Related Experiment Video
Updated: Aug 14, 2026

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
Growth hormone response to growth hormone releasing factor in sickle cell disease
S E Oberfield1, D L Wethers, J L Kirkland
1Pediatric Service, St. Luke's-Roosevelt Hospital Center, Columbia University College of Physicians and Surgeons, New York, NY 10021.
Insights
Children with sickle cell disease (SCD) often experience impaired growth. This study found that their growth hormone (GH) response to growth hormone releasing factor (GRF) is normal, suggesting other causes for growth issues.
Area of Science:
- Pediatrics
- Endocrinology
- Hematology
Background:
- Children with sickle cell disease (SCD) frequently exhibit growth impairment.
- Growth patterns in SCD can resemble constitutional delay in growth and pubertal development (CDGD).
Purpose of the Study:
- To investigate the growth hormone (GH) secretory capacity in children with SCD and CDGD-like growth patterns.
- To determine if impaired GH response to growth hormone releasing factor (GRF) contributes to growth deficits in SCD.
Main Methods:
- Evaluated the GH response to an intravenous infusion of GRF (1-44) in six children with SCD.
- Compared GH response in SCD patients to a control group of seven children.
Main Results:
- Peak GH response to GRF in SCD patients (29.2 +/- 14.3 ng/ml) was not significantly different from controls (29.0 +/- 6.3 ng/ml).
- These results indicate intact pituicyte GH response to GRF in children with SCD.
Conclusions:
- The observed impaired growth in children with SCD is unlikely due to a deficient GH response to GRF.
- Further research is needed to identify the specific mechanisms causing growth delay in pediatric SCD patients.
Abstract:
Many children with sickle cell disease (SCD) have impaired growth during childhood and adolescence, with patterns of growth consistent with constitutional delay in growth and pubertal development (CDGD). We evaluated the growth hormone (GH) response to a rapid intravenous (i.v.) infusion of growth hormone releasing factor (GRF, 1-44, 1 microgram/kg) in six children with SCD whose growth patterns and bone ages were consistent with CDGD. The peak GH response of the SCD patients to GRF (29.2 +/- 14.3 ng/ml, mean +/- SD, n = 6) was not statistically significantly different from the peak GH response of the control children (29.0 +/- 6.3 ng/ml, mean +/- SD, n = 7). These findings suggest that pituicyte GH response to GRF is intact and is not the cause of the observed impaired growth in patients with SCD.
Related Concept Videos
Regulation of Angiogenesis and Blood Supply
Multipotency of Hematopoietic Stem Cells
Regulation of Hematopoietic Stem Cells
Overview of Hematopoiesis
Developmental Phases of Hematopoiesis
Initially, HSCs are formed in the embryonic yolk sac, a critical site for early blood cell production. These stem cells subsequently migrate to other...
Role of Hematopoietic Growth Factors
Thrombopoietin (TPO), mainly released by the liver,...
Factors Affecting Erythropoiesis
Several factors influence the erythrocyte production rate, with tissue oxygen level being among the most critical. Intense exercise or high altitudes can cause tissue hypoxia, which triggers the kidneys to release more erythropoietin (EPO) into the bloodstream.
EPO then...

