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Proteinuria is associated with elevated tricuspid regurgitant jet velocity in children with sickle cell disease
Suzanne Forrest1, Ashley Kim, Judith Carbonella
1Yale University School of Medicine, New Haven, CT, USA.
Insights
Elevated pulmonary artery pressures are linked to proteinuria in children with sickle cell disease (SCD). This finding suggests a connection between pulmonary hypertension and kidney issues in pediatric SCD patients.
Area of Science:
- Pediatric Nephrology
- Cardiology in Sickle Cell Disease
- Echocardiography in Pediatric Practice
Background:
- Sickle cell disease (SCD) impacts multiple organ systems, with pulmonary hypertension (PHT) and sickle cell nephropathy (SCN) being serious complications.
- PHT and SCN share risk factors, and in adults, PHT is associated with albuminuria, a marker of SCN.
- Data on the association between PHT and SCN markers in children with SCD is lacking.
Purpose of the Study:
- To investigate the association between elevated pulmonary artery systolic pressures and proteinuria in pediatric patients with SCD.
- To determine if echocardiogram-estimated pulmonary artery pressures correlate with kidney damage markers in children with SCD.
Main Methods:
- Retrospective chart review of pediatric SCD patients screened via echocardiogram between June 2005 and July 2010.
- Inclusion criteria: initial echocardiogram and urine analysis within one year, with longitudinal data collection.
- Analysis focused on tricuspid regurgitant jet velocity (TRV) and presence of proteinuria.
Main Results:
- Eighty-five pediatric SCD patients were included; 32.9% had elevated TRV (≥2.5 m/s) on initial echocardiogram.
- Proteinuria was observed in 7.14% of patients with elevated TRV versus 1.75% without elevated TRV at initial screening.
- On follow-up, 19.08% of repeat urinalyses showed proteinuria in patients with elevated baseline TRV, compared to 12.35% in those with normal TRV (P=0.04).
Conclusions:
- Elevated tricuspid regurgitant jet velocity (TRV) ≥2.5 m/s is significantly associated with proteinuria in children with SCD.
- This association suggests a potential link between pulmonary hypertension and kidney dysfunction in pediatric SCD.
- Findings highlight the importance of monitoring for SCN in children with SCD and signs of PHT.
Background:
Sickle cell disease (SCD) affects multiple organ systems. Complications of SCD such as pulmonary hypertension (PHT) and sickle cell nephropathy (SCN) are associated with an increased mortality. Both PHT and SCN have some common risk factors. In adults, PHT has been found to be associated with albuminuria, a manifestation of SCN. There is no data on this association in children. We conducted a study to determine if elevated pulmonary artery systolic pressures estimated on echocardiogram was associated with proteinuria in children with SCD.
Methods:
A detailed retrospective chart review was conducted on a cohort of sickle cell patients screened with echocardiograms from June 2005 to July 2010. Patients who had an initial screening echocardiogram and urine analysis within 1 year were included. Longitudinal data from all subsequent echocardiograms and urine analyses were collected.
Results:
Eighty-five patients were included. On initial echocardiograms 32.9% had an elevated tricuspid regurgitant jet velocity (TRV) ≥2.5 m/second. On follow up, in the 28 patients with elevated TRV, 49.27% of all repeat echocardiograms showed persistent elevation. In the 57 patients with normal baseline TRV, 73.6% of all repeat echocardiograms continued to have normal TRV. On initial screening 7.14% of patients with elevated TRV had proteinuria compared to 1.75% without elevated TRV. On follow up, 19.08% of repeat urinalysis had proteinuria in patients with elevated baseline TRV compared to 12.35% in patients with normal baseline TRV (P = 0.04).
Conclusions:
Elevated TRV ≥ 2.5 m/second is significantly associated with proteinuria on longitudinal follow up in children with SCD.
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