The aim of this study was to explore the chronergy of intravenous recombinant streptokinase (r-SK) in patients with acute myocardial infarction (AMI). A total of 114 patients were divided into two groups according to the time of AMI onset: the morning onset (6:01–12:00, n=53) and non-morning onset (12:01–06:00, n=61) groups. The recanalization rate was recorded, as well as anticoagulant and fibrinolytic indices. Statistical analysis was performed to evaluate the recanalization rate following thrombolysis, as well as the anticoagulant and fibrinolytic activities. The recanalization rates following thrombolysis in the morning onset and non-morning onset groups were 60.4 and 82.0%, respectively (P<0.05). The level of plasminogen activator inhibitor-1 (PAI-1) antigen was significantly higher in the morning onset group compared with that in the non-morning onset group (P<0.05). This indicated a resistance to r-SK thrombolysis in the morning at the early stage of AMI, which possibly correlates with increased PAI-1 antigen levels and activity.
acute myocardial infarctionchronergy of onsetthrombolytic therapymorning resistance to thrombolysisIntroduction
Through more than ten years of extensive studies concerning reperfusion therapy, particularly through stage three clinical trials of thrombolytic therapy for myocardial infarction, it has been identified that coronary artery recanalization plays a crucial role in the prognosis of patients with acute myocardial infarction (AMI). It is well known that AMI onset presents characteristic circadian variations involving a definite morning peak between 6:00 and 12:00 a.m., particularly between 9:00 and 10:00 a.m. (1). One important factor accounting for the high incidence of AMI onset in the morning is the rapid increase in physical and/or mental activities, as well as in blood pressure, in the first few hours after awakening (2–4).
Percutaneous coronary intervention (PCI) and systemic intravenous thrombolytic therapy have been recognized as effective methods for clearing the affected blood vessel. However, the benefit of PCI is less than that of thrombolysis with regard to mortality reduction when the PCI-related time is longer than 62 min (5,6). If the ‘prime time’ of reperfusion is missed, the survival rate drops and recanalizing the affected blood vessel as soon as possible allows for a 25% reduction in the fatality rate (7). As PCI is not available for patients with AMI in a number of hospitals in China, the recanalization rate of systemic intravenous thrombolytic therapy in the treatment of coronary artery disease is extremely low. Along with the comprehensive development of thrombolytic efficacy for AMI, increasing attention has been drawn to a factor that affects thrombolytic efficacy: resistance to thrombolysis in the morning (8–10). Our previous study focused on the chronergy of thrombolytic therapy for AMI, which to date, has been limited to recombinant tissue plasminogen activator (rt-PA) and urokinase (UK). It was identified that the recanalization rate of thrombolysis with streptokinase (SK) is high. However, SK has been utilized as a drug to treat myocardial infarction only since the 1960s (11). Currently, the main SK thrombolytic drugs officially approved worldwide for clinical use include SK and recombinant SK (r-SK). Whether resistance to r-SK intravenous thrombolysis exists in the morning has not yet been reported.
The current study aims to explore whether morning resistance exists in r-SK intravenous thrombolysis in the treatment of AMI and to investigate the related anticoagulant and fibrinolytic indices.
Materials and methodsSubjects
A total of 114 study subjects with AMI were selected from patients at the General Hospital of North China Petroleum Administration affiliated to Hebei Medical University between July 2008 and December 2010. This study was conducted in accordance with the Declaration of Helsinki and with approval from the Ethics Committee of the General Hospital of North China Petroleum Administration affiliated to Hebei Medical University. Written informed consent was obtained from all participants. These subjects accorded with the following conditions: i) diagnostic standard of AMI; ii) thrombolytic therapy within 4 h of AMI onset; iii) exclusion of chronic myocardial infarction, taking aspirin or β-receptor blockers prior to onset, serious lung infection and serious liver disease. The selected patients were divided into two groups according to the time of AMI onset: the morning onset group (6:01–12:00, n=53) with 35 males and 18 females aged 39–80 years, and the non-morning onset group (12:01–06:00, n=61) with 42 males and 19 females aged 36–79 years. There were no statistical differences in gender, history of high blood pressure, history of diabetes or infarction position and heart function (P>0.05).
