TY - JOUR
T1 - 3T MRI signal intensity profiles and thicknesses of transient zones in human fetal brain at mid-gestation
AU - Pogledic, Ivana
AU - Schwartz, Ernst
AU - Bobić-Rasonja, Mihaela
AU - Mitter, Christian
AU - Baltzer, Pascal
AU - Gruber, Gerlinde Maria
AU - Milković-Periša, Marija
AU - Haberler, Christine
AU - Bettelheim, Dieter
AU - Kasprian, Gregor
AU - Judaš, Miloš
AU - Prayer, Daniela
AU - Jovanov-Milošević, Nataša
N1 - Publisher Copyright:
© 2021
PY - 2021/11
Y1 - 2021/11
N2 - In this study we compare temporal lobe (TL) signal intensity (SI) profiles, along with the average thicknesses of the transient zones obtained from postmortem MRI (pMRI) scans and corresponding histological slices, to the frontal lobe (FL) SI and zone thicknesses, in normal fetal brains. The purpose was to assess the synchronization of the corticogenetic processes in different brain lobes. Nine postmortem human fetal brains without cerebral pathologies, from 19 to 24 weeks of gestation (GW) were analyzed on T2-weighted 3T pMRI, at the coronal level of the thalamus and basal ganglia. The SI profiles of the transient zones in the TL correlate well spatially and temporally to the signal intensity profile of the FL. During the examined period, in the TL, the intermediate and subventricular zone are about the size of the subplate zone (SP), while the superficial SP demonstrates the highest signal intensity. The correlation of the SI profiles and the distributions of the transient zones in the two brain lobes, indicates a time-aligned histogenesis during this narrow time window. The 3TpMRI enables an assessment of the regularity of lamination patterns in the fetal telencephalic wall, upon comparative evaluation of sizes of the transient developmental zones and the SI profiles of different cortical regions. A knowledge of normal vs. abnormal transient lamination patterns and the SI profiles is a prerequisite for further advancement of the MR diagnostic tools needed for early detection of developmental brain pathologies prenatally, especially mild white matter injuries such as lesions of TL due to prenatal cytomegalovirus infections, or cortical malformations.
AB - In this study we compare temporal lobe (TL) signal intensity (SI) profiles, along with the average thicknesses of the transient zones obtained from postmortem MRI (pMRI) scans and corresponding histological slices, to the frontal lobe (FL) SI and zone thicknesses, in normal fetal brains. The purpose was to assess the synchronization of the corticogenetic processes in different brain lobes. Nine postmortem human fetal brains without cerebral pathologies, from 19 to 24 weeks of gestation (GW) were analyzed on T2-weighted 3T pMRI, at the coronal level of the thalamus and basal ganglia. The SI profiles of the transient zones in the TL correlate well spatially and temporally to the signal intensity profile of the FL. During the examined period, in the TL, the intermediate and subventricular zone are about the size of the subplate zone (SP), while the superficial SP demonstrates the highest signal intensity. The correlation of the SI profiles and the distributions of the transient zones in the two brain lobes, indicates a time-aligned histogenesis during this narrow time window. The 3TpMRI enables an assessment of the regularity of lamination patterns in the fetal telencephalic wall, upon comparative evaluation of sizes of the transient developmental zones and the SI profiles of different cortical regions. A knowledge of normal vs. abnormal transient lamination patterns and the SI profiles is a prerequisite for further advancement of the MR diagnostic tools needed for early detection of developmental brain pathologies prenatally, especially mild white matter injuries such as lesions of TL due to prenatal cytomegalovirus infections, or cortical malformations.
KW - Autopsy
KW - Brain/diagnostic imaging
KW - Female
KW - Humans
KW - Magnetic Resonance Imaging
KW - Pregnancy
UR - http://www.scopus.com/inward/record.url?scp=85116945548&partnerID=8YFLogxK
U2 - 10.1016/j.ejpn.2021.09.014
DO - 10.1016/j.ejpn.2021.09.014
M3 - Journal article
C2 - 34653829
SN - 1090-3798
VL - 35
SP - 67
EP - 73
JO - European Journal of Paediatric Neurology
JF - European Journal of Paediatric Neurology
ER -