4.7 Article

Myocardial reperfusion reverses the J-curve association of cardiovascular risk and diastolic blood pressure in patients with left ventricular dysfunction and heart failure after myocardial infarction: insights from the EPHESUS trial

期刊

EUROPEAN HEART JOURNAL
卷 41, 期 17, 页码 1673-1683

出版社

OXFORD UNIV PRESS
DOI: 10.1093/eurheartj/ehaa132

关键词

Acute myocardial infarction; Heart failure; Systolic blood pressure; Diastolic blood pressure; J-curve; Blood pressure risk association; Coronary perfusion

资金

  1. Deutsche Forschungsgemeinschaft (DFG) [TTR 219, S-01, M-03, M-05]
  2. French National Research Agency Fighting Heart Failure [ANR-15-RHU-0004]
  3. French PIA project <> GEENAGE [ANR-15-IDEX-04-LUE]
  4. Contrat de Plan Etat Region Lorraine
  5. Pfizer
  6. FEDER IT2MP

向作者/读者索取更多资源

Aims The described association of low diastolic blood pressure (DBP) with increased cardiovascular outcomes could be due to reduced coronary perfusion or is simply due to reverse causation. If DBP is physiologically relevant, coronary reperfusion after myocardial infarction (MI) might influence DBP risk association. Methods and results The relation of achieved DBP with cardiovascular death or cardiovascular hospitalization, cardiovascular death, and all-cause death was explored in 5929 patients after acute myocardial infarction (AMI) with impaired left ventricular function, signs and symptoms of heart failure, or diabetes in the EPHESUS trial according to their reperfusion status. Cox regression models were used to assess the impact of reperfusion status on the association of DBP and systolic blood pressure (SBP) with outcomes in an adjusted fashion. In patients without reperfusion, tower DBP <70 mmHg was associated with increased risk for all-cause death [adjusted hazard ratios (HRs) 1.80, 95% confidence interval (CI) 1.41-2.30; P < 0.001], cardiovascular death (HR 1.70, 95% CI 1.3-3.22; P<0.001), cardiovascular death or cardiovascular hospitalization (HR 1.54, 95% CI 126-1.87; P < 0.001). In patients with reperfusion, the risk increase at low DBP was not observed. At low SBP, risk increased independently of reperfusion. A sensitivity analysis in the subgroup of patients with optimal SBP of 120-130 mmHg showed again risk reduction of reperfusion at low DBP. Adding the treatment allocation to eplerenone or placebo into the models had no effects on the results. Conclusion Patients after AMIs with a low DBP had an increased risk, which was sensitive to reperfusion therapy. Low blood pressure after MI identifies in patients with particular higher risk. These data support the hypothesis that low DBP in patients with stenotic coronary lesions is associated with risk, potentially involving coronary perfusion pressure and the recommendations provided by guidelines suggesting lower DBP boundaries for these high-risk patients.

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