NIH, National Cancer Institute, Division of Cancer Treatment and Diagnosis (DCTD) NIH - National Institutes of Health National Cancer Institute DCTD - Division of Cancer Treatment and Diagnosis

Collection and storage of urine specimens for measurement of urolithiasis risk factors.

Author(s): Wu W, Yang D, Tiselius HG, Ou L, Mai Z, Chen K, Zhu H, Xu S, Zhao Z, Zeng G

Publication: Urology, 2015, Vol. 85, Page 299-303

PubMed ID: 25623670 PubMed Review Paper? No

Purpose of Paper

This paper investigated the effects of preservation with thymol, toluene, hydrochloric acid, or sodium azide and storage at 4˚C or room temperature on levels of eight urine biomarkers.

Conclusion of Paper

Levels of calcium, magnesium, phosphate, sodium, oxalate, and urate were not affected by preservative type or storage, but citrate levels were lower in specimens preserved with hydrochloric acid than in unpreserved specimens. pH increased with increasing storage duration, regardless of preservative type, and generally pH was higher in specimens stored at room temperature than 4˚C. 

Studies

  1. Study Purpose

    This study investigated the effects of preservation with thymol, toluene, hydrochloric acid, or sodium azide and storage for up to 48 h at 4˚C or room temperature on levels of urine biomarkers in spot urine from 21 healthy patients. Specimens were aliquoted and two were stored with each preservative (thymol, toluene, hydrochloric acid, or sodium azide), two were left unpreserved, and one aliquot of each pair was stored at 4˚C and the other was stored at room temperature. All eight analytes were analyzed in unpreserved specimens and specimens preserved with thymol or toluene immediately after preservation and again after 24 and 48 h.  Specimens preserved with hydrochloric acid were not analyzed for pH and urate  and sodium azide-preserved specimens were analyzed only for pH and urate levels.  Levels of oxalate and citrate were determined by ion-exchange chromatography. Calcium, magnesium, and sodium levels were determined by atomic absorption spectrophotometer.

    Summary of Findings:

    Citrate levels were lower in specimens preserved with hydrochloric acid than in unpreserved specimens (P<0.05, all timepoints at both temperatures), but there was no effect of storage temperature or duration.  pH levels increased with increasing storage at room temperature or 4˚C, regardless of preservative (P<0.05, 0 versus 24 h at both temperatures and all preservatives). pH was significantly higher after 24 h in specimens stored at room temperature than 4˚C (P<0.05, all), regardless of preservative, and higher after 48 h in specimens preserved with sodium azide, thymol, or toluene (P<0.05, all). Preservative type, storage duration, and storage temperature had no impact on the levels of calcium, magnesium, phosphate, sodium, oxalate, citrate, or urate.

    Biospecimens
    Preservative Types
    • Other Preservative
    • None (Fresh)
    Diagnoses:
    • Normal
    Platform:
    AnalyteTechnology Platform
    Small molecule Ion exchange chromatography
    Electrolyte/Metal Atomic absorption spectroscopy
    Small molecule Clinical chemistry/auto analyzer
    Pre-analytical Factors:
    ClassificationPre-analytical FactorValue(s)
    Storage Storage duration 0 h
    24 h
    48 h
    Biospecimen Preservation Type of fixation/preservation Hydrochloric acid
    Thymol
    Toluene
    Sodium azide
    None (fresh)
    Storage Storage temperature 4˚C
    Room temperature

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