Related Experiment Video
Updated: Jun 21, 2026

09:33
Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
Published on: July 28, 2013
Correlation of diffusion tensor imaging with histology in the developing human frontal cerebrum
Richa Trivedi1, Nuzhat Husain, Ram K S Rathore
1Department of Radiodiagnosis, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Developmental Neuroscience
|July 23, 2009
Summary
Fractional anisotropy (FA) in fetal brain scans correlates with histological markers of neurodevelopment. This suggests FA can noninvasively track early brain development in the frontal lobe.
Area of Science:
- Neuroscience
- Developmental Biology
- Medical Imaging
Background:
- Early human brain development involves transient cerebral laminar organization.
- Diffusion Tensor Imaging (DTI) studies suggest Fractional Anisotropy (FA) differentiates laminar structures based on cellular density and fiber alignment.
- Histology confirms these developmental events but is invasive.
Purpose of the Study:
- To correlate Fractional Anisotropy (FA) values in transient fetal brain zones with histological findings.
- To investigate FA as a noninvasive marker for early neurodevelopmental events.
Main Methods:
- Brain DTI was performed on 50 human fetuses (12-42 weeks gestational age).
- Regions of interest (cortical plate, subplate, intermediate zone, germinal matrix) were analyzed for FA values.
- Immunohistochemical analysis (GFAP, NF, NSE) was conducted on corresponding fetal brain tissues.
Main Results:
- Positive correlation between FA and GFAP in the cortical plate for fetuses ≤28 weeks (r=0.56, p=0.01).
- Positive correlation between FA and NF in the intermediate zone (r=0.54, p=0.05).
- Positive correlation between FA and NSE in the germinal matrix (r=0.76, p<0.01) and subplate (r=0.59, p=0.03) zones.
Conclusions:
- FA values in specific fetal brain regions correlate significantly with histological markers of neurodevelopment.
- Fractional Anisotropy (FA) shows potential as a noninvasive biomarker for tracking early neurodevelopmental events in the human fetal frontal lobe.

