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Limited Utility of Biochemical Screening for Pituitary Deficiencies and Adverse Effects in Idiopathic GH Deficiency
Stephen Zborovski1, Mark R Palmert1, Jennifer Harrington1
1Division of Endocrinology, Department of Pediatrics, Hospital for Sick Children, University of Toronto, Toronto, Canada.
Insights
Routine screening for multiple pituitary hormone deficiencies (MPHD) in children with isolated growth hormone (GH) deficiency is rarely necessary. Biochemical screening for MPHD should be reserved for children with an abnormal MRI.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
- Pituitary Disorders
Background:
- Routine biochemical screening for multiple pituitary hormone deficiencies (MPHD) and GH treatment complications is common in children with isolated GH deficiency (GHD).
- Evidence supporting this practice is limited.
Purpose of the Study:
- To determine the incidence of MPHD development in children initially diagnosed with isolated GHD.
- To assess the effectiveness of screening tests in detecting GH therapy complications.
Main Methods:
- Retrospective analysis of 328 children treated with GH since 2005.
- Included subjects with GHD, idiopathic short stature, and SHOX deficiency.
- Excluded subjects with GHD associated with acquired disorders or known pituitary abnormalities.
Main Results:
- MPHD developed in 4.2% of children with isolated GHD after a mean of 35.4 months.
- MRI abnormalities were associated with a 6.3-fold increased risk of developing MPHD.
- Dysglycemia occurred in 0.9% of subjects; no persistent liver or renal function abnormalities were noted.
Conclusions:
- Routine biochemical screening for MPHD in children with isolated GHD has a limited role.
- Screening for MPHD should be prioritized for children with abnormal MRI findings.
- Routine screening for adverse effects of GH therapy is not generally warranted in otherwise healthy children.
Context:
In children with isolated growth hormone (GH) deficiency (GHD), routine biochemical screening for multiple pituitary hormone deficiencies (MPHD) and adverse effects related to growth hormone (GH) treatment are frequently performed. More evidence is needed to support this practice.
Objectives:
To evaluate the rate of development of MPHD among children initially diagnosed with isolated GHD and to assess the utility of screening tests to identify complications of GH therapy.
Design:
Retrospective analysis of subjects treated with GH since 2005. For the first objective, only subjects diagnosed with GHD were included. Subjects were excluded if GHD was associated with an acquired disorder or condition known to be associated with pituitary abnormalities. For the second objective, other GH-treated diagnoses were included.
Patients:
A total of 328 subjects (171 with GHD, 154 with idiopathic short stature, and three with SHOX deficiency).
Results:
In subjects with isolated GHD, MPHD was diagnosed in seven (4.2%) after a mean of 35.4 months (range, 9.4 to 68.0). Sex, age at diagnosis, duration of GH, and peak stimulated GH levels were not associated with developing MPHD. Among subjects with an MRI abnormality, 13.9% developed MPHD (OR, 6.3; 95% CI, 1.2 to 33.7). In the entire cohort, three subjects (0.9%) developed dysglycemia, and no subject had persistently abnormal liver or renal function tests.
Conclusions:
There is a limited role for routine biochemical screening for MPHD in children with idiopathic isolated GHD or for adverse effects in otherwise healthy children. Routine biochemical screening for MPHD should be limited to those with an abnormal MRI.
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