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DOI 10.5114/pedm.2026.163264

Медицинская библиотека · Pediatric endocrinology, diabetes, and metabolism · 2026

Medium-chain acyl-CoA dehydrogenase deficiency in the neonatal period: a case report.

Wądołowska Aleksandra, Suda-Całus Magdalena Alicja, Gulczyńska Ewa Matylda

СтатьяКлинический случайПеревод пока не подготовлен

Аннотация

OBJECTIVE

To determine whether gestational diabetes mellitus (GDM) is associated with increased incidence of neonatal hyperthyrotropinemia.

STUDY

DESIGN

In a retrospective study, maternal characteristics, infant outcome and cord blood thyrotropin (TSH) concentration were compared between 469 diet-treated GDM pregnancies diagnosed by the World Health Organization 75 g oral glucose tolerance test (OGTT) with 474 non-diabetic pregnancies with normal OGTT results.

RESULTS

Hyperthyrotropinemia (TSH >16 mIU/l) was found in 7.2% of the GDM pregnancies and 2.1% of the controls (p < 0.001), but there was no difference in the birth weight or gestational age. The TSH concentration was correlated with the OGTT 2-hour glucose value (rho = 0.0948, p = 0.029) and Apgar score at the fifth minute (rho = -0.1197, p = 0.009). There was no difference in the TSH or free thyroxine concentrations between the hyperthyrotropinemic newborns of the GDM and control groups. In the GDM group, the hyperthyrotropinemic newborns had a higher incidence (p = 0.017) of neonatal jaundice.

CONCLUSIONS

Neonatal hyperthyrotropinemia is more frequently found in pregnancies with GDM, and this could have reflected increased fetal in-utero hypoxic stress in these pregnancies.

Для цитирования: Wądołowska Aleksandra, Suda-Całus Magdalena Alicja, Gulczyńska Ewa Matylda. Medium-chain acyl-CoA dehydrogenase deficiency in the neonatal period: a case report.. Pediatric endocrinology, diabetes, and metabolism. 2026. DOI: 10.5114/pedm.2026.163264.

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