IgM-phosphorylcholine autoantibodies and outcome in acute coronary syndromes

被引:35
作者
Caidahl, Kenneth [1 ,5 ,7 ]
Hartford, Marianne [8 ]
Karlsson, Thomas [8 ]
Herlitz, Johan [9 ]
Pettersson, Knut [6 ]
de Faire, Ulf [2 ,4 ]
Frostegard, Johan [3 ]
机构
[1] Karolinska Inst, Dept Mol Med & Surg, Stockholm, Sweden
[2] Karolinska Inst, Div Cardiovasc Epidemiol, IMM, Stockholm, Sweden
[3] Karolinska Inst, Inst Environm Med, Unit Immunol & Chron Dis, S-10401 Stockholm, Sweden
[4] Karolinska Univ Hosp Stockholm, Dept Cardiol, Stockholm, Sweden
[5] Karolinska Univ Hosp Stockholm, Dept Clin Physiol, Stockholm, Sweden
[6] Athera Biotechnol, Solna, Sweden
[7] Sahlgrens Univ Hosp, Dept Clin Physiol, Gothenburg, Sweden
[8] Sahlgrens Univ Hosp, Dept Mol & Clin Med, Gothenburg, Sweden
[9] Univ Boras, Ctr Prehosp Res Western Sweden, Boras, Sweden
基金
瑞典研究理事会;
关键词
Angina; Antibodies; Immune system; Myocardial infarction; Prognosis; SECRETORY PHOSPHOLIPASE A(2); OXIDATION-SPECIFIC EPITOPES; C-REACTIVE PROTEIN; INTERCELLULAR-ADHESION MOLECULE-1; OXIDIZED LDL; NATURAL ANTIBODIES; PROTECTIVE FACTORS; APOPTOTIC CELLS; T15; IDIOTYPE; GROUP IIA;
D O I
10.1016/j.ijcard.2012.01.018
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Antibodies against proinflammatory phosphorylcholine (anti-PC) seem to be protective and reduce morbidity. We sought to determine whether low levels of immunoglobulin-M (IgM) autoantibodies against PC add prognostic information in acute coronary syndromes (ACS). Methods: IgM anti-PC titers were measured in serum obtained within 24 h of admission from 1185 ACS patients (median age 66 years, 30% women). We evaluated major acute cardiovascular events (MACE) and all-cause mortality short- (6 months), intermediate- (18 months) and long- (72 months) terms. Results: Low anti-PC titers were associated with MACE and all-cause mortality at all follow-up times. After adjusting for clinical variables, plasma troponin-I, proBNP and CRP levels, associations remained at all times with MACE, short and intermediate terms also with all-cause mortality. With anti-PC titers below median, adjusted hazard ratios at 18 months were for MACE 1.79 (95% confidence interval [CI]: 1.31 to 2.44; p=0.0002) and for all-cause mortality 2.28 (95% CI: 1.32 to 3.92; p=0.003). Anti-PC and plasma CRP were unrelated and added to risk prediction. Conclusions: Serum IgM anti-PC titers provide prognostic information above traditional risk factors in ACS. The ease of measurement and potential therapeutic perspective indicate that it may be a valuable novel biomarker in ACS. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:464 / 469
页数:6
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