FOCUS FEATURE:
Biomarkers in Network Neuroscience
Structure-function coupling as a correlate and
potential biomarker of cognitive impairment
in multiple sclerosis
Shanna D. Kulik1*
, Ilse M. Nauta2*, Prejaas Tewarie2,3, Ismail Koubiyr4, Edwin van Dellen5,
Aurelie Ruet4,6, Kim A. Meijer1, Brigit A. de Jong2, Cornelis J. Stam2,3, Arjan Hillebrand3,
Jeroen J. G. Geurts1, Linda Douw1, and Menno M. Schoonheim1
1Department of Anatomy and Neurosciences, Amsterdam UMC, Vrije Universiteit Amsterdam, MS Center Amsterdam,
Amsterdam Neuroscience, Amsterdam, The Netherlands
2Department of Neurology, Amsterdam UMC, Vrije Universiteit Amsterdam, MS Center Amsterdam,
Amsterdam Neuroscience, Amsterdam, The Netherlands
3Department of Clinical Neurophysiology and MEG center, Amsterdam UMC, Vrije Universiteit Amsterdam,
MS Center Amsterdam, Amsterdam Neuroscience, Amsterdam, The Netherlands
4University of Bordeaux, Bordeaux, France; Inserm U1215 – Neurocentre Magendie, Bordeaux, France
5Department of Psychiatry and UMC Utrecht Brain Center, University Medical Center Utrecht,
Utrecht University, The Netherlands
6University of Bordeaux, Bordeaux, France; Inserm U1215 – Neurocentre Magendie, Bordeaux, France;
CHU Pellegrin Bordeaux, Bordeaux, France
*Equal contribution.
Keywords: Magnetoencephalography, Diffusion tensor imaging, Structural connectivity, Functional
connectivity, Cognition, Multiple sclerosis
ABSTRACT
Multiple sclerosis (MS) features extensive connectivity changes, but how structural and
functional connectivity relate, and whether this relation could be a useful biomarker for
cognitive impairment in MS is unclear. This study included 79 MS patients and 40 healthy
controls (HCs). Patients were classified as cognitively impaired (CI) or cognitively preserved
(CP). Structural connectivity was determined using diffusion MRI and functional connectivity
using resting-state magnetoencephalography (MEG) dati (theta, alpha1, and alpha2 bands).
Structure-function coupling was assessed by correlating modalities, and further explored in
frequency bands that significantly correlated with whole-brain structural connectivity.
Functional correlates of short- and long-range structural connections (based on tract length)
were then specifically assessed. Receiving operating curve analyses were performed on
coupling values to identify biomarker potential. Only the theta band showed significant
correlations between whole-brain structural and functional connectivity (rho = −0.26,
p = 0.023, only in MS). Long-range structure-function coupling was stronger in CI patients
compared to HCs ( p = 0.005). Short-range coupling showed no group differences. Structure-
function coupling was not a significant classifier of cognitive impairment for any tract length
(short-range area under the curve (AUC) = 0.498, p = 0.976, long-range AUC = 0.611, p =
0.095). Long-range structure-function coupling was stronger in CI MS compared to HCs, Ma
more research is needed to further explore this measure as biomarkers in MS.
AUTHOR SUMMARY
Cognitive impairment in multiple sclerosis (MS) is common and relates to structural and
functional connectivity. Tuttavia, it remains unclear whether the interplay (coupling) between
a n o p e n a c c e s s
j o u r n a l
Citation: Kulik, S. D., Nauta, IO. M., Tewarie,
P., Koubiyr, I., van Dellen, E., Ruet, A.,
Meijer, K. A., de Jong, B. A., Stam, C. J.,
Hillebrand, A., Geurts, J. J. G., Douw, L., &
Schoonheim, M. M. (2022). Structure-
function coupling as a correlate and
potential biomarker of cognitive
impairment in multiple sclerosis. Network
Neuroscience, 6(2), 339–356. https://doi
.org/10.1162/netn_a_00226
DOI:
https://doi.org/10.1162/netn_a_00226
Received: 1 ottobre 2021
Accepted: 21 Dicembre 2021
Competing Interests: The authors have
declared that no competing interests
exist.
