Myocardial Flow Reserve, an Independent Prognostic Marker of All-Cause Mortality Assessed by 82Rb PET Myocardial Perfusion Imaging: A Danish Multicenter Study

被引:6
|
作者
Hojstrup, Signe [1 ,2 ,4 ]
Hansen, Kim W. [2 ,4 ]
Talleruphuus, Ulrik [3 ,5 ]
Marner, Lisbeth [3 ,5 ]
Bjerking, Louise [2 ]
Jakobsen, Lars [6 ]
Christiansen, Evald H. [6 ]
Bouchelouche, Kirsten [7 ,8 ]
Wiinberg, Niels [3 ,5 ]
Guldbrandsen, Kasper [3 ,5 ,9 ]
Galatius, Soren [2 ,4 ]
Prescott, Eva [2 ,4 ]
机构
[1] Copenhagen Univ Hosp, Dept Cardiol, Bispebjerg & Frederiksberg, Nordre Fasanvej 57, Vej 4, 3, DK-2000 Frederiksberg, Denmark
[2] Copenhagen Univ Hosp, Dept Cardiol, Bispebjerg, Denmark
[3] Copenhagen Univ Hosp, Dept Clin Physiol & Nucl Med, Bispebjerg, Denmark
[4] Copenhagen Univ Hosp, Dept Cardiol, Frederiksberg, Denmark
[5] Copenhagen Univ Hosp, Dept Clin Physiol & Nucl Med, Frederiksberg, Denmark
[6] Aarhus Univ Hosp, Dept Cardiol, Aarhus, Denmark
[7] Aarhus Univ Hosp, Dept Nucl Med, Aarhus, Denmark
[8] Aarhus Univ Hosp, PET Ctr, Aarhus, Denmark
[9] Rigshosp, Copenhagen Univ Hosp, Dept Clin Physiol Nucl Med & PET, Copenhagen, Denmark
关键词
coronary circulation; microcirculation; myocardial perfusion imaging; positron-emission tomography; Rubidium-82; survival; POSITRON-EMISSION-TOMOGRAPHY; CORONARY-ARTERY-DISEASE; BLOOD-FLOW; MICROVASCULAR DYSFUNCTION; REPRODUCIBILITY; QUANTIFICATION; ACCURACY;
D O I
10.1161/CIRCIMAGING.122.015184
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND:Rubidium-82 positron emission tomography (Rb-82 PET) myocardial perfusion imaging is used in clinical practice to quantify regional perfusion defects. Additionally, Rb-82 PET provides a measure of absolute myocardial flow reserve (MFR), describing the vasculature state of health. We assessed whether Rb-82 PET-derived MFR is associated with all-cause mortality independently of the extent of perfusion defects. METHODS:We conducted a multicenter clinical registry-based study of patients undergoing Rb-82 PET myocardial perfusion imaging on suspicion of chronic coronary syndromes. Patients were followed up in national registries for the primary outcome of all-cause mortality. Global MFR & LE;2 was considered reduced. RESULTS:Among 7169 patients studied, 38.1% were women, the median age was 69 (IQR, 61-76) years, and 39.0% had MFR & LE;2. A total of 667 (9.3%) patients died during a median follow-up of 3.1 (IQR, 2.6-4.0) years, more in patients with MFR & LE;2 versus MFR >2 (15.7% versus 5.2%; P<0.001). MFR & LE;2 was associated with all-cause mortality across subgroups defined by the extent of perfusion defects (all P<0.05). In a Cox survival regression model adjusting for sex, age, comorbidities, kidney function, left ventricular ejection fraction, and perfusion defects, MFR & LE;2 was a robust predictor of mortality with a hazard ratio of 1.62 (95% CI, 1.31-2.02; P<0.001). Among patients with no reversible perfusion defects (n=3101), MFR & LE;2 remained strongly associated with mortality (hazard ratio, 1.86 [95% CI, 1.26-2.73]; P<0.01). The prognostic value of impaired MFR was similar for cardiac and noncardiac death. CONCLUSIONS:MFR & LE;2 predicts all-cause mortality independently of the extent of perfusion defects. Our results support the inclusion of MFR when assessing the prognosis of patients suspected of chronic coronary syndromes.
引用
收藏
页码:645 / 654
页数:10
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