Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome

Background Hypercortisolemia results in changes of the immune system and elevated infection risk, but data on the WBC changes in pediatric Cushing syndrome (CS) are not known. We describe the changes of the WBC lineages in pediatric endogenous hypercortisolemia, their associations with the markers o...

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Veröffentlicht in:Pediatric research 2018-02, Vol.83 (2), p.431-437
Hauptverfasser: Tatsi, Christina, Boden, Rebecca, Sinaii, Ninet, Keil, Meg, Lyssikatos, Charalampos, Belyavskaya, Elena, Rosenzweig, Sergio D, Stratakis, Constantine A, Lodish, Maya B
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Sprache:eng
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Zusammenfassung:Background Hypercortisolemia results in changes of the immune system and elevated infection risk, but data on the WBC changes in pediatric Cushing syndrome (CS) are not known. We describe the changes of the WBC lineages in pediatric endogenous hypercortisolemia, their associations with the markers of disease severity, and the presence of infections. Methods We identified 197 children with endogenous CS. Clinical and biochemical data were recorded. Sixty-six children with similar age and gender, and normocortisolemia served as controls. Results The absolute lymphocyte count of CS patients was significantly lower than that of controls, while the total WBC and the absolute neutrophil counts were significantly higher. These changes correlated with several markers of CS severity and improved after resolution of hypercortisolemia. Infections were identified in 35 patients (17.8%), and their presence correlated to elevated serum morning cortisol, midnight cortisol, and urinary free cortisol levels, as well as with the decrease in absolute lymphocyte count. Conclusions Children with endogenous CS have abnormal WBC counts, which correlate with the severity of CS, and normalize after cure. Infections are common in this population; clinicians should be aware of this complication of CS and have low threshold in diagnosis and treating infections in CS.
ISSN:0031-3998
1530-0447
DOI:10.1038/pr.2017.278