Corresponding Author:
Shanna D. Kulik
s.kulik@amsterdamumc.nl
Handling Editor:
Olaf Sporns
Copyright: © 2022
Istituto di Tecnologia del Massachussetts
Pubblicato sotto Creative Commons
Attribuzione 4.0 Internazionale
(CC BY 4.0) licenza
The MIT Press
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Long-range coupling is related to cognitive impairment in MS
structural and functional connectivity could be a biomarker of MS-related cognitive
impairment. This study investigated the cognitive relevance of structure-function coupling in
79 MS patients and 40 healthy controls using diffusion MRI and magnetoencephalography.
Results show that coupling was stronger in cognitively impaired MS patients compared to
controls, but only when considering long-distance connections. Nonetheless, classifier
analyses indicated only weak biomarker potential in terms of sensitivity and specificity. Future
studies should include additional operationalization of coupling as well as longitudinal and
regional or network level data.
INTRODUCTION
Patients with multiple sclerosis (MS) commonly experience deficits in cognitive performance,
which profoundly affect quality of life (Chiaravalloti & DeLuca, 2008). Both structural and
functional brain alterations seem to correlate with cognitive impairment in MS (Chard et al.,
2021; Fleischer et al., 2019; Nauta et al., 2020). Previous studies have indicated that beside
structural brain damage, such as gray matter atrophy, disruptions in both structural and func-
tional networks are important correlates of cognitive impairment (Eijlers et al., 2018B; Faivre
et al., 2016; Fleischer et al., 2019; Nauta et al., 2020). Structural and functional connectivity
are commonly measured using statistical approaches and algorithms, thereby providing an
estimation of true connections. Structural connectivity (SC) estimates the likelihood that white
matter tracts physically interconnect brain regions based on diffusion measurements, whereas
functional connectivity (FC) reflects statistical interdependencies between time series that
describe activity measurements (Aertsen, Gerstein, Habib, & Palm, 1989). È interessante notare, MS
patients with cognitive problems may show functional network changes without severe struc-
tural damage (Eijlers et al., 2018UN). How these two network modalities are related, and whether
there is an important interplay between structural and functional networks that pertains to cog-
nitive function, has rarely been studied in MS.
In healthy populations, several studies have shown a relationship between SC and FC,
although varying directions of this relationship have been found: higher SC has been related
to lower FC, but also vice versa (Hermundstad et al., 2013; Honey et al., 2009; Skudlarski
et al., 2008). While intuitively one might expect that FC would be severely constrained by
the presence of direct structural connections, previous work found strong FC without a direct
structural connection (Honey et al., 2009; Robinson, 2012). Overall, in the healthy situation,
the functional repertoire seems extensive despite a limited structural backbone, indicating a
potentially low overlap between structure and function (van Dam, Hulst, & Schoonheim,
2021). Infatti, it has become clear that there are regional variations in SC-FC correspondence,
which relate to cognition in healthy controls (HCs) (Gu, Jamison, Sabuncu, & Kuceyeski,
2021). In MS, it was found that more similarity between SC and FC (cioè., structure-function
coupling) related with poorer cognitive performance (Koubiyr et al., 2020), indicating that
greater correspondence between structural and functional networks of MS patients could
potentially be of use as a biomarker for cognitive impairment.
Recentemente, it was found that particularly damage to long-range white matter tracts is impor-
tant for cognitive problems in MS, which warrants a focus on the interplay between SC and FC
for specifically these connections in the brain (Meijer, Steenwijk, Douw, Schoonheim, &
Geurts, 2020). Our study aimed to investigate the interplay between SC and FC and its relation
with cognition in MS. It was examined whether MS patients with cognitive impairment
Structural connectivity:
Estimation of white matter tracts that
physically interconnect brain regions
based on diffusion measurements.
Functional connectivity:
Statistical interdependencies
between time series that describe
activity measurements.
Biomarker:
An indicator of a biological state
(per esempio., disease) or process that can be
measured via various means.
