AI Article Synopsis

  • The study investigates differences in colorimetric albumin assays (BCP vs. BCG) in chronic kidney disease, suggesting carbamylated albumin may alter dye binding.
  • Various factors were analyzed including uremic toxins, acute phase proteins, and Kt/V related to hemodialysis efficiency.
  • Results indicated that total para-cresyl sulfate (PCS) positively correlates with the BCP/BCG ratio, while serum α1-acid glycoprotein and Kt/V negatively correlate with this ratio, highlighting the complexity of serum albumin measurements in renal insufficiency.

Article Abstract

Background: Colorimetric albumin assays based on binding to bromocresol purple (BCP) and bromocresol green (BCG) yield different results in chronic kidney disease. Altered dye binding of carbamylated albumin has been suggested as a cause. In the present study, a detailed analysis was carried out in which uremic toxins, acute phase proteins and Kt/V, a parameter describing hemodialysis efficiency, were compared with colorimetrically assayed (BCP and BCG) serum albumin.

Methods: Albumin was assayed using immunonephelometry on a BN II nephelometer and colorimetrically based on, respectively, BCP and BCG on a Modular P analyzer. Uremic toxins were assessed using high-performance liquid chromatography. Acute phase proteins (C-reactive protein and α1-acid glycoprotein) and plasma protein α2-macroglobulin were assayed nephelometrically. In parallel, Kt/V was calculated.

Results: Sixty-two serum specimens originating from hemodialysis patients were analyzed. Among the uremic toxins investigated, total para-cresyl sulfate (PCS) showed a significant positive correlation with the BCP/BCG ratio. The serum α1-acid glycoprotein concentration correlated negatively with the BCP/BCG ratio. The BCP/BCG ratio showed also a negative correlation with Kt/V.

Conclusions: In renal insufficiency, the BCP/BCG ratio of serum albumin is affected by multiple factors: next to carbamylation, uremic toxins (total PCS) and α1-acid glycoprotein also play a role.

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Source
http://dx.doi.org/10.1515/cclm-2017-0444DOI Listing

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