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Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Adding Glucagon-Stimulated GH Testing to the Diagnostic Fast Increases the Detection of GH-Sufficient Children
Colin P Hawkes1, Adda Grimberg, Vivian E Dzata
1Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, Pa., USA.
Insights
Serial growth hormone (GH) testing after glucagon administration during a diagnostic fast helps identify children without GH deficiency (GHD). This approach reduces the need for further GH stimulation tests and potential GH treatment.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Hormone Testing
Background:
- Diagnostic fasting is used to evaluate unexplained hypoglycemia in children.
- Low growth hormone (GH) levels during hypoglycemia are not specific for GH deficiency (GHD).
Purpose of the Study:
- To assess if serial GH measurements after glucagon administration improve GHD identification in children undergoing diagnostic fasting.
- To reduce unnecessary GH stimulation testing and treatment.
Main Methods:
- Retrospective chart review of children undergoing diagnostic fasting.
- Glucagon administration at the end of the fast.
- Serial GH measurements every 30 minutes for 210 minutes post-glucagon.
Main Results:
- Only 10% of children had GH >7 ng/ml at baseline after the fast.
- Serial GH testing post-glucagon increased the detection rate of children without GHD to 55%.
- GH levels showed significant increases during the serial testing period.
Conclusions:
- Serial GH measurements after glucagon administration enhance the diagnosis of children without GHD.
- This method can prevent unnecessary further testing and treatment for GHD.
- Optimizes diagnostic protocols for pediatric endocrine evaluations.
Background/Aims:
The evaluation of children with unexplained hypoglycemia may include a diagnostic fast. However, low growth hormone (GH) concentration during hypoglycemia is not specific to GH deficiency (GHD). The aim of this study was to determine if serial GH measurement following glucagon administration, in the setting of a diagnostic fast, would increase the number of children identified as not having GHD.
Methods:
We conducted a retrospective chart review of children who had serial GH measurements performed after glucagon administration at the end of a diagnostic fast. Glucagon was administered at the end of the fasting study, and GH was measured every 30 min for 210 min.
Results:
Of the 29 children in this series, only 3 (10%) had GH concentrations >7 ng/ml at the end of the fast, which increased by 16 (55%) after serial GH testing. The percentages of samples with GH concentrations >7 ng/ml were: 10% at baseline, and 25, 39, 41, 41, 33, 43, and 0% every 30 min thereafter.
Conclusion:
Additional GH measurements after glucagon administration following a diagnostic fast can improve the identification of children without GHD and thereby save them unnecessary GH stimulation testing and potential GH treatment.
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