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Clin Chim Acta. 2017 Aug;471:107-112. doi: 10.1016/j.cca.2017.05.032. Epub 2017 May 26.

Sensitive albuminuria analysis using dye-binding based test strips.

Author information

1
Department of Clinical Chemistry, Ghent University Hospital, Gent, Belgium. Electronic address: joris.delanghe@ugent.be.
2
Department of Clinical Chemistry, Ghent University Hospital, Gent, Belgium.
3
Department of Nephrology, Ghent University Hospital, Gent, Belgium.

Abstract

BACKGROUND:

Populations at increased risk for chronic kidney disease should be screened for albuminuria. Possibilities of advanced urine strip readers based on complementary metal oxide semiconductor (CMOS) sensor technology were investigated for obtaining quantitative albuminuria results.

METHODS:

Reflectance data of test strips (Sysmex UFC 3500 reader+CMOS) were compared with albuminuria (BNII) and with proteinuria (Cobas 8000). Urinary creatinine was assayed using a Jaffe-based creatinine assay (Cobas 8000).

RESULTS:

Calibration curve was made between 11.5 and 121.5mg/L with detection limit of 5.5mg/L. Within-run CV values of reflectance data were 0.21% (UC-Control L; 10mg/L) and 0.37% (UC-Control H; >150mg/L) for albumin, and 0.71%/3.97% for creatinine. Between-run CV values were 0.24%/0.42% for albumin and 0.93%/5.13% for creatinine. A strong correlation (r=0.92) was obtained between albuminuria (BNII) and protein strip reflectance data. Creatinine reflectance data correlated well with Jaffe-based urinary creatinine data (r=0.90). Albumin:creatinine ratio obtained by test strip and by wet chemistry showed a good correlation (r=0.59). Carbamylated, glycated and partially hydrolyzed isoforms of albumin could be detected by test strip.

CONCLUSIONS:

Dye-binding based albumin test strip assay in combination with a CMOS based reader would potentially allow quantitative analysis of albuminuria and determination of albumin:creatinine ratio.

KEYWORDS:

Albuminuria; Chronic kidney disease; Diabetes mellitus; Reflectance data; Test strips

PMID:
28554541
DOI:
10.1016/j.cca.2017.05.032
[Indexed for MEDLINE]

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