ESPE Abstracts (2015) 84 P-1-126

aDepartment of Biochemical Laboratories, Institute of Child Health, Athens, Greece; bFirst Department of Pediatrics, Division of Endocrinology, Metabolism and Diabetes, Medical School, National and Kapodistrian University of Athens, Athens, Greece


Background: In vitro fertilisation (IVF) has been widely used during the last decades. Increased susceptibility to birth defects and a higher cardiometabolic risk in children born after IVF than naturally conceived (NC) children have been reported. Also, a higher incidence of hyperthyrotropinemia has been noted in children born after IVF with respect to NC children and has been attributed to an epigenetic modification of the TSH set-point.

Objective and hypotheses: To retrospectively evaluate the main characteristics and outcome of children born after IVF and diagnosed with CH.

Method: Data from the medical records of children diagnosed with CH by the Greek national screening program were reviewed.

Results: A total of 1 051 children with CH were analyzed. Of these, 152 neonates (14.5%) were born following IVF (88 boys and 64 girls; ratio 1.4:1). 89.5% of neonates born after IVF were premature (<37 gestational week) and 79.5% had a birthweight below 2500 g With respect to TSH values at diagnosis, 10% had a TSH >20 mIU/ml, 11% between 10 and 20 mIU/ml and 79% between 6 and 10 miU/ml. With respect to thyroid ultrasonography, only 4% had absence of or a very small thyroid gland. Pertinent longterm data were available in 62 boys and 48 girls. With respect to the outcome, LT4 substitution therapy was discontinued only in 50% of boys and 37% of girls.

Conclusion: Children born after IVF constitute a relatively large subgroup of children with CH, with a notable male predominance. Anatomical thyroid defects are rare. Although hypothyroidism at diagnosis is mild based on TSH values, in 50% of boys and 63% of girls born after IVF, a certain degree of dysfunction of the Hypothalamic-Pituitary-Thyroid-axis seems to persist. The reason of the gender dimorphism is not apparent.

Volume 84

54th Annual ESPE (ESPE 2015)

Barcelona, Spain
01 Oct 2015 - 03 Oct 2015

European Society for Paediatric Endocrinology 

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