno, UKB Kamenice 5/A18, 625 00, Brno, Czech Republic.
700    1_
$a Pácal, Lukáš $u Department of Pathophysiology, Faculty of Medicine, Masaryk University Brno, UKB Kamenice 5/A18, 625 00, Brno, Czech Republic. $7 xx0084072
700    1_
$a Dvořáková, Veronika $u Department of Pathophysiology, Faculty of Medicine, Masaryk University Brno, UKB Kamenice 5/A18, 625 00, Brno, Czech Republic.
700    1_
$a Bělobrádková, Jana $u Diabetes Centre, Department of Internal Medicine - Gastroenterology, University Hospital Brno, Jihlavská 20, 625 00, Brno, Czech Republic. $7 mzk2007382258
700    1_
$a Tomandlová, Marie $u Department of Biochemistry, Faculty of Medicine, Masaryk University Brno, Kamenice 5, 625 00, Brno, Czech Republic. $7 xx0230817
700    1_
$a Tomandl, Josef, $u Department of Biochemistry, Faculty of Medicine, Masaryk University Brno, Kamenice 5, 625 00, Brno, Czech Republic. $d 1964- $7 mzk2003175507
700    1_
$a Kaňková, Kateřina, $u Department of Pathophysiology, Faculty of Medicine, Masaryk University Brno, UKB Kamenice 5/A18, 625 00, Brno, Czech Republic. kankov@med.muni.cz. $d 1971- $7 mzk2003190820
773    0_
$w MED00006846 $t Glycoconjugate journal $x 1573-4986 $g Roč. 33, č. 4 (2016), s. 591-598
856    41
$u https://pubmed.ncbi.nlm.nih.gov/27287225 $y Pubmed
910    __
$a ABA008 $b sig $c sign $y a $z 0
990    __
$a 20180515 $b ABA008
991    __
$a 20191002081929 $b ABA008
999    __
$a ok $b bmc $g 1300837 $s 1014053
BAS    __
$a 3
BAS    __
$a PreBMC
BMC    __
$a 2016 $b 33 $c 4 $d 591-598 $e 20160610 $i 1573-4986 $m Glycoconjugate journal $n Glycoconj J $x MED00006846
GRA    __
$a NT13198 $p MZ0
LZP    __
$a Pubmed-20180515

Najít záznam

Citační ukazatele

Nahrávání dat ...

Možnosti archivace

Nahrávání dat ...