Key result
Undiagnosed dysglycemia linked to ~76% higher CRS-1 risk in acute heart failure.
Why the study?
Early and accurate prediction of cardiorenal syndrome type 1 in patients with acute heart failure remains a challenge despite reported biomarkers.
Cohort (n=1,059)
No
Odds Ratio: 1.76 (95% CI 1.16–2.66)
Absolute Event Rate: 28.6% vs 17.7%
May inform CRS1 risk stratification via glycemic phenotyping in AHF; leaves open causal and therapeutic implications from observational data.
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.
No takes yet. Share an insight, caveat, or question.
Fan et al. (2018) conducted a cohort in Acute Heart Failure (n=1,059). Dysglycemic phenotype without prior diagnosis vs. No diabetes was evaluated on Cardiorenal syndrome type 1 (CRS-1) (OR 1.76, 95% CI 1.16-2.66). A dysglycemic phenotype without prior diagnosis was associated with a significantly higher risk of cardiorenal syndrome type 1 compared to no diabetes in patients hospitalized for acute heart failure (OR 1.76).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: