Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.

In clinical states associated with systemic oxidative stress (OS) and inflammation such as chronic kidney disease (CKD), oxidative modifications of serum albumin impair its quantification, resulting in apparent hypoalbuminemia. As the maintenance of oncotic pressure/colloid osmotic pressure (COP) is...

Full description

Bibliographic Details
Main Authors: Regina Michelis, Shifra Sela, Teuta Zeitun, Ronit Geron, Batya Kristal
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4959682?pdf=render
id doaj-c8757f4a52684d4195aaf294a59f5e71
record_format Article
spelling doaj-c8757f4a52684d4195aaf294a59f5e712020-11-24T22:03:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01117e015983910.1371/journal.pone.0159839Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.Regina MichelisShifra SelaTeuta ZeitunRonit GeronBatya KristalIn clinical states associated with systemic oxidative stress (OS) and inflammation such as chronic kidney disease (CKD), oxidative modifications of serum albumin impair its quantification, resulting in apparent hypoalbuminemia. As the maintenance of oncotic pressure/colloid osmotic pressure (COP) is a major function of albumin, this study examined the impact of albumin oxidation on COP, both in-vivo and in-vitro.Patients with proteinuria and patients on chronic hemodialysis (HD) with systemic inflammation and OS were enrolled. Blood samples were collected from 134 subjects: 32 healthy controls (HC), proteinuric patients with high (n = 17) and low (n = 31) systemic inflammation and from 54 patients on chronic hemodialysis (HD) with the highest levels of OS and inflammation.In-vitro oxidized albumin showed significantly higher COP values than non-oxidized albumin at identical albumin levels. In vivo, in hypoalbuminemic HD patients with the highest OS and inflammation, COP values were also higher than expected for the low albumin levels. The contribution to COP by other prevalent plasma proteins, such as fibrinogen and immunoglobulins was negligible. We imply that the calculation of COP based on albumin levels should be revisited in face of OS and inflammation. Hence, in hypoalbuminemic proteinuric patients with systemic OS and inflammation the assumption of low COP should be verified by its measurements.http://europepmc.org/articles/PMC4959682?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Regina Michelis
Shifra Sela
Teuta Zeitun
Ronit Geron
Batya Kristal
spellingShingle Regina Michelis
Shifra Sela
Teuta Zeitun
Ronit Geron
Batya Kristal
Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.
PLoS ONE
author_facet Regina Michelis
Shifra Sela
Teuta Zeitun
Ronit Geron
Batya Kristal
author_sort Regina Michelis
title Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.
title_short Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.
title_full Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.
title_fullStr Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.
title_full_unstemmed Unexpected Normal Colloid Osmotic Pressure in Clinical States with Low Serum Albumin.
title_sort unexpected normal colloid osmotic pressure in clinical states with low serum albumin.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description In clinical states associated with systemic oxidative stress (OS) and inflammation such as chronic kidney disease (CKD), oxidative modifications of serum albumin impair its quantification, resulting in apparent hypoalbuminemia. As the maintenance of oncotic pressure/colloid osmotic pressure (COP) is a major function of albumin, this study examined the impact of albumin oxidation on COP, both in-vivo and in-vitro.Patients with proteinuria and patients on chronic hemodialysis (HD) with systemic inflammation and OS were enrolled. Blood samples were collected from 134 subjects: 32 healthy controls (HC), proteinuric patients with high (n = 17) and low (n = 31) systemic inflammation and from 54 patients on chronic hemodialysis (HD) with the highest levels of OS and inflammation.In-vitro oxidized albumin showed significantly higher COP values than non-oxidized albumin at identical albumin levels. In vivo, in hypoalbuminemic HD patients with the highest OS and inflammation, COP values were also higher than expected for the low albumin levels. The contribution to COP by other prevalent plasma proteins, such as fibrinogen and immunoglobulins was negligible. We imply that the calculation of COP based on albumin levels should be revisited in face of OS and inflammation. Hence, in hypoalbuminemic proteinuric patients with systemic OS and inflammation the assumption of low COP should be verified by its measurements.
url http://europepmc.org/articles/PMC4959682?pdf=render
work_keys_str_mv AT reginamichelis unexpectednormalcolloidosmoticpressureinclinicalstateswithlowserumalbumin
AT shifrasela unexpectednormalcolloidosmoticpressureinclinicalstateswithlowserumalbumin
AT teutazeitun unexpectednormalcolloidosmoticpressureinclinicalstateswithlowserumalbumin
AT ronitgeron unexpectednormalcolloidosmoticpressureinclinicalstateswithlowserumalbumin
AT batyakristal unexpectednormalcolloidosmoticpressureinclinicalstateswithlowserumalbumin
_version_ 1725831279408054272