Neonatology Department, University Medical Center Utrecht, Utrecht, The Netherlands.
Neonatology. 2013;104(2):143-50. doi: 10.1159/000351017. Epub 2013 Jul 24.
Detection of white matter (WM) abnormalities on MRI is important regarding the neurodevelopmental outcome in preterm infants. The long-term neurodevelopmental outcome of preterm infants with postnatal cytomegalovirus (CMV) infection has not been studied extensively.
We aimed to assess WM microstructure in preterm infants with postnatal CMV infection using diffusion tensor imaging.
Infants <32 weeks' gestational age (GA) admitted to our hospital between 2007 and 2010, who had cerebral diffusion tensor imaging at term-equivalent age (40 weeks' GA) were included. CMV PCR in urine collected at term-equivalent age was performed to diagnose postnatal CMV infection. Congenital infection was excluded. In the frontal, parietal and occipital WM mean diffusivity, fractional anisotropy (FA), radial and axial diffusivity were calculated. Neurodevelopmental outcome was assessed at 16 months' corrected age using Griffiths' Mental Developmental Scales.
Twenty-one postnatally infected and 61 noninfected infants were eligible. Both groups were comparable regarding GA, birth weight and age at MRI. There was a significant difference in median FA of the occipital WM between infected and noninfected infants (0.13 [IQR 0.11-0.16] versus 0.16 [IQR 0.14-0.18], p = 0.002). There were no differences in short-term neurodevelopmental outcome between infected and noninfected infants.
A significantly reduced FA suggests microstructural changes in the occipital WM of postnatally infected infants. These microstructural changes do not appear to result in impaired neurodevelopmental outcome at 16 months' corrected age.
MRI 上检测到的脑白质(WM)异常与早产儿的神经发育结局有关。患有后天性巨细胞病毒(CMV)感染的早产儿的长期神经发育结局尚未得到广泛研究。
我们旨在使用弥散张量成像评估患有后天性 CMV 感染的早产儿的 WM 微观结构。
纳入 2007 年至 2010 年期间我院收治的胎龄<32 周且在校正胎龄 40 周时进行脑弥散张量成像的婴儿。通过在校正胎龄 40 周时收集的尿液进行 CMV PCR 以诊断后天性 CMV 感染。排除先天性感染。在额、顶和枕叶 WM 中计算平均弥散度、分数各向异性(FA)、径向和轴向弥散度。在 16 个月的校正年龄使用 Griffiths 精神发育量表评估神经发育结局。
21 例后天性感染和 61 例非感染婴儿符合条件。两组的胎龄、出生体重和 MRI 年龄均相似。感染组和非感染组之间枕叶 WM 的 FA 中位数存在显著差异(0.13 [IQR 0.11-0.16]与 0.16 [IQR 0.14-0.18],p = 0.002)。感染组和非感染组的短期神经发育结局无差异。
FA 显著降低提示后天性感染婴儿的枕叶 WM 微观结构发生改变。这些微观结构变化似乎不会导致 16 个月校正年龄时神经发育结局受损。