Neonatal hydrocortisone treatment related to 1H-MRS of the hippocampus and short-term memory at school age in preterm born children

• Published in: Pediatric research Vol. 59; no. 2; pp. 309 - 313
• Main Authors: RADEMAKER, Karin J, RIJPERT, Maarten, UITERWAAL, Cuno S. P. M, LIEFTINK, Arno F, VAN BEL, Frank, GROBBEE, Diederick E, DE VRIES, Linda S, GROENENDAAL, Floris
• Format: Journal Article
• Language: English
• Published: Hagerstown, MD Lippincott Williams & Wilkins 01.02.2006
• Subjects: Biological and medical sciences; General aspects; Hippocampus - anatomy & histology; Hippocampus - physiology; Humans; Infant, Newborn; Infant, Premature - physiology; Intelligence; Magnetic Resonance Spectroscopy; Medical sciences; Memory, Short-Term; Mental Recall; Human; Short term; Premature; Corticosteroid; Pediatrics; Neonatal; Steroid hormone; Memory; Central nervous system; Antiinflammatory agent; Hydrocortisone; Birth; Glucocorticoid; Encephalon; Pregnancy; School age; Newborn; Treatment; Prematurity; Adrenal hormone; Child; Hippocampus
• ISSN: 0031-3998; 1530-0447
• DOI: 10.1203/01.pdr.0000196377.13816.61

Animal studies have shown that corticosteroids (dexamethasone) cause neuronal loss in the hippocampus and deficits in short term memory. Proton magnetic resonance spectroscopy can measure brain metabolites in vivo and give an indication of neuronal integrity. We investigated whether prolonged administration of hydrocortisone during the neonatal period for bronchopulmonary dysplasia (BPD) in preterm born children changes the metabolism in the hippocampus, measured at school age. Secondly, we investigated whether hippocampal metabolism and short-term memory and neurodevelopmental outcome are related. In this observational study 37 preterm born children (< or = 32 wk (range 25.0-33.0) and/or a birth weight < or = 1500 g) underwent proton spectroscopy of the hippocampus at school age. Eighteen children were treated with hydrocortisone for BPD (starting dose 5 mg/kg/d tapered over a minimum period of 22 d, median duration 28 d) and 19 never received corticosteroids during the perinatal period. N-acetyl aspartate/ Choline + Creatine/phosphocreatine (NAA/(Cho + Cr)) ratios were determined. A 15-word recall memory test and an IQ measurement were obtained on the same day. Hydrocortisone treated children were younger, lighter and sicker than their nonsteroid treated counterparts. Mean NAA/(Cho + Cr) ratios in the hippocampus were not significantly different in the hydrocortisone group compared with the non-steroid group. Performance on the 15-word memory test and IQ were similar in the two groups. There was no relation between NAA/(Cho + Cr) ratios and memory nor between NAA/(Cho + Cr) ratios and IQ. We conclude that hydrocortisone in the mentioned dose, administered in the neonatal period for BPD, does not appear to have any long-term effects on memory and/or hippocampal metabolism.