Answers to previous TC issues:

Answers to previous TC issues:- Demographic features of the selected subjects (age, sex, disease, ApoE)- Check for SIEMENS-Allegra scans at 3T for the selected benchmark images

Activities update:- III Delphi round- Abstract for AAN 2011- Test of the Qualification Platform

Prospective:Divulgation of Harmonized Protocol project and preliminary results to interested fields (psychiatry, epilepsy..).

II PMT meeting – Sept 28 2011

Benchmark Harmonized hippos:1.5T ADNI scans2 x each of the 5

Scheltens’s atrophy score x 2 sides(SAME on 3T ADNI scans)

(total for each rater: 40 hippos)

5 expert tracers

20 naive tracers

The best 5 naive tracers

Harmonized Protocol:1.5T ADNI scans

2 sides x 5 Scheltens’s atrophy scores x 3 time points (0-12°month-24°month)

x 3 scanners + retracing for timepoint 1(SAME on 3T ADNI scans)

(total for each rater: 240 hippos – including40 hippos already traced)

GOLD STANDARD

Qualification(10 tracers each SU;10 whole hippo)

global and local 95% confidence intervals

RM-ANOVA: test of rater and rater by center terms

RM-ANOVA: test of main effects side, trace-retrace, atrophy, time, scanner, rater

Local Protocol:Experimental set (1.5T ADNI):2 x each of the 5 Scheltens’s

atrophy score x 2 sides (SAME on 3T ADNI scans)


Harmonized Protocol:Experimental set (1.5T ADNI): 2 x each of the 5 Scheltens’s

atrophy score x 2 sides(SAME on 3T ADNI scans)


VARIABILITY EVALUATION

Benchmark Images(20 scans)

Validation Phase(90 scans)

Age, years 77.5 (5.10) 74.5 (6.46)

Gender, female 8 (40%) 51 (56.7%)

Diagnosis, AD/MCIc/MCInc/CTRc/CTR

2/6/4/0/8(10%,30%,20%,0%,40%)

37/14/15/4/20 (41%,15.5%,17%,22%,4.5%)

E4, carriers 6 (30%) 42 (46.7%)

Scans selection

Considered as “scans”, not as “subjects”

Scans selection – Benchmark (10 sbj, 1.5T+3T= 20 scans)

Gender, Fisher’s: p=0.429; E4-carriers: p=0.283age, ANOVA one-way: p=0.756

Considered as “subjects”

Scans selection – Validation(16* sbj, 1.5T + 3T, 3 time points = 90 scans)

*one subject: no match 1.5-3TGender, Fisher’s: p=0.179; E4, Fisher’s: p=1age, ANOVA one-way: p=0.641

Considered as “subjects” at BASELINE

Age, Mean (SD)

Gender, female/male

E4, carriers/non-carriers

AD 75.6 (5.73) 4/1 2/3

MCIc 70 (10.23) 1/3 2/2

MCInc 69.67 (6.81) 1/2 1/2

CTRc 76 (/) 0/1 1/0

CTRL 75.33 (2.08) 3/0 1/2

TOT 73.06 (6.71) 9/7 7/9

Age, Mean (SD)

Gender, female/male


AD 77.14 (4.85) 4/3 3/4

MCIc 63.5 (9.19) 1/1 1/1

MCInc 75.33 (2.08) 1/2 2/1

CTRc --- 0/0 0/0

CTRL 73 (6.88) 3/1 1/3

TOT 74.06 (6.71) 9/7 7/9


*one subject: no match 1.5-3TGender, Fisher’s: p=0.89 ; E4, Fisher’s: p=0.89age, ANOVA one-way: 0.063

Considered as “subjects” at TIME 2


*one subject: no match 1.5-3TGender, Fisher’s: p=0.711; E4, Fisher’s: p=0.711age, ANOVA one-way: p=0.946

Considered as “subjects” at TIME 3

Age, Mean (SD)

Gender, female/male


AD 75.63 (8.42) 5/3 3/5

MCIc 71 (/) 0/1 1/0

MCInc 75.5 (2.12) 1/1 1/1

CTRc 78 (/) 0/1 1/0

CTRL 74 (6.88) 3/1 1/3

TOT 75.06 (6.71) 9/7 7/9

Manufacter Scanner Type

SIEMENS TrioTim

SIEMENS Trio

SIEMENS TrioTim

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

SIEMENS TrioTim

SIEMENS TrioTim

SIEMENS TrioTim

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

SIEMENS Trio

Scanner: no 3T Siemens Allegra

I section:

LANDMARKS DEFINITION

Delphi Panel – III Round

Delphi Panel – Preliminary Results from I and II rounds

P=0.021

P=0.057

P=0.035

This preliminary model:

Covers 100% of hippocampus proper

Captures 100% of AD-related atrophy

Has a global inter-rater of 0.94(preliminary value across

FBF-Mayo-LONI-Mainz)

P for agreement

among panelists)

Covers 100% of hippocampus properCaptures 100% of AD-related atrophy

Preliminary inter-rater ICC (FBF-Mayo-LONI-Mainz): 0.94

Covers 99.5% of hippocampus properCaptures 99.6% of AD-related atrophy Preliminary inter-rater ICC (FBF-Mayo-

LONI-Mainz): 0.93

A model of the hippocampus, as chosen by the majority so far, but using the Horizontal criterion as first choice for the medial boundary of the hippocampal body, has the following features (right panel):

Preliminary Harmonized Hippo resulting from the first two Delphi rounds

Preliminary Harmonized Hippo resulting from the first two Delphi rounds but using Horizontal criterion

Based on this information, and on the values relating to the global preliminary models of the Harmonized Protocol, to what extent do you agree with the use of the Morphology criterion as first choice in the Harmonized Protocol?

