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...
Gespeichert in:
Veröffentlicht in: | Pediatric research 2018-02, Vol.83 (2), p.431-437 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5866174</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1973460683</sourcerecordid><originalsourceid>FETCH-LOGICAL-c446t-20df2def6e76f74f1f00df6dddafe09fef808583a0ec6ec4b2c027c8932a0c703</originalsourceid><addsrcrecordid>eNptkUFv1DAQhS0EokvhxB1Z4oIEWcaxkziXSmiBFqkSFzhbrj3e9ZLYwU6Q9t_jsm1pESeP5316M6NHyEsGawZcvp_SugbWretOPiIr1nCoQIjuMVkBcFbxvpcn5FnOewAmGimekpO6rxmDRq7I_iOahDqjpcNhnHbRHGbMVAdLfbhVks8_qIuptBya2cdAdUJq4jiW0geKwcYthrhkOqH1ek7e0M2Sdz5saT4Em-KIz8kTp4eML27eU_L986dvm4vq8uv5l82Hy8oI0c5VDdbVFl2LXes64ZiD0mmttdoh9A6dBNlIrgFNi0Zc1Qbqzsie1xpMB_yUnB19p-VqRGswzEkPakp-1OmgovbqoRL8Tm3jL9XItmWdKAZvbgxS_LlgntXos8Fh0AHLiYr1HRcttJIX9PU_6D4uKZTz1HUmwIE3TaHeHimTYs4J3d0yDNR1huX_h1clw0K_ur__HXsbWgHeHYFcpLDF9Hfo__x-Aw-vqSI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2017030355</pqid></control><display><type>article</type><title>Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome</title><source>SpringerLink Journals</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Tatsi, Christina ; Boden, Rebecca ; Sinaii, Ninet ; Keil, Meg ; Lyssikatos, Charalampos ; Belyavskaya, Elena ; Rosenzweig, Sergio D ; Stratakis, Constantine A ; Lodish, Maya B</creator><creatorcontrib>Tatsi, Christina ; Boden, Rebecca ; Sinaii, Ninet ; Keil, Meg ; Lyssikatos, Charalampos ; Belyavskaya, Elena ; Rosenzweig, Sergio D ; Stratakis, Constantine A ; Lodish, Maya B</creatorcontrib><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.</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 & 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. 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><subject>631/250/1619</subject><subject>692/420/254</subject><subject>692/699/2743/1279</subject><subject>692/700/1720/3187</subject><subject>clinical-investigation</subject><subject>Cushing syndrome</subject><subject>Hormones</subject><subject>Infections</subject><subject>Lymphocytes</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Pediatric Surgery</subject><subject>Pediatrics</subject><issn>0031-3998</issn><issn>1530-0447</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNptkUFv1DAQhS0EokvhxB1Z4oIEWcaxkziXSmiBFqkSFzhbrj3e9ZLYwU6Q9t_jsm1pESeP5316M6NHyEsGawZcvp_SugbWretOPiIr1nCoQIjuMVkBcFbxvpcn5FnOewAmGimekpO6rxmDRq7I_iOahDqjpcNhnHbRHGbMVAdLfbhVks8_qIuptBya2cdAdUJq4jiW0geKwcYthrhkOqH1ek7e0M2Sdz5saT4Em-KIz8kTp4eML27eU_L986dvm4vq8uv5l82Hy8oI0c5VDdbVFl2LXes64ZiD0mmttdoh9A6dBNlIrgFNi0Zc1Qbqzsie1xpMB_yUnB19p-VqRGswzEkPakp-1OmgovbqoRL8Tm3jL9XItmWdKAZvbgxS_LlgntXos8Fh0AHLiYr1HRcttJIX9PU_6D4uKZTz1HUmwIE3TaHeHimTYs4J3d0yDNR1huX_h1clw0K_ur__HXsbWgHeHYFcpLDF9Hfo__x-Aw-vqSI</recordid><startdate>20180201</startdate><enddate>20180201</enddate><creator>Tatsi, Christina</creator><creator>Boden, Rebecca</creator><creator>Sinaii, Ninet</creator><creator>Keil, Meg</creator><creator>Lyssikatos, Charalampos</creator><creator>Belyavskaya, Elena</creator><creator>Rosenzweig, Sergio D</creator><creator>Stratakis, Constantine A</creator><creator>Lodish, Maya B</creator><general>Nature Publishing Group US</general><general>Nature Publishing Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180201</creationdate><title>Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome</title><author>Tatsi, Christina ; Boden, Rebecca ; Sinaii, Ninet ; Keil, Meg ; Lyssikatos, Charalampos ; Belyavskaya, Elena ; Rosenzweig, Sergio D ; Stratakis, Constantine A ; Lodish, Maya B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-20df2def6e76f74f1f00df6dddafe09fef808583a0ec6ec4b2c027c8932a0c703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>631/250/1619</topic><topic>692/420/254</topic><topic>692/699/2743/1279</topic><topic>692/700/1720/3187</topic><topic>clinical-investigation</topic><topic>Cushing syndrome</topic><topic>Hormones</topic><topic>Infections</topic><topic>Lymphocytes</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Pediatric Surgery</topic><topic>Pediatrics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><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><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Pediatric research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tatsi, Christina</au><au>Boden, Rebecca</au><au>Sinaii, Ninet</au><au>Keil, Meg</au><au>Lyssikatos, Charalampos</au><au>Belyavskaya, Elena</au><au>Rosenzweig, Sergio D</au><au>Stratakis, Constantine A</au><au>Lodish, Maya B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased lymphocytes and increased risk for infection are common in endogenous pediatric Cushing syndrome</atitle><jtitle>Pediatric research</jtitle><stitle>Pediatr Res</stitle><addtitle>Pediatr Res</addtitle><date>2018-02-01</date><risdate>2018</risdate><volume>83</volume><issue>2</issue><spage>431</spage><epage>437</epage><pages>431-437</pages><issn>0031-3998</issn><eissn>1530-0447</eissn><abstract>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.</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> |
fulltext | fulltext |
identifier | ISSN: 0031-3998 |
ispartof | Pediatric research, 2018-02, Vol.83 (2), p.431-437 |
issn | 0031-3998 1530-0447 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5866174 |
source | SpringerLink Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection |
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 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-02T14%3A45%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Decreased%20lymphocytes%20and%20increased%20risk%20for%20infection%20are%20common%20in%20endogenous%20pediatric%20Cushing%20syndrome&rft.jtitle=Pediatric%20research&rft.au=Tatsi,%20Christina&rft.date=2018-02-01&rft.volume=83&rft.issue=2&rft.spage=431&rft.epage=437&rft.pages=431-437&rft.issn=0031-3998&rft.eissn=1530-0447&rft_id=info:doi/10.1038/pr.2017.278&rft_dat=%3Cproquest_pubme%3E1973460683%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2017030355&rft_id=info:pmid/29211058&rfr_iscdi=true |