Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-08 Thread Anastasia Yendiki


Fantastic! I love problems that solve themselves :) I won't be at ISMRM, 
but I'd be interested in seeing your results.


On Sun, 7 Apr 2013, Sean Hatton wrote:


I reinitialised the tracts and they all make sense now :) Hope to see you
all at ISMRM.

Sean Hatton
Brain and Mind Research Institute
University of Sydney.




On 5/04/13 7:21 AM, Anastasia Yendiki ayend...@nmr.mgh.harvard.edu
wrote:



It's the pathstats.byvoxel.txt file.

On Thu, 4 Apr 2013, Sean Hatton wrote:


There are no extreme outliers (only 3 moderate outliers). Regarding the
position, is that the FA center measures?

Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


The increase in FA in patients is strange indeed. Are there any outliers
in the tract averages? (Sorry if you've already mentioned this.)

There are definitely situations in which TBSS and tracula would give you
different results, since tracula gives you average FA in a large bundle,
whereas TBSS gives voxel-based differences, where the voxels are on the
skeleton of the white matter. So you could imagine a situation where
part
of a tract shows a decrease and other parts don't. Have you looked at
the
FA as a function of position along the tract from tracula (the other
stats
file that it gives you)?

On Thu, 4 Apr 2013, Sean Hatton wrote:


Yes, TBSS has reductions in FA in the patients' ATR cf controls (TFCE
corrected, p. 05), but extracting the path stats in Tracula have the
patients' ATR FA increased cf controls (independent t test, p. 05,
uncorrected as per Yendiki et al. 2011).

Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


Hm, it doesn't sound like a failure in the tract reconstruction then.
What
areas does TBSS give you differences in? Is it in the area of the same
tracts?

On Thu, 4 Apr 2013, Sean Hatton wrote:



Hi Anastasia,

An independent T-test on the aseg.stats WM-Hypointensties (SegId
77) showed that the
mean WM hypointensities volume of the patient group (1378.8mm3, SD
650mm3) did not
significantly differ from the controls (1120.8mm3, SD 372mm3;
p=.111). A Pearson and
Spearman correlation analysis found no correlation of WMH volume with
tract volumes
but did find a correlation with FA in three of the nine tracts of
interest (Forceps
minor, left ATR, left ILF). I reviewed the T2-FLAIRs for the subjects
with the highest
volumes of WM lesions and they were all dirty-appearing white matter
around the
ventricles rather than punctate WMH within the regions of these
tracts.

The tracts look reasonable in FreeviewŠ scratching head

Sean




On 4/04/13 7:17 AM, Anastasia Yendiki
ayend...@nmr.mgh.harvard.edu wrote:


Hi Sean - Can you check their freesurfer aseg's and see if any of the
white matter was classified as a hypointensity there?

a.y

On Wed, 3 Apr 2013, Sean Hatton wrote:

  This is Tracula 5.2 with FLIRT and the vectors are correctly
aligned
  (V1 over FA).
From the literature and what is seen in my TBSS is reduced FA in the
minor
forceps and
ATR.
These are young (23yo) psychiatric so age related atrophy is not
expected.
However,
they are known to have WM hypointensities even at a young age, I can
review their T2s.
A few are on mood stabilizers, but if this affected FA I would also
see it
in TBSS.
Thoughts?
Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:
Oh, another question: do your patients have white-mater
hypo/hyper-intensities, in other words any voxels in the white matter
that
are classified as something other than white matter in the freesurfer
aseg?
On Wed, 3 Apr 2013, Sean Hatton wrote:

Hi Freesurfer gurus,

I have been using Tracula to investigate white matter abnormalities
in a

patient

cohort (n=20) compared to matched controls (n=40). In line with the

literature, we

expected to see reductions in FA in the patients' tracts but instead

they have

significantly higher FA means. To double-check, we ran TBSS over the

same cohorts
and

got the results as per the literature (I.e. reduced FA in the patient

group). The
FA,

RD, AD, MD and volume outputs are normally distributed and there are
no

extreme

outliners. So wondering:
  1. The patient group had significantly reduced tract volumes. If
this

volume

 calculation is incorrect I expect it could influence the
calculation

of the mean

 FA, RD, AD etc. Is there a way of checking the volume and
subsequent
 calculations?
  2. Yendiki et al 2011 had no corrections ­ do I need corrections?
  3. Should I be thresholding tract stats?
Thank you in advance,

Sean Hatton
Brain and Mind Research Institute
University of Sydney








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contains patient information, please contact the Partners Compliance
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Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-06 Thread Sean Hatton
I reinitialised the tracts and they all make sense now :) Hope to see you
all at ISMRM.