Recording methods
Symptom onset, duration and start time of thrombolysis in patients were recorded. The thrombolysis was performed according to ‘References of acute myocardial infarction intravenous thrombolytic therapy’ edited by the editorial committee of Cardiovascular Disease magazine in 1996. Briefly, 300 mg aspirin was chewed immediately and 20,000 U/kg 0.9% sodium chloride solution with r-SK solution (Qingdao Guoda Biopharmaceutical Co., Ltd., Qingdao, China) was intravenously administered to the patients within 60 min. An 18-lead electrocardiogram (ECG) was utilized to continuously monitor ECG parameters at 0, 30, 60, 90, 120 min after thrombolysis. Myocardial enzymes and troponin T were measured 6, 12, 14, 16, 24 h after the onset. Two blood samples (each 1.8 ml) were collected from the antecubital vein without tourniquet at 30 and 120 min after thrombolysis, into anticoagulant tubes containing 0.38% citric acid. The blood samples were immediately centrifuged at 3,000 rpm for 20 min and the plasma was stored at −70°C for further detection. Other pharmaceuticals, including nitric acid ester, statins, β-receptor blockers and angiotensin-converting enzyme (ACE) inhibitors were administered to patients with acute myocardial infarction. The standard of coronary artery recanalization (indirect indications 120 min after thrombolysis) was as described in a previous study (12). The anticoagulant activity was evaluated by measuring the antithrombin III (AT III) activity. Fibrinolytic activity was assessed using a dynamic method, that is, by measuring PAI-1 antigen and α2-antiplasmin (α2-APL) antigen levels. Additionally, the PAI-1 dissolubility was detected using a double antibody sandwich enzyme-linked immunosorbent assay (ELISA). Levels of D-dimer (D-D) were quantified using a double antibody sandwich ELISA with monoclonal antibodies.
Statistical analysis
Data were analyzed with SPSS 10.0 software (SPSS Inc., Chicago, IL, USA) and were presented as mean ± standard deviation. The variation of means was assessed by analysis of variance or F-test. Chi-square test was performed using cross-tabulation (RxC) multiple group comparison to analyze the recanalization rate.
ResultsGeneral information
The recanalization rates following thrombolysis in the morning onset and non-morning onset groups were 60.4 (32/53 cases) and 82.0% (50/61 cases), respectively, which were significantly different (P<0.05).
Anticoagulant and fibrinolytic activities prior to thrombolysis
The comparison of anticoagulant and fibrinolytic activities in the two groups prior to thrombolysis is summarized in Table I.
Anticoagulant and fibrinolytic activities following thrombolysis
The comparison of anticoagulant and fibrinolytic activities in the recanalized and non-recanalized patients before and at 30 and 120 min after thrombolysis is shown in Table II. At these three time-points, the PAI-1 antigen level and PAI-1 activity in non-recanalized patients were significantly higher than in recanalized patients, respectively (P<0.01).
Discussion
The aim of our study was to observe whether resistance to r-SK thrombolysis exists in the morning; however, the results of this study are contrary to our expectations. The recanalization rate following r-SK intravenous thrombolysis in the morning onset group was significantly lower than that in the non-morning onset group, which indicates that resistance to r-SK thrombolysis for the treatment of AMI exists in the morning. The level of PAI-1 antigen and its activity is significantly higher in non-recanalized patients than in recanalized patients. In addition, the higher level of PAI-1 antigen and its activity in non-recanalized patients are indicated by i) the differences in anticoagulant and fibrinolytic activities prior to thrombolysis between recanalized and non-recanalized patients and ii) the changes in anticoagulant and fibrinolytic activities that occur after thrombolysis. Thrombolytic therapy should be considered instead of PCI when the patients have a long history of AMI (13–15); however, it is difficult to dissolve thrombi in the coronary artery due to the decreased fibrinolytic activity induced by an increased level of PAI-1. Therefore, the recanalization rate of r-SK may be higher than that of UK at times other than the morning.
Our study reveals a relatively high level of PAI-1 in the morning onset group. When the coronary artery is injured, the release of PA is reduced, while physiological and pathological PAI-1 levels are higher in the morning regardless of the health of the patient. During this period the platelet activity enhances and fibrinolytic activity weakens, which facilitates thrombosis of the coronary artery (16–18). Due to the circadian variation of PAI-1, the thrombolytic efficacy is improved in the afternoon compared with that in the morning and the rhythm of thrombolytic resistance is not related to differences in the thrombolytic preparations. The timely and accurate understanding of AMI chronergy helps to confirm thrombolytic therapy and improve the prognosis following PCI (19). There is no significant difference in heart function between direct PCI and PCI following thrombolytic recanalization (20–22). The thrombolytic time was not consistent with the onset time in a number of cases, which may have affected the results to a certain extent. The optimal solution for AMI patients with a morning onset is to perform PCI or transfer the patients to a tertiary hospital where PCI may be conducted directly.
