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Thyroid function in short children born small-for-gestational age (SGA) before and during GH treatment
S W K de Kort1, R H Willemsen, D C M van der Kaay
1Department Paediatrics, Division of Endocrinology, Erasmus MC-Sophia, Rotterdam, The Netherlands. s.dekort@erasmusmc.nl
Insights
Preterm small-for-gestational age (SGA) children show higher thyroid-stimulating hormone (TSH) levels. Growth hormone (GH) treatment slightly decreases FT4 but does not impact TSH or growth response, suggesting monitoring is unnecessary.
Area of Science:
- Pediatric Endocrinology
- Neonatology
- Thyroidology
Background:
- Thyroid function disturbances are noted in small-for-gestational age (SGA) children, but the impact of prematurity remains unclear.
- The effect of growth hormone (GH) treatment on thyroid function in short SGA children has not been previously investigated.
Purpose of the Study:
- To compare thyroid-stimulating hormone (TSH) levels in short SGA children versus controls.
- To assess the influence of gestational age on TSH levels in SGA children.
- To determine if GH treatment affects thyroid function in these children.
Main Methods:
- Studied 264 prepubertal, non-GH deficient short SGA children (116 preterm).
- Measured serum free thyroxine (FT4) and TSH at baseline and after 6, 12, and 24 months of GH treatment.
Main Results:
- Preterm short SGA children had higher baseline TSH than controls; FT4 levels were similar.
- GH treatment led to a significant decrease in FT4 within 6 months, remaining within normal limits.
- TSH levels did not change during GH treatment, and FT4 changes did not correlate with height SDS response.
Conclusions:
- Preterm short SGA children exhibit elevated, though normal, TSH levels not correlated with gestational age or birth size.
- GH treatment causes a mild FT4 decrease without affecting TSH or growth outcomes.
- These minor thyroid function changes are not clinically significant, obviating the need for routine thyroid monitoring during GH therapy in short SGA children.
Context:
Disturbances in thyroid function have been described in small-for-gestational age (SGA) children but the influence of prematurity is unclear. In addition, the effect of GH treatment on thyroid function has not been studied in short SGA children.
Objectives:
To determine whether short SGA children have higher TSH levels compared to age-matched controls and evaluate the influence of gestational age. To investigate whether GH treatment alters thyroid function.
Patients:
A total of 264 short SGA children (116 preterm), prepubertal and non-GH deficient.
Measurements:
Serum FT4 and TSH at baseline and after 6, 12 and 24 months of GH treatment.
Results:
Baseline mean TSH was higher in preterm short SGA children than in age-matched controls (P < 0.05). Mean FT4 was not significantly different between short SGA children and controls. Baseline FT4 or TSH did not correlate with gestational age, or SDS for birth weight, birth length, height, body mass index, IGF-I or IGFBP-3. Mean FT4 decreased significantly during the first 6 months of GH treatment, but remained within the normal range. TSH did not change during treatment. The change in FT4 did not correlate with the change in height SDS during 24 months of GH treatment.
Conclusion:
Preterm short SGA children have higher, although within the normal range, TSH levels than controls. The level of TSH does not correlate with gestational age, birth weight SDS or birth length SDS. FT4 decreases during GH treatment, but is neither associated with an increase in TSH nor does it affect the response to GH treatment. As these mild alterations in thyroid function do not appear clinically relevant, frequent monitoring of thyroid function during GH therapy is not warranted in short SGA children.
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