Sean Hatton
Brain and Mind Research Institute
University of Sydney.




On 5/04/13 7:21 AM, Anastasia Yendiki ayend...@nmr.mgh.harvard.edu
wrote:


It's the pathstats.byvoxel.txt file.

On Thu, 4 Apr 2013, Sean Hatton wrote:

 There are no extreme outliers (only 3 moderate outliers). Regarding the
position, is that the FA center measures?

 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


 The increase in FA in patients is strange indeed. Are there any outliers
 in the tract averages? (Sorry if you've already mentioned this.)

 There are definitely situations in which TBSS and tracula would give you
 different results, since tracula gives you average FA in a large bundle,
 whereas TBSS gives voxel-based differences, where the voxels are on the
 skeleton of the white matter. So you could imagine a situation where
part
 of a tract shows a decrease and other parts don't. Have you looked at
the
 FA as a function of position along the tract from tracula (the other
stats
 file that it gives you)?

 On Thu, 4 Apr 2013, Sean Hatton wrote:

 Yes, TBSS has reductions in FA in the patients' ATR cf controls (TFCE
corrected, p. 05), but extracting the path stats in Tracula have the
patients' ATR FA increased cf controls (independent t test, p. 05,
uncorrected as per Yendiki et al. 2011).

 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


 Hm, it doesn't sound like a failure in the tract reconstruction then.
What
 areas does TBSS give you differences in? Is it in the area of the same
 tracts?

 On Thu, 4 Apr 2013, Sean Hatton wrote:


 Hi Anastasia,

 An independent T-test on the aseg.stats WM-Hypointensties (SegId
77) showed that the
 mean WM hypointensities volume of the patient group (1378.8mm3, SD
650mm3) did not
 significantly differ from the controls (1120.8mm3, SD 372mm3;
p=.111). A Pearson and
 Spearman correlation analysis found no correlation of WMH volume with
tract volumes
 but did find a correlation with FA in three of the nine tracts of
interest (Forceps
 minor, left ATR, left ILF). I reviewed the T2-FLAIRs for the subjects
with the highest
 volumes of WM lesions and they were all dirty-appearing white matter
around the
 ventricles rather than punctate WMH within the regions of these
tracts.

 The tracts look reasonable in FreeviewŠ scratching head

 Sean




 On 4/04/13 7:17 AM, Anastasia Yendiki
ayend...@nmr.mgh.harvard.edu wrote:


 Hi Sean - Can you check their freesurfer aseg's and see if any of the
 white matter was classified as a hypointensity there?

 a.y

 On Wed, 3 Apr 2013, Sean Hatton wrote:

   This is Tracula 5.2 with FLIRT and the vectors are correctly
aligned
   (V1 over FA).
 From the literature and what is seen in my TBSS is reduced FA in the
minor
 forceps and
 ATR.
 These are young (23yo) psychiatric so age related atrophy is not
expected.
 However,
 they are known to have WM hypointensities even at a young age, I can
 review their T2s.
 A few are on mood stabilizers, but if this affected FA I would also
see it
 in TBSS.
 Thoughts?
 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:
 Oh, another question: do your patients have white-mater
 hypo/hyper-intensities, in other words any voxels in the white matter
that
 are classified as something other than white matter in the freesurfer
 aseg?
 On Wed, 3 Apr 2013, Sean Hatton wrote:
 Hi Freesurfer gurus,

