Hi Dr Greve,
>
> Dear Dr Greve,
>
> Thank you very much for the great explanation. I
will definitely
> correct for PVC using PET surfer.
>
> Kindly I have one follow-up question and I highly
appreciate your input.
>
> I have PET data for two groups. I studied the
difference in PET signal
> using voxel-wise ( FSL/randomise) and surface-based using PET surfer.
>
> My question is about PVC. We correct for PVC in
surface based because
> we re-sample PET data to the brain surface which is
an output of
> segmentation process, meaning we expect partial
volume effects between
> the grey/white for a possible contamination between them during
> segmentation.
>
> We don't do PVE in voxel-wise because we don't worry
about the
> contamination meaning there are no segmentation
lines to separate
> between brain regions.
>
> Kindly is my understanding for this fact correct (
i.e. why we correct
> in surface based and we don't correct in
voxel-wise).
It is not correct. You do PVC to remove interactions
between the anatomy and the PET through PVEs. Those will be there in both
surface-based and volume-based analysis. If you perform smoothing in volume-based analysis, you will make the
PVEs worse. Doing MG PVC then volume-based smoothing will result in a disaster.
In my opinion, the only way to do PVC in a map-based analysis (vs ROI) is to do
it on the surface. For subcortical, you can do volume-based smoothing within a
GM mask.
> By the way, I ran voxel-wise using randomise with
TFCE and 5000
> permutations.
For the surface, you can use mri_glmfit with the --perm
option.
>
> Thank you again for any clarification
> John
>
>
>
>
> The PET signalcan change with a lot of anatomical
changes in the brain
> including thickness, surface area, and gyrification.
There is no known
> regressor that will account for this. Right right
way to account for
> it is with partialvolume correction (PVC). It is
best to do PVC
> simultaneously with the recon, but software is not
available to
> perform this. You can do it on a post-hoc basis in
PETsurfer using the
> PVC options in mri_gtmpvc. See the wiki.
>
>
>
> On 08/10/2017 04:11 AM, John Anderson wrote:
>
> >
>
> > Hi Dr Greve,
>
> >
>
> > I have PET data for two groups and I used PET
surfer in FSV 6.0 to
> > run
>
> > the analyses. The pipeline is straightforward
and the analysis ran
>
> > smoothly without any issues.
>
> >
>
> > Is it correct procedure to adjust PET signal to
differences in gray
>
> > matter volume or cortical thinness between two
groups?
>
> >
>
> > In other words, is it correct if gray matter
volume or cortical
>
> > thickness for subjects be included as EVs in
GLM or a nausiance
> > factor
>
> > in QDEC?
>
> >
>
> > Specifically, is the PET signal changeable
depending ondifferences
>
> > in cortical thickness.
>
> > or differences in gray matter volume?
>
> >
>
> > Thank youfor any clarification
>
> >
>
> >> Thank you !
>
> >> Jon
>
> >>
>
> >
>
> >
>
> >
>
> > _______________________________________________
>
> > Freesurfer mailing list
>
> > Freesurfer@nmr.mgh.harvard.edu
> > <mailto:Freesurfer@nmr.mgh.harvard.edu>
>
> > https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
>
>
> --
>
> Douglas N. Greve, Ph.D.
>
> MGH-NMR Center
>
> greve@nmr.mgh.harvard.edu <mailto:greve@nmr.mgh.harvard.edu>
>
> Phone Number: 617-724-2358
>
> Fax: 617-726-7422
>
>
> Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
> <http://surfer.nmr.mgh.harvard.edu/fswiki/BugReporting>
>
> FileDrop: https://gate.nmr.mgh.harvard.edu/filedrop2
>
> www.nmr.mgh.harvard.edu/facility/filedrop/index.html
> <http://www.nmr.mgh.harvard.edu/facility/filedrop/index.html>
>
> Outgoing:
> ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/
>
>
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>
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>
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>
>
>> -------- Original Message --------
>> Subject: PET surfer
>> Local Time: August 10, 2017 4:11 AM
>> UTC Time: August 10, 2017 8:11 AM
>> From: John.anderso@protonmail.com
>> To: Freesurfer support list <freesurfer@nmr.mgh.harvard.edu>
>>
>> Hi Dr Greve,
>>
>> I have PET data for two groups and I used PET
surfer in FSV 6.0 to
>> run the analyses. The pipeline is
straightforward and the analysis
>> ran smoothly without any issues.
>>
>> Is it correct procedure to adjust PET signal to
differences in gray
>> matter volume or cortical thinness between two
groups?
>>
>> In other words, is it correct if gray matter
volume or cortical
>> thickness for subjects be included as EVs in GLM
or a nausiance
>> factor in QDEC?
>>
>> Specifically, is the PET signal changeable
depending on differences
>> in cortical thickness.
>> or differences in gray matter volume?
>>
>> Thank you for any clarification
>>
>>> Thank you !
>>> Jon
>>>
>>
>
>
>
> _______________________________________________
> Freesurfer mailing list
> Freesurfer@nmr.mgh.harvard.edu
> https://mail.nmr.mgh.harvard.edu/mailman/listinfo/freesurfer
--
Douglas N. Greve, Ph.D.
MGH-NMR Center
Phone Number: 617-724-2358
Fax: 617-726-7422
Bugs: surfer.nmr.mgh.harvard.edu/fswiki/BugReporting
FileDrop: https://gate.nmr.mgh.harvard.edu/filedrop2
www.nmr.mgh.harvard.edu/facility/filedrop/index.html
Outgoing: ftp://surfer.nmr.mgh.harvard.edu/transfer/outgoing/flat/greve/
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