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Updated: Jun 27, 2026

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Drug-Induced Sleep Endoscopy (DISE) with Target Controlled Infusion (TCI) and Bispectral Analysis in Obstructive Sleep Apnea
Published on: December 6, 2016
Reticulocytes in untreated obstructive sleep apnoea.
O Marrone1, A Salvaggio, M Gioia
1National Research Council, Institute of Biomedicine and Molecular Immunology (IBIM), Palermo. marrone@ibim.cnr.it
Summary
Obstructive sleep apnea (OSA) may increase immature red blood cells, but erythropoietin does not mediate this effect. Hypoxemia, not EPO, influences reticulocyte release in OSA patients.
Area of Science:
- Hematology
- Sleep Medicine
- Cardiopulmonary Physiology
Background:
- Repetitive hypoxemic episodes in Obstructive Sleep Apnea (OSA) may affect red blood cell production.
- The impact of OSA on reticulocyte release and maturation remains unclear.
- This study investigates alterations in circulating reticulocytes in OSA patients.
Purpose of the Study:
- To determine if OSA influences the number and maturation of circulating reticulocytes.
- To explore the potential role of erythropoietin (EPO) in mediating these changes.
- To correlate reticulocyte parameters with OSA severity and other physiological markers.
Main Methods:
- Fifty male adult patients with suspected OSA underwent polysomnography.
- Blood samples were analyzed for reticulocyte count, immaturity (Immature Reticulocyte Fraction - IRF), erythropoietin, iron, and transferrin.
- Statistical analyses, including univariate and multiple regression, were performed.
Main Results:
- Patients exhibited a wide range of OSA severity (AHI: 44.3 ± 30.4).
- Both reticulocyte count and IRF were slightly elevated above normal ranges.
- Lowest nocturnal oxygen saturation was a significant predictor of IRF, independent of EPO levels.
Conclusions:
- Hypoxemia associated with OSA appears to influence the release of immature reticulocytes.
- The observed effect on reticulocyte release is not mediated by erythropoietin.
- Further research is needed to elucidate the precise mechanisms linking hypoxemia to reticulocyte maturation in OSA.