 I have been using Tracula to investigate white matter abnormalities
in a
 patient
 cohort (n=20) compared to matched controls (n=40). In line with the
 literature, we
 expected to see reductions in FA in the patients' tracts but instead
 they have
 significantly higher FA means. To double-check, we ran TBSS over the
 same cohorts
 and
 got the results as per the literature (I.e. reduced FA in the patient
 group). The
 FA,
 RD, AD, MD and volume outputs are normally distributed and there are
no
 extreme
 outliners. So wondering:
   1. The patient group had significantly reduced tract volumes. If
this
 volume
  calculation is incorrect I expect it could influence the
calculation
 of the mean
  FA, RD, AD etc. Is there a way of checking the volume and
subsequent
  calculations?
   2. Yendiki et al 2011 had no corrections ­ do I need corrections?
   3. Should I be thresholding tract stats?
 Thank you in advance,

 Sean Hatton
 Brain and Mind Research Institute
 University of Sydney







 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
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 properly
 dispose of the e-mail.










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Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-04 Thread Sean Hatton

Hi Anastasia,

An independent T-test on the aseg.stats WM-Hypointensties (SegId 77) showed 
that the mean WM hypointensities volume of the patient group (1378.8mm3, SD 
650mm3) did not significantly differ from the controls (1120.8mm3, SD 372mm3; 
p=.111). A Pearson and Spearman correlation analysis found no correlation of 
WMH volume with tract volumes but did find a correlation with FA in three of 
the nine tracts of interest (Forceps minor, left ATR, left ILF). I reviewed the 
T2-FLAIRs for the subjects with the highest volumes of WM lesions and they were 
all dirty-appearing white matter around the ventricles rather than punctate WMH 
within the regions of these tracts.

The tracts look reasonable in Freeview… scratching head

Sean




On 4/04/13 7:17 AM, Anastasia Yendiki 
ayend...@nmr.mgh.harvard.edumailto:ayend...@nmr.mgh.harvard.edu wrote:


Hi Sean - Can you check their freesurfer aseg's and see if any of the
white matter was classified as a hypointensity there?

a.y

On Wed, 3 Apr 2013, Sean Hatton wrote:

This is Tracula 5.2 with FLIRT and the vectors are correctly aligned (V1 over 
FA).
From the literature and what is seen in my TBSS is reduced FA in the minor 
forceps and
ATR.
These are young (23yo) psychiatric so age related atrophy is not expected. 
However,
they are known to have WM hypointensities even at a young age, I can review 
their T2s.
A few are on mood stabilizers, but if this affected FA I would also see it in 
TBSS.
Thoughts?
Anastasia Yendiki 
ayend...@nmr.mgh.harvard.edumailto:ayend...@nmr.mgh.harvard.edu wrote:
Oh, another question: do your patients have white-mater
hypo/hyper-intensities, in other words any voxels in the white matter that
are classified as something other than white matter in the freesurfer
aseg?
On Wed, 3 Apr 2013, Sean Hatton wrote:
 Hi Freesurfer gurus,

 I have been using Tracula to investigate white matter abnormalities in a 
 patient
 cohort (n=20) compared to matched controls (n=40). In line with the 
 literature, we
 expected to see reductions in FA in the patients' tracts but instead they have
 significantly higher FA means. To double-check, we ran TBSS over the same 
 cohorts
and
 got the results as per the literature (I.e. reduced FA in the patient group). 
 The
FA,
 RD, AD, MD and volume outputs are normally distributed and there are no 
 extreme
 outliners. So wondering:
  1. The patient group had significantly reduced tract volumes. If this volume
 calculation is incorrect I expect it could influence the calculation of 
 the mean
 FA, RD, AD etc. Is there a way of checking the volume and subsequent
 calculations?
  2. Yendiki et al 2011 had no corrections – do I need corrections?
  3. Should I be thresholding tract stats?
 Thank you in advance,

 Sean Hatton
 Brain and Mind Research Institute
 University of Sydney







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.

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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
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but does not contain patient information, please contact the sender and properly
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Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-04 Thread Anastasia Yendiki


Hm, it doesn't sound like a failure in the tract reconstruction then. What 
areas does TBSS give you differences in? Is it in the area of the same 
tracts?


