Changes in circulating ApoJ-Glyc levels in patients with suspected acute coronary syndrome: The EDICA trial

Myocardial ischemia induces intracellular accumulation of non-glycosylated apolipoprotein J that results in a reduction of circulating glycosylated ApoJ (ApoJ-Glyc). The latter has been suggested to be a marker of transient myocardial ischemia. This proof-of-concept clinical study aimed to assess wh...

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Veröffentlicht in:International journal of cardiology 2023-11, Vol.391, p.131291-131291, Article 131291
Hauptverfasser: Kaski, Juan Carlos, Lluch, Nuria, Lopez-Sendon, Jose-Luis, Gorog, Diana A., Antorrena-Miranda, Isabel, Avanzas, Pablo, Herrero Puente, Pablo, Sionis, Alessandro, González-Juanatey, José R., Íñiguez, Andrés, Cordero, Alberto, Ako, Emmanuel, Fernández-Avilés, Francisco, Atienza, Felipe, Recio-Mayoral, Alejandro, Wu, Alan H.B., Crea, Filippo, Storey, Robert, Badimon, Lina, Cubedo, Judit
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container_title International journal of cardiology
container_volume 391
creator Kaski, Juan Carlos
Lluch, Nuria
Lopez-Sendon, Jose-Luis
Gorog, Diana A.
Antorrena-Miranda, Isabel
Avanzas, Pablo
Herrero Puente, Pablo
Sionis, Alessandro
González-Juanatey, José R.
Íñiguez, Andrés
Cordero, Alberto
Ako, Emmanuel
Fernández-Avilés, Francisco
Atienza, Felipe
Recio-Mayoral, Alejandro
Wu, Alan H.B.
Crea, Filippo
Storey, Robert
Badimon, Lina
Cubedo, Judit
description Myocardial ischemia induces intracellular accumulation of non-glycosylated apolipoprotein J that results in a reduction of circulating glycosylated ApoJ (ApoJ-Glyc). The latter has been suggested to be a marker of transient myocardial ischemia. This proof-of-concept clinical study aimed to assess whether changes in circulating ApoJ-Glyc could detect myocardial ischemia in patients attending the emergency department (ED) with chest pain suggestive of acute coronary syndrome (ACS). In suspected ACS patients, EDICA (Early Detection of Myocardial Ischemia in Suspected Acute Coronary Syndromes by ApoJ-Glyc a Novel Pathologically based Ischemia Biomarker), a multicentre, international, cohort study assessed changes in 2 glycosylated variants of ApoJ-Glyc, (ApoJ-GlycA2 and ApoJ-GlycA6), in serum samples obtained at ED admission (0 h), and 1 h and 3 h thereafter, blinded to the clinical diagnosis (i.e. STEMI, NSTEMI, unstable angina, non-ischemic). 404 patients were recruited; 291 were given a clinical diagnosis of “non-ischemic” chest pain and 113 were considered to have had an ischemic event. ApoJ-GlycA6 was lower on admission in ischemic compared with “non-ischemic” patients (66 [46–90] vs. 73 [56–95] μg/ml; P = 0.04). 74% of unstable angina patients (all with undetectable hs-Tn), had ischemic changes in ApoJ-Glyc at 0 h and 89% at 1 h. Initially low ApoJ-Glyc levels in 62 patients requiring coronary revascularization increased significantly after successful percutaneous intervention. Circulating ApoJ-Glyc concentrations decrease early in ED patients with myocardial ischemia compared with “non-ischemic” patients, even in the absence of troponin elevations. ApoJ-Glyc may be a useful marker of myocardial ischemia in the ED setting. •ApoJ-Glyc detects reversible myocardial ischemia and the restoration of perfusion.•ApoJ-Glyc is a dynamic marker of transient/reversible myocardial ischemia.•ApoJ-Glyc might complement the diagnostic role of hs-Tn in the Emergency Department.
doi_str_mv 10.1016/j.ijcard.2023.131291
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The latter has been suggested to be a marker of transient myocardial ischemia. This proof-of-concept clinical study aimed to assess whether changes in circulating ApoJ-Glyc could detect myocardial ischemia in patients attending the emergency department (ED) with chest pain suggestive of acute coronary syndrome (ACS). In suspected ACS patients, EDICA (Early Detection of Myocardial Ischemia in Suspected Acute Coronary Syndromes by ApoJ-Glyc a Novel Pathologically based Ischemia Biomarker), a multicentre, international, cohort study assessed changes in 2 glycosylated variants of ApoJ-Glyc, (ApoJ-GlycA2 and ApoJ-GlycA6), in serum samples obtained at ED admission (0 h), and 1 h and 3 h thereafter, blinded to the clinical diagnosis (i.e. STEMI, NSTEMI, unstable angina, non-ischemic). 404 patients were recruited; 291 were given a clinical diagnosis of “non-ischemic” chest pain and 113 were considered to have had an ischemic event. ApoJ-GlycA6 was lower on admission in ischemic compared with “non-ischemic” patients (66 [46–90] vs. 73 [56–95] μg/ml; P = 0.04). 74% of unstable angina patients (all with undetectable hs-Tn), had ischemic changes in ApoJ-Glyc at 0 h and 89% at 1 h. Initially low ApoJ-Glyc levels in 62 patients requiring coronary revascularization increased significantly after successful percutaneous intervention. Circulating ApoJ-Glyc concentrations decrease early in ED patients with myocardial ischemia compared with “non-ischemic” patients, even in the absence of troponin elevations. ApoJ-Glyc may be a useful marker of myocardial ischemia in the ED setting. •ApoJ-Glyc detects reversible myocardial ischemia and the restoration of perfusion.•ApoJ-Glyc is a dynamic marker of transient/reversible myocardial ischemia.•ApoJ-Glyc might complement the diagnostic role of hs-Tn in the Emergency Department.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.ijcard.2023.131291</doi><tpages>1</tpages></addata></record>
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subjects Acute coronary syndrome
Acute myocardial ischemia
Angina
Glycosylated ApoJ
Ischemia
title Changes in circulating ApoJ-Glyc levels in patients with suspected acute coronary syndrome: The EDICA trial
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