-
Je něco špatně v tomto záznamu ?
Characterization of iron metabolism and erythropoiesis in erythrocyte membrane defects and thalassemia traits
L. Sulovska, D. Holub, Z. Zidova, M. Divoka, M. Hajduch, V. Mihal, J. Vrbkova, M. Horvathova, D. Pospisilova
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
Grantová podpora
NT13587
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
PubMed
26592557
DOI
10.5507/bp.2015.054
Knihovny.cz E-zdroje
- MeSH
- analýza rozptylu MeSH
- dědičná eliptocytóza krev MeSH
- dědičná sférocytóza krev MeSH
- dítě MeSH
- erytrocytární membrána metabolismus MeSH
- erytropoéza fyziologie MeSH
- hemostáza fyziologie MeSH
- hepcidiny metabolismus MeSH
- lidé MeSH
- mladiství MeSH
- předškolní dítě MeSH
- talasemie metabolismus MeSH
- železo metabolismus MeSH
- Check Tag
- dítě MeSH
- lidé MeSH
- mladiství MeSH
- předškolní dítě MeSH
- Publikační typ
- časopisecké články MeSH
BACKGROUND AND AIMS: Erythropoiesis is closely related to iron metabolism in a balanced homeostasis. Analyses of diverse erythroid and iron metabolism disorders have shown that disrupted erythropoiesis negatively affects iron homeostasis and vice versa. The aim of this study was to characterize the relationship between erythropoietic activity and iron homeostasis in pediatric patients with erythrocyte membrane defects and thalassemia traits. METHODS: Selected markers of erythropoietic activity (erythropoietin, soluble transferrin receptor - sTfR and growth differentiation factor 15) and iron status parameters (serum iron, ferritin and hepcidin) were evaluated in pediatric patients with erythrocyte membrane defects and thalassemia traits. RESULTS: The patients with erythrocyte membrane defects and thalassemia traits had altered iron homeostasis due to disturbed erythropoiesis. In comparison with healthy controls, they had a normal to low hepcidin/ferritin ratio and concomitantly elevated sTfR. CONCLUSION: The findings suggest that pediatric patients with erythrocyte membrane defects and thalassemia traits are more susceptible to iron overload than the general population and that the (hepcidin/ferritin)/sTfR ratio can be used to monitor any worsening of the disease.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17012982
- 003
- CZ-PrNML
- 005
- 20190919082747.0
- 007
- ta
- 008
- 170413s2016 xr f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.5507/bp.2015.054 $2 doi
- 035 __
- $a (PubMed)26592557
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Sulovská, Lucie $u Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic $7 xx0144823
- 245 10
- $a Characterization of iron metabolism and erythropoiesis in erythrocyte membrane defects and thalassemia traits / $c L. Sulovska, D. Holub, Z. Zidova, M. Divoka, M. Hajduch, V. Mihal, J. Vrbkova, M. Horvathova, D. Pospisilova
- 520 9_
- $a BACKGROUND AND AIMS: Erythropoiesis is closely related to iron metabolism in a balanced homeostasis. Analyses of diverse erythroid and iron metabolism disorders have shown that disrupted erythropoiesis negatively affects iron homeostasis and vice versa. The aim of this study was to characterize the relationship between erythropoietic activity and iron homeostasis in pediatric patients with erythrocyte membrane defects and thalassemia traits. METHODS: Selected markers of erythropoietic activity (erythropoietin, soluble transferrin receptor - sTfR and growth differentiation factor 15) and iron status parameters (serum iron, ferritin and hepcidin) were evaluated in pediatric patients with erythrocyte membrane defects and thalassemia traits. RESULTS: The patients with erythrocyte membrane defects and thalassemia traits had altered iron homeostasis due to disturbed erythropoiesis. In comparison with healthy controls, they had a normal to low hepcidin/ferritin ratio and concomitantly elevated sTfR. CONCLUSION: The findings suggest that pediatric patients with erythrocyte membrane defects and thalassemia traits are more susceptible to iron overload than the general population and that the (hepcidin/ferritin)/sTfR ratio can be used to monitor any worsening of the disease.
- 650 _2
- $a mladiství $7 D000293
- 650 _2
- $a analýza rozptylu $7 D000704
- 650 _2
- $a dítě $7 D002648
- 650 _2
- $a předškolní dítě $7 D002675
- 650 _2
- $a dědičná eliptocytóza $x krev $7 D004612
- 650 _2
- $a erytrocytární membrána $x metabolismus $7 D004910
- 650 _2
- $a erytropoéza $x fyziologie $7 D004920
- 650 _2
- $a hemostáza $x fyziologie $7 D006487
- 650 _2
- $a hepcidiny $x metabolismus $7 D064451
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a železo $x metabolismus $7 D007501
- 650 _2
- $a dědičná sférocytóza $x krev $7 D013103
- 650 _2
- $a talasemie $x metabolismus $7 D013789
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Holub, Dušan $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc, Czech Republic $7 xx0169439
- 700 1_
- $a Židová, Zuzana $u Department of Biology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Czech Republic $7 xx0207826
- 700 1_
- $a Divoká, Martina $u Department of Hemato-oncology, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic $7 xx0066076
- 700 1_
- $a Hajdúch, Marián $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc, Czech Republic $7 xx0050218
- 700 1_
- $a Mihál, Vladimír, $u Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic $d 1951- $7 nlk19990073561
- 700 1_
- $a Vrbková, J. $u Institute of Molecular and Translational Medicine, Faculty of Medicine and Dentistry, Palacky University Olomouc, Czech Republic $7 _AN085567
- 700 1_
- $a Horváthová, Monika $u Department of Biology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Czech Republic $7 ntk2011644397
- 700 1_
- $a Pospíšilová, Dagmar $u Department of Pediatrics, Faculty of Medicine and Dentistry, Palacky University Olomouc and University Hospital Olomouc, Czech Republic $7 xx0052603
- 773 0_
- $w MED00012606 $t Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czech Republic $x 1213-8118 $g Roč. 160, č. 2 (2016), s. 231-237
- 910 __
- $a ABA008 $b A 1502 $c 958 $y 4 $z 0
- 990 __
- $a 20170413 $b ABA008
- 991 __
- $a 20190919083138 $b ABA008
- 999 __
- $a ok $b bmc $g 1205378 $s 973755
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2016 $b 160 $c 2 $d 231-237 $e 20151027 $i 1213-8118 $m Biomedical papers of the Medical Faculty of the University Palacký, Olomouc Czech Republic $n Biomed. Pap. Fac. Med. Palacký Univ. Olomouc Czech Repub. (Print) $x MED00012606
- GRA __
- $a NT13587 $p MZ0
- LZP __
- $b NLK118 $a Pubmed-20170413