On Thu, 4 Apr 2013, Sean Hatton wrote:



Hi Anastasia,

An independent T-test on the aseg.stats WM-Hypointensties (SegId 77) showed 
that the
mean WM hypointensities volume of the patient group (1378.8mm3, SD 650mm3) did 
not
significantly differ from the controls (1120.8mm3, SD 372mm3; p=.111). A 
Pearson and
Spearman correlation analysis found no correlation of WMH volume with tract 
volumes
but did find a correlation with FA in three of the nine tracts of interest 
(Forceps
minor, left ATR, left ILF). I reviewed the T2-FLAIRs for the subjects with the 
highest
volumes of WM lesions and they were all dirty-appearing white matter around the
ventricles rather than punctate WMH within the regions of these tracts.

The tracts look reasonable in Freeview… scratching head

Sean




On 4/04/13 7:17 AM, Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


Hi Sean - Can you check their freesurfer aseg's and see if any of the
white matter was classified as a hypointensity there?

a.y

On Wed, 3 Apr 2013, Sean Hatton wrote:

  This is Tracula 5.2 with FLIRT and the vectors are correctly aligned
  (V1 over FA).
From the literature and what is seen in my TBSS is reduced FA in the minor
forceps and
ATR.
These are young (23yo) psychiatric so age related atrophy is not expected.
However,
they are known to have WM hypointensities even at a young age, I can
review their T2s.
A few are on mood stabilizers, but if this affected FA I would also see it
in TBSS.
Thoughts?
Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:
Oh, another question: do your patients have white-mater
hypo/hyper-intensities, in other words any voxels in the white matter that
are classified as something other than white matter in the freesurfer
aseg?
On Wed, 3 Apr 2013, Sean Hatton wrote:
 Hi Freesurfer gurus,

 I have been using Tracula to investigate white matter abnormalities in a
patient
 cohort (n=20) compared to matched controls (n=40). In line with the
literature, we
 expected to see reductions in FA in the patients' tracts but instead
they have
 significantly higher FA means. To double-check, we ran TBSS over the
same cohorts
and
 got the results as per the literature (I.e. reduced FA in the patient
group). The
FA,
 RD, AD, MD and volume outputs are normally distributed and there are no
extreme
 outliners. So wondering:
  1. The patient group had significantly reduced tract volumes. If this
volume
 calculation is incorrect I expect it could influence the calculation
of the mean
 FA, RD, AD etc. Is there a way of checking the volume and subsequent
 calculations? 
  2. Yendiki et al 2011 had no corrections – do I need corrections? 
  3. Should I be thresholding tract stats?
 Thank you in advance,

 Sean Hatton
 Brain and Mind Research Institute
 University of Sydney







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.


___
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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.


Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-04 Thread Anastasia Yendiki


The increase in FA in patients is strange indeed. Are there any outliers 
in the tract averages? (Sorry if you've already mentioned this.)


There are definitely situations in which TBSS and tracula would give you 
different results, since tracula gives you average FA in a large bundle, 
whereas TBSS gives voxel-based differences, where the voxels are on the 
skeleton of the white matter. So you could imagine a situation where part 
of a tract shows a decrease and other parts don't. Have you looked at the 
FA as a function of position along the tract from tracula (the other stats 
file that it gives you)?


On Thu, 4 Apr 2013, Sean Hatton wrote:


Yes, TBSS has reductions in FA in the patients' ATR cf controls (TFCE corrected, 
p. 05), but extracting the path stats in Tracula have the patients' ATR FA 
increased cf controls (independent t test, p. 05, uncorrected as per Yendiki et 
al. 2011).

Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


Hm, it doesn't sound like a failure in the tract reconstruction then. What
areas does TBSS give you differences in? Is it in the area of the same
tracts?

On Thu, 4 Apr 2013, Sean Hatton wrote:



Hi Anastasia,

An independent T-test on the aseg.stats WM-Hypointensties (SegId 77) showed 
that the
mean WM hypointensities volume of the patient group (1378.8mm3, SD 650mm3) did 
not
significantly differ from the controls (1120.8mm3, SD 372mm3; p=.111). A 
Pearson and
Spearman correlation analysis found no correlation of WMH volume with tract 
volumes
but did find a correlation with FA in three of the nine tracts of interest 
(Forceps
minor, left ATR, left ILF). I reviewed the T2-FLAIRs for the subjects with the 
highest
volumes of WM lesions and they were all dirty-appearing white matter around the
ventricles rather than punctate WMH within the regions of these tracts.

