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An Ex vivo Culture System to Study Thyroid Development
Published on: June 6, 2014
Final height in long-term primary hypothyroid children
A Chiesa1, L Gruñeiro de Papendieck, A Keselman
1Centro de Investigaciones Endocrinológicas, Hospital de Niños R. Gutiérrez, Buenos Aires, Argentina.
Insights
Children with primary hypothyroidism treated before puberty achieved normal adult height relative to their target height. However, those treated during puberty did not achieve catch-up growth, indicating puberty
Area of Science:
- Pediatric Endocrinology
- Growth and Development
- Thyroid Disorders
Background:
- Primary hypothyroidism in children can significantly impair statural growth.
- Early diagnosis and treatment are crucial for optimizing growth outcomes.
- Understanding the impact of treatment timing on final height is essential.
Purpose of the Study:
- To retrospectively analyze the statural growth and bone maturation in children with primary hypothyroidism.
- To correlate final height with chronological age, height deficit, and bone age at treatment initiation.
- To evaluate the influence of treatment timing (prepubertal vs. pubertal) on achieving target height.
Main Methods:
- Retrospective study of 32 children diagnosed with primary hypothyroidism.
- Patients were categorized into three groups based on age at treatment initiation: early childhood (G1), late childhood (G2), and puberty (G3).
- Final height was compared to target height, with analysis of height deficits and bone age progression.
Main Results:
- Children treated before puberty (G1 and G2) achieved final heights comparable to their target heights (SDS G1: -1.05 +/- 0.89; G2: -1.2 +/- 1).
- Children treated during puberty (G3) did not reach their target height (SDS G3: -2 +/- 1.5), with a statistically significant difference (p < 0.04).
- Bone age advancement varied, with prepubertal groups showing better catch-up potential.
Conclusions:
- Treatment of primary hypothyroidism initiated before puberty allows for attainment of normal adult height relative to genetic potential.
- Puberty is a critical period, and its onset in untreated or inadequately treated hypothyroid children significantly hinders catch-up growth.
- Timely intervention in pediatric hypothyroidism is paramount for achieving optimal growth outcomes.
Objective:
We studied retrospectively the statural growth and bone maturation of 32 children with primary hypothyroidism in order to relate their final heights to their chronological ages, height deficits and bone ages at the beginning of treatment. Patients were grouped according to age when treatment was started: Group 1 (G1) (n = 17): (15 girls, 1 boy) 3.09 +/- 0.8 yr; Group 2 (G2) (n = 9): (7 girls, 2 boys) 9.1 +/- 1.2 yr, and Group 3 (G3) (n = 6): (5 girls, 1 boy) 13.58 +/- 1.13 yr. At diagnosis G1 and G2 were prepubertal and G3 children were in puberty. In 10 patients of G1, 7 of G2 and 6 (all) of G3 final height was compared with target height.
Results:
(SDS) Initial height: G1: -3.74 +/- 1.2; G2: -3.94 +/- 1.32; G3 -3.65 +/- 1. Height at onset of puberty: G1: -1.06 +/- 1.1; G2: -2.5 +/- 1.4. Height menarche stage 5: G1: -0.63 +/- 1.1; G2: -1.76 +/- 1.2; G3: -2.6 +/- 1.7. Final height: (whole group) G1: -0.85 +/- 0.91; G2: -1.6 +/- 1.3; G3: -2 +/- 1.5. Final height G1 (n = 10): -1.05 +/- 0.89; G2 (n = 7) 1.2 +/- 1. Target height G1 (n = 10): -1.22 +/- 0.78; G2 (n = 7): -0.8 +/- 1.2; G3 (n = 6): -1.07 +/- 1.5. Initial bone age: G1: -4.9 +/- 0.85; G2: -7.2 +/- 2.6; G3: -4.5 +/- 1.9. Bone age (onset of puberty) G1: -0.26 +/- 1.74; G2: -2 +/- 1.7; Bone age (menarche) G1: 0.09 +/- 0.6; G2: -0.5 +/- 0.6; G3: -0.76 +/- 0.82.
Conclusion:
G1 and G2, prepubertal at diagnosis, reached a normal adult height with respect to target height; G3 did not, the difference being statistically significant (p < 0.04). Puberty plays a decisive role in the incomplete catch-up growth of longstanding hypothyroid patients.
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