1 2 3 4 5 6 7 8 9

Choice justification and comments:

If the agreement about the morphology criterion as first choice will be confirmed in this round, we further need to define which kind of arbitrary line should be used in a Harmonized protocol as second choice, for those images where no morphological details can be detected on the coronal plane. The possible options, as obtained from the surveyed protocols, are the oblique and the horizontal line. More exactly:

The Oblique line criterion consists in continuing, using the same inclination, the oblique line delineating the boundary between the parahippocampal white matter and the hippocampal gray matter, up to the CSF of the quadrigeminal cistern, and then close the segmentation with the reset of the hippocampal tracing.

The Horizontal line criterion consist in drawing a horizontal line starting from the upper point of the parahippocampal white matter, to the CSF of the quadrigeminal cistern, and then closing with reset of the hippocampal tracing.

Subiculum - Horizontal

Subiculum - Oblique

TAIL END

Significant agreement has been achieved on the inclusion of the whole hippocampal Tail in the Harmonized Protocol, in the second Delphi round (p<0.035). Main reason for this agreement was that most caudal tissue is proper hippocampal tissue, with large contribution to global hippocampal volume and to AD related difference. (find the quantitative data about all Segmentation Units here). This may add sensitivity to a Harmonized Protocol. Other reasons were that caudal hippocampus can be reliably identified with 3D navigation, and that without the tail, the volume might be more dependent on individual hippocampal angulation. Some panelists note that the Crura criterion is slightly more reliable and may be easier to standardize (find all anonymous individual answers here).(You can download the presentation reporting the data from both delphi rounds and statistics here).







A model of the hippocampus, as chosen by the majority so far, but using the Crura criterion for the segmentation of the most caudal hippocampal tissue, has the following features (right panel):

Preliminary Harmonized Hippo resulting from the first two Delphi rounds

Preliminary Harmonized Hippo resulting from the first two Delphi rounds but using Crura criterion

Delphi Panel – III Round

II section:

SEGMENTATION MODALITIES

Separation of the fimbria from the fornix

“Include the white matter as fimbria as long as it runs parallel to the parahippocampal white matter located at the ventral border of the hippocampus (a,

b, c), and exclude it as fornix when its inclination, in the coronal view, takes a different angle (d, e). This usually happens only in the last two slices, just caudal to

the slice offering simultaneous visualization of both the inferior and superior colliculi, and before the visualization of the fornix in its full length.”

a b c d e

To what extent you agree with the above definition for the segmentation of the most caudal slice that includes the fimbria in the Harmonized Protocol?

If you do not agree with the above definition, please propose an alternative definition in the box below:

Alternative definition, or comments to the limits of the above:

1 2 3 4 5 6 7 8 9

3D model indicating the Andrea Retzius (AR; red) and Fasciolar gyrus (FG; yellow) within the proper hippocampal tissue. The model is built using the manual segmentation of the cytoarchitectonic boundaries of the single subject’s brain reported in the atlas by Mai JK et al., 1997 Some portions of AR and FG run internally within the hippocampal gray matter.

The dorso-medial portion of the hippocampus at this level is often excluded by hippocampal segmentors, based on differences of gray matter intensity, and often independently on explicit mention of this exclusion by the protocol that is formally adopted.

In our investigation, we could not find a demonstration that these different gray shades do correspond to the anatomical AR and FG. Nonetheless, when comparing the sagittal view, this tissue denoted by different gray intensity does fall in the scythe shape contiguous to the corpus callosum, that corresponds to the AR and FG as independently inferred from the Duvernoy’s atlas of the hippocampus (Duvernoy HM, 1998).

3D reconstruction from Mai, J.K., Assheuer, J., Paxinos, G., 1997. Atlas of the Human Brain. Academic Press, San Diego, CA

Yellow: Fasciolar gyrus

Red: Andreas Retzius gyrus head

tail

head tail

Frontal view

Medial view

Now, different options are possible:

Option n. 1) The Harmonized Protocol may include the whole vestigial tissue (Figure 1)

Option n. 2) The Harmonized Protocol may exclude the vestigial tissue when, on the coronal plane, this looks different based on gray matter intensity and morphology (i.e., boundaries of regions with different gray matter intensity) (Figure 2)

Delphi III Round – Vestigial Tissue

Delphi III Round – Internal CSF

Significant agreement (p=0.004) was achieved in the previous Delphi rounds about the fact that the CSF located internal to the hippocampus should be excluded from segmentation. Nonetheless, the criterion of connection of the CSF in the coronal plane, voted by the majority (63%), did not achieve a significant agreement.

