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Subclinical inflammation in paediatric patients with primary hypertension and white coat hypertension
Introduction and objective: Evaluation of subclinical inflammation in patients with primary hypertension (PH) and white coat hypertension (WCH). Materials and methods: In 56 untreated paediatric patients with PH, 40 with WCH, and 30 healthy individuals (control group, CG), we evaluated high sensitiv...
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Published in: | Paediatrics and Family Medicine 2024-01, Vol.20 (2), p.215-224 |
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description | Introduction and objective: Evaluation of subclinical inflammation in patients with primary hypertension (PH) and white coat hypertension (WCH). Materials and methods: In 56 untreated paediatric patients with PH, 40 with WCH, and 30 healthy individuals (control group, CG), we evaluated high sensitivity C-reactive protein (hsCRP), interleukin 18 (IL-18) levels, complete blood count-derived markers of inflammation, office and ambulatory blood pressure, and selected clinical and biochemical parameters. Results: hsCRP was significantly higher in PH patients compared to CG, and neutrophil and monocyte counts were significantly higher in PH and WCH patients compared to CG. Receiver operating characteristic analysis revealed good prognostic profiles for hsCRP, neutrophil, lymphocyte, monocyte, and platelet counts, as well as neutrophil-to-lymphocyte ratio (NLR), monocyte-to-neutrophil ratio, and platelet-to-mean platelet volume ratio as predictors of the presence of PH. In multivariate analysis, monocyte-to-lymphocyte ratio (MLR) and platelet count (β = 0.217, β = 0.191) were significant predictors of office diastolic blood pressure Z-score, while neutrophil count predicted 24 h systolic blood pressure Z-score (β = 0.365), MLR, lymphocyte count, IL-18, and NLR predicted 24 h diastolic blood pressure Z-score (β = 0.305, β = 0.253, β = −0.197, β = −0.189), and neutrophil count together with IL-18 predicted 24 h mean arterial pressure Z-score (β = 0.210, β = −0.209). Conclusions: 1. Patients with PH and WCH are characterised by similar levels of subclinical inflammation, which are significantly higher compared to healthy peers. 2. Complete blood count-derived indices, especially neutrophil count and MLR, can serve as important adjuncts to the clinical evaluation of paediatric patients with PH. |
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Materials and methods: In 56 untreated paediatric patients with PH, 40 with WCH, and 30 healthy individuals (control group, CG), we evaluated high sensitivity C-reactive protein (hsCRP), interleukin 18 (IL-18) levels, complete blood count-derived markers of inflammation, office and ambulatory blood pressure, and selected clinical and biochemical parameters. Results: hsCRP was significantly higher in PH patients compared to CG, and neutrophil and monocyte counts were significantly higher in PH and WCH patients compared to CG. Receiver operating characteristic analysis revealed good prognostic profiles for hsCRP, neutrophil, lymphocyte, monocyte, and platelet counts, as well as neutrophil-to-lymphocyte ratio (NLR), monocyte-to-neutrophil ratio, and platelet-to-mean platelet volume ratio as predictors of the presence of PH. In multivariate analysis, monocyte-to-lymphocyte ratio (MLR) and platelet count (β = 0.217, β = 0.191) were significant predictors of office diastolic blood pressure Z-score, while neutrophil count predicted 24 h systolic blood pressure Z-score (β = 0.365), MLR, lymphocyte count, IL-18, and NLR predicted 24 h diastolic blood pressure Z-score (β = 0.305, β = 0.253, β = −0.197, β = −0.189), and neutrophil count together with IL-18 predicted 24 h mean arterial pressure Z-score (β = 0.210, β = −0.209). Conclusions: 1. Patients with PH and WCH are characterised by similar levels of subclinical inflammation, which are significantly higher compared to healthy peers. 2. Complete blood count-derived indices, especially neutrophil count and MLR, can serve as important adjuncts to the clinical evaluation of paediatric patients with PH.</description><identifier>ISSN: 1734-1531</identifier><identifier>EISSN: 2451-0742</identifier><identifier>DOI: 10.15557/PiMR.2024.0031</identifier><language>eng</language><publisher>Warsaw: Medical Communications Sp. z o.o</publisher><subject>Blood platelets ; Blood pressure ; Blood tests ; Hypertension ; Inflammation ; Lymphocytes ; Neutrophils ; Pediatrics ; Standard scores</subject><ispartof>Paediatrics and Family Medicine, 2024-01, Vol.20 (2), p.215-224</ispartof><rights>Copyright Medical Communications Sp. z o.o. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c153t-282ac1e4e74db2f1cc7567002d35b253b2485f24c1865d10ae4395e75d9f12693</cites><orcidid>0009-0007-1369-8304 ; 0000-0002-1959-8255 ; 0000-0002-7336-7327 ; 0000-0003-3667-1220</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Dziedzic-Jankowska, Katarzyna</creatorcontrib><creatorcontrib>Bujanowicz, Adam</creatorcontrib><creatorcontrib>Szyszka, Michał</creatorcontrib><creatorcontrib>Stelmaszczyk-Emmel, Anna</creatorcontrib><creatorcontrib>Skrzypczyk, Piotr</creatorcontrib><title>Subclinical inflammation in paediatric patients with primary hypertension and white coat hypertension</title><title>Paediatrics and Family Medicine</title><description>Introduction and objective: Evaluation of subclinical inflammation in patients with primary hypertension (PH) and white coat hypertension (WCH). Materials and methods: In 56 untreated paediatric patients with PH, 40 with WCH, and 30 healthy individuals (control group, CG), we evaluated high sensitivity C-reactive protein (hsCRP), interleukin 18 (IL-18) levels, complete blood count-derived markers of inflammation, office and ambulatory blood pressure, and selected clinical and biochemical parameters. Results: hsCRP was significantly higher in PH patients compared to CG, and neutrophil and monocyte counts were significantly higher in PH and WCH patients compared to CG. Receiver operating characteristic analysis revealed good prognostic profiles for hsCRP, neutrophil, lymphocyte, monocyte, and platelet counts, as well as neutrophil-to-lymphocyte ratio (NLR), monocyte-to-neutrophil ratio, and platelet-to-mean platelet volume ratio as predictors of the presence of PH. In multivariate analysis, monocyte-to-lymphocyte ratio (MLR) and platelet count (β = 0.217, β = 0.191) were significant predictors of office diastolic blood pressure Z-score, while neutrophil count predicted 24 h systolic blood pressure Z-score (β = 0.365), MLR, lymphocyte count, IL-18, and NLR predicted 24 h diastolic blood pressure Z-score (β = 0.305, β = 0.253, β = −0.197, β = −0.189), and neutrophil count together with IL-18 predicted 24 h mean arterial pressure Z-score (β = 0.210, β = −0.209). Conclusions: 1. Patients with PH and WCH are characterised by similar levels of subclinical inflammation, which are significantly higher compared to healthy peers. 2. Complete blood count-derived indices, especially neutrophil count and MLR, can serve as important adjuncts to the clinical evaluation of paediatric patients with PH.</description><subject>Blood platelets</subject><subject>Blood pressure</subject><subject>Blood tests</subject><subject>Hypertension</subject><subject>Inflammation</subject><subject>Lymphocytes</subject><subject>Neutrophils</subject><subject>Pediatrics</subject><subject>Standard scores</subject><issn>1734-1531</issn><issn>2451-0742</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpVkE1rwzAMhs3YYKXredfAzmkt2a6T4yj7KHRs7ONsHMehHqmT2S6l_37J2stOktArvdJDyC3QOQgh5OLNvbzPkSKfU8rggkyQC8ip5HhJJiAZz0EwuCazGF1FqSwYlwVOiP3YV6Z13hndZs43rd7tdHKdH4qs17Z2OgVnhjQ561PMDi5tsz64nQ7HbHvsbUjWx3FA-zo7bF2ymel0-te7IVeNbqOdneOUfD0-fK6e883r03p1v8nNcF3KsUBtwHIreV1hA8ZIsZSUYs1EhYJVyAvRIDdQLEUNVFvOSmGlqMsGcFmyKbk77e1D97O3Manvbh_8YKkYcAklIIVBtTipTOhiDLZR538UUPWHU4041YhTjTjZL_W4aXU</recordid><startdate>20240101</startdate><enddate>20240101</enddate><creator>Dziedzic-Jankowska, Katarzyna</creator><creator>Bujanowicz, Adam</creator><creator>Szyszka, Michał</creator><creator>Stelmaszczyk-Emmel, Anna</creator><creator>Skrzypczyk, Piotr</creator><general>Medical Communications Sp. z o.o</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PHGZM</scope><scope>PHGZT</scope><scope>PIMPY</scope><scope>PJZUB</scope><scope>PKEHL</scope><scope>PPXIY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0009-0007-1369-8304</orcidid><orcidid>https://orcid.org/0000-0002-1959-8255</orcidid><orcidid>https://orcid.org/0000-0002-7336-7327</orcidid><orcidid>https://orcid.org/0000-0003-3667-1220</orcidid></search><sort><creationdate>20240101</creationdate><title>Subclinical inflammation in paediatric patients with primary hypertension and white coat hypertension</title><author>Dziedzic-Jankowska, Katarzyna ; Bujanowicz, Adam ; Szyszka, Michał ; Stelmaszczyk-Emmel, Anna ; Skrzypczyk, Piotr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c153t-282ac1e4e74db2f1cc7567002d35b253b2485f24c1865d10ae4395e75d9f12693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Blood platelets</topic><topic>Blood pressure</topic><topic>Blood tests</topic><topic>Hypertension</topic><topic>Inflammation</topic><topic>Lymphocytes</topic><topic>Neutrophils</topic><topic>Pediatrics</topic><topic>Standard scores</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dziedzic-Jankowska, Katarzyna</creatorcontrib><creatorcontrib>Bujanowicz, Adam</creatorcontrib><creatorcontrib>Szyszka, Michał</creatorcontrib><creatorcontrib>Stelmaszczyk-Emmel, Anna</creatorcontrib><creatorcontrib>Skrzypczyk, Piotr</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Proquest Health & Medical Complete</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</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)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>PML(ProQuest Medical Library)</collection><collection>ProQuest Central (New)</collection><collection>ProQuest One Academic (New)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Research Collection</collection><collection>ProQuest One Academic Middle East (New)</collection><collection>ProQuest One Health & Nursing</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><jtitle>Paediatrics and Family Medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dziedzic-Jankowska, Katarzyna</au><au>Bujanowicz, Adam</au><au>Szyszka, Michał</au><au>Stelmaszczyk-Emmel, Anna</au><au>Skrzypczyk, Piotr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Subclinical inflammation in paediatric patients with primary hypertension and white coat hypertension</atitle><jtitle>Paediatrics and Family Medicine</jtitle><date>2024-01-01</date><risdate>2024</risdate><volume>20</volume><issue>2</issue><spage>215</spage><epage>224</epage><pages>215-224</pages><issn>1734-1531</issn><eissn>2451-0742</eissn><abstract>Introduction and objective: Evaluation of subclinical inflammation in patients with primary hypertension (PH) and white coat hypertension (WCH). Materials and methods: In 56 untreated paediatric patients with PH, 40 with WCH, and 30 healthy individuals (control group, CG), we evaluated high sensitivity C-reactive protein (hsCRP), interleukin 18 (IL-18) levels, complete blood count-derived markers of inflammation, office and ambulatory blood pressure, and selected clinical and biochemical parameters. Results: hsCRP was significantly higher in PH patients compared to CG, and neutrophil and monocyte counts were significantly higher in PH and WCH patients compared to CG. Receiver operating characteristic analysis revealed good prognostic profiles for hsCRP, neutrophil, lymphocyte, monocyte, and platelet counts, as well as neutrophil-to-lymphocyte ratio (NLR), monocyte-to-neutrophil ratio, and platelet-to-mean platelet volume ratio as predictors of the presence of PH. In multivariate analysis, monocyte-to-lymphocyte ratio (MLR) and platelet count (β = 0.217, β = 0.191) were significant predictors of office diastolic blood pressure Z-score, while neutrophil count predicted 24 h systolic blood pressure Z-score (β = 0.365), MLR, lymphocyte count, IL-18, and NLR predicted 24 h diastolic blood pressure Z-score (β = 0.305, β = 0.253, β = −0.197, β = −0.189), and neutrophil count together with IL-18 predicted 24 h mean arterial pressure Z-score (β = 0.210, β = −0.209). Conclusions: 1. Patients with PH and WCH are characterised by similar levels of subclinical inflammation, which are significantly higher compared to healthy peers. 2. Complete blood count-derived indices, especially neutrophil count and MLR, can serve as important adjuncts to the clinical evaluation of paediatric patients with PH.</abstract><cop>Warsaw</cop><pub>Medical Communications Sp. z o.o</pub><doi>10.15557/PiMR.2024.0031</doi><tpages>10</tpages><orcidid>https://orcid.org/0009-0007-1369-8304</orcidid><orcidid>https://orcid.org/0000-0002-1959-8255</orcidid><orcidid>https://orcid.org/0000-0002-7336-7327</orcidid><orcidid>https://orcid.org/0000-0003-3667-1220</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Blood platelets Blood pressure Blood tests Hypertension Inflammation Lymphocytes Neutrophils Pediatrics Standard scores |
title | Subclinical inflammation in paediatric patients with primary hypertension and white coat hypertension |
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