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Published on: June 16, 2020
Longitudinal changes in lung function and somatic growth in children with sickle cell disease
Anastassios C Koumbourlis1, Donna J Lee, Ada Lee
1Division of Pediatric Pulmonology, Morgan Stanley Children's Hospital of New York Presbyterian, Columbia University Medical Center, New York, NY, USA. Akoumbou@LIJ.edu
Insights
Children with sickle cell disease (SCD) show worsening lung function over time, with an increase in obstructive patterns. Somatic growth did not appear to directly impact lung function changes in this study.
Area of Science:
- Pulmonology
- Pediatrics
- Hematology
Background:
- Sickle cell disease (SCD) significantly impacts multiple organ systems, including the lungs.
- Longitudinal studies are crucial to understand the progression of lung function changes in pediatric SCD patients.
Purpose of the Study:
- To investigate the longitudinal changes in lung function and somatic growth patterns in children and adolescents with hemoglobin SS (Hb-SS) sickle cell disease (SCD).
Main Methods:
- 45 children with Hb-SS SCD underwent two lung function and somatic growth assessments, separated by approximately 42 months.
- Spirometry was used to evaluate lung volumes and airflow indices, including FEV1, FVC, and FEF25-75.
- Body Mass Index (BMI) was assessed to categorize somatic growth patterns.
Main Results:
- Lung volumes slightly decreased but remained borderline normal; however, significant declines in spirometric indices indicated developing lower airway obstruction (P<0.001).
- The prevalence of obstructive lung function patterns increased from 22% to 44%, while normal patterns decreased from 56% to 29% over time.
- Abnormal BMI (high or low) was associated with abnormal lung function, but only normal BMI patients exhibited lung function decline.
Conclusions:
- Sickle cell disease is associated with a progressive obstructive pattern of lung function in children and adolescents.
- No direct causal relationship was identified between somatic growth patterns and the observed changes in lung function in this cohort.
Background:
We studied the changes in the patterns of lung function and somatic growth over time in children and adolescents (10.6 +/- 3.5 years at first test) with hemoglobin SS (Hb-SS) sickle cell disease (SCD).
Methods:
Lung function and somatic growth were measured twice with an interval of 42.3 +/- 23.3 months in 45 children (25 females and 20 males) with Hb-SS SCD.
Results:
The lung volumes slightly decreased but remained borderline normal in both tests. All spirometric indices were within the normal range but significantly decreased (P<0.001) at the time of the second test indicating development of lower airway obstruction (forced expiratory volume in the first second (FEV(1)): 87 +/- 21 vs. 80 +/- 15; FEV(1)/forced vital capacity (FVC): 89 +/- 7 vs. 85 +/- 6; FEF(25-75): 89 +/- 32 vs. 76 +/- 24). "Normal" pattern of lung function was initially found in 56% of the patients, but in only 29% in the second test. In contrast, those with "obstructive" pattern increased from 22 to 44%, and those with "restrictive" pattern from 22 to 27%. There was no association between history of asthma and pattern of lung function. "Normal" Body Mass Index (BMI) was found in 64% of the patients, whereas 13% had "High" BMI and 22% "Low" BMI. The two latter patterns were associated with abnormal lung function but only patients with normal BMI showed actual decline overtime.
Conclusion:
SCD is characterized by a predominantly obstructive pattern of lung function that increases in prevalence over time. There was no apparent causal relationship between the pattern of somatic growth and the pattern of lung function.
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