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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container_end_page 437
container_issue 2
container_start_page 431
container_title Pediatric research
container_volume 83
creator Tatsi, Christina
Boden, Rebecca
Sinaii, Ninet
Keil, Meg
Lyssikatos, Charalampos
Belyavskaya, Elena
Rosenzweig, Sergio D
Stratakis, Constantine A
Lodish, Maya B
description 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.
doi_str_mv 10.1038/pr.2017.278
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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.</description><identifier>ISSN: 0031-3998</identifier><identifier>EISSN: 1530-0447</identifier><identifier>DOI: 10.1038/pr.2017.278</identifier><identifier>PMID: 29211058</identifier><language>eng</language><publisher>New York: Nature Publishing Group US</publisher><subject>631/250/1619 ; 692/420/254 ; 692/699/2743/1279 ; 692/700/1720/3187 ; clinical-investigation ; Cushing syndrome ; Hormones ; Infections ; Lymphocytes ; Medicine ; Medicine &amp; Public Health ; Pediatric Surgery ; Pediatrics</subject><ispartof>Pediatric research, 2018-02, Vol.83 (2), p.431-437</ispartof><rights>International Pediatric Research Foundation, Inc. 2018</rights><rights>Copyright Nature Publishing Group Feb 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-20df2def6e76f74f1f00df6dddafe09fef808583a0ec6ec4b2c027c8932a0c703</citedby><cites>FETCH-LOGICAL-c446t-20df2def6e76f74f1f00df6dddafe09fef808583a0ec6ec4b2c027c8932a0c703</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1038/pr.2017.278$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1038/pr.2017.278$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29211058$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tatsi, Christina</creatorcontrib><creatorcontrib>Boden, Rebecca</creatorcontrib><creatorcontrib>Sinaii, Ninet</creatorcontrib><creatorcontrib>Keil, Meg</creatorcontrib><creatorcontrib>Lyssikatos, Charalampos</creatorcontrib><creatorcontrib>Belyavskaya, Elena</creatorcontrib><creatorcontrib>Rosenzweig, Sergio D</creatorcontrib><creatorcontrib>Stratakis, Constantine A</creatorcontrib><creatorcontrib>Lodish, Maya B</creatorcontrib><title>Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome</title><title>Pediatric research</title><addtitle>Pediatr Res</addtitle><addtitle>Pediatr Res</addtitle><description>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. 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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.</abstract><cop>New York</cop><pub>Nature Publishing Group US</pub><pmid>29211058</pmid><doi>10.1038/pr.2017.278</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects 631/250/1619
692/420/254
692/699/2743/1279
692/700/1720/3187
clinical-investigation
Cushing syndrome
Hormones
Infections
Lymphocytes
Medicine
Medicine & Public Health
Pediatric Surgery
Pediatrics
title Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome
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