Optimal carbohydrate antigen 125 cutpoint for identifying low-risk patients after admission for acute heart failure

Julio Núñez1, Antoni Bayés-Genís2, Elena Revuelta-López3

  • 1Servicio de Cardiología, Hospital Clínico Universitario de Valencia, INCLIVA, Valencia, Spain; Departamento de Medicina, Universitat de Valencia, València, Spain; Centro de Investigación Biomédica en Red Enfermedades Cardiovaculares (CIBERCV), Spain.

Insights

A low Carbohydrate Antigen 125 (CA125) level below 23 U/mL in acute heart failure (AHF) patients identifies those at low risk for 1-month death or readmission. This finding suggests these patients may not need intensive post-discharge monitoring.

Area of Science:

  • Cardiology
  • Biomarkers
  • Clinical Risk Stratification

Background:

  • Carbohydrate Antigen 125 (CA125) is a valuable biomarker for risk stratification in patients with acute heart failure (AHF).
  • Accurate identification of low-risk patients is crucial for optimizing post-discharge care strategies.

Purpose of the Study:

  • To establish a specific CA125 cutoff value for identifying patients with AHF at low risk of 1-month mortality or the composite outcome of death/heart failure readmission.
  • To validate this cutoff in an external cohort to confirm its predictive accuracy.

Main Methods:

  • A derivation cohort of 3231 AHF patients was analyzed to identify CA125 cutoff values with high negative predictive value (NPV) and sensitivity.
  • The optimal cutoff was selected based on its ability to predict 1-month adverse events and validated in an independent cohort of 1583 AHF patients from BIOSTAT-CHF.
  • Multivariate survival analyses and the Royston-Parmar method were employed to assess risk prediction.

Main Results:

  • An optimal CA125 cutoff of <23 U/mL was identified, present in 21.5% of the derivation cohort.
  • This cutoff demonstrated high NPVs: 99.3% for death and 94.1% for the composite endpoint (death/HF readmission) at 1 month.
  • CA125 <23 U/mL was independently associated with significantly lower risks of death and the composite endpoint, a finding consistent in the validation cohort with NPVs of 98.6% and 96.6% respectively.

Conclusions:

  • A CA125 level below 23 U/mL effectively identifies a subgroup of AHF patients at low risk for short-term adverse events.
  • This low-risk population may benefit from less intensive post-discharge monitoring, potentially improving resource allocation.
  • The predictive value of this CA125 cutoff extends to 6 months of follow-up, reinforcing its utility in risk stratification.
Abstract

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