Thompson Deanne K, Cai Shirley, Kelly Claire E, Alexander Bonnie, Matthews Lillian G, Mainzer Rheanna, Doyle Lex W, Cheong Jeanie L Y, Inder Terrie E, Yang Joseph Y M, Anderson Peter J
Victorian Infant Brain Studies, Murdoch Children's Research Institute, Parkville, VIC, 3052, Australia.
Developmental Imaging, Murdoch Children's Research Institute, Parkville, VIC, 3052, Australia.
Pediatr Res. 2025 Feb;97(2):744-750. doi: 10.1038/s41390-024-03407-w. Epub 2024 Jul 13.
Associations of neonatal infection with brain growth and later neurodevelopmental outcomes in very preterm (VP) infants are unclear. This study aimed to assess associations of neonatal sepsis in VP infants with (1) brain growth from term-equivalent age to 13 years; and (2) 13-year brain volume and neurodevelopmental outcomes.
224 infants born VP ( < 30 weeks' gestation/<1250 g birthweight) were recruited. Longitudinal brain volumes for 68 cortical and 14 subcortical regions were derived from MRI at term-equivalent, 7 and/or 13 years of age for 216 children (79 with neonatal sepsis and 137 without). 177 children (79%) had neurodevelopmental assessments at age 13. Of these, 63 with neonatal sepsis were compared with 114 without. Brain volumetric growth trajectories across time points were compared between sepsis and no-sepsis groups using mixed effects models. Linear regressions compared brain volume and neurodevelopmental outcome measures at 13 years between sepsis and no sepsis groups.
Growth trajectories were similar and there was little evidence for differences in brain volumes or neurodevelopmental domains at age 13 years between those with or without sepsis.
Neonatal sepsis in children born VP does not appear to disrupt subsequent brain development, or to have functional consequences in early adolescence.
Neonatal sepsis has been associated with poorer short-term neurodevelopmental outcomes and reduced brain volumes in very preterm infants. This manuscript provides new insights into the long-term brain development and neurodevelopmental outcomes of very preterm-born children who did or did not have neonatal sepsis. We found that regional brain volumes up to 13 years, and neurodevelopmental outcomes at age 13, were similar between those with and without neonatal sepsis. The links between neonatal sepsis and long-term neurodevelopment remain unclear.
极早产儿(VP)的新生儿感染与脑生长及后期神经发育结局之间的关联尚不清楚。本研究旨在评估VP婴儿的新生儿败血症与以下方面的关联:(1)从足月等效年龄到13岁的脑生长;(2)13岁时的脑容量和神经发育结局。
招募了224名出生时为VP(孕周<30周/出生体重<1250g)的婴儿。对216名儿童(79名有新生儿败血症,137名无)在足月等效年龄、7岁和/或13岁时通过MRI获得了68个皮质区域和14个皮质下区域的纵向脑容量。177名儿童(79%)在13岁时进行了神经发育评估。其中,将63名有新生儿败血症的儿童与114名无新生儿败血症的儿童进行了比较。使用混合效应模型比较了败血症组和无败血症组在各时间点的脑容量增长轨迹。线性回归比较了败血症组和无败血症组在13岁时的脑容量和神经发育结局指标。
生长轨迹相似,几乎没有证据表明有或无败血症的儿童在13岁时脑容量或神经发育领域存在差异。
出生时为VP的儿童发生新生儿败血症似乎不会干扰随后的脑发育,也不会在青春期早期产生功能后果。
新生儿败血症与极早产儿较差的短期神经发育结局和脑容量减少有关。本手稿为有或无新生儿败血症的极早产儿的长期脑发育和神经发育结局提供了新的见解。我们发现,有和无新生儿败血症的儿童在13岁时的区域脑容量以及13岁时的神经发育结局相似。新生儿败血症与长期神经发育之间的联系仍不清楚。