SuPAR predicts postoperative complications and mortality in patients with asymptomatic aortic stenosis
Hodges, Gethin W; Bang, Casper N; Eugen-Olsen, Jesper; Olsen, Michael H; Boman, Kurt; Ray, Simon; Kesäniemi, Antero Y; Jeppesen, Jørgen L; Wachtell, Kristian (2018-01-13)
Hodges GW, Bang CN, Eugen-Olsen J, et al SuPAR predicts postoperative complications and mortality in patients with asymptomatic aortic stenosis Open Heart 2018;5:e000743. doi: 10.1136/openhrt-2017-000743
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https://urn.fi/URN:NBN:fi-fe2018042518491
Tiivistelmä
Abstract
Background: We evaluated whether early measurement of soluble urokinase plasminogen activator receptor (suPAR) could predict future risk of postoperative complications in initially asymptomatic patients with mild-moderate aortic stenosis (AS) undergoing aortic valve replacement (AVR) surgery.
Methods: aseline plasma suPAR levels were available in 411 patients who underwent AVR surgery during follow-up in the Simvastatin and Ezetimibe in Aortic Stenosis (SEAS) study. Cox analyses were used to evaluate suPAR in relation to all-cause mortality and the composite endpoint of postoperative complications (all-cause mortality, congestive heart failure, stroke and renal impairment) occurring in the 30-day postoperative period.
Results: Patients with initially higher levels of suPAR were at increased risk of postoperative mortality with a HR of 3.5 (95% CI 1.4 to 9.0, P=0.008) and postoperative complications with a HR of 2.7 (95% CI 1.5 to 5.1, P=0.002), per doubling in suPAR. After adjusting for the European System for Cardiac Operative Risk Evaluation or Society of Thoracic Surgeons risk score, suPAR remained associated with postoperative mortality with a HR 3.2 (95% CI 1.2 to 8.6, P=0.025) and 2.7 (95% CI 1.0 to 7.8, P=0.061); and postoperative complications with a HR of 2.5 (95% CI 1.3 to 5.0, P=0.007) and 2.4 (95% CI 1.2 to 4.8, P=0.011), respectively.
Conclusions: Higher baseline suPAR levels are associated with an increased risk for postoperative complications and mortality in patients with mild-moderate, asymptomatic AS undergoing later AVR surgery. Further validation in other subsets of AS individuals are warranted.
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