Literature DB >> 11018189

Prognostic value of plasma levels of secretory type II phospholipase A2 in patients with unstable angina pectoris.

K Kugiyama1, Y Ota, S Sugiyama, H Kawano, H Doi, H Soejima, S Miyamoto, H Ogawa, K Takazoe, H Yasue.   

Abstract

Plasma levels of secretory nonpancreatic type II phospholipase A2 (sPLA2) are increased in various chronic inflammatory diseases; this increase is correlated with disease severity. sPLA2 plays a possible role in atherogenesis and is highly expressed in atheromatous plaques. Thus, this study prospectively examined whether plasma levels of sPLA2 may have a prognostic value in patients with unstable angina, which is known to have inflammatory features. Plasma levels of sPLA2 were measured in 52 patients with unstable angina, in 107 patients with stable angina, and in 96 control subjects by radioimmunoassay. sPLA2 levels were significantly higher in patients with unstable angina than in those with stable angina and in control subjects. sPLA2 remained elevated after stabilization of disease. The levels were not increased in the blood in the coronary sinus. Kaplan-Meier analysis demonstrated that patients with unstable angina and with the higher sPLA2 levels had a significantly higher probability of developing clinical coronary events during a follow-up period of 2 years compared with those with the lower levels. In multivariate Cox hazard analysis, the higher levels of sPLA2 were a significant predictor of developing coronary events in patients with unstable angina, independent of other risk factors, including C-reactive protein levels, an established inflammatory predictor. In conclusion, the increase in circulating levels of sPLA2 predicts clinical coronary events independently of other risk factors in patients with unstable angina. sPLA2 levels were persistently elevated but the elevated levels may not be derived from coronary circulation.

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Year:  2000        PMID: 11018189     DOI: 10.1016/s0002-9149(00)01069-9

Source DB:  PubMed          Journal:  Am J Cardiol        ISSN: 0002-9149            Impact factor:   2.778


  19 in total

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2.  Group IIA Secretory Phospholipase A2, Vascular Inflammation, and Incident Cardiovascular Disease.

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3.  Phospholipase A2 group IIA expression in gastric adenocarcinoma is associated with prolonged survival and less frequent metastasis.

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Journal:  Proc Natl Acad Sci U S A       Date:  2002-11-27       Impact factor: 11.205

Review 4.  Biomarkers of plaque instability.

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6.  Novel genetic approach to investigate the role of plasma secretory phospholipase A2 (sPLA2)-V isoenzyme in coronary heart disease: modified Mendelian randomization analysis using PLA2G5 expression levels.

Authors:  Michael V Holmes; Holly J Exeter; Lasse Folkersen; Christopher P Nelson; Montse Guardiola; Jackie A Cooper; Reecha Sofat; S Matthijs Boekholdt; Kay-Tee Khaw; Ka-Wah Li; Andrew J P Smith; Ferdinand Van't Hooft; Per Eriksson; Anders Franco-Cereceda; Folkert W Asselbergs; Jolanda M A Boer; N Charlotte Onland-Moret; Marten Hofker; Jeanette Erdmann; Mika Kivimaki; Meena Kumari; Alex P Reiner; Brendan J Keating; Steve E Humphries; Aroon D Hingorani; Ziad Mallat; Nilesh J Samani; Philippa J Talmud
Journal:  Circ Cardiovasc Genet       Date:  2014-02-21

7.  Secretory Phospholipase A2 Is Associated with the Odds of Acute Coronary Syndromes through Elevation of Serum Amyloid-A Protein.

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Journal:  Int J Angiol       Date:  2013-03

8.  Secretory phospholipase A2 in patients with coronary artery disease.

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Journal:  J Thromb Thrombolysis       Date:  2009-05-17       Impact factor: 2.300

9.  Generation in human plasma of misfolded, aggregation-prone electronegative low density lipoprotein.

Authors:  Giulia Greco; Gabor Balogh; Roberto Brunelli; Graziella Costa; Marco De Spirito; Laura Lenzi; Giampiero Mei; Fulvio Ursini; Tiziana Parasassi
Journal:  Biophys J       Date:  2009-07-22       Impact factor: 4.033

10.  Increased type IIA secretory phospholipase A(2) expression contributes to oxidative stress in end-stage renal disease.

Authors:  Markus van der Giet; Markus Tölle; Domenico Pratico; Volkmar Lufft; Mirjam Schuchardt; Matthias P Hörl; Walter Zidek; Uwe J F Tietge
Journal:  J Mol Med (Berl)       Date:  2009-10-02       Impact factor: 4.599

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