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Text to brain: predicting the spatial distribution of neuroimaging observations from text reports (submitted to MICCAI 2018) Jérôme Dockès, Russel Poldrack, Demian Wassermann, Fabian Suchanek, Bertrand Thirion, Gaël Varoquaux INRIA, Télécom Paris, Stanford University 2018-05-16 1 / 22
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Page 1: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Text to brain: predicting the spatial distributionof neuroimaging observations from text

reports (submitted to MICCAI 2018)

Jérôme Dockès, Russel Poldrack, Demian Wassermann,Fabian Suchanek, Bertrand Thirion, Gaël Varoquaux

INRIA, Télécom Paris, Stanford University

2018-05-16

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Page 2: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Text to brain images

I Many neuroimaging observations are stored in unstructuredtext.

I e.g “[...] in the anterolateral temporal cortex, especially thetemporal pole and inferior and middle temporal gyri”

I It would be good to have them in the form of images and dostatistics with them

I our objective: transform a medical publication into abrain image

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Page 3: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

text to brain image

Title:“Where sound position in-fluences sound object repre-sentations: a 7-T fMRI study”[5] Abstract: “Evidence fromhuman and non-human pri-mate studies supports a dual-pathway model of audition, withpartially segregated cortical net-works for sound recognition andsound localisation, referred toas the What and Where pro-cessing streams. In normalsubjects, these two networksoverlap partially on the supra-temporal......”

L R

probability density function(pdf) over the brain (subsetof R3)

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Page 4: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

How we transform text into a brain image(a spatial pdf)

Page 5: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Supervised learning approach

I Simple heuristics don’t workI Some articles e.g. fMRI (functional Magnetic Resonance

Imaging) studies provide text and coordinates in the brainI We extract those coordinates and exploit the pairs (text,

coordinates) in a supervised learning setting

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Page 6: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Example fMRI study

LaCroix et al. Neural computations for speech and music perception

FIGURE 1 | (A) Representative sagittal slices of the ALE for passive listening to speech, p < 0.05, corrected, overlaid on top of the passive music listening ALE.

(B) Speech vs. music passive listening contrasts results, p < 0.05 corrected.

Music Tasks vs. Speech TasksThe passive listening ALE results identify distinct andoverlapping regions of speech and music processing. Wenow turn to the question of how do these distinctions changeas a function of the type of task employed? First, ALEs werecomputed for each music task condition, p < 0.05 FDRcorrected (Figure 1, Table 2). The music task conditions’ ALEsall significantly identified bilateral STG and bilateral precentralgyrus, and inferior parietal regions, overlapping with thepassive listening music ALE (Figure 2). The tasks also activatedadditional inferior frontal and inferior parietal regions notidentified by the passive listening music ALE; these differencesare discussed in a subsequent section.

To compare the brain regions activated by each musictask to those activated by speech in similar tasks, pairwisecontrasts of the ALEs for each music task vs. its correspondingspeech task group were calculated (Figure 3, Table 2). Musicdiscrimination > speech discrimination identified regionsincluding bilateral inferior frontal gyri (pars opercularis),bilateral pre and postcentral gyri, bilateral medial frontalgyri, left inferior parietal lobule, and left cerebellum, whereasspeech discrimination>music discrimination identified bilateralregions in the anterior superior temporal sulci (including bothsuperior and middle temporal gyri). Music detection > speechdetection identified a bilateral group of clusters spanning thesuperior temporal gyri, bilateral precentral gyri, bilateral insulaand bilateral inferior parietal regions, as well as clusters in theright middle frontal gyrus. Speech detection > music detection

identified bilateral superior temporal sulci regions as well as leftinferior frontal regions (pars triangularis and pars opercularis).Music memory > speech memory identified a left posteriorsuperior temporal/inferior parietal region and bilateral medialfrontal regions; speech memory > music memory identified leftinferior frontal gyrus (pars opercularis and pars triangularis) andbilateral superior and middle temporal gyri.