Based on the comments of panelists, the question is:

To what extent do you agree with the following instruction for the Harmonized Protocol:

“The CSF located internal to the hippocampus must be excluded from the segmentation when the tracer is sufficiently sure that it is CSF and not partial volume effect. This needs to be ascertained through the connection of the hypointense voxels with the CSF located external to the hippocampus, or with other hypointense voxels in rostro-caudal direction, as detected using the 3D navigation and scrolling contiguous slices. CSF spaces presumably belonging to individual differences in the morphology of the hippocampal fissure should also be excluded from segmentation”

1 2 3 4 5 6 7 8 9


Delphi III Round – Hardly visible structures

In the previous Delphi rounds, comments of panelists were consistent with the statement that only visible tissue must be segmented in slices where structures can not be consistently seen in different raters, due to atrophy.

To what extent do you agree with the following instruction for the Harmonized Protocol:

“Hippocampal tissue must be segmented based on its being visible on MRI, and not based on a priori knowledge of hippocampal morphology. Nonetheless, a priori knowledge of hippocampal morphology must be used to ascertain whether hippocampal tissue can be detected in atrophic patients. For example, in some cases the subiculum is so atrophic that sometimes it can be noted only if actually searched for, adjusting image contrast and monitor settings specifically for that aim (Figure). If, after specific search guided by anatomical knowledge, thin portions of tissue can be detected, these will be segmented with a thin trace, trying not to overestimate its volume. If no tissue can be detected in such search, the segmentation should not complete the hippocampal shape based on a priori knowledge, but should only include the tissue that is actually visible after all possible checks.”

1 2 3 4 5 6 7 8 9


Delphi III Round – Image orientation

A) Parallel to the long axis of one of the two hippocampi (say, the left) of each subject (same orientation for both hippocampi in each subject).

B) Parallel to the long axis of the currently segmented hippocampus, in each subject (two orientations used in each subject).

C) Along the axis representing the mean angle among the right and the left long axes of the hippocampi of each subject (same orientation for both hippocampi in each subject).

Significant agreement (p=0.012) was achieved on the fact that the image orientation for hippocampal segmentation should be aligned parallel to the long axis of the hippocampus.

Now, it should be defined whether the MRI images should be oriented:

*

*

*


AAN 2012

“Definition of landmarks for a Harmonized Protocol for the manual segmentation of the hippocampus on MRI: preliminary results from the EADC-ADNI working group”

Marina Boccardi, Martina Bocchetta, Liana Apostolova, Josephine Barnes, George Bartzokis, Gabriele Corbetta, Charles deCarli, Leyla DeToledo-Morrell, Michael Firbank, Rossana Ganzola, Lotte Gerritsen, Wouter Henneman, Ronald Killiani, Nikolai Malykhin, Patrizio Pasqualetti, Jens Pruessner, Alberto Redolfi, Nicolas Robitaille, Hilkka Soininen, Daniele Tolomeo, Lei Wang, Craig Watson, Henrike Wolf, Simon Duchesne, Clifford R. Jack Jr, Giovanni B. Frisoni.

Platform preliminary test?

Benchmark Harmonized hippos:1.5T ADNI scans2 x each of the 5

Scheltens’s atrophy score x 2 sides(SAME on 3T ADNI scans)


5 expert tracers

20 naive tracers

The best 5 naive tracers

Harmonized Protocol:1.5T ADNI scans

2 sides x 5 Scheltens’s atrophy scores x 3 time points (0-12°month-24°month)

x 3 scanners + retracing for timepoint 1(SAME on 3T ADNI scans)

(total for each rater: 240 hippos – including40 hippos already traced)

GOLD STANDARD

Local Protocol:1.5T 3D T1-weighted scans from (Bobinski et al., 2000)pathologically verified set(total for rater: 30 hippos)

1 tracer

Qualification(10 tracers each SU;10 whole hippo)

Qualification

global and local 95% confidence intervals

RM-ANOVA: test of rater and rater by center terms

RM-ANOVA: test of main effects side, trace-retrace, atrophy, time, scanner, rater

Local Protocol:Experimental set (1.5T ADNI):2 x each of the 5 Scheltens’s

atrophy score x 2 sides (SAME on 3T ADNI scans)


Harmonized Protocol:Experimental set (1.5T ADNI): 2 x each of the 5 Scheltens’s

atrophy score x 2 sides(SAME on 3T ADNI scans)


Harmonized Protocol:1.5T 3D T1-weighted scans from (Bobinski et al., 2000)pathologically verified set(total for rater: 30 hippos)

RM-ANOVA: test of protocol main effect

VARIABILITY EVALUATION

VALIDATION vsPATHOLOGY

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Divulgation of Harmonized Protocol project and preliminary results to interested fields (psychiatry, epilepsy..)

Society of Biological Psychiatry (SOBP) Philadelphia May 2012 – Deadline for symposium is Oct 24, 2011(Csernansky?)

Epilepsy/Neurology meeting other than AAN?

Other?

Next: symposia

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Answers to previous TC issues:

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