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dc.contributor.authorDeligözoğlu, Duygu
dc.contributor.authorKasap Demir, Belde
dc.contributor.authorAlparslan, Caner
dc.contributor.authorErbak, Huriye
dc.contributor.authorÇatlı, Gönül
dc.contributor.authorMutlubaş, Fatma
dc.contributor.authorAlaygut, Demet
dc.contributor.authorSoyaltın, Eren
dc.contributor.authorArslansoyu Çamlar, Seçil
dc.contributor.authorYavaşcan, Önder
dc.date.accessioned2021-01-07T11:22:18Z
dc.date.available2021-01-07T11:22:18Z
dc.date.issued2020en_US
dc.identifier.citationDeligözoğlu, D., Kasap Demir, B., Alparslan, C., Erbak, H., Çatlı, G., Mutlubaş, F. ... Yavaşcan, Ö. (2020). Can we use copeptin as a biomarker for masked hypertension or metabolic syndrome in obese children and adolescents? Journal of Pediatric Endocrinology and Metabolism, 33(12), 1551-1561. https://dx.doi.org/10.1515/jpem-2020-0240en_US
dc.identifier.issn0334-018X
dc.identifier.issn2191-0251
dc.identifier.urihttps://dx.doi.org/10.1515/jpem-2020-0240
dc.identifier.urihttps://hdl.handle.net/20.500.12511/6200
dc.description.abstractObjectives: Copeptin, the C-terminal part of arginine-vasopressin, is increased in hypertensive adolescents and closely associated with metabolic syndrome (MS). We aimed to investigate whether serum copeptin can be used to differentiate masked hypertension (MHT) and MS, and the role of sodium intake, natriuretic peptide response and renin-angiotensin-aldosterone system in MHT and MS in obese youth.Methods: Obese children aged 10-18 years with normal office blood pressure measurements were included. Patients with MHT and normotension and those with MS and non-MS were evaluated separately. Biochemical parameters, copeptin, brain natriuretic peptide (BNP), aldosterone, renin, urine sodium, and protein were evaluated. Echocardiography, fundoscopic examination, and ambulatory blood pressure monitoring were performed.Results: There were 80 (M/F=39/41) obese patients with a mean age of 13.78 +/- 1.93 years. The cases with MHT, MS, and concomitant MHT and MS were 53,24, and 13%, respectively. Copeptin levels were similar among patients with and without MHT or MS (p>0.05). However, multivariate analysis revealed that copeptin significantly increased the probability of MHT (OR 1.01, 95% CI=1.001-1.018, p=0.033). Copeptin was positively correlated with daytime systolic and diastolic load, aldosterone, BNP, and urine microalbumin/creatinine levels (p<0.05). Linear regression analyses revealed that copeptin was significantly correlated with BNP regardless of having MHT or MS in obese youth. In the MHT group, 24-h sodium excretion was not significantly correlated with BNP.Conclusion: Copeptin may be a beneficial biomarker to discriminate MHT, but not MS in obese children and adolescents. An insufficient BNP response to sodium intake might be one of the underlying causes of MHT in obese cases.en_US
dc.description.sponsorshipIzmir Katip Celebi University Scientific Research Projects Coordination Uniten_US
dc.language.isoengen_US
dc.publisherWalter de Gruyter GMBHen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectChildrenen_US
dc.subjectCopeptinen_US
dc.subjectMasked Hypertensionen_US
dc.subjectMetabolic Syndromeen_US
dc.subjectObesityen_US
dc.titleCan we use copeptin as a biomarker for masked hypertension or metabolic syndrome in obese children and adolescents?en_US
dc.typearticleen_US
dc.relation.ispartofJournal of Pediatric Endocrinology and Metabolismen_US
dc.departmentİstanbul Medipol Üniversitesi, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Çocuk Sağlığı ve Hastalıkları Ana Bilim Dalıen_US
dc.authorid0000-0002-3582-5075en_US
dc.identifier.volume33en_US
dc.identifier.issue12en_US
dc.identifier.startpage1551en_US
dc.identifier.endpage1561en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.doi10.1515/jpem-2020-0240en_US
dc.identifier.wosqualityQ3en_US
dc.identifier.scopusqualityQ3en_US


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