In sum, the task pairwise contrasts in many ways mirrorthe passive listening contrast: music tasks activated moredorsal/medial superior temporal and inferior parietal regions,while speech tasks activated superior temporal sulcus regions,particularly in the anterior temporal lobe. In addition, notabledifferences were found in Broca’s area and its right hemispherehomolog: in discrimination tasks music significantly activatedBroca’s area (specifically the pars opercularis) more than speech.However, in detection and memory tasks speech activated Broca’sarea (pars opercularis and pars triangularis) more than music.The right inferior frontal gyrus responded equally to speechand music in both detection and memory tasks, but respondedmore to music than speech in discrimination tasks. Alsonotably, in the memory tasks, music activated a lateral superiortemporal/inferior parietal cluster (in the vicinity of Hickok andPoeppel’s “area Spt”) more than speech while an inferior frontalcluster including the pars opercularis was activated more forspeech than music. Both area Spt and the pars opercularispreviously have been implicated in a variety of auditory workingmemory tasks (including speech and pitch working memory) inboth lesion patients and control subjects (Koelsch and Siebel,

Frontiers in Psychology | www.frontiersin.org 5 August 2015 | Volume 6 | Article 1138

LaCroix et al. Neural computations for speech and music perception

TABLE 2 | Locations, peaks and cluster size for significant voxel clusters for each condition’s ALE and for each contrast of interest.

Condition Anatomical locations Peak coordinates Voxels

Music passive listening Left inferior frontal gyrus (pars opercularis)* −46, 10, 26 32

Left medial frontal gyrus*, left subcallosal gyrus −2, 26,−14 65

Left medial frontal gyrus* −2, 2, 62 48

Left postcentral gyrus*, left inferior parietal lobule −34,−36, 54 27

Left superior temporal gyrus*, left transverse temporal gyrus, left middle temporal gyrus, left insula −52,−20, 6 2073

Right inferior frontal gyrus* 48, 10, 28 43

Right precentral gyrus*, right postcentral gyrus, right middle frontal gyrus 52,−2, 44 173

Right superior temporal gyrus*, right transverse temporal gyrus, right middle temporal gyrus, right

insula

58,−20, 6 2154

Right insula*, right inferior frontal gyrus, right precentral gyrus 42, 14, 0 206

Right lingual gyrus*, right culmen 16,−54,−2 27

Music discrimination Left medial frontal gyrus*, left middle frontal gyrus −8,−4, 58 224

Left precentral gyrus*, left postcentral gyrus, left inferior parietal lobule −48,−12, 48 259

Left precentral gyrus*, left inferior frontal gyrus (pars opercularis) −50, 2, 26 67

Left superior temporal gyrus*, left transverse temporal gyrus, left precentral gyrus −54,−16, 8 239

Left superior temporal gyrus*, left middle temporal gyrus −58,−34, 8 92

Left insula*, left inferior frontal gyrus (pars triangularis) −34, 22, 2 48

Left cerebellum* −28,−62,−24 127

Right inferior frontal gyrus*, right middle frontal gyrus 52, 12, 28 58

Right precentral gyrus*, right middle frontal gyrus 46,−6, 44 170

Right superior temporal gyrus*, right middle temporal gyrus 62,−24, 8 310

Right superior temporal gyrus*, right precentral gyrus, right insula 50, 6,−2 91

Music error detection Left medial frontal gyrus* −4,−4, 58 49

Left superior temporal gyrus*,

Let transverse temporal gyrus,

Left postcentral gyrus, left insula

−50,−18, 8 1448

Left inferior parietal lobule*, left supramarginal gyrus, left angular gyrus −40,−48, 40 41

Left lentiform nucleus*, left putamen −22, 6, 10 263

Right middle frontal gyrus* 36, 42, 18 43

Right middle frontal gyrus*, right precentral gyrus 32,−4, 56 35

Right superior frontal gyrus*, right medial frontal gyrus, left superior frontal gyrus, left medial frontal

gyrus

2, 10, 52 95

Right superior temporal gyrus*, right transverse temporal gyrus, right insula, right precentral gyrus,

right middle temporal gyrus, right claustrum

50,−18, 6 1228

Right parahippocampal gyrus* 22,−14,−12 36

Right inferior parietal lobule*, right supramarginal gyrus 36,−44, 40 103

Right insula*, right inferior frontal gyrus 32, 22, 12 329

Right lentiform nucleus*, right putamen, right caudate 18, 6, 12 144

Right thalamus* 12,−16, 8 33

Right cerebellum* 26,−50,−26 28

Music memory Left inferior frontal gyrus (pars opercularis)*, left precentral gyrus, left middle frontal gyrus −50, 4, 26 206

Left inferior frontal gyrus (pars triangularis*, pars orbitalis), left insula −34, 24,−2 57

Left inferior frontal gyrus (pars triangularis)* −44, 26, 10 25

Left medial frontal gyrus* −4, 52, 12 31

Left middle frontal gyrus* −32, 4, 54 29

Left precentral gyrus* −44,−10, 42 33

Left superior frontal gyrus*, left medial frontal gyrus, right superior frontal gyrus, right medial frontal

gyrus

−0, 12, 50 373

Left middle temporal gyrus* −50,−20,−10 72

Left middle temporal gyrus*, left superior temporal gyrus −46, 4,−18 35

(Continued)

Frontiers in Psychology | www.frontiersin.org 6 August 2015 | Volume 6 | Article 1138

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Page 7: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Example fMRI study

LaCroix et al. Neural computations for speech and music perception

TABLE 2 | Locations, peaks and cluster size for significant voxel clusters for each condition’s ALE and for each contrast of interest.

