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Status: Bibliographieeintrag

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Verfasst von:Stamatelopoulos, Kimon [VerfasserIn]   i
 Müller-Hennessen, Matthias [VerfasserIn]   i
 Georgiopoulos, Georgios [VerfasserIn]   i
 Sachse, Marco [VerfasserIn]   i
 Boeddinghaus, Jasper [VerfasserIn]   i
 Sopova, Kateryna [VerfasserIn]   i
 Gatsiou, Aikaterini [VerfasserIn]   i
 Amrhein, Carolin [VerfasserIn]   i
 Biener, Moritz [VerfasserIn]   i
 Vafaie, Mehrshad [VerfasserIn]   i
 Athanasouli, Fani [VerfasserIn]   i
 Stakos, Dimitrios [VerfasserIn]   i
 Pateras, Konstantinos [VerfasserIn]   i
 Twerenbold, Raphael [VerfasserIn]   i
 Badertscher, Patrick [VerfasserIn]   i
 Nestelberger, Thomas [VerfasserIn]   i
 Dimmeler, Stefanie [VerfasserIn]   i
 Katus, Hugo [VerfasserIn]   i
 Zeiher, Andreas M. [VerfasserIn]   i
 Mueller, Christian [VerfasserIn]   i
 Giannitsis, Evangelos [VerfasserIn]   i
 Stellos, Konstantinos [VerfasserIn]   i
Titel:Amyloid-β (1-40) and mortality in patients with non-ST-segment elevation acute coronary syndrome
Titelzusatz:a cohort study
Verf.angabe:Kimon Stamatelopoulos, Matthias Mueller-Hennessen, Georgios Georgiopoulos, Marco Sachse, Jasper Boeddinghaus, Kateryna Sopova, Aikaterini Gatsiou, Carolin Amrhein, Moritz Biener, Mehrshad Vafaie, Fani Athanasouli, Dimitrios Stakos, Konstantinos Pateras, Raphael Twerenbold, Patrick Badertscher, Thomas Nestelberger, Stefanie Dimmeler, Hugo A. Katus, Andreas M. Zeiher, Christian Mueller, Evangelos Giannitsis and Konstantinos Stellos
E-Jahr:2018
Jahr:19 June 2018
Umfang:11 S.
Fussnoten:Gesehen am 08.04.2020
Titel Quelle:Enthalten in: Annals of internal medicine
Ort Quelle:Philadelphia, Pa. : Coll., 1927
Jahr Quelle:2018
Band/Heft Quelle:168(2018), 12, Seite 855-865
ISSN Quelle:1539-3704
Abstract:Background: Amyloid-β (1-40) (Aβ40) is implicated in mechanisms related to plaque destabilization and correlates with adverse outcomes in stable coronary artery disease. - Objective: To determine the prognostic and reclassification value of baseline circulating levels of Aβ40 after adjustment for the Global Registry of Acute Coronary Events (GRACE) score, which is widely recommended for risk stratification in non-ST-segment elevation acute coronary syndrome (NSTE-ACS). - Design: Retrospective cohort study using data from 2 independent prospective cohorts, the Heidelberg study (n = 1145) and the validation multicenter international APACE (Advantageous Predictors of Acute Coronary Syndrome Evaluation) study (n = 734). - Setting: Academic hospitals in 7 European countries. - Participants: Patients with adjudicated NSTE-ACS followed for a median of 21.9 and 24.9 months in the Heidelberg and APACE studies, respectively. - Measurements: All-cause mortality was the primary end point. - Results: Amyloid-β (1-40) was associated with mortality after multivariate adjustment for age, sex, diabetes mellitus, high-sensitivity cardiac troponin T and C-reactive protein, revascularization, and ACS type (Heidelberg cohort hazard ratio [HR] for 80th vs. 20th percentiles, 1.66 [95% CI, 1.06 to 2.61; P = 0.026]; APACE cohort HR, 1.50 [CI, 1.15 to 1.96; P = 0.003]). It was also associated with mortality after adjustment for the GRACE score (Heidelberg cohort HR for 80th vs. 20th percentiles, 1.11 [CI, 1.04 to 1.18; P = 0.001]; APACE cohort HR, 1.39 [CI, 1.02 to 1.88; P = 0.036]). Amyloid-β (1-40) correctly reclassified risk for death over the GRACE score (net reclassification index, 33.4% and 47.1% for the Heidelberg and APACE cohorts, respectively) (P < 0.05). - Limitation: At low concentrations of Aβ40, dose-response associations with mortality differed between cohorts, possibly because of varying blood preparations used to measure Aβ40. - Conclusion: Circulating Aβ40 is a predictor of mortality and improves risk stratification of patients with NSTE-ACS over the GRACE score recommended by clinical guidelines. The clinical application of Aβ40 as a novel biomarker in NSTE-ACS should be further explored and validated. - Primary Funding Source: German Cardiac Society.
DOI:doi:10.7326/M17-1540
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.7326/M17-1540
 Volltext: https://annals.org/aim/article-abstract/2681795
 DOI: https://doi.org/10.7326/M17-1540
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Acute Coronary Syndrome
 Aged
 Amyloid beta-Peptides
 Biomarkers
 Female
 Humans
 Male
 Peptide Fragments
 Prognosis
 Retrospective Studies
 Risk Factors
K10plus-PPN:169424816X
Verknüpfungen:→ Zeitschrift

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