The tracts look reasonable in Freeview… scratching head

Sean




On 4/04/13 7:17 AM, Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


Hi Sean - Can you check their freesurfer aseg's and see if any of the
white matter was classified as a hypointensity there?

a.y

On Wed, 3 Apr 2013, Sean Hatton wrote:

  This is Tracula 5.2 with FLIRT and the vectors are correctly aligned
  (V1 over FA).
From the literature and what is seen in my TBSS is reduced FA in the minor
forceps and
ATR.
These are young (23yo) psychiatric so age related atrophy is not expected.
However,
they are known to have WM hypointensities even at a young age, I can
review their T2s.
A few are on mood stabilizers, but if this affected FA I would also see it
in TBSS.
Thoughts?
Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:
Oh, another question: do your patients have white-mater
hypo/hyper-intensities, in other words any voxels in the white matter that
are classified as something other than white matter in the freesurfer
aseg?
On Wed, 3 Apr 2013, Sean Hatton wrote:

Hi Freesurfer gurus,

I have been using Tracula to investigate white matter abnormalities in a

patient

cohort (n=20) compared to matched controls (n=40). In line with the

literature, we

expected to see reductions in FA in the patients' tracts but instead

they have

significantly higher FA means. To double-check, we ran TBSS over the

same cohorts
and

got the results as per the literature (I.e. reduced FA in the patient

group). The
FA,

RD, AD, MD and volume outputs are normally distributed and there are no

extreme

outliners. So wondering:
  1. The patient group had significantly reduced tract volumes. If this

volume

 calculation is incorrect I expect it could influence the calculation

of the mean

 FA, RD, AD etc. Is there a way of checking the volume and subsequent
 calculations?
  2. Yendiki et al 2011 had no corrections – do I need corrections?
  3. Should I be thresholding tract stats?
Thank you in advance,

Sean Hatton
Brain and Mind Research Institute
University of Sydney








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.






___
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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
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but does not contain patient information, please contact the sender and properly
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Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-04 Thread Sean Hatton
There are no extreme outliers (only 3 moderate outliers). Regarding the 
position, is that the FA center measures?

Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


The increase in FA in patients is strange indeed. Are there any outliers
in the tract averages? (Sorry if you've already mentioned this.)

There are definitely situations in which TBSS and tracula would give you
different results, since tracula gives you average FA in a large bundle,
whereas TBSS gives voxel-based differences, where the voxels are on the
skeleton of the white matter. So you could imagine a situation where part
of a tract shows a decrease and other parts don't. Have you looked at the
FA as a function of position along the tract from tracula (the other stats
file that it gives you)?

On Thu, 4 Apr 2013, Sean Hatton wrote:

 Yes, TBSS has reductions in FA in the patients' ATR cf controls (TFCE 
 corrected, p. 05), but extracting the path stats in Tracula have the 
 patients' ATR FA increased cf controls (independent t test, p. 05, 
 uncorrected as per Yendiki et al. 2011).

 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


 Hm, it doesn't sound like a failure in the tract reconstruction then. What
 areas does TBSS give you differences in? Is it in the area of the same
 tracts?

 On Thu, 4 Apr 2013, Sean Hatton wrote:


 Hi Anastasia,

 An independent T-test on the aseg.stats WM-Hypointensties (SegId 77) 
 showed that the
 mean WM hypointensities volume of the patient group (1378.8mm3, SD 650mm3) 
 did not
 significantly differ from the controls (1120.8mm3, SD 372mm3; p=.111). A 
 Pearson and
 Spearman correlation analysis found no correlation of WMH volume with tract 
 volumes
 but did find a correlation with FA in three of the nine tracts of interest 
 (Forceps
 minor, left ATR, left ILF). I reviewed the T2-FLAIRs for the subjects with 
 the highest
 volumes of WM lesions and they were all dirty-appearing white matter around 
 the
 ventricles rather than punctate WMH within the regions of these tracts.