Condition Anatomical locations Peak coordinates Voxels

Music passive listening Left inferior frontal gyrus (pars opercularis)* −46, 10, 26 32

Left medial frontal gyrus*, left subcallosal gyrus −2, 26,−14 65

Left medial frontal gyrus* −2, 2, 62 48

Left postcentral gyrus*, left inferior parietal lobule −34,−36, 54 27

Left superior temporal gyrus*, left transverse temporal gyrus, left middle temporal gyrus, left insula −52,−20, 6 2073

Right inferior frontal gyrus* 48, 10, 28 43

Right precentral gyrus*, right postcentral gyrus, right middle frontal gyrus 52,−2, 44 173

Right superior temporal gyrus*, right transverse temporal gyrus, right middle temporal gyrus, right

insula

58,−20, 6 2154

Right insula*, right inferior frontal gyrus, right precentral gyrus 42, 14, 0 206

Right lingual gyrus*, right culmen 16,−54,−2 27

Music discrimination Left medial frontal gyrus*, left middle frontal gyrus −8,−4, 58 224

Left precentral gyrus*, left postcentral gyrus, left inferior parietal lobule −48,−12, 48 259

Left precentral gyrus*, left inferior frontal gyrus (pars opercularis) −50, 2, 26 67

Left superior temporal gyrus*, left transverse temporal gyrus, left precentral gyrus −54,−16, 8 239

Left superior temporal gyrus*, left middle temporal gyrus −58,−34, 8 92

Left insula*, left inferior frontal gyrus (pars triangularis) −34, 22, 2 48

Left cerebellum* −28,−62,−24 127

Right inferior frontal gyrus*, right middle frontal gyrus 52, 12, 28 58

Right precentral gyrus*, right middle frontal gyrus 46,−6, 44 170

Right superior temporal gyrus*, right middle temporal gyrus 62,−24, 8 310

Right superior temporal gyrus*, right precentral gyrus, right insula 50, 6,−2 91

Music error detection Left medial frontal gyrus* −4,−4, 58 49

Left superior temporal gyrus*,

Let transverse temporal gyrus,

Left postcentral gyrus, left insula

−50,−18, 8 1448

Left inferior parietal lobule*, left supramarginal gyrus, left angular gyrus −40,−48, 40 41

Left lentiform nucleus*, left putamen −22, 6, 10 263

Right middle frontal gyrus* 36, 42, 18 43

Right middle frontal gyrus*, right precentral gyrus 32,−4, 56 35

Right superior frontal gyrus*, right medial frontal gyrus, left superior frontal gyrus, left medial frontal

gyrus

2, 10, 52 95

Right superior temporal gyrus*, right transverse temporal gyrus, right insula, right precentral gyrus,

right middle temporal gyrus, right claustrum

50,−18, 6 1228

Right parahippocampal gyrus* 22,−14,−12 36

Right inferior parietal lobule*, right supramarginal gyrus 36,−44, 40 103

Right insula*, right inferior frontal gyrus 32, 22, 12 329

Right lentiform nucleus*, right putamen, right caudate 18, 6, 12 144

Right thalamus* 12,−16, 8 33

Right cerebellum* 26,−50,−26 28

Music memory Left inferior frontal gyrus (pars opercularis)*, left precentral gyrus, left middle frontal gyrus −50, 4, 26 206

Left inferior frontal gyrus (pars triangularis*, pars orbitalis), left insula −34, 24,−2 57

Left inferior frontal gyrus (pars triangularis)* −44, 26, 10 25

Left medial frontal gyrus* −4, 52, 12 31

Left middle frontal gyrus* −32, 4, 54 29

Left precentral gyrus* −44,−10, 42 33

Left superior frontal gyrus*, left medial frontal gyrus, right superior frontal gyrus, right medial frontal

gyrus

−0, 12, 50 373

Left middle temporal gyrus* −50,−20,−10 72

Left middle temporal gyrus*, left superior temporal gyrus −46, 4,−18 35

(Continued)

