Key result
High hsCRP levels (>3 mg/L) were independently associated with significantly higher odds of congestive heart failure (adjusted OR 2.03; 95% CI 1.45-2.91; p<0.01) among US adults.
Why the study?
Does high hsCRP (>3 mg/L) predict congestive heart failure in US adults in the post-pandemic period?
Cross-Sectional (n=5,571)
Yes
Does high hsCRP (>3 mg/L) predict congestive heart failure in US adults in the post-pandemic period?
Odds Ratio: 2.03 (95% CI 1.45–2.91)
p-value: p=< 0.01
High hsCRP (>3 mg/L) remains a strong independent predictor of congestive heart failure in the post-pandemic US population, supporting its continued utility in cardiovascular risk stratification.
Introduction: High sensitivity C-reactive protein (hsCRP) has been widely used as a biomarker for cardiovascular risk stratification, including congestive heart failure (CHF). However, its predictive value in the context of post-pandemic, as characterized by heightened population-level baseline inflammation, remains unexplored. Hence, we aim to assess the predictive value of hsCRP to CHF among United States (US) populations in 2021-2023. Methods: A total of 5571 adults from the National Health and Nutrition Examination Survey (NHANES) 2021-2023 were assessed. Multivariable logistic regression was performed to evaluate the association between hsCRP and CHF, adjusting for age, sex, race, and education. Non-linear association was explored using restricted cubic spline. Model performance was evaluated using area under the receiver operating characteristic (ROC) curve (AUC). Results: High hsCRP level (>3 mg/L) was independently associated with significantly higher odds of CHF (adjusted odds ratio (OR) = 2.03, 95% CI: 1.45-2.91, p-value < 0.01). The predictive model demonstrated strong discriminatory performance with an AUC of 0.782 after adjusting for covariates. Adjustment for age and sex alone yielded an AUC of 0.761. Restricted cubic spline analysis revealed a non-linear relationship between hsCRP and CHF odds, with an inflection in risk observed at hsCRP levels exceeding 1.82 mg/L. Discussion: Despite elevated baseline inflammation following the pandemic, hsCRP remains a clinically valuable biomarker for CHF prediction in the US population. hsCRP promotes CHF event by playing a critical role in atherogenesis, complement activation, and monocyte infiltration to the vascular wall. Conclusion: The hs-CRP level is significantly positively correlated with CHF among American adults. Preventive strategies to maintain the hsCRP levels should be employed to reduce CHF burden in the US. Findings highlight the potential clinical benefit of incorporating routine monitoring and targeted-hsCRP lowering strategies to improve clinical decision-making.
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Nugrahani et al. (2026) conducted a cross-sectional in Congestive heart failure (n=5,571). High sensitivity C-reactive protein (hsCRP) >3 mg/L was evaluated on Congestive heart failure (OR 2.03, 95% CI 1.45-2.91, p=< 0.01). High hsCRP levels (>3 mg/L) were independently associated with significantly higher odds of congestive heart failure (adjusted OR 2.03; 95% CI 1.45-2.91; p<0.01) among US adults.
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