TY - JOUR
T1 - Plasma oxalate levels in prevalent hemodialysis patients and potential implications for ascorbic acid supplementation
AU - Liu, Yuguan
AU - Weisberg, Lawrence S.
AU - Langman, Craig B.
AU - Logan, Amanda
AU - Hunter, Krystal
AU - Prasad, Deepali
AU - Avila, Jose
AU - Venkatchalam, Thaliga
AU - Berns, Jeffrey S.
AU - Handelman, Garry J.
AU - Sirover, William D.
N1 - Funding Information:
The Cooper Foundation of Cooper University Hospital (WDS, grant C310500005 ) and a fellowship from the University of Massachusetts Lowell (YL) provided funding for this study. CBL was supported in parts by grants from the National Institutes of Health 1 RO1 HD074596-01 (NICHD); 1U54DK083908-01 (NIDDK)
Publisher Copyright:
© 2016 The Canadian Society of Clinical Chemists
PY - 2016/10/1
Y1 - 2016/10/1
N2 - Objectives Ascorbic acid (AA) supplementation may increase hemoglobin levels and decrease erythropoiesis-stimulating agent dose requirement in patients with end stage renal disease (ESRD). While plasma AA levels > 100 μM may be supratherapeutic, levels of at least 30 μM may be needed to improve wound healing and levels may need to reach 70 μM to optimize erythropoiesis. Of concern, oxalate (Ox), an AA metabolite, can accumulate in ESRD. Historically, if plasma Ox levels remain ≥ 30 μM, oxalosis was of concern. Contemporary hemodialysis (HD) efficiencies may decrease the risk of oxalosis by maintaining pre-HD Ox levels < 30 μM. This study focuses on the plasma Ox levels in HD patients. Design and methods A prospective, observational study of 197 HD patients with pre-HD AA levels and pre-HD and post-HD Ox levels. Results Mean plasma Ox levels decreased 71% during the intradialytic period (22.3 ± 11.1 μM to 6.4 ± 3.2 μM, P < 0.001). In regression analysis, pre-HD plasma AA levels ≤ 100 μM were not associated with a pre-HD plasma Ox level ≥ 30 μM, even if ferritin levels were increased. Pre-HD plasma Ox levels ≥ 20 or ≥ 30 μM were not associated with lower cumulative 4-year survival. Conclusions Pre-HD plasma AA levels up to 100 μM in HD patients do not appear to be associated with an increased risk of developing secondary oxalosis, as the corresponding pre-HD plasma Ox level appears to be maintained at tolerable levels.
AB - Objectives Ascorbic acid (AA) supplementation may increase hemoglobin levels and decrease erythropoiesis-stimulating agent dose requirement in patients with end stage renal disease (ESRD). While plasma AA levels > 100 μM may be supratherapeutic, levels of at least 30 μM may be needed to improve wound healing and levels may need to reach 70 μM to optimize erythropoiesis. Of concern, oxalate (Ox), an AA metabolite, can accumulate in ESRD. Historically, if plasma Ox levels remain ≥ 30 μM, oxalosis was of concern. Contemporary hemodialysis (HD) efficiencies may decrease the risk of oxalosis by maintaining pre-HD Ox levels < 30 μM. This study focuses on the plasma Ox levels in HD patients. Design and methods A prospective, observational study of 197 HD patients with pre-HD AA levels and pre-HD and post-HD Ox levels. Results Mean plasma Ox levels decreased 71% during the intradialytic period (22.3 ± 11.1 μM to 6.4 ± 3.2 μM, P < 0.001). In regression analysis, pre-HD plasma AA levels ≤ 100 μM were not associated with a pre-HD plasma Ox level ≥ 30 μM, even if ferritin levels were increased. Pre-HD plasma Ox levels ≥ 20 or ≥ 30 μM were not associated with lower cumulative 4-year survival. Conclusions Pre-HD plasma AA levels up to 100 μM in HD patients do not appear to be associated with an increased risk of developing secondary oxalosis, as the corresponding pre-HD plasma Ox level appears to be maintained at tolerable levels.
KW - Ascorbic acid
KW - Hemodialysis
KW - Nutrition
KW - Oxalate
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U2 - 10.1016/j.clinbiochem.2016.05.025
DO - 10.1016/j.clinbiochem.2016.05.025
M3 - Article
C2 - 27265723
AN - SCOPUS:84991575694
VL - 49
SP - 1133
EP - 1139
JO - Clinical Biochemistry
JF - Clinical Biochemistry
SN - 0009-9120
IS - 15
ER -