Literature DB >> 26857252

Urine oxalate biological variation in patients with primary hyperoxaluria.

Oliver Clifford-Mobley1, Anna Sjögren2, Elisabeth Lindner2, Gill Rumsby3.   

Abstract

Hyperoxaluria is a well-recognised risk factor for urolithiasis and patients with primary hyperoxaluria (PH) gradually build up calcium oxalate deposits leading to chronic kidney disease. Efforts to improve treatment for PH have focused on reducing urine oxalate excretion and thus decreasing lithogenesis. To determine the efficacy of treatments designed to alter a biochemical parameter it is necessary to know the biological and analytical variation of that parameter. In this study, we estimated the intra-individual biological variation of urine oxalate excretion in patients with PH, and from this determined what would constitute a significant change in the form of a reference change value (RCV). Each patient collected four 24-h urines on consecutive weeks. The intra-individual biological variation of oxalate excretion calculated from these samples ranged from 0 to 36 % with a mean of 14 %. The corresponding RCVs were 4-84 % with a mean of 32 %. This result implies that, on average, a reduction of almost one-third in urine oxalate excretion is required to prove an effect from treatment. The wide range of biological variation between individuals may reflect other, as yet unknown, determinants of oxaluria in PH, as well as inaccuracies in urine collection. The data suggest that it is more appropriate to use individual RCVs established prior to treatment to determine its efficacy: a relatively small fall in urine oxalate excretion may be outside the biological variation of some patients but not of others.

Entities:  

Keywords:  Biological variation; Primary hyperoxaluria; Reference change value; Urine oxalate

Mesh:

Substances:

Year:  2016        PMID: 26857252     DOI: 10.1007/s00240-016-0860-2

Source DB:  PubMed          Journal:  Urolithiasis        ISSN: 2194-7228            Impact factor:   3.436


  21 in total

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6.  Transplantation outcomes in primary hyperoxaluria.

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Journal:  Ann Clin Biochem       Date:  1988-05       Impact factor: 2.057

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Review 3.  Genetic assessment in primary hyperoxaluria: why it matters.

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4.  ePHex: a phase 3, double-blind, placebo-controlled, randomized study to evaluate long-term efficacy and safety of Oxalobacter formigenes in patients with primary hyperoxaluria.

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5.  Endogenous Oxalate Production in Primary Hyperoxaluria Type 1 Patients.

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6.  Size-dependent cellular uptake mechanism and cytotoxicity toward calcium oxalate on Vero cells.

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7.  Efficacy of Hydroxy-L-proline (HYP) analogs in the treatment of primary hyperoxaluria in Drosophila Melanogaster.

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8.  Diet-related urine collections: assistance in categorization of hyperoxaluria.

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9.  Subsequent urinary stone events are predicted by the magnitude of urinary oxalate excretion in enteric hyperoxaluria.

Authors:  Matthew R D'Costa; Annamaria T Kausz; Kevin J Carroll; Jóhann P Ingimarsson; Felicity T Enders; Kristin C Mara; Ramila A Mehta; John C Lieske
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10.  Development and Validation of a New Gas Chromatography-Tandem Mass Spectrometry Method for the Measurement of Enrichment of Glyoxylate Metabolism Analytes in Hyperoxaluria Patients Using a Stable Isotope Procedure.

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Journal:  Anal Chem       Date:  2020-01-03       Impact factor: 6.986

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