Key result
Elevated TRV linked to ~5.3-fold higher odds of elevated NT-proBNP in pediatric sickle cell disease.
Why the study?
Cardiopulmonary complications are leading causes of morbidity and mortality in children with sickle cell disease, but data on NT-proBNP levels and echocardiographic assessment in this population are limited.
Cross-Sectional (n=73)
No
Routine screening with NT-proBNP and echocardiography reveals a high prevalence of subclinical cardiopulmonary involvement in children with sickle cell disease, driven primarily by severe anemia, diastolic dysfunction, and elevated pulmonary pressures.
May flag subclinical cardiopulmonary involvement in pediatric sickle cell disease; leaves open whether NT-proBNP screening alters outcomes.
Background: Sickle cell disease (SCD) is among the most common single-gene disorders globally, classified as an autosomal recessive condition causing chronic anemia, painful vaso-occlusive crises, progressive multi-organ damage, and reduced lifespan. Cardiopulmonary complications are leading causes of morbidity and mortality.Objective: To evaluate cardiopulmonary risk using serum NT-proBNP levels and transthoracic echocardiography in children with sickle cell disease at a tertiary care center in Jharkhand.Methods: A hospital-based cross-sectional study was conducted on 73 children (aged 5–18 years) with confirmed SCD. Detailed clinical, laboratory, and standardized echocardiographic evaluations were performed, alongside quantitative measurements of serum NT-proBNP levels.Results: Elevated NT-proBNP levels (>100 pg/mL) were found in 63% of participants, with a mean level of 142.6 ± 98.4 pg/mL. Echocardiography revealed left ventricular hypertrophy (LVH) in 35.6%, diastolic dysfunction in 42.5%, and pulmonary hypertension (elevated tricuspid regurgitant velocity, TRV >= 2.5 m/s) in 38.4% of patients. Left ventricular systolic function remained largely preserved (mean EF 64.2% ± 5.8%). NT-proBNP levels correlated significantly with lower hemoglobin (r = -0.486, p < 0.001), reticulocytosis (r = +0.396, p = 0.001), elevated TRV (r = +0.642, p < 0.001), and high E/e' ratio (r = +0.568, p < 0.001). Multivariate analysis identified TRV >= 2.5 m/s (OR 5.26), hemoglobin < 7 g/dL (OR 3.84), and diastolic dysfunction (OR 2.98) as independent predictors of elevated NT-proBNP levels.Conclusion: Subclinical cardiopulmonary involvement is highly prevalent in pediatric sickle cell disease in Jharkhand. Routine screening with echocardiography and NT-proBNP can aid in early risk stratification and target timely therapeutic interventions.
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Rai et al. (2026) conducted a cross-sectional in Sickle cell disease (n=73). Tricuspid regurgitant velocity (TRV) ≥ 2.5 m/s vs. TRV < 2.5 m/s was evaluated on Elevated NT-proBNP (>160 pg/mL) (OR 5.26, 95% CI 2.14-12.94, p=<0.001). Elevated tricuspid regurgitant velocity (≥2.5 m/s) was strongly associated with elevated NT-proBNP levels (OR 5.26) in children with sickle cell disease.
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