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dc.contributor.authorAnarat, Ali
dc.contributor.authorHARAMBAT, Jerome
dc.contributor.authorKUNZMANN, Kevin
dc.contributor.authorAZUKAITIS, Karolis
dc.contributor.authorBayazit, Aysun K.
dc.contributor.authorDOYON, Anke
dc.contributor.authorDÜZOVA, ALİ
dc.contributor.authorNIEMIRSKA, Anna
dc.contributor.authorSozeri, Betul
dc.contributor.authorTHURN-VALSASSINA, Daniela
dc.contributor.authorBESSENAY, Lucie
dc.contributor.authorCandan, Cengiz
dc.contributor.authorPECO-ANTIC, Amira
dc.contributor.authorTschumi, Sibylle
dc.contributor.authorTESTA, Sara
dc.contributor.authorJankauskiene, Augustina
dc.contributor.authorARBEITER, Klaus
dc.contributor.authorMENCARELLI, Francesca
dc.contributor.authorKIYAK, Aysel
dc.contributor.authorDonmez, Osman
dc.contributor.authorDROZDZ, Dorota
dc.contributor.authorMELK, Anette
dc.contributor.authorQUERFELD, Uwe
dc.contributor.authorSCHAEFER, Franz
dc.contributor.authorERDOGAN, Hakan
dc.contributor.authorROSALES, Alejandra
dc.contributor.authorAlpay, Harika
dc.contributor.authorLUGANI, Francesca
dc.contributor.authorYilmaz, Alev
dc.contributor.authorCanpolat, Nur
dc.date.accessioned2021-03-05T14:19:45Z
dc.date.available2021-03-05T14:19:45Z
dc.date.issued2017
dc.identifier.citationHARAMBAT J., KUNZMANN K., AZUKAITIS K., Bayazit A. K. , Canpolat N., DOYON A., DÜZOVA A., NIEMIRSKA A., Sozeri B., THURN-VALSASSINA D., et al., "Metabolic acidosis is common and associates with disease progression in children with chronic kidney disease", KIDNEY INTERNATIONAL, cilt.92, ss.1507-1514, 2017
dc.identifier.issn0085-2538
dc.identifier.othervv_1032021
dc.identifier.otherav_b6964b8d-b52a-4a3e-88d8-f439970b368b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/121539
dc.identifier.urihttps://doi.org/10.1016/j.kint.2017.05.006
dc.description.abstractRecent studies in adult chronic kidney disease (CKD) suggest that metabolic acidosis is associated with faster decline in estimated glomerular filtration rate (eGFR). Alkali therapies improve the course of kidney disease. Here we investigated the prevalence and determinants of abnormal serum bicarbonate values and whether metabolic acidosis may be deleterious to children with CKD. Associations between follow-up serum bicarbonate levels categorized as under 18, 18 to under 22, and 22 or more mmol/l and CKD outcomes in 704 children in the Cardiovascular Comorbidity in Children with CKD Study, a prospective cohort of pediatric patients with CKD stages 3-5, were studied. The eGFR and serum bicarbonate were measured every six months. At baseline, the median eGFR was 27 ml/min/1.73m(2) and median serum bicarbonate level 21 mmol/l. During a median follow-up of 3.3 years, the prevalence of metabolic acidosis (serum bicarbonate under 22 mmol/l) was 43%, 60%, and 45% in CKD stages 3, 4, and 5, respectively. In multivariable analysis, the presence of metabolic acidosis as a time-varying covariate was significantly associated with log serum parathyroid hormone through the entire follow-up, but no association with longitudinal growth was found. A total of 211 patients reached the composite endpoint (ESRD or 50% decline in eGFR). In a multivariable Cox model, children with time-varying serum bicarbonate under 18 mmol/l had a significantly higher risk of CKD progression compared to those with a serum bicarbonate of 22 or more mmol/l (adjusted hazard ratio 2.44; 95% confidence interval 1.43-4.15). Thus, metabolic acidosis is a common complication in pediatric patients with CKD and may be a risk factor for secondary hyperparathyroidism and kidney disease progression.
dc.language.isoeng
dc.subjectDahili Tıp Bilimleri
dc.subjectÜROLOJİ VE NEFROLOJİ
dc.subjectKlinik Tıp
dc.subjectKlinik Tıp (MED)
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectNefroloji
dc.titleMetabolic acidosis is common and associates with disease progression in children with chronic kidney disease
dc.typeMakale
dc.relation.journalKIDNEY INTERNATIONAL
dc.contributor.departmentCHU Bordeaux , ,
dc.identifier.volume92
dc.identifier.issue6
dc.identifier.startpage1507
dc.identifier.endpage1514
dc.contributor.firstauthorID91336


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