Abnormal levels of serum anti-elastin antibodies in patients with symptomatic carotid stenosis

Abstract Background and objective A correlation between the levels of antibodies to alpha-elastin (alpha-AEAb) and tropoelastin (tropo-AEAb) and the corresponding peptide concentration is found in human serum in health and disease. Serum elastin peptide and anti-elastin antibodies (AEAb) levels are...

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Veröffentlicht in:Clinical neurology and neurosurgery 2014-01, Vol.116 (C), p.9-12
Hauptverfasser: Tzvetanov, Plamen, Hegde, Vish, Al-Hashel, Jasem Y, Atanasova, Milena, Sohal, Aman P.S, Rousseff, Rossen T
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Sprache:eng
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Zusammenfassung:Abstract Background and objective A correlation between the levels of antibodies to alpha-elastin (alpha-AEAb) and tropoelastin (tropo-AEAb) and the corresponding peptide concentration is found in human serum in health and disease. Serum elastin peptide and anti-elastin antibodies (AEAb) levels are age-related and vary with the stages of atherosclerotic vascular damage. This study aims to determine if elastin metabolism (assessed by the ratio of tropo-AEAb to alpha-AEAb) differs in patients with symptomatic carotid stenosis versus subjects with asymptomatic stenosis. Patients and methods Alpha-AEAb and tropo-AEAb were measured by ELISA in blood sera of 65 patients with ultrasound verified high-grade symptomatic carotid stenosis (resulting in stroke 1–7 days before measurement) compared to 51 patients with asymptomatic stenosis. Results Serum anti-alpha-elastin IgG levels are extremely increased in symptomatic versus asymptomatic carotid stenosis. The ratio of tropo-AEAb (reflecting elastin synthesis) to alpha-AEAb (a function of elastin degradation) was 3.7 in symptomatic stenosis versus 14.2 in asymptomatic stenosis ( p < 0.001). Conclusions There is a significant difference in elastin metabolism in patients with symptomatic carotid stenosis versus asymptomatic stenosis. The ratio of tropo-AEAb to alpha-AEAb as an index of elastin synthesis/degradation proves useful in investigation of atherosclerotic lesions and may represent a new immunologic marker for carotid plaque destabilization.
ISSN:0303-8467
1872-6968
DOI:10.1016/j.clineuro.2013.11.011