Thank you Michael!

LT


On Mon, Mar 11, 2013 at 8:54 AM, Michael Harms <mha...@conte.wustl.edu>wrote:

>
> Hi Laura,
> If you're looking for another reference that has used this approach, you
> could see our 2010 paper:
> http://www.ncbi.nlm.nih.gov/pubmed/20118463
>
> cheers,
> -MH
>
> --
> Michael Harms, Ph.D.
> -----------------------------------------------------------
> Conte Center for the Neuroscience of Mental Disorders
> Washington University School of Medicine
> Department of Psychiatry, Box 8134
> 660 South Euclid Ave. Tel: 314-747-6173
> St. Louis, MO  63110 Email: mha...@wustl.edu
>
> From: "Laura M. Tully" <tully.la...@googlemail.com>
> Date: Saturday, March 9, 2013 5:58 PM
> To: "Anderson M. Winkler" <wink...@fmrib.ox.ac.uk>
> Cc: free <freesurfer@nmr.mgh.harvard.edu>
> Subject: Re: [Freesurfer] mean thickness covariate, mean area covariate,
> & mri_anatomical_stats for multiple subjects
>
> Hi Anderson,
>
> Thanks, that reference is particularly helpful.
>
> Re: the usage of the white versus pial area question - I believe that the
> default area calculation in freesurfer is the white surface area, so unless
> one specifies the pial in calculations, the standard surface area output
> for surface area by parcellation will be white. This suggests the use of
> the global measurement of white surface area as a covariate would be an
> appropriate, whereas if one was specifically using pial surface area in the
> aparc calculations, it may make more sense to use the global measure of
> pial surface area as a covariate, correct? As for which one to use in
> analysis, I'm not sure - conceptually it might be that the pial surface
> area is more sensitive to atrophy but I don't know if that is born out in
> the data...
>
> Laura.
>
>
> On Sat, Mar 9, 2013 at 11:49 AM, Anderson M. Winkler <
> wink...@fmrib.ox.ac.uk> wrote:
>
>> Hi Laura,
>>
>>
>>
>>>    1. Is there a paper that I could cite that recommends using mean
>>>    cortical thickness rather than ICV?
>>>
>>>
>> If it helps, we used cortical thickness and area as covariate for the
>> respective analysis of regional thickness and area. Brain volume, which is
>> more closely related to ICV, correlates well with area, but not with
>> thickness. We computed a global thickness average by weighting the
>> thickness of each region by their respective areas. The paper is this:
>> http://surfer.nmr.mgh.harvard.edu/ftp/articles/Winkler2010_Neuroimage.pdf
>>
>>
>>>
>>>    1. Would the same logic be applied to surface area analyses? i.e.
>>>    would it make more sense to use mean surface area as a covariate in 
>>> surface
>>>    area analyses? If so, which mean surface area calculation should be used?
>>>    mri_anatomical_stats can produce both pial and white matter mean surface
>>>    area stats.
>>>
>>>
>> Yes, I think so. It seems more logical to have a global measurement of
>> area in the model than a measurement of brain volume. On the other hand,
>> area and thickness are not correlated one to another (as shown in the paper
>> above and also in Panizzon et al, 2009, in Cereb Cortex). I don't think
>> there is a clear answer on which, pial or white, should be used. I'd
>> probably go with the white, as I think it may be more robust to image
>> quality, but I admit this is a rather weak justification and if the images
>> are good, perhaps the pial could be just as good, despite the fact that it
>> somewhat depends on the white for its construction.
>>
>>
>>
>>>
>>>    1. Is there a way to run mri_anatomical_stats on multiple subjects
>>>    at once and write to a tablefile (similar to asegstats2table output)?
>>>
>>>
>> I think you can use aparcstats2table, then add up all regions in a
>> spreadsheet (or even with awk/gawk). Alternatively, you can use "grep" to
>> pick the WhiteSurfArea for each hemisphere from the ?h.aparc.stats file for
>> each subject.
>>
>> Hope this helps!
>>
>> All the best,
>>
>> Anderson
>>
>>
>
>
> --
> --
> Laura M. Tully, MA
> Social Neuroscience & Psychopathology, Harvard University
> Center for the Assessment and Prevention of Prodromal States, UCLA Semel
> Institute of Neuroscience
> ltu...@mednet.ucla.edu
> ltu...@fas.harvard.edu
> 310-267-0170
> --
> My musings as a young clinical scientist:
> http://theclinicalbrain.blogspot.com/
> Follow me on Twitter: @tully_laura
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-- 
--
Laura M. Tully, MA
Social Neuroscience & Psychopathology, Harvard University
Center for the Assessment and Prevention of Prodromal States, UCLA Semel
Institute of Neuroscience
ltu...@mednet.ucla.edu
ltu...@fas.harvard.edu
310-267-0170
--
My musings as a young clinical scientist:
http://theclinicalbrain.blogspot.com/
Follow me on Twitter: @tully_laura
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