Angiopoietin-2 and angiopoietin-like 4 protein provide prognostic information in patients with suspected acute coronary syndrome

被引:8
作者
Aarsetoy, Reidun [1 ,2 ]
Ueland, Thor [3 ]
Aukrust, Pal [3 ,4 ]
Michelsen, Annika E. [3 ]
de la Fuente, Ricardo Leon [5 ]
Ponitz, Volker [1 ]
Brugger-Andersen, Trygve [1 ]
Grundt, Heidi [2 ,6 ]
Staines, Harry [7 ]
Nilsen, Dennis W. T. [1 ,2 ]
机构
[1] Stavanger Univ Hosp, Dept Cardiol, POB 8100, N-4068 Stavanger, Norway
[2] Univ Bergen, Dept Clin Sci, Bergen, Norway
[3] Oslo Univ Hosp, Res Inst Internal Med, Rikshosp, Oslo, Norway
[4] Oslo Univ Hosp, Sect Clin Immunol & Infect Dis, Rikshosp, Oslo, Norway
[5] Ctr Cardiovasc Salta, Salta, Argentina
[6] Stavanger Univ Hosp, Dept Resp Med, Stavanger, Norway
[7] Sigma Stat Serv, Balmullo, Scotland
关键词
acute coronary syndrome; all-cause mortality; angiopoietin-2; angiopoietin-like; 4; protein; prognostic biomarkers; cardiac death; SOLUBLE RECEPTOR TIE-2; CARDIOVASCULAR MORTALITY; ANGPTL4; DISEASE; RISK; ANGIOGENESIS; BIOMARKER; EVENTS;
D O I
10.1111/joim.13339
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Plasma levels of angiopoietin-2 (ANGPT2) and angiopoietin-like 4 protein (ANGPTL4) reflect different pathophysiological aspects of cardiovascular disease. We evaluated their association with outcome in a hospitalized Norwegian patient cohort (n = 871) with suspected acute coronary syndrome (ACS) and validated our results in a similar Argentinean cohort (n = 982). Methods A cox regression model, adjusting for traditional cardiovascular risk factors, was fitted for ANGPT2 and ANGPTL4, respectively, with all-cause mortality and cardiac death within 24 months and all-cause mortality within 60 months as the dependent variables. Results At 24 months follow-up, 138 (15.8%) of the Norwegian and 119 (12.1%) of the Argentinian cohort had died, of which 86 and 66 deaths, respectively, were classified as cardiac. At 60 months, a total of 259 (29.7%) and 173 (17.6%) patients, respectively, had died. ANGPT2 was independently associated with all-cause mortality in both cohorts at 24 months [hazard ratio (HR) 1.27 (95% confidence interval (CI), 1.08-1.50) for Norway, and HR 1.57 (95% CI, 1.27-1.95) for Argentina], with similar results at 60 months [HR 1.19 (95% CI, 1.05-1.35) (Norway), and HR 1.56 (95% CI, 1.30-1.88) (Argentina)], and was also significantly associated with cardiac death [HR 1.51 (95% CI, 1.14-2.00)], in the Argentinean population. ANGPTL4 was significantly associated with all-cause mortality in the Argentinean cohort at 24 months [HR 1.39 (95% CI, 1.15-1.68)] and at 60 months [HR 1.43 (95% CI, 1.23-1.67)], enforcing trends in the Norwegian population. Conclusions ANGPT2 and ANGPTL4 were significantly associated with outcome in similar ACS patient cohorts recruited on two continents. Clinical Trial Registration ClinicalTrials.gov Identifier: NCT00521976. ClinicalTrials.gov Identifier: NCT01377402.
引用
收藏
页码:894 / 909
页数:16
相关论文
共 34 条
[1]   Rationale and design of the GRACE (Global Registry of Acute Coronary Events) Project:: A multinational registry of patients hospitalized with acute coronary syndromes [J].
Agnelli, G ;
Avezum, A ;
Brieger, D ;
Budaj, A ;
Cannon, CP ;
Goldberg, RJ ;
Goodman, S ;
Gulba, DC ;
Granger, C ;
Kennelly, BM ;
Gurfinkel, E ;
López-Sendón, J ;
Klein, W ;
Montalescot, G ;
Van de Werf, F .
AMERICAN HEART JOURNAL, 2001, 141 (02) :190-199
[2]   Control of vascular morphogenesis and homeostasis through the angiopoietin-Tie system [J].
Augustin, Hellmut G. ;
Koh, Gou Young ;
Thurston, Gavin ;
Alitalo, Kari .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (03) :165-177
[3]   B-type natriuretic peptide is a long-term predictor of all-cause mortality, whereas high-sensitive C-reactive protein predicts recurrent short-term troponin T positive cardiac events in chest pain patients: a prognostic study [J].
Brugger-Andersen, Trygve ;
Poenitz, Volker ;
Staines, Harry ;
Pritchard, David ;
Grundt, Heidi ;
Nilsen, Dennis W. T. .
BMC CARDIOVASCULAR DISORDERS, 2008, 8 (1)
[4]   Inactivating Variants in ANGPTL4 and Risk of Coronary Artery Disease [J].
Dewey, Frederick F. ;
Gusarova, Viktoria ;
O'Dushlaine, Colm ;
Gottesman, Omri ;
Trejos, Jesus ;
Hunt, Charleen ;
Van Hout, Cristopher V. ;
Habegger, Lukas ;
Buckler, David ;
Lai, Ka-Man V. ;
Leader, Joseph B. ;
Murray, Michael F. ;
Ritchie, Marylyn D. ;
Kirchner, H. Lester ;
Ledbetter, David H. ;
Penn, John ;
Lopez, Alexander ;
Borecki, Ingrid B. ;
Overton, John D. ;
Reid, Jeffrey G. ;
Carey, David J. ;
Murphy, Andrew J. ;
Yancopoulos, George D. ;
Baras, Aris ;
Gromada, Jesper ;
Shuldiner, Alan R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 374 (12) :1123-1133
[5]   Regulation of lipoprotein lipase by AngptI4 [J].
Dijk, Wieneke ;
Kersten, Sander .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2014, 25 (03) :146-155
[6]   Angiopoietin-Tie signalling in the cardiovascular and lymphatic systems [J].
Eklund, Lauri ;
Kangas, Jaakko ;
Saharinen, Pipsa .
CLINICAL SCIENCE, 2017, 131 (01) :87-103
[7]   Angiopoietin signaling in the vasculature [J].
Eklund, Lauri ;
Saharinen, Pipsa .
EXPERIMENTAL CELL RESEARCH, 2013, 319 (09) :1271-1280
[8]   Prognostic value of angiopoietin-2 in patients with chronic heart failure [J].
Eleuteri, Ermanno ;
Di Stefano, Antonino ;
Giordano, Andrea ;
Corra, Ugo ;
Genta, Franco Tarro ;
Gnemmi, Isabella ;
Giannuzzi, Pantaleo .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2016, 212 :364-368
[9]   Development and Validation of a Protein-Based Risk Score for Cardiovascular Outcomes Among Patients With Stable Coronary Heart Disease [J].
Ganz, Peter ;
Heidecker, Bettina ;
Hveem, Kristian ;
Jonasson, Christian ;
Kato, Shintaro ;
Segal, Mark R. ;
Sterling, David G. ;
Williams, Stephen A. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2016, 315 (23) :2532-2541
[10]  
Goenka L, 2017, THER ADV CARDIO DIS, V11, P261, DOI 10.1177/1753944717723311