Related Experiment Video
Updated: Sep 2, 2025

5/6 Nephrectomy Using Sharp Bipolectomy Via Midline Laparotomy in Rats
Published on: April 4, 2025
Mineral and bone disorder and longterm survival in a chronic kidney disease grade 3b-4cohort
Pablo Rios1, Ricardo Silvariño1,2, Laura Sola1
1Comisión Asesora Programa de Salud Renal, Fondo Nacional de Recursos, Montevideo, Uruguay.
Insights
Mineral and bone disorder biomarkers impact mortality in chronic kidney disease (CKD) G3b-4 patients. Higher phosphate, iPTH, and lower vitamin D levels increase mortality risk, while vitamin D treatment reduces it.
Area of Science:
- Nephrology
- Endocrinology
- Clinical Biochemistry
Background:
- Mineral and bone disorder (MBD) biomarker reference ranges in chronic kidney disease (CKD) are debated.
- CKD patients experience high mortality rates, often linked to MBD.
- Accurate MBD biomarker levels are crucial for predicting mortality risk in CKD.
Purpose of the Study:
- To investigate the association between serum calcium (Ca), phosphate (P), intact parathyroid hormone (iPTH), and 25(OH) vitamin D levels and mortality risk.
- To evaluate these associations in a cohort of CKD G3b-4 patients.
- To inform precise MBD biomarker level definitions for CKD G3b-4.
Main Methods:
- Analysis of a large CKD cohort (n=6473) from the Uruguayan National Renal Healthcare Program (NRHP-UY).
- Inclusion period: October 2004 - March 2020, follow-up until March 2021.
- Bivariate and multivariate Cox regression analyses adjusted for multiple clinical factors were performed.
Main Results:
- Higher mortality risk was significantly associated with serum phosphate > 4.00 mg/dl (HR 1.668), iPTH > 105 pg/ml (HR 1.386), and 25(OH) vitamin D ≤ 10 ng/ml (HR 1.958).
- Lower mortality risk was observed with 1,25(OH)2 vitamin D treatment (HR 0.639).
- Bivariate analysis indicated optimal ranges for reduced mortality: Ca 9.01-10.25 mg/dl, P 2.76-4.0 mg/dl, iPTH ≤ 105 pg/ml, and 25(OH) vitamin D > 10 ng/ml.
Conclusions:
- Serum phosphate, iPTH, and 25(OH) vitamin D levels are significant predictors of mortality in CKD G3b-4 patients.
- Maintaining optimal levels of these biomarkers and considering vitamin D treatment may reduce mortality risk.
- These findings support refining target ranges for MBD biomarkers in CKD management.
Abstract:
Mineral and bone disorder biomarkers 'normal ranges' are controversial. The aim of the study was to evaluate the association between serum calcium (Ca), phosphate (P), intact parathyroid hormone (iPTH), and 25(OH) vitamin D levels and mortality risk, in a chronic kidney disease (CKD) grade (G) 3b-4 cohort. The Uruguayan National Renal Healthcare Program (NRHP-UY) CKD patients' cohort, included between 1 October 2004 and 1 March 2020 and followed-up until 1 March 2021, was analyzed with the Ethics Committee approval. A total of 6473 patients were analyzed: 56% men, median age 73 (65-79) years, 55% on CKD G3b. At the end of the follow-up, 2459 (37.7%) patients had died (6.4/100 patient-year). There were iPTH data on 2013 patients (younger, with lower estimated glomerular filtration rate (eGFR) and lesser comorbidities). By bivariate Cox analysis the lowest death risk was observed with mean Ca between 9.01 and 10.25 mg/dl, P between 2.76 and 4.0 mg/dl, iPTH ≤ 105 pg/ml, and 25(OH) vitamin D >10 ng/ml. The multivariate Cox regression mortality risk adjusted to age, sex, CKD etiology, diabetes, smoking, cardiovascular comorbidity, blood pressure, proteinuria, eGFR, renin-angiotensin system blockers and vitamin D treatments, serum Ca, P, iPTH, and 25(OH) vitamin D (n = 964) showed that a higher mortality risk was associated with p > 4.00 mg/dl (HR 1.668, CI 95%: 1.201-2.317), iPTH >105 pg/ml (HR 1.386, CI 95%: 1.012-1.989), and 25(OH) vitamin D ≤ 10 ng/ml (HR 1.958, CI 95%: 1.238-3.098) and a lower mortality risk with 1,25(OH)2 vitamin D treatment (HR 0.639, CI 95%: 0.451-0.906). These data may contribute to the precise G3b-4 CKD-MBD biomarkers levels definition.
Related Concept Videos
Chronic Kidney Disease III: Interprofessional Care
Chronic Kidney Disease II: Clinical Manifestations
Acute Kidney Injury III: Clinical Manifestations
Chronic Kidney Disease IV: Nursing Management
Chronic Kidney Disease I: Introduction
Acute Kidney Injury IV: Diagnostic Studies and Prevention

