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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
Όλο το DSpace
  • Κοινότητες & Συλλογές
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Erythropoietin levels in children with obstructive sleep apnea

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Συγγραφέας
Kalogritsas N.D., Lachanas V.A., Liakos P., Alexopoulos E.I., Beka D., Petinaki E., Hajiioannou J., Simos G., Skoulakis C.E.
Ημερομηνία
2021
Γλώσσα
en
DOI
10.1016/j.ijporl.2021.110932
Λέξη-κλειδί
biological marker
erythropoietin
biological marker
erythropoietin
Article
child
controlled study
correlational study
diagnostic test accuracy study
diagnostic value
disease severity
female
human
major clinical study
male
oxygen saturation
pediatric patient
predictive value
prospective study
protein blood level
sleep disordered breathing
sleep time
adult
polysomnography
preschool child
Adult
Biomarkers
Child
Child, Preschool
Erythropoietin
Humans
Polysomnography
Prospective Studies
Sleep Apnea, Obstructive
Elsevier Ireland Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Objective: High serum erythropoietin (EPO) levels have been reported in adult patients with obstructive sleep apnea (OSA), however there is a lack of related literature in children with OSA. The main objective of this study was to explore the potential use of EPO as a pediatric OSA biomarker by exploring the relationship between serum EPO levels and the presence of pediatric OSA. Methods and materials: A prospective study was conducted on children (4–12 years old) referred for overnight PSG. Thirty (30) consecutive children with mild. 30 consecutives with moderate, and 30 consecutives with severe OSA (OSA group), as well as 30 consecutive children with AHI≤1 (non-OSA group) were recruited. Morning blood specimens after PSG studies were obtained in order to compare EPO levels. Results: Finally, 115 children included for analysis. Non-OSA group consisted of 29 children (mean age: 6.93 ± 2.10) and OSA-group of 86 children (mean age: 6.78 ± 2.53). Mean EPO values for the non-OSA and OSA groups were 5.46 ± 2.29 mIU/ml and 8.33 ± 4.10 mIU/ml respectively. OSA-group had significant higher EPO levels than non-OSA (P: 0.01) while EPO levels were significantly correlated with AHI (p < 0.001). Conclusion: Our study showed that serum EPO levels of children with OSA are significantly higher than those without OSA and correlate significantly with AHI. These results suggest that EPO may be considered as a biomarker candidate for pediatric OSA. Since this may be the first study on the topic further research is needed. © 2021
URI
http://hdl.handle.net/11615/74209
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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