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Redox Biol. 2013 Oct 8;1:483-91. doi: 10.1016/j.redox.2013.07.006.

Biological markers of oxidative stress: Applications to cardiovascular research and practice.

Author information

1
North Shore Heart Research Group, Kolling Institute of Medical Research, University of Sydney, Sydney, Australia.

Abstract

Oxidative stress is a common mediator in pathogenicity of established cardiovascular risk factors. Furthermore, it likely mediates effects of emerging, less well-defined variables that contribute to residual risk not explained by traditional factors. Functional oxidative modifications of cellular proteins, both reversible and irreversible, are a causal step in cellular dysfunction. Identifying markers of oxidative stress has been the focus of many researchers as they have the potential to act as an "integrator" of a multitude of processes that drive cardiovascular pathobiology. One of the major challenges is the accurate quantification of reactive oxygen species with very short half-life. Redox-sensitive proteins with important cellular functions are confined to signalling microdomains in cardiovascular cells and are not readily available for quantification. A popular approach is the measurement of stable by-products modified under conditions of oxidative stress that have entered the circulation. However, these may not accurately reflect redox stress at the cell/tissue level. Many of these modifications are "functionally silent". Functional significance of the oxidative modifications enhances their validity as a proposed biological marker of cardiovascular disease, and is the strength of the redox cysteine modifications such as glutathionylation. We review selected biomarkers of oxidative stress that show promise in cardiovascular medicine, as well as new methodologies for high-throughput measurement in research and clinical settings. Although associated with disease severity, further studies are required to examine the utility of the most promising oxidative biomarkers to predict prognosis or response to treatment.

KEYWORDS:

Biomarker; CVD, cardiovascular disease; Cardiovascular disease; GSH, glutathione (reduced); Glutathionylation; H2O2, hydrogen peroxide; HO2•, hydroperoxyl radical; HOCl, hypochlorous acid; IsoP, isoprostane; MDA, malondialdehyde; MPO, myeloperoxidase; NO2, nitrogen dioxide; O2•−, superoxide; ONOO−, peroxynitrite; OxLDL, Oxidized low-density lipoprotein; Oxidative stress; Prognosis; ROS, reactive oxygen species; TBARS, thiobarbituric acid reacting substance; •OH, hydroxyl radical

PMID:
24251116
PMCID:
PMC3830063
DOI:
10.1016/j.redox.2013.07.006
[Indexed for MEDLINE]
Free PMC Article

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