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Title:

Is serum pregnancy-associated plasma protein A really a potential marker of atherosclerotic carotid plaque stability?

Document type:
Journal Article; Article
Author(s):
Heider, P; Pfäffle, N; Pelisek, J; Wildgruber, M; Poppert, H; Rudelius, M; Eckstein, HH
Abstract:
OBJECTIVES: The search for markers predicting risk of plaque rupture in carotid atherosclerosis is still ongoing. Previous findings showed that pregnancy-associated plasma protein-A (PAPP-A) levels correlate with an adverse plaque morphology. However, the role of PAPP-A in plaque destabilisation is still uncertain. MATERIAL AND METHODS: Patients with carotid artery stenosis involved in the study were asymptomatic (n=29) and symptomatic (n=37). Carotid plaques were characterised by histology (n=33). Immunohistochemistry (n=17) was used to determine expression of PAPP-A and CD68 within the plaques. Serum levels of PAPP-A were measured by the enzyme-linked immunosorbent assay (ELISA). RESULTS: Circulating PAPP-A levels were significantly higher in patients with unstable versus stable plaques (0.10+/-0.06 vs. 0.07+/-0.04 microg ml(-1), p=0.047) and interestingly, in asymptomatic versus symptomatic patients (0.11+/-0.05 vs. 0.069+/-0.09 microg ml(-1), p=0.025). These differences remained statistically significant after adjustment for age, gender and degree of stenosis (p=0.050). PAPP-A expression in plaques correlated significantly with CD68 positive macrophages, cap-thickness and its serological values (r=+0.291, p<0.001, r=-0.639, p<0.001 and r=0.618, p<0.008, respectively). Furthermore, PAPP-A serum values demonstrated a significant positive predictive value of 68.8% for unstable plaques. CONCLUSION: Our present data confirmed the close relationship between expression of PAPP-A and plaque instability and furthermore correlated significantly with cap thickness. However, the question whether PAPP-A is a useful predictive marker of plaque instability remains unresolved.
Journal title abbreviation:
Eur J Vasc Endovasc Surg
Year:
2010
Journal volume:
39
Journal issue:
6
Pages contribution:
668-75
Language:
eng
Fulltext / DOI:
doi:10.1016/j.ejvs.2010.03.012
Pubmed ID:
http://view.ncbi.nlm.nih.gov/pubmed/20399126
Print-ISSN:
1078-5884
TUM Institution:
Fachgebiet Gefäßchirurgie (Prof. Eckstein); Institut für Allgemeine Pathologie und Pathologische Anatomie; Neurologische Klinik und Poliklinik
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