Network Neuroscience
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Long-range coupling is related to cognitive impairment in MS
displayed a disruption of structure-function coupling and whether this effect was more apparent
in specific tracts according to their length. Because structural and functional brain connectivity
are inseparably connected, studying the relationship between SC and FC (cioè., coupling) could
provide more sensitive and specific measures of individual response to MS-related damage
compared to studying SC and FC separately, and could lead to the development of better
biomarkers thereof (Honey, Thivierge, & Sporns, 2010; van den Heuvel et al., 2013).
MATERIALS AND METHODS
Participants
MEG:
Magnetoencephalography; recording
the magnetic fields produced by
electrical currents generated by
neural populations.
dMRI:
Specific MRI sequence that quantifies
the diffusion of water molecules in
different directions, which can be
used for probabilistic tractography.
All MS patients and HCs were part of the Amsterdam MS cohort (Eijlers et al., 2018B). Subsamples
of the magnetoencephalography (MEG) and diffusion magnetic resonance imaging (dMRI) data of
this cohort has been published previously (Meijer et al., 2020; Nauta et al., 2020), but have never
been analyzed together. In the present study participants were included who underwent cognitive
assessment as well as both MEG and dMRI measurements between 2010 E 2013, resulting in
the inclusion of 79 patients with a diagnosis of MS (72.2% women, age 53.77 ± 10.7 years;
Tavolo 1) E 40 HCs (62.5% women, age 50.72 ± 6.11 years; Tavolo 1). Disability was estimated
using the Expanded Disability Status Scale (EDSS) (Kurtzke, 1983). Level of education was mea-
sured on a scale of 1 (did not finish primary school) A 7 (acquired a university degree) (Verhage,
1964) and categorized as low (categories 1–4) or high (categories 5–7). Ethics approval was granted
by the institutional ethics review board of the Amsterdam UMC, and written informed consent was
obtained from all participants prior to participation.
Tavolo 1. Demographic, clinical, cognitive, and MRI outcomes of MS patients and healthy controls
Demographics
Age; years, mean (SD)
Sex; % females
Education; % low/high
Clinical characteristics
Disease duration; years, mean (SD)
MS type; RR/SP/PP (%)
EDSS; median (range)
MRI characteristics
Healthy Controls
N = 40
Total Group
N = 79
MS Patients
CP Patients
N = 46
CI Patients
N = 33
50.7 (6.11)
53.8 (10.7)
53.4 (10.8)
54.3 (10.8)
63%
40/60%
72%
50/50%
74%
46/54%
70%
56/44%
n/a
n/a
n/a
18.1 (6.93)
18.0 (6.77)
18.3 (7.3)
71/20/9%
3.50 (1–8)
76/17/7%
3.25 (1–8)
64/24/12%
4.00 (2.5–7.5)
Cortical gray matter volume; l, mean (SD)
0.764 (0.033)*
0.732 (0.050)
0.740 (0.047)
0.721 (0.052)
Deep gray mater volume; mL, mean (SD)
61.5 (2.71)*
54.2 (7.00)
56.4 (5.58)
51.3 (7.62)
White matter lesion load; mL, median (range)
n/a
12.6 (2.47–85.5)
11.0 (3.17–61.0)
18.7 (2.47–85.5)
Note. Disease duration represents the disease duration since symptom onset. CI = cognitively impaired; CP = cognitively preserved; EDSS = Expanded Disability
Status Scale; MS = multiple sclerosis; n/a = not applicable; PP = primary progressive; SD = standard deviation; RR = relapsing remitting; SP = secondary
progressive.
* Significantly different from MS patients (P < 0.05).
