A cross-sectional study of the association between heat shock protein 27 antibody titers, pro-oxidant–antioxidant balance and metabolic syndrome in patients with angiographically-defined coronary artery disease
To investigate the association between serum antibody titers to Hsp27 (anti-Hsp27) and pro-oxidant–antioxidant balance (PAB) in patients with angiographically-defined coronary artery disease (CAD) with or without the metabolic syndrome (MS). Subjects ( n = 243) were classified into MS+ ( n = 161) an...
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Veröffentlicht in: | Clinical biochemistry 2011-12, Vol.44 (17), p.1390-1395 |
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Sprache: | eng |
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Zusammenfassung: | To investigate the association between serum antibody titers to Hsp27 (anti-Hsp27) and pro-oxidant–antioxidant balance (PAB) in patients with angiographically-defined coronary artery disease (CAD) with or without the metabolic syndrome (MS).
Subjects (
n
=
243) were classified into MS+ (
n
=
161) and MS− (
n
=
82) subgroups, based on the AHA/NHBLI criteria.
Serum anti-Hsp27 titers were found to be significantly higher in the MS+ vs. MS− group. However, no significant difference was observed in serum PAB values. When assessed for individual components of MS, increased serum anti-Hsp27 was found to be higher in subgroups with elevated triglycerides, elevated blood pressure and reduced high-density lipoprotein cholesterol (HDL-C). Subgroups of patients with elevated triglycerides had higher PAB values. HDL-C was the only significant predictor of anti-Hsp27 in the population as a whole.
The evidence from this investigation indicates the presence of elevated anti-Hsp27 in patients with concurrent CAD and MS compared to those with CAD alone.
► Anti-Hsp27 titres were elevated in patients with concurrent CAD and metabolic syndrome compared to those with only CAD. ► Serum prooxidant-antioxidant balance was not elevated in the metabolic syndrome group beyond what is caused by CAD. ► Accumulation of MS features in patients with CAD could be associated with increased risk of vascular complications. |
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ISSN: | 0009-9120 1873-2933 |
DOI: | 10.1016/j.clinbiochem.2011.09.011 |