TY - JOUR
T1 - Comparison of Mineral Metabolites as Risk Factors for Adverse Clinical Outcomes in CKD
AU - Isakova, Tamara
N1 - Funding Information:
Financial support: supported by a grant ( K23DK087858 ) from the National Institutes of Health .
Copyright:
Copyright 2013 Elsevier B.V., All rights reserved.
PY - 2013/3
Y1 - 2013/3
N2 - Patients with chronic kidney disease are at increased risk for progressing to end-stage renal disease, developing cardiovascular disease, and dying prematurely. Recent evidence has suggested that disordered mineral metabolism, which includes hyperphosphatemia, secondary hyperparathyroidism, vitamin D deficiency, and fibroblast growth factor 23 excess, may contribute to the high rates of adverse outcomes in this population. However, marked within-subject variability for some of these biochemical parameters exists, potentially detracting from the utility of certain metabolites as prognostic tools. This review summarizes the available data on the epidemiology of phosphate, parathyroid hormone, vitamin D, and fibroblast growth factor 23, and their relationships with adverse clinical outcomes in chronic kidney disease, compares the performance of each as a biomarker of risk and introduces recent insights into the pathophysiology behind some of the observed relationships.
AB - Patients with chronic kidney disease are at increased risk for progressing to end-stage renal disease, developing cardiovascular disease, and dying prematurely. Recent evidence has suggested that disordered mineral metabolism, which includes hyperphosphatemia, secondary hyperparathyroidism, vitamin D deficiency, and fibroblast growth factor 23 excess, may contribute to the high rates of adverse outcomes in this population. However, marked within-subject variability for some of these biochemical parameters exists, potentially detracting from the utility of certain metabolites as prognostic tools. This review summarizes the available data on the epidemiology of phosphate, parathyroid hormone, vitamin D, and fibroblast growth factor 23, and their relationships with adverse clinical outcomes in chronic kidney disease, compares the performance of each as a biomarker of risk and introduces recent insights into the pathophysiology behind some of the observed relationships.
KW - Fibroblast growth factor 23
KW - Parathyroid hormone
KW - Phosphate
KW - Vitamin D
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U2 - 10.1016/j.semnephrol.2012.12.012
DO - 10.1016/j.semnephrol.2012.12.012
M3 - Article
C2 - 23465498
AN - SCOPUS:84875250860
SN - 0270-9295
VL - 33
SP - 106
EP - 117
JO - Seminars in nephrology
JF - Seminars in nephrology
IS - 2
ER -