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The effect of thyroid functions on osteopenia of prematurity in preterm infants
1Division of Neonatology, Zekai Tahir Burak Women's Health Training and Research Hospital, Faculty of Medicine, University of Health Sciences, Altıntag, Ankara, Turkey.
Insights
This study found no link between congenital hypothyroidism and osteopenia of prematurity in preterm infants. Further research is needed to understand bone development in premature babies.
Area of Science:
- Neonatology
- Pediatric Endocrinology
- Bone Metabolism
Background:
- Thyroid hormones influence bone development.
- The impact of thyroid hormones on osteopenia of prematurity (OOP) in preterm infants remains under-explored.
- Congenital hypothyroidism (CH) is a potential factor affecting bone health in neonates.
Purpose of the Study:
- To investigate the association between congenital hypothyroidism (CH) and osteopenia of prematurity (OOP) in preterm infants.
- To determine if thyroid hormone levels correlate with the incidence of OOP.
- To identify risk factors for OOP in very low birth weight (VLBW) infants.
Main Methods:
- Study included 543 very low birth weight (VLBW) infants (<1500 g).
- TSH and fT4 levels measured on postnatal day 5; calcium, phosphorus, and ALP on postnatal week 4.
- OOP defined by serum ALP >700 IU/L.
Main Results:
- OOP occurred in 14.9% of VLBW infants.
- No significant difference in OOP prevalence between infants with and without CH (p=0.632).
- Lower gestational age, preeclampsia, SGA, respiratory support, LOS, BPD, and feeding time were associated with OOP.
Conclusions:
- Thyroid hormones do not appear to affect the development of OOP in preterm infants.
- Gestational age and other neonatal complications are more significantly associated with OOP.
- Further randomized controlled and long-term outcome studies are warranted.
Abstract:
Background It is known that thyroid hormones have effects on bone development. In particular, the effect of thyroid hormones on osteopenia of prematurity (OOP) has not been examined in preterm infants. Our study aimed to examine the relationship between OOP and congenital hypothyroidism (CH) in preterm infants. Methods Very low birth weight infants (VLBW, <1500 g) were included in the study. Thyroid-stimulating hormone (TSH) and free thyroxine (fT4) levels were measured on postnatal day 5. Serum calcium, phosphorus and alkaline phosphatase (ALP) levels were studied as standard screening parameters for OOP at postnatal week 4. Patients with serum ALP level >700 IU/L were included in the OOP group. We intended to figure out the relationship between OOP and CH in infants. Results In our study, OOP frequency was 14.9% among 543 VLBW infants. There was no statistically significant difference between groups with and without CH (21.7% and 14.8%, respectively) in terms of OOP (p=0.632). Gestational age (GA) was significantly lower in infants with diagnosed OOP (p<0.001, p<0.001, respectively). In addition, the prevalence rates of mothers with preeclampsia, small for gestational age (SGA), respiratory support requirement, late-onset neonatal sepsis (LOS), bronchopulmonary dysplasia (BPD) and full enteral feeding time were found to be higher in the OOP group (p<0.05). Conclusions We found that thyroid hormones had no effect on OOP in preterm infants. Therefore, future randomized controlled studies as well as long-term outcome studies are warranted on this topic.
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