 The tracts look reasonable in Freeview… scratching head

 Sean




 On 4/04/13 7:17 AM, Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


 Hi Sean - Can you check their freesurfer aseg's and see if any of the
 white matter was classified as a hypointensity there?

 a.y

 On Wed, 3 Apr 2013, Sean Hatton wrote:

   This is Tracula 5.2 with FLIRT and the vectors are correctly aligned
   (V1 over FA).
 From the literature and what is seen in my TBSS is reduced FA in the minor
 forceps and
 ATR.
 These are young (23yo) psychiatric so age related atrophy is not expected.
 However,
 they are known to have WM hypointensities even at a young age, I can
 review their T2s.
 A few are on mood stabilizers, but if this affected FA I would also see it
 in TBSS.
 Thoughts?
 Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:
 Oh, another question: do your patients have white-mater
 hypo/hyper-intensities, in other words any voxels in the white matter that
 are classified as something other than white matter in the freesurfer
 aseg?
 On Wed, 3 Apr 2013, Sean Hatton wrote:
 Hi Freesurfer gurus,

 I have been using Tracula to investigate white matter abnormalities in a
 patient
 cohort (n=20) compared to matched controls (n=40). In line with the
 literature, we
 expected to see reductions in FA in the patients' tracts but instead
 they have
 significantly higher FA means. To double-check, we ran TBSS over the
 same cohorts
 and
 got the results as per the literature (I.e. reduced FA in the patient
 group). The
 FA,
 RD, AD, MD and volume outputs are normally distributed and there are no
 extreme
 outliners. So wondering:
   1. The patient group had significantly reduced tract volumes. If this
 volume
  calculation is incorrect I expect it could influence the calculation
 of the mean
  FA, RD, AD etc. Is there a way of checking the volume and subsequent
  calculations?
   2. Yendiki et al 2011 had no corrections – do I need corrections?
   3. Should I be thresholding tract stats?
 Thank you in advance,

 Sean Hatton
 Brain and Mind Research Institute
 University of Sydney







 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.







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Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-04 Thread Anastasia Yendiki


It's the pathstats.byvoxel.txt file.

On Thu, 4 Apr 2013, Sean Hatton wrote:


There are no extreme outliers (only 3 moderate outliers). Regarding the position, is that 
the FA center measures?

Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


The increase in FA in patients is strange indeed. Are there any outliers
in the tract averages? (Sorry if you've already mentioned this.)

There are definitely situations in which TBSS and tracula would give you
different results, since tracula gives you average FA in a large bundle,
whereas TBSS gives voxel-based differences, where the voxels are on the
skeleton of the white matter. So you could imagine a situation where part
of a tract shows a decrease and other parts don't. Have you looked at the
FA as a function of position along the tract from tracula (the other stats
file that it gives you)?

On Thu, 4 Apr 2013, Sean Hatton wrote:


Yes, TBSS has reductions in FA in the patients' ATR cf controls (TFCE corrected, 
p. 05), but extracting the path stats in Tracula have the patients' ATR FA 
increased cf controls (independent t test, p. 05, uncorrected as per Yendiki et 
al. 2011).

Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


Hm, it doesn't sound like a failure in the tract reconstruction then. What
areas does TBSS give you differences in? Is it in the area of the same
tracts?

On Thu, 4 Apr 2013, Sean Hatton wrote:



Hi Anastasia,

An independent T-test on the aseg.stats WM-Hypointensties (SegId 77) showed 
that the
mean WM hypointensities volume of the patient group (1378.8mm3, SD 650mm3) did 
not
significantly differ from the controls (1120.8mm3, SD 372mm3; p=.111). A 
Pearson and
Spearman correlation analysis found no correlation of WMH volume with tract 
volumes
but did find a correlation with FA in three of the nine tracts of interest 
(Forceps
minor, left ATR, left ILF). I reviewed the T2-FLAIRs for the subjects with the 
highest
volumes of WM lesions and they were all dirty-appearing white matter around the
ventricles rather than punctate WMH within the regions of these tracts.