Frontiers in Psychology | www.frontiersin.org 6 August 2015 | Volume 6 | Article 1138

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Predict the distribution of coordinates, given text

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Page 9: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Details

I text is vectorized by counting word frequenciesI functions over the brain are turned into vectors of weights

over a set of regions (atlas regions or voxels){Rk , k = 1 . . .m}

I true pdf is estimated from the reported coordinates

p =1c

m∑k=1

ckIk

|Ik |1, (1)

where ck is the number of coordinates in Rk and c =∑

k ck

I (possibly p is smoothed with a Gaussian kernel)I we fit a linear regression: (either least squares or least

deviations) + `2 penalty on the coefficients

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Page 10: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Details: regression model

I We are trying to predict a pdfI a common distance between probability measures is Total

Variation:

TV(P,Q) = supA⊂R

|P(A)−Q(A)| (2)

the sup is attained by taking A = {Rk |P(Rk ) > Q(Rk )}and:

TV(P,Q) = 12

m∑k=1

|P(Rk )−Q(Rk )| =12

∫R3|p(z)−q(z)|dz .

(3)I hence the least-deviations regressionI we also compare it to least squares because it is popular

and easy to solve

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Page 11: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Details: regression model

β = argminβ

(‖Y − Xβ‖1 + λ‖β‖22

)(4)

I particular case of penalized quantile regressionI can be solved efficiently as the dual only involves box

constraints (and X is sparse)

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Page 12: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Results: prediction on left-out articles andmodel inspection

Page 13: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Evaluation

I metric: log-likelihood given coordinates reported in left-outarticles

I if q : R3 → [0, 1] is our prediction, and L are the coordinatesreported in the study,

1|L|∑`∈L

log(q(`))

is our score

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Page 14: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Results

I baseline: human-labelled atlasesI an atlas is a segmentation of the brain, with labels such as

“parietal lobe” or “hippocampus”I for this baseline, we set the probability of a region to be

proportional to the frequency of its label in the text

10.3 10.2 10.1 10.0 9.9 9.8 9.7 9.6Log-likelihood of coordinates in left-out articles

Atlas

Least-squares

Least deviations

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Regression coefficients link words to voxels

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Page 16: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Results: regression coefficients

“anterior cingulate”

L R

y=-6

L R

y=-6

L R

y=-2

“left amygdala”, “amygdala”,“right amygdala”

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Page 17: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Results: regression coefficients as word embeddings

word2vec:emotionnegative emotionemotion expressionexpressing emotionsemotion regulationdisturbing emotionsemotive face recognition

brain maps:emotionamygdalabasolateral amygdalafearanxietyaffectionanger

fusiform gyrusinferior temporal gyrustemporal fusiform gyrusoccipitotemporal sulcusinferior occipital gyrioccipito temporal sulcusmiddle occipital gyrus

fusiform gyrusobject recognitionface recognitionface perceptionba37prosopagnosiaidentity gender

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Page 18: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Example (proof-of-concept) application

Page 19: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

Application

I we want to know which brain areas are related toHuntington’s disease.

I in our labelled corpus, almost no article (only 21) mention itI we learn term-location associations on this small, labelled

corpus.I we use the learned mapping to encode articles found in a

larger, unlabelled corpus (140K articles, over 400 mentionhuntington), find the putamen and caudate nucleus

L R

y=-34

L R

y=2

L R

z=-12

L R

z=0

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Application

parkinson (motor cortex, brain stem, thalamus):L R

y=-34

L R

y=2

L R

z=-12

L R

z=0

aphasia (Broca’s and Wernicke’s areas):L R

y=14

L R

z=14

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Page 21: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

conclusion

I framework for translating text into spatial pdfs over the brainI quantitative validation; voxel-wise encoding is much better

than atlases and least-deviations is better thanleast-squares.

I allows pooling together text-only studies and doing statisticson their results in brain space

I yields interesting embeddings of words related to anatomy,cognition and brain diseases

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Page 22: Text to brain: predicting the spatial distribution of ...Text to brain images I Many neuroimaging observations are stored in unstructured text. I e.g “[...] in the anterolateral

conclusion

I framework for translating text into spatial pdfs over the brainI quantitative validation; voxel-wise encoding is better than

atlases and least-deviations is (a bit) better thanleast-squares.

I allows pooling together text-only studies and doing statisticson their results in brain space

I yields interesting embeddings of words related to anatomy,cognition and brain diseases

Thank you for your attention!

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