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Linear growth, growth-hormone secretion and IGF-I generation in children with neglected hypothyroidism before and
Ashraf T Soliman1, Magdy Omar, Ahmad El Awwa
1Department of Pediatrics, University of Alexandria Children's Hospital, El Chatby, Alexandria, Egypt. ATSOLIMAN@yahoo.com
Insights
Thyroxine (T4) replacement therapy in children with congenital hypothyroidism (CH) significantly improved height and the growth hormone (GH)-insulin-like growth factor-I (IGF-I) axis, indicating partial catch-up growth.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Disorders
- Congenital Hypothyroidism
Background:
- Congenital hypothyroidism (CH) can impair growth and the growth hormone (GH)-insulin-like growth factor-I (IGF-I) axis.
- Long-term effects of neglected CH on growth and endocrine function require further investigation.
Purpose of the Study:
- To evaluate the impact of thyroxine (T4) replacement on growth parameters and the GH-IGF-I axis in children with neglected CH.
- To assess the recovery of GH and IGF-I generation after T4 treatment.
Main Methods:
- Studied 15 children with neglected CH (mean age 6.4 years).
- Measured growth parameters, GH stimulation (clonidine), and IGF-I generation tests before and after >1 year of T4 replacement.
- Analyzed correlations between height SDS increments and basal free T4 levels.
Main Results:
- Height SDS improved significantly from -4.3 to -2.7 after one year of T4 treatment.
- Peak GH response to clonidine increased from 3.2 to 7.62 ng/mL.
- Basal and peak IGF-I levels showed substantial increases, indicating improved GH-IGF-I axis function. Height SDS increments correlated with basal free T4.
Conclusions:
- T4 replacement therapy in children with neglected CH promotes significant catch-up growth.
- Treatment partially restores the GH-IGF-I axis function, underscoring the importance of early diagnosis and management.
- The degree of catch-up growth is linked to basal free T4 concentrations during treatment.
Abstract:
We studied growth hormone (GH) stimulation and insulin-like growth factor -I (IGF-I) generation tests in 15 children with neglected congenital hypothyroidism (CH) (age = 6.4 +/- 4.2 years) and measured their growth parameters for >1 years after starting thyroxine (T4) replacement. One year after treatment, height SDS (HtSDS) increased from -4.3 +/- 2.5 to -2.7 +/- 2.3. Peak GH response to clonidine increased from 3.2 +/- 1.2 ng ml(-1) to 7.62 +/- 1.38 ng ml(-1) after treatments. Basal and peak IGF-I response to GH increased from (34.66 +/- 17.3 ng ml(-1) and 58.4 +/- 36.99 ng ml(-1), respectively) before treatment to (130.6 +/- 97.8 ng ml(-1) and 193.75 +/- 122.5 ng ml(-1), respectively). HtSDS increments were correlated significantly with basal free T4 concentrations (r = 0.622, P < 0.01). In summary, after long period of hypothyroidism, T4 replacement produced significant, although incomplete, catch-up growth through a partial recovery of GH- IGF-I axis.
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