The tracts look reasonable in Freeview… scratching head

Sean




On 4/04/13 7:17 AM, Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:


Hi Sean - Can you check their freesurfer aseg's and see if any of the
white matter was classified as a hypointensity there?

a.y

On Wed, 3 Apr 2013, Sean Hatton wrote:

  This is Tracula 5.2 with FLIRT and the vectors are correctly aligned
  (V1 over FA).
From the literature and what is seen in my TBSS is reduced FA in the minor
forceps and
ATR.
These are young (23yo) psychiatric so age related atrophy is not expected.
However,
they are known to have WM hypointensities even at a young age, I can
review their T2s.
A few are on mood stabilizers, but if this affected FA I would also see it
in TBSS.
Thoughts?
Anastasia Yendiki ayend...@nmr.mgh.harvard.edu wrote:
Oh, another question: do your patients have white-mater
hypo/hyper-intensities, in other words any voxels in the white matter that
are classified as something other than white matter in the freesurfer
aseg?
On Wed, 3 Apr 2013, Sean Hatton wrote:

Hi Freesurfer gurus,

I have been using Tracula to investigate white matter abnormalities in a

patient

cohort (n=20) compared to matched controls (n=40). In line with the

literature, we

expected to see reductions in FA in the patients' tracts but instead

they have

significantly higher FA means. To double-check, we ran TBSS over the

same cohorts
and

got the results as per the literature (I.e. reduced FA in the patient

group). The
FA,

RD, AD, MD and volume outputs are normally distributed and there are no

extreme

outliners. So wondering:
  1. The patient group had significantly reduced tract volumes. If this

volume

 calculation is incorrect I expect it could influence the calculation

of the mean

 FA, RD, AD etc. Is there a way of checking the volume and subsequent
 calculations?
  2. Yendiki et al 2011 had no corrections – do I need corrections?
  3. Should I be thresholding tract stats?
Thank you in advance,

Sean Hatton
Brain and Mind Research Institute
University of Sydney








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Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-03 Thread Anastasia Yendiki


Hi Sean - Are you using 5.1 or 5.2? What registration options are you 
using? Does your patient population have pronounced anatomical changes 
(e.g. atrophy) compared to controls? Which pathways did you expect to show

reduced anisotropy in your patient population?

Thanks,
a.y

On Wed, 3 Apr 2013, Sean Hatton wrote:


Hi Freesurfer gurus,

I have been using Tracula to investigate white matter abnormalities in a patient
cohort (n=20) compared to matched controls (n=40). In line with the literature, 
we
expected to see reductions in FA in the patients' tracts but instead they have
significantly higher FA means. To double-check, we ran TBSS over the same 
cohorts and
got the results as per the literature (I.e. reduced FA in the patient group). 
The FA,
RD, AD, MD and volume outputs are normally distributed and there are no extreme
outliners. So wondering:
 1. The patient group had significantly reduced tract volumes. If this volume
calculation is incorrect I expect it could influence the calculation of the 
mean
FA, RD, AD etc. Is there a way of checking the volume and subsequent
calculations? 
 2. Yendiki et al 2011 had no corrections – do I need corrections? 
 3. Should I be thresholding tract stats?
Thank you in advance,

Sean Hatton
Brain and Mind Research Institute
University of Sydney






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contains patient information, please contact the Partners Compliance HelpLine at
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Re: [Freesurfer] Tracula the inverse of TBSS results

2013-04-03 Thread Anastasia Yendiki


Oh, another question: do your patients have white-mater 
hypo/hyper-intensities, in other words any voxels in the white matter that 
are classified as something other than white matter in the freesurfer 
aseg?


On Wed, 3 Apr 2013, Sean Hatton wrote:


Hi Freesurfer gurus,

I have been using Tracula to investigate white matter abnormalities in a patient
cohort (n=20) compared to matched controls (n=40). In line with the literature, 
we
expected to see reductions in FA in the patients' tracts but instead they have
significantly higher FA means. To double-check, we ran TBSS over the same 
cohorts and
got the results as per the literature (I.e. reduced FA in the patient group). 
The FA,
RD, AD, MD and volume outputs are normally distributed and there are no extreme
outliners. So wondering:
 1. The patient group had significantly reduced tract volumes. If this volume
calculation is incorrect I expect it could influence the calculation of the 
mean
FA, RD, AD etc. Is there a way of checking the volume and subsequent
calculations? 
 2. Yendiki et al 2011 had no corrections – do I need corrections? 
 3. Should I be thresholding tract stats?
Thank you in advance,

Sean Hatton
Brain and Mind Research Institute
University of Sydney






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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
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but does not contain patient information, please contact the sender and properly
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