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Associations between Early Thyroid-Stimulating Hormone Levels and Morbidities in Extremely Preterm Neonates
Li-Wen Chen1, Chi-Hsiang Chu2, Yung-Chieh Lin3
1Department of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan, muffychen@gmail.com.
Insights
Low thyroid-stimulating hormone (TSH) levels in extremely preterm infants are linked to severe respiratory distress syndrome and brain injuries. Further research is needed to understand thyroid function in these vulnerable neonates.
Area of Science:
- Neonatal Medicine
- Endocrinology
- Pediatric Neurology
Background:
- High-end cutoffs for thyroid-stimulating hormone (TSH) are established for hypothyroidism therapy in extremely preterm infants.
- The clinical significance of low TSH levels in this population remains largely unknown.
- This study investigated the relationship between TSH levels and neonatal morbidities.
Purpose of the Study:
- To determine if the spectrum of TSH levels at newborn screening correlates with specific morbidities in extremely preterm neonates.
- To analyze the association between different TSH level categories and neonatal outcomes.
Main Methods:
- A multicenter cohort study analyzed 434 extremely preterm neonates.
- Neonates were screened for TSH levels within 24-96 hours of birth and categorized into four groups based on TSH values.
- Neonatal morbidities were assessed using the modified Neonatal Therapeutic Intervention Scoring System.
Main Results:
- Groups with lower TSH levels showed significant differences in gestational age, birth weight, and postnatal age at sampling.
- Lower TSH groups had higher incidences of mechanical ventilation, hypoxic respiratory failure, intraventricular hemorrhage, and periventricular leukomalacia.
- Specifically, the lowest TSH group (<0.5 µU/mL) exhibited significantly higher severity scores for respiratory distress syndrome and brain injury compared to the next TSH group, even after adjusting for confounding factors.
Conclusions:
- Low TSH levels in extremely preterm neonates are associated with increased severity of respiratory distress syndrome and brain injuries.
- Further research with larger cohorts and comprehensive thyroid function data is required to elucidate the interactions within the hypothalamic-pituitary-thyroid axis in this population.
Introduction:
High-end cutoffs of thyroid-stimulating hormone (TSH) have been emphasized for hypothyroidism therapy in extremely preterm infants, but the significance of low TSH levels remains unknown. This study hypothesized that the spectrum of TSH levels by newborn screening after birth signifies specific morbidities in extremely preterm neonates.
Methods:
The multicenter population cohort analyzed 434 extremely preterm neonates receiving TSH screening at 24-96 h of age in 2008-2019. Neonates were categorized by blood TSH levels into group 1: TSH <0.5 µU/mL, group 2: 0.5 ≤ TSH <2 µU/mL, group 3: 2 ≤ TSH <4 µU/mL, and group 4: TSH ≥4 µU/mL. Neonatal morbidities were categorized using the modified Neonatal Therapeutic Intervention Scoring System.
Results:
The four groups differed in gestational age, birth weight, and the postnatal age at blood sampling so did the proportions of mechanical ventilation usage (p = 0.01), hypoxic respiratory failure (p = 0.005), high-grade intraventricular hemorrhage (p = 0.007), and periventricular leukomalacia (p = 0.048). Group 1 had higher severity scores for respiratory distress syndrome (RDS; effect size 0.39 [95% confidence interval [CI]: 0.18-0.59]) and brain injury (0.36 [0.15-0.57]) than group 2, which remained significant after adjusting for gestational age, birth weight, dopamine usage, and the postnatal age at TSH screening (RDS: mean + 0.45 points [95% CI: 0.11-0.79]; brain injury: +0.32 [0.11-0.54]).
Conclusions:
Low TSH levels in extremely preterm neonates are associated with severe RDS and brain injuries. Studies recruiting more neonates with complete thyroid function data are necessary to understand central-peripheral interactions of the hypothalamic-pituitary-thyroid axis.
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