TY - JOUR
T1 - Endothelial function predicts 1-year adverse clinical outcome in patients hospitalized in the emergency department chest pain unit
AU - Shechter, Michael
AU - Matetzky, Shlomi
AU - Prasad, Megha
AU - Goitein, Orly
AU - Goldkorn, Ronen
AU - Naroditsky, Michael
AU - Koren-Morag, Nira
AU - Lerman, Amir
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2017/8/1
Y1 - 2017/8/1
N2 - Background Endothelial function is a marker for cardiovascular risk. Thus, abnormal endothelial function may be associated with adverse 1-year outcome in patients presenting to the emergency department chest pain unit (CPU). Methods Following endothelial function testing, using EndoPAT 2000 in 300 consecutive subjects with chest pain and no history of coronary artery disease (CAD) presenting to CPU, patients underwent coronary computerized tomographic angiography (CCTA) or single-photon emission computed tomography according to availability. Results Mean 10-year Framingham risk score (FRS) was 6.6 ± 5.9%, median reactive hyperemia index (RHI) as a measure of endothelial function 2.08 and mean was 2.0 ± 0.4. During a 1-year follow-up, the 20 (6.6%) patients who developed major adverse cardiovascular end-points (MACE), including all-cause mortality, non-fatal myocardial infarction, hospitalization for heart failure or angina pectoris, stroke, coronary artery bypass grafting and percutaneous coronary interventions, had higher 10-year FRS (10.5 ± 8.2% vs 6.3 ± 5.7%; p < 0.001), lower baseline RHI (1.43 ± 0.41 vs 2.10 ± 0.44; p < 0.001) and a greater extent of coronary atherosclerosis lesions (70% vs 3.9%, p < 0.001) in the CPU CCTA, compared to those without MACE. RHI ≤ the median was associated with higher 1-year MACE (13% vs 0.7%, p < 0.001) compared to RHI > the median. Multivariate analysis demonstrated that RHI ≤ the median is an independent predictor of coronary atherosclerosis lesions in the CPU CCTA (OR 5.98, 95% CI 03.29-10.88; p < 0.001) and 1-year MACE (OR 15.207, 95% CI 2.00-115.33; p < 0.01). Conclusions Our findings suggest that non-invasive endothelial function testing may have clinical utility in triaging patients in the CPU and in predicting 1-year MACE.
AB - Background Endothelial function is a marker for cardiovascular risk. Thus, abnormal endothelial function may be associated with adverse 1-year outcome in patients presenting to the emergency department chest pain unit (CPU). Methods Following endothelial function testing, using EndoPAT 2000 in 300 consecutive subjects with chest pain and no history of coronary artery disease (CAD) presenting to CPU, patients underwent coronary computerized tomographic angiography (CCTA) or single-photon emission computed tomography according to availability. Results Mean 10-year Framingham risk score (FRS) was 6.6 ± 5.9%, median reactive hyperemia index (RHI) as a measure of endothelial function 2.08 and mean was 2.0 ± 0.4. During a 1-year follow-up, the 20 (6.6%) patients who developed major adverse cardiovascular end-points (MACE), including all-cause mortality, non-fatal myocardial infarction, hospitalization for heart failure or angina pectoris, stroke, coronary artery bypass grafting and percutaneous coronary interventions, had higher 10-year FRS (10.5 ± 8.2% vs 6.3 ± 5.7%; p < 0.001), lower baseline RHI (1.43 ± 0.41 vs 2.10 ± 0.44; p < 0.001) and a greater extent of coronary atherosclerosis lesions (70% vs 3.9%, p < 0.001) in the CPU CCTA, compared to those without MACE. RHI ≤ the median was associated with higher 1-year MACE (13% vs 0.7%, p < 0.001) compared to RHI > the median. Multivariate analysis demonstrated that RHI ≤ the median is an independent predictor of coronary atherosclerosis lesions in the CPU CCTA (OR 5.98, 95% CI 03.29-10.88; p < 0.001) and 1-year MACE (OR 15.207, 95% CI 2.00-115.33; p < 0.01). Conclusions Our findings suggest that non-invasive endothelial function testing may have clinical utility in triaging patients in the CPU and in predicting 1-year MACE.
KW - Atherosclerosis
KW - Coronary artery disease
KW - Endothelial function
KW - Prognosis
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U2 - 10.1016/j.ijcard.2017.04.101
DO - 10.1016/j.ijcard.2017.04.101
M3 - Article
C2 - 28477961
AN - SCOPUS:85018957882
SN - 0167-5273
VL - 240
SP - 14
EP - 19
JO - International Journal of Cardiology
JF - International Journal of Cardiology
ER -