Functional Diffusion Tensor Imaging: Measuring Task-Related Fractional Anisotropy Changes in the Human Brain along White Matter Tracts
2008

Measuring Changes in Brain White Matter Activity with fDTI

Sample size: 8 publication 10 minutes Evidence: moderate

Author Information

Author(s): Mandl René C. W., Schnack Hugo G., Zwiers Marcel P., van der Schaaf Arjen, Kahn René S., Hulshoff Pol Hilleke E.

Primary Institution: Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht

Hypothesis

We hypothesize that fractional anisotropy changes relate to morphological changes of glial cells induced by axonal activity.

Conclusion

The results indicate that these fractional anisotropy changes may serve as a functional contrast mechanism for white matter.

Supporting Evidence

  • Activation in the sensory thalamocortical tract and optic radiation was found during tactile and visual stimulation, respectively.
  • A substantial increase in signal-to-noise ratio was achieved by pooling the signal over the complete fiber tract.
  • The fDTI method allows for the detection of task-related changes in white matter activity.

Takeaway

This study shows a new way to see how brain connections work when we do things, by looking at tiny changes in the brain's wiring.

Methodology

The study used functional diffusion tensor imaging (fDTI) to measure task-related changes in fractional anisotropy along white matter tracts in healthy subjects during tactile and visual stimulation.

Potential Biases

The sign-test used may lead to an overestimation of fiber activation due to the assumption of independence among neighboring voxels.

Limitations

The relatively large voxel size used limits the detection of tract activation to major tracts, and the study's low temporal resolution may affect the interpretation of results.

Participant Demographics

Eight healthy right-handed subjects participated in the study.

Statistical Information

P-Value

0.000000001

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0003631

Want to read the original?

Access the complete publication on the publisher's website

View Original Publication