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Factors associated with permanent hypothyroidism in infants with congenital hypothyroidism
Eun Sil Park1,2, Ju Young Yoon3,4
1Department of Pediatrics, Gyeongsang National University College of Medicine, Jinju, South Korea.
Insights
Higher levothyroxine doses at discontinuation may indicate permanent congenital hypothyroidism (CH). Most infants, including those discontinuing early, successfully stopped treatment, suggesting potential for earlier CH management.
Area of Science:
- Pediatric Endocrinology
- Neonatal Health
- Genetics and Development
Background:
- Congenital hypothyroidism (CH) is a common childhood endocrine disorder.
- Distinguishing transient CH from permanent CH (PCH) is crucial for management.
- Predictive factors for PCH and outcomes of early levothyroxine discontinuation are not well-established.
Purpose of the Study:
- To identify predictive factors for transient CH in infants.
- To evaluate the outcomes of early levothyroxine discontinuation in CH patients.
Main Methods:
- Retrospective chart review of infants diagnosed with CH between 2005 and 2015.
- Exclusion of infants with structural thyroid abnormalities.
- Definition of an early discontinuation subgroup (levothyroxine stopped before 30 months).
Main Results:
- Nine out of 80 infants (11.3%) had PCH.
- PCH cases required higher levothyroxine doses at discontinuation compared to transient CH (4.3 vs 2.9 μg/kg).
- A levothyroxine dose of 2.86 μg/kg predicted PCH with 88.9% sensitivity and 71.0% specificity.
Conclusions:
- Most CH patients, including those discontinuing levothyroxine early, successfully managed their condition.
- A higher levothyroxine dose at discontinuation is a significant predictive factor for PCH.
Background:
Congenital hypothyroidism (CH) is one of the most common endocrine diseases in childhood. A significant proportion of CH cases are transient, but the risk factors for permanent CH (PCH) are not yet well established. The current guidelines suggest using levothyroxine until the age of 3 years, but some studies suggest the possibility of earlier discontinuation. However, few, if any, studies have followed up on the results of early discontinuation. This study aimed to identify predictive factors of transient CH among infants with CH. We also investigated the results in patients who underwent a trial of early discontinuation.
Methods:
We gathered data regarding infants diagnosed with CH between July 2005 and July 2015 by retrospective chart review. Those with aplastic, hypoplastic or ectopic glands on thyroid ultrasonography or scan were excluded. Among them, early discontinuation subgroup was defined as those who discontinued levothyroxine before 30 months of age.
Results:
From the 80 infants (40 males, 40 females) enrolled in this study, 51 were preterm. Nine (11.3%) were diagnosed with PCH. Compared with transient cases, those with PCH were on higher levothyroxine dose at discontinuation (4.3 vs 2.9 μg/kg, P < 0.001). There was no difference in the proportion of permanent cases between preterm and full-term groups. In preterm group,infants with PCH required higher levothyroxine dose at discontinuation than those with transient CH (3.8 vs 2.5 μg/kg, P = 0.018). Levothyroxine discontinuation at a dose of 2.86 μg/kg could suggest PCH (sensitivity, 88.9%; specificity, 71.0%). Among the 9 patients who underwent a trial of early discontinuation, 8 successfully discontinued levothyroxine.
Conclusion:
The majority of CH patients discontinued levothyroxine successfully, including those who underwent a trial of early discontinuation. Higher levothyroxine dose at the time of discontinuation was found to be a predictive factor for PCH.
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