Subclinical cardiovascular disease and its association with risk factors in children with steroid-resistant nephrotic syndrome

dc.contributor.authorCandan, Cengiz
dc.contributor.authorCanpolat, Nur
dc.contributor.authorGökalp, Selman
dc.contributor.authorYildiz, Nurdan
dc.contributor.authorTurhan, Pinar
dc.contributor.authorTaşdemir, Mehmet
dc.contributor.authorSever, Lale
dc.date.accessioned2025-05-10T15:23:59Z
dc.date.issued2014
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractBackground: The aim of this study was to evaluate the presence of subclinical cardiovascular disease (CVD) and its relation to risk factors in pediatric patients with steroid-resistant nephrotic syndrome (NS). Methods: Thirty-seven patients with normal renal function were compared with 22 healthy controls regarding the presence of subclinical CVD. Measurements included aortic pulse wave velocity (PWV), carotid intima media thickness (IMT), and left ventricular mass (LVM). Patients were additionally assessed for blood pressure (BP) pattern and the presence of hypertension by 24-h ambulatory blood pressure monitoring. Results: Compared with the controls, patients had significantly higher mean aortic PWV-standard deviation scores (SDS), mean carotid IMT-SDS, and LVM index (p < 0.001 for all). Increased aortic PWV was noted in 5 % of patients, increased carotid IMT in 22 %, and increased LVM index in 19 %. Five patients (14 %) were hypertensive, and mean BP indexes, SDS, and BP loads during nighttime were significantly higher than those during daytime (p < 0.001 for all). Multivariate analysis revealed a significant relationship between PWV-SDS and ferritin (R 2 = 0.269, p = 0.006) and between carotid IMT-SDS and proteinuria (R 2 = 0.141, p = 0.022). The LVM index was independently associated only with higher body mass index SDS (R 2 = 0.317, p < 0.001). In addition, six patients (16 %) had multiple abnormal subclinical CVD markers, and increased subclinical CVD risk was independently associated only with higher low-density lipoprotein cholesterol (R 2 = 0.292, p = 0.044). Conclusions: Based on these results, steroid-resistant NS children generally are at high risk of cardiovascular complications, but the increased risk is likely to be multifactorial. © 2013 IPNA.
dc.identifier.doi10.1007/s00467-013-2608-3
dc.identifier.endpage102
dc.identifier.issn1432-198X
dc.identifier.issue1
dc.identifier.pmid24037224
dc.identifier.scopus2-s2.0-84890546585
dc.identifier.scopusqualityQ1
dc.identifier.startpage95
dc.identifier.urihttps://doi.org/10.1007/s00467-013-2608-3
dc.identifier.urihttps://hdl.handle.net/20.500.14730/6580
dc.identifier.volume29
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.relation.ispartofPediatric Nephrology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_Scopus_20250302
dc.subjectAortic stiffness; Atherosclerosis; Cardiovascular disease; Childhood; Steroid-resistant nephrotic syndrome
dc.titleSubclinical cardiovascular disease and its association with risk factors in children with steroid-resistant nephrotic syndrome
dc.typeArticle

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