Background: Adverse neurodevelopmental outcomes and MRI alterations are reported in infants born after fetal growth restriction (FGR). This study evaluates the additional role of FGR over prematurity in determining brain impairment. Methods: Retrospective observational study comparing 48 FGR and 36 appropriate for gestational age infants born between 26 and 32 weeks’ gestation who underwent a cerebral MRI at term equivalent age. Exclusion criteria were twins, congenital anomalies, and findings of overt brain lesions. Main outcomes were total maturation score (TMS) and cerebral areas independently measured by two neuro-radiologists and Griffiths or Bayley scale III scores at median age of 2 years. Results: TMS was not significantly different between the groups. Inner calvarium and parenchyma’s areas were significantly smaller in FGR cases. There were no significant differences in the average quotient scores. A positive correlation between parenchyma area and cognitive score was found (r = 0.372, p = 0.0078) and confirmed after adjusting for sex, gestational age, and birth weight (p = 0.0014). Among FGR, the subgroup with umbilical arterial Doppler velocimetry alterations had significantly worse gross motor scores (p = 0.005). Conclusions: FGR plays additional role over prematurity in determining brain impairment. An early structural dimensional MRI evaluation may identify infants who are at higher risk. Impact: Fetal growth-restricted infants showed smaller cerebral parenchymal areas than preterm controls.There is a positive correlation between the parenchyma area and the cognitive score.These results highlight the already known link between structure and function and add importance to the role of a structural dimensional MRI evaluation even in the absence of overt brain lesions.
Neuroimaging and neurodevelopmental outcome after early fetal growth restriction: NEUROPROJECT—FGR / G. Brembilla, A. Righini, B. Scelsa, G. Lista, M. Balestriero, E. Cesari, F.M. Castoldi, M. Di Stasi, C. Ciardi, E. Ligato, E. Taricco, I. Cetin. - In: PEDIATRIC RESEARCH. - ISSN 0031-3998. - 90:4(2021), pp. 869-875. [10.1038/s41390-020-01333-1]
Neuroimaging and neurodevelopmental outcome after early fetal growth restriction: NEUROPROJECT—FGR
G. BrembillaPrimo
;E. Ligato;I. CetinUltimo
2021
Abstract
Background: Adverse neurodevelopmental outcomes and MRI alterations are reported in infants born after fetal growth restriction (FGR). This study evaluates the additional role of FGR over prematurity in determining brain impairment. Methods: Retrospective observational study comparing 48 FGR and 36 appropriate for gestational age infants born between 26 and 32 weeks’ gestation who underwent a cerebral MRI at term equivalent age. Exclusion criteria were twins, congenital anomalies, and findings of overt brain lesions. Main outcomes were total maturation score (TMS) and cerebral areas independently measured by two neuro-radiologists and Griffiths or Bayley scale III scores at median age of 2 years. Results: TMS was not significantly different between the groups. Inner calvarium and parenchyma’s areas were significantly smaller in FGR cases. There were no significant differences in the average quotient scores. A positive correlation between parenchyma area and cognitive score was found (r = 0.372, p = 0.0078) and confirmed after adjusting for sex, gestational age, and birth weight (p = 0.0014). Among FGR, the subgroup with umbilical arterial Doppler velocimetry alterations had significantly worse gross motor scores (p = 0.005). Conclusions: FGR plays additional role over prematurity in determining brain impairment. An early structural dimensional MRI evaluation may identify infants who are at higher risk. Impact: Fetal growth-restricted infants showed smaller cerebral parenchymal areas than preterm controls.There is a positive correlation between the parenchyma area and the cognitive score.These results highlight the already known link between structure and function and add importance to the role of a structural dimensional MRI evaluation even in the absence of overt brain lesions.File | Dimensione | Formato | |
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