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Nomogram Model to Predict Cardiorenal Syndrome Type 1 in Patients with Acute Heart Failure
Zeyuan Fan1, Yang Li2, Hanhua Ji2
1Department of Cardiovascular Diseases, Civil Aviation General Hospital, Civil Aviation Clinical Medical College of Peking University, Beijing, China, fanzy_mhzyy@163.com.
Insights
A new nomogram accurately predicts individualized risk for cardiorenal syndrome type 1 (CRS1) in acute heart failure (AHF) patients. This tool aids early identification and management of CRS1, improving clinical outcomes.
Area of Science:
- Cardiology
- Nephrology
- Biomarkers
Background:
- Cardiorenal syndrome type 1 (CRS1) in acute heart failure (AHF) patients leads to poor outcomes.
- Early and accurate prediction of CRS1 remains a clinical challenge.
- Existing biomarkers have limitations for timely CRS1 identification.
Purpose of the Study:
- To develop and validate an individualized predictive nomogram for CRS1 risk in AHF patients.
- To improve early detection and risk stratification of CRS1.
- To provide a clinically applicable tool for managing AHF patients at risk of CRS1.
Main Methods:
- A cohort of 1235 AHF patients was analyzed.
- Patients were divided into training (n=823) and validation (n=412) sets.
- Multivariate logistic regression identified predictors; a nomogram was developed and validated using AUC and calibration plots.
Main Results:
- The incidence of CRS1 was 31.7%.
- Independent predictors identified were age, diabetes, NYHA class, eGFR, hs-CRP, and uAGT.
- The nomogram achieved AUCs of 0.885 (internal) and 0.823 (external) with good calibration.
Conclusions:
- The developed nomogram accurately predicts individualized CRS1 risk in AHF patients.
- The nomogram demonstrates high discrimination and good predictive accuracy.
- This tool has potential clinical applicability for AHF patient management.
Background/Aims:
Cardiorenal syndrome type 1(CRS1) is a serious clinical condition in patients with acute heart failure (AHF) associated with adverse clinical outcomes. Although several biomarkers for identifying CRS1 have been reported, early and accurate predicting CRS1 still remains a challenge. This study was aimed to develop and validate an individualized predictive nomogram for the risk of CRS1 in patients with AHF.
Methods:
A total of 1235 AHF patients between 2013 and 2018 were included in this study. The patients were randomly classified into training set (n=823) and validation set (n=412). All data of the training set were used to screen the predictors of CRS1 via univariate and multivariate analyses. A nomogram was developed based on these predictors and validated by internal and external validation. The nomogram validation comprised discriminative ability determined by the area under the curve (AUC) of receiver-operating characteristic (ROC) curve and the predictive accuracy by calibration plots.
Results:
The overall incidence of CRS1 was 31.7%. Multivariate logistic regression revealed that age, diabetes, NYHA class, eGFR, hs-CRP and uAGT were independently associated with CRS1. A nomogram developed based on the six variables was with the AUC 0.885 and 0.823 on internal and external validation, respectively. Calibration plots showed that the predicted and actual CRS1 probabilities were fitted well on both internal and external validation.
Conclusion:
The proposed nomogram could predict the individualized risk of CRS1 with good accuracy, high discrimination, and potential clinical applicability in patients with AHF.
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