ReferencesKonoTMoritaHNishinaTCircadian variations of onset of acute myocardial infarction and efficacy of thrombolytic therapyJ Am Coll Cardiol277747781996ParkerJDTestaMAJimenezAHMorning increase in ambulatory ischemia in patients with stable coronary artery disease. Importance of physical activity and increased cardiac demandCirculation896046141994KannelWBRisk stratification in hypertension: new insights from the Framingham studyAm J Hypertens133S10S2000GierachGLJohnsonBDBairey MerzCNHypertension, menopause and coronary artery disease risk in the Women’s Ischemia Syndrome Evaluation (WISE) studyJ Am Coll Cardiol47Suppl 3S50S582006NallamothuBKBatesERPercutaneous coronary intervention versus fibrinolytic therapy in acute myocardial infarction: is timing (almost) everything?Am J Cardiol928248262003BoersmaEMaasACDeckersJWSimoonsMLEarly thrombolytic treatment in acute myocardial infarction: reappraisal of the golden hourLancet2177l7751996AntmanEMAnbeDTArmstrongPWACC/AHA guidelines for the management of patients with ST-elevation myocardial infarction-executive summary. A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to revise the 1999 guidelines for the management of patients with acute myocardial infarction)J Am Coll Cardiol446717192004BeckerRCCorraoJMBakerSPCircadian variation in thrombolytic response to recombinant tissue-type plasminogen activator in acute myocardial infarctionJAPPL Cardiol32132211998BraunwaldEMorning resistance to thrombolytic therapyCirculation91160416061995KurnikPBCircadian variation in the efficacy of tissue-type plasminogen activatorCirculation91134113461995BeldarrainALópez-LaccombaJLKutyshenkoVPSerranoRCortijoMMultidomain structure of a recombinant streptokinase. A differential scanning calorimetry studyJ Protein Chem209172001PolackBSchvedJFBoneuBGroupe d’Etude sur l’Hémostase et la Thrombose (GEHT)Preanalytical recommendations of the ‘Groupe d’Etude sur l’Hemostase et la Thrombose’ (GEHT) for venous blood testing in hemostasis laboratoriesHaemostasis3161682001RosenfeldAGWomen’s risk of decision delay in acute myocardial infarction: implications for research and practiceAACN Clin Issues1229392001HerlitzJWireklintsundströmBBángABerglundASvenssonLBlomstrandCEarly identification and delay to treatment in myocardial infarction and stroke: differences and similaritiesScand J Trauma Resusc Emerg Med18482010ChenWWoodsSLPuntilloKAGender differences in symptoms associated with acute myocardial infarction: a review of the researchHeart Lung342402472005KrantzDSKopWJGabbayFHCircadian variation of ambulatory myocardial ischemia. Triggering by daily activities and evidence for an endogenous circadian componentCirculation93136413711996MullerJEToflerGHCircadian variation and cardiovascular diseaseN Engl J Med325103810391991GuoYFSteinPKCircadian rhythm in the cardiovascular system: chronocardiologyAm Heart J1457797862003TrigoJMimosoJGagoPFemale gender: an independent factor in ST-elevation myocardial infarctionRev Port Cardiol29138313942010CantorWJFitehettDBotgundvaagBRoutine early angioplasty after fibrinolysis for acute myocardial infarctionN Engl J Med360270527182009YanATYonRTCantorWJRelationship between risk stratification at admission and treatment effects of early invasive management following fibrinolysis: insights from the trial of routine angioplasty and stenting after fibrinolysis to enhance reperfusion in acute myocardial infarction (TRANSFER-AMI)Eur Heart J32199420022011ArmstrongPWWEST Steering CommitteeA comparison of pharmacologic therapy with/without timely coronary intervention vs. primary percutaneous intervention early after ST-elevation myocardial infarction: the WEST (Which Early ST-elevation myocardial infarction Therapy) studyEur Heart J27153015382006Tables
Comparison of anticoagulant fibrinolytic activity in the two groups prior to thrombolysis.
Testing index
Morning onset group (n=53)
Non-morning onset group (n=61)
AT-III activity (%)
93.64±12.22
93.89±11.91
PAI-1 antigen (μg/l)
39.73±4.63a
37.31±4.61
PAI-1 activity (AU/ml)
17.08±3.59
17.16±3.57
α2-APL antigen (μg/l)
90.28±15.30
90.30±14.72
D-D (mg/l)
0.25±0.13
0.25±0.10
Data are presented as mean ± standard deviation.
P<0.05, compared with the non-morning onset group. AT-III, antithrombin III; PAI-1, plasminogen activator inhibitor 1; APL, antiplasmin; D-D, D-dimer.
Comparison of anticoagulant fibrinolytic activity in the recanalized and non-recanalized patients before and at 30 and 120 min after thrombolysis.