PMID- 34481261 OWN - NLM STAT- MEDLINE DCOM- 20211228 LR - 20211228 IS - 1532-8171 (Electronic) IS - 0735-6757 (Linking) VI - 50 DP - 2021 Dec TI - The additive value of copeptin for early diagnosis and prognosis of acute coronary syndromes. PG - 413-421 LID - S0735-6757(21)00709-9 [pii] LID - 10.1016/j.ajem.2021.08.069 [doi] AB - BACKGROUND: One promising biomarker that has received substantial interest for the evaluation of suspected acute coronary syndromes (ACS) is copeptin. Therefore, our goal was to assess the additive value of copeptin for early diagnosis and prognosis of Non-ST segment acute coronary syndromes (NSTE-ACS). METHODS: The study included ninety patients with suspected ACS. Patients with typical ischemic chest pain within six hours of symptom onset and without ST-segment elevation on electrocardiograph (ECG) were included. In addition to cardiac troponin I (cTnI), copeptin was assayed from venous blood samples obtained on admission, followed by serial troponin measurements six and twelve hours later. One year follow-up was performed for any major adverse cardiac events (MACEs) including cardiac death, re-infarction, re- hospitalization for ischemic events, heart failure, stroke and target lesion revascularization (TLR). RESULTS: Of seventy nine patients included in the final analysis, Forty (50.6%) were diagnosed as unstable angina (UA), while thirty nine (49.4%) had a non-ST elevation myocardial infarction (NSTEMI). Copeptin level on admission was significantly higher among NSTEMI patients than those with UA. With regard to the correlation analyses, copeptin was positively correlated with each of, Global Registry of Acute Coronary Events (GRACE), Thrombolysis In Myocardial Infarction (TIMI) and synergy between percutaneous coronary intervention with taxus and cardiac surgery (SYNTAX) scores. The sensitivity and negative predictive value (NPV) of the combination of admission copeptin and cTn-I were 100% and 100%, respectively, versus 57% and 70%, respectively, with admission of cTn-I alone. The area under curve (AUC) of the combination of copeptin and cTn-I was (0.975, p < 0.001) and was significantly higher than the AUC of cTn-I alone (0.888, p < 0.001). Admission copeptin was an independent predictor for MACEs by multiple regression analysis (OR: 0.01, 95% CI: 0.0-0.8, P = 0.04). High values of copeptin had the highest rate of MACEs and coronary revascularization during one year of follow up. CONCLUSION: The combination of copeptin and conventional troponin I aids in early rule out of NSTEMI virtually independent of chest pain onset (CPO) with high NPV in patients presenting within three hours from chest pain onset with excellent prognostic value for risk stratification and prediction of MACEs. CI - Copyright (c) 2021 Elsevier Inc. All rights reserved. FAU - Ahmed, Tarek A N AU - Ahmed TAN AD - Cardiology Department, Assiut University Heart Hospital, Egypt. FAU - Johny, John S AU - Johny JS AD - Cardiology Department, Assiut University Heart Hospital, Egypt. Electronic address: Johnsafwatjohny91@yahoo.com. FAU - Abdel-Malek, Mohamed Y AU - Abdel-Malek MY AD - Clinical Pathology Department, Assiut University Hospital, Egypt. FAU - Fouad, Doaa A AU - Fouad DA AD - Cardiology Department, Assiut University Heart Hospital, Egypt. LA - eng PT - Journal Article PT - Observational Study DEP - 20210830 PL - United States TA - Am J Emerg Med JT - The American journal of emergency medicine JID - 8309942 RN - 0 (Biomarkers) RN - 0 (Glycopeptides) RN - 0 (Troponin) RN - 0 (copeptins) SB - IM MH - Acute Coronary Syndrome/*diagnosis MH - Biomarkers/blood MH - Early Diagnosis MH - Electrocardiography MH - Female MH - Glycopeptides/*blood MH - Humans MH - Male MH - Middle Aged MH - Prognosis MH - Prospective Studies MH - Troponin/blood OTO - NOTNLM OT - Acute coronary syndrome OT - Cardiac troponin I OT - Copeptin COIS- Declaration of Competing Interest None EDAT- 2021/09/05 06:00 MHDA- 2021/12/29 06:00 CRDT- 2021/09/04 20:23 PHST- 2021/06/16 00:00 [received] PHST- 2021/08/21 00:00 [revised] PHST- 2021/08/24 00:00 [accepted] PHST- 2021/09/05 06:00 [pubmed] PHST- 2021/12/29 06:00 [medline] PHST- 2021/09/04 20:23 [entrez] AID - S0735-6757(21)00709-9 [pii] AID - 10.1016/j.ajem.2021.08.069 [doi] PST - ppublish SO - Am J Emerg Med. 2021 Dec;50:413-421. doi: 10.1016/j.ajem.2021.08.069. Epub 2021 Aug 30.