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Plasma CA125 Levels as a Predictor of Major Adverse Cardiac Events in Patients With Acute Coronary Syndrome: A
Nazlı Dilek Çolak1, Turgut Karabağ2, Onuralp Çalışkan3
1Clinical Pharmacy, Marmara University, Institute of Health Sciences, 34854, Istanbul, Turkey.
Insights
Carbohydrate antigen 125 (CA125) levels correlate with cardiac biomarkers in acute coronary syndrome (ACS) patients. Elevated CA125 may predict major adverse cardiac events (MACE) within six months.
Area of Science:
- Cardiology
- Biomarkers
- Clinical Research
Background:
- Carbohydrate antigen 125 (CA125) is linked to cardiovascular conditions.
- Understanding CA125's role in acute coronary syndrome (ACS) is crucial.
Purpose of the Study:
- To determine CA125 levels in ACS patients.
- To investigate the relationship between CA125 and major adverse cardiac events (MACE) in the short term.
Main Methods:
- Prospective cohort study in a coronary care unit.
- Plasma CA125 measured upon admission; patients followed for six months.
- MACE included mortality, recurrent ACS, revascularization, heart failure, stroke, and atrial fibrillation.
Main Results:
- 127 ACS patients included; median CA125 was 14.6 KU/L.
- CA125 positively correlated with hs-cTn and pro-BNP.
- CA125 showed a weak negative correlation with left ventricular ejection fraction (LVEF).
Conclusions:
- Plasma CA125 correlates with established ACS biomarkers (pro-BNP, hs-cTn).
- Elevated CA125 may identify ACS patients at higher risk for short-term MACE.
- CA125 warrants further investigation as a prognostic marker in ACS.
Objectives:
Carbohydrate antigen 125 (CA125) is associated with different cardiovascular conditions. This study aimed to determine CA125 levels in patients with acute coronary syndrome (ACS) and the potential relationship between major adverse cardiac events (MACE) in the short-term following.
Methods:
This prospective cohort study was conducted in a coronary care unit between May and November 2022. Plasma CA125 levels were measured only once upon hospital admission. Patients were followed for six months. All-cause mortality, recurrent acute coronary syndrome, requirement for revascularization, decompensated heart failure, cardiogenic pulmonary edema, atrial fibrillation, and stroke were recorded as MACE.
Results:
A total of 127 patients were included in this study. The mean left ventricular ejection fraction (LVEF) was 50.5 %. The median plasma CA125 level was 14.6 KU/L. There was a, significant positive relationship between CA125 and high-sensitivity cardiac troponin (hs-cTn) (r = 0.315, p < 0.001) and pro-B-type natriuretic peptide (proBNP) (r = 0.423, p < 0.001), and a weak negative relationship with LVEF (r = -0.186, p = 0.037) value.
Conclusions:
Plasma CA125 levels were correlated with the pro-BNP and hs-cTn, established ACS biomarkers. An additional notable finding was the weak correlation with LVEF. Elevated plasma CA125 levels might be used to identify patients with ACS who are at higher risk of MACE at six months.
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