from Tom....

---------- Forwarded message ----------
Date: Thu, 12 Jul 2018 16:51:31 +0100
From: Thomas Nichols <thomas.nich...@bdi.ox.ac.uk>
To: Bruce Fischl <fis...@nmr.mgh.harvard.edu>
Cc: freesurfer@nmr.mgh.harvard.edu
Subject: Re: [Freesurfer] Cortical Thickness at Individual Vertices


        External Email - Use Caution        

Hi Bruce!
James: I don't have any particular deep thoughts except, all things equal, if 
you have a tenable
continuous summary of the mTBI deficits it will probably be more sensitivity 
than a discrete
count-based summary of the deficits.

Bruce's idea of comparing distributions is sound but probably will only work 
well for mTBI effect
that are diffuse.  For localised effects (that are not spatially consistent), 
finding some summary
measure of the deficits are probably the best way forward.

-Tom

On Thu, Jul 12, 2018 at 4:31 PM Bruce Fischl <fis...@nmr.mgh.harvard.edu> wrote:
      Hi James

      you could use techniques that compare the whole distribution of
      thicknesses across subject populations. You could do a t-test or something
      non-parametric like a Kolmogorov-Smirnov or use permutation testing. I'll
      cc Tom Nichols so he can chime in with something more sophisticated or
      specific.

      cheers
      Bruce



      On Wed, 11 Jul 2018, James Gullickson
      wrote:

      >
      >         External Email - Use Caution        
      >
      > All,
      > I am comparing cortical thickness between subjects with and without 
mild traumatic
      brain injury
      > (mTBI). So far the contrasts in QDEC have not been significant after 
correcting for
      multiple
      > comparisons. I am not necessarily surprised at this due to the 
heterogeneous nature of
      mTBI in our
      > sample, i.e. we do not expect any two subjects to have damage in the 
same area. I am
      interested in
      > ways to compare cortical thickness that are not dependent on a single 
ROI having an
      effect across
      > subjects. One way I have tried is calculating z-scores for the values 
in the
      aparc.stats file, and
      > using the number of abnormally low ROIs as a dependant variable to 
compare between
      groups. 
      >
      > Is there a way to look at thickness differences at an even more general 
level? E.g. by
      comparing the
      > number of vertices with abnormally low thickness? If so how would one 
go about that
      with Freesurfer
      > data?
      >
      > This paper takes a similar approach with DTI. I'd like to do something 
analogous to
      their "number of
      > voxels with low FA" analysis.
      > https://www.sciencedirect.com/science/article/pii/S1053811911012146
      >
      > Thanks,
      >
      > James
      >
      >


      The information in this e-mail is intended only for the person to whom it 
is
      addressed. If you believe this e-mail was sent to you in error and the 
e-mail
      contains patient information, please contact the Partners Compliance 
HelpLine at
      http://www.partners.org/complianceline . If the e-mail was sent to you in 
error
      but does not contain patient information, please contact the sender and 
properly
      dispose of the e-mail.



--
__________________________________________________________
Thomas Nichols, PhD
Professor of Neuroimaging Statistics
Nuffield Department of Population Health | University of Oxford
Big Data Institute | Li Ka Shing Centre for Health Information and Discovery
Old Road Campus | Headington | Oxford | OX3 7LF | United Kingdom
T: +44 1865 743590 | E: thomas.nich...@bdi.ox.ac.uk
W: http://nisox.org | http://www.bdi.ox.ac.uk
_______________________________________________
Freesurfer mailing list
Freesurfer@nmr.mgh.harvard.edu
https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer


The information in this e-mail is intended only for the person to whom it is
addressed. If you believe this e-mail was sent to you in error and the e-mail
contains patient information, please contact the Partners Compliance HelpLine at
http://www.partners.org/complianceline . If the e-mail was sent to you in error
but does not contain patient information, please contact the sender and properly
dispose of the e-mail.

Reply via email to