Network Neuroscience
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Long-range coupling is related to cognitive impairment in MS
Magnetic Resonance Imaging
Participants were scanned on a 3T scanner (GE Signa HDxt) using an eight-channel phased-array
head coil. Volumetry and registration were based on a 3D T1-weighted inversion-prepared fast
spoiled gradient recall sequence (repetition time 7.8 ms, echo time 3 ms, inversion time 450 ms,
flip angle 12°, sagittal 1.0-mm sections, 0.94 × 0.94 mm2 in-plane resolution). Lesion filling
(using LEAP) was performed and deep gray matter volumes were estimated using FIRST
(FSL5). SIENAX (FSL5) was used to calculate cortical gray matter volumes by masking deep gray
matter areas from total gray matter segmentations. To normalize brain volumes, differences in
skull size of each participant compared to the skull of the standard brain were computed by
multiplying all gray matter volumes with the V-scaling factor (FSL5). SC was based on dMRI
covering the entire brain using five volumes without directional weighting (i.e., b = 0 s/mm2)
and 30 volumes with noncollinear diffusion gradients (echo planar imaging (EPI), b =
1,000 s/mm2, repetition time 13,000 ms, echo time 91 ms, flip angle 90°, 2.4-mm contiguous
axial slices, 2 × 2 mm2 in-plane resolution). Automatic segmentation of hyperintense lesions was
applied on FLAIR images and they were filled on the 3D T1 using LEAP (Chard, Jackson,
Miller, & Wheeler-Kingshott, 2010; Steenwijk et al., 2013).
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Tractography:
Method for tracking the trajectory of
the axonal pathways that exploits the
anisotropy of the diffusion MRI
signal.
Fractional anisotropy:
Scalar value between zero and one
that describes the degree of
anisotropy of a diffusion process.
Structural Connectivity
All dMRI preprocessing was performed as previously reported (Meijer et al., 2020), using the
FMRIB Diffusion Toolbox with standard settings (FDT; part of FSL5), including brain extraction,
eddy current, and motion correction. Images were then fed into MRtrix 3.0 to perform prob-
abilistic tractography, using the fiber orientation distribution (Tournier, Calamante, & Connelly,
2012). Through this algorithm, SC in the form of number of streamlines was reconstructed by
randomly putting seeds in the white matter. In order to determine possible paths (fibers)
between regions, the local fiber orientation distribution was estimated using constrained spher-
ical deconvolution (Tournier, Calamante, & Connelly, 2007). The 30 noncollinear diffusion
directions in the data were adjusted by restricting the maximum spherical harmonic order
(lmax) to six. Then, whole-brain probabilistic tractography was performed by randomly seed-
ing 100 million fibers within the brain mask for each participant. Subsequently, these whole-
brain maps were converted to atlas-specific maps; all connections remained unthresholded for
further analyses. Cortical gray matter nodes were defined by processing the 3D T1-weighted
image of each participant with the FreeSurfer 5.3 pipeline, after lesion filling (Meijer et al.,
2020). The automated anatomical labeling (AAL) atlas (Tzourio-Mazoyer et al., 2002) was
used to define 78 cortical nodes on the native cortical surface (Meijer et al., 2020). Subse-
quently, cortical regions were coregistered to dMRI space by using FLIRT (part of FSL), where
MRtrix was used to visualize structural tracts between all atlas regions by using the aforemen-
tioned processed streamline data. Finally, mean fractional anisotropy (FA) was calculated and
used as our measure of whole-brain SC within each tract. FA is commonly used as a measure
of connectivity in the MS field (Lopez-Soley et al., 2020; Pardini et al., 2015). Importantly, the
reliability of raw fiber count as a measure of SC is understudied in MS. However, concerns
remain regarding the use of this approach in MS due to effects of MS pathology, which could
induce false positive and/or negative connections. As such, it has been recommended that
average diffusion measures (such as FA) could be a better candidate than fiber count for SC
to avoid this particular issue (Lipp et al., 2020). Additionally, different types of tractography
have different error types (false positive or false negatives), but tract-averaged diffusion mea-
sures were recently proposed to deal with MS-specific noise (Lipp et al., 2020). From this
point, SC thus refers to the mean FA within a given tract.
Network Neuroscience
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Long-range coupling is related to cognitive impairment in MS
Magnetoencephalography
Eyes-closed, resting-state MEG measurements of 5 minutes were analyzed. Acquisition and
preprocessing of the MEG data was performed as described previously (Derks et al., 2018).
In short, measurements were performed in a magnetically shielded room ( Vacuum Schmelze
GmbH, Hanua, Germany) with a 306-channel MEG system (Elekta Neuromag Oy, Helsinki,
Finland). Data were sampled at 1250 Hz, and a high-pass filter (0.1 Hz) and anti-aliasing filter
(410 Hz) were employed online. The extended Signal Space Separation method (xSSS) (van
Klink et al., 2017) was applied to facilitate visual inspection of malfunctioning channels, after
which a maximum of 12 malfunctioning channels were excluded (SK, LD). Artifact removal
was performed offline with the temporal extension of the SSS in MaxFilter software (Elekta
Neuromag Oy, version 2.2.15) (Taulu & Simola, 2006). MEGs were subsequently coregistered
with participants’ MRI using a surface-matching procedure. The outline of the scalp and four
or five head localization coils were digitized and continuously monitored using a 3D digitizer
(3Space Fastrak, Polhemus, Colchester, VT, USA), which was matched to the MRI scalp sur-
face. Subsequently, the coregistered MRI was spatially normalized to a template MRI. Centroid
voxels (Hillebrand et al., 2016) in the 78 cortical regions of the AAL atlas (Gong et al., 2009)
were selected for further analyses after inverse transformation to the participant’s coregistered
MRI. An atlas-based beamformer implementation (Elekta Neuromag Oy, version 2.1.28) was
then applied to reconstruct broadband (0.5–48 Hz) time series of neural activity for these 78
centroids (Hillebrand, Barnes, Bosboom, Berendse, & Stam, 2012).
For each patient and HC, the first 13 consecutive epochs of 13.10 s (16,384 samples) were
selected (Liuzzi et al., 2017). The number of included epochs was based on the participant
with the lowest number of epochs available. All epochs were concatenated such that the
included time series were analyzed as a whole.
Functional Connectivity
FC was calculated for theta, alpha1, and alpha2 bands only, based on previous results showing
relations with cognition in MS (Schoonheim et al., 2013; Tewarie et al., 2014a, 2014b, 2015).
It should be noted that although there are papers that use the corrected amplitude envelope
correlation (AECc) in HCs (Messaritaki et al., 2021), none have investigated cognition in MS,
thus this choice was based on other FC metrics. Time series were therefore filtered in the theta
(4–8 Hz), alpha1 (8–10 Hz), and alpha2 (10–13 Hz) bands by digital band-pass filtering using
a fast Fourier transform, after which all bins outside the pass bands were set to zero, and an
inverse Fourier transform was performed.
To estimate FC between time series of each pair of AAL regions, the AEC (Brookes et al.,
2011; Hipp, Hawellek, Corbetta, Siegel, & Engel, 2012) was calculated. The AEC measures
amplitude-based connectivity between each pair of brain regions, based on correlations
between their amplitude envelopes. To calculate the AEC, the Hilbert transform was performed
on the band-pass filtered time series. Subsequently, since source-reconstructed MEG data is
contaminated by signal leakage (Stam, Nolte, & Daffertshofer, 2007), the AEC was computed
after pairwise orthogonalization of time series in the time domain, resulting in the corrected
AEC (AECc). To avoid negative values in the FC matrices, values were rescaled according to
AECcþ1
. FC was calculated in Matlab (version 2018.b, Mathworks, Natick, MA, USA) using in-
2
house scripts. Whole-brain FC was calculated by averaging the FC matrices over all regions.
Short- and Long-Range Connections
Short- and long-range connections of both SC and FC matrices were determined as previously
described (Meijer et al., 2020). Structural connections were divided into short- (first quartile
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Long-range coupling is related to cognitive impairment in MS
(Q1), <96.765 mm) and long- (fourth quartile (Q4), >172.056 mm) connections (see Figure 1D),
based on the histogram of tract lengths of HCs (Guarda la figura 2), as calculated on dMRI by MRtrix.
Subsequently, to determine short- and long-range FC, only functional connections with a direct
underlying structural connection (cioè., short- or long-range connection) were taken into account.
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Figura 1. Overview of the applied methods to calculate structure-function relationships. (UN) Sche-
matic representation of SC and FC. (B) Between-subject correlations were calculated by first aver-
aging all connections in the upper triangle of each individual subject’s matrix for both SC (blue M)
and FC (orange M). Subsequently, these averaged values for SC and FC were correlated across sub-
jects within the HC and MS groups separately. (C) Within-subject correlations were calculated by
first vectorizing all short- and long-range connections (see panel D) in the upper triangle of each
subject’s matrix for both SC and FC. Secondo, these SC and FC vectors were correlated within each
subject to determine structure-function coupling. (D) Schematic representation of short- (Q1) E
long-range (Q4) connections, based on the first and fourth quartiles of the histogram of tract lengths
in HCs. SC = structural connectivity; FC = functional connectivity; M = mean, Q1 = first quartile;
Q4 = fourth quartile.
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Long-range coupling is related to cognitive impairment in MS
Figura 2. Distribution of tract lengths in healthy controls. Structural connections of both HCs and
MS patients were categorized into short-range (<96.765 mm) and long-range connections
(>172.056 mm) based on first and fourth quartile thresholds. Q1 = first quartile; Q2 = second quar-
tile; Q3 = third quartile; Q4 = fourth quartile.
Structure-Function Relationships
Figura 1 represents an overview of how the structure-function relationships were constructed.
Between-subject correlations (Figure 1B): To determine the group-level correlation between
mean SC and mean FC within HCs and MS, SC and FC were first averaged for each subject
across all connections in the upper triangles of the respective matrices. Subsequently, this aver-
aged SC value and averaged FC value per subject were correlated across all subjects in the MS
and HC groups separately, using Pearson’s correlation coefficients. This approach therefore
provided one correlation coefficient per group indicating how individual differences in global
functional and SC are related. Between-subject correlations were calculated for whole-brain,
short-, and long-range connections.
The within-subject correlations (Figure 1C) measure of structure-function coupling was cal-
culated for each individual subject by first vectorizing the short- and long-range connection
weights of both SC and FC matrices within each participant (cioè., the short- and long-range
connections weights in the upper triangle of the matrix were transformed into one column).
Secondo, these SC and FC vectors were correlated within each participant using Pearson’s cor-
relations, resulting in one structure-function coupling value per participant for both short- E
long-range connections. This measure therefore indicates whether connectivity weights corre-
late across the structural and functional network of an individual.
Neuropsychological Evaluation
Neuropsychological assessment was based on an expanded Brief Repeatable Battery of Neu-
ropsychological tests (BRB-N), as described previously (Eijlers et al., 2018B). The assessment
consisted of seven neuropsychological tests: (1) the Selective Reminding Test (verbal memory);
(2) IL 10/36 Spatial Recall Test (visuospatial memory); (3) the Symbol Digit Modalities Test
(information processing speed); (4) the paper and pencil Memory Comparison Test (working
memory); (5) the Word List Generation Test (semantic verbal fluency); (6) the Concept Shifting
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Long-range coupling is related to cognitive impairment in MS
Test (executive function); E (7) the Stroop Color-Word Test (attention and executive func-
zione). Details on the raw test scores that have been used were described previously (Eijlers
et al., 2018B). Based on a normative sample of HCs, the raw test scores were adjusted for
age, sex, and education, as described previously (Amato et al., 2006; Eijlers et al., 2018B).
These adjusted scores were converted into z-scores based on the means and standard devi-
ations of the HCs and subsequently averaged into test-specific z-scores.
The MS patients were categorized as cognitively impaired (CI; 2 SDs (cioè., z ≤ −2) below
the average of the HCs on at least two cognitive domains) or cognitively preserved
(CP; remainder).
Classification Analyses
Receiving operating curve (ROC) analyses were performed to determine whether structure-
function coupling in whole-brain, short-, and long-range connections could classify CI patients
among MS patients. The areas under the curve (AUCs) were reported and optimal cutoff scores
(cioè., the highest value for sensitivity and specificity combined) were defined.
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Statistical Analyses
Statistical analyses were performed in SPSS 26.0 (Chicago, IL, USA) and in Matlab. All out-
come measures were checked for normal distributions using histogram inspection.
To test whether the sparsity of the SC matrices differed between groups, which could
potentially have affected subsequent analyses, the sparsity of the SC matrices was calculated
per subject. Subsequently, these sparsity values were compared between HCs, CP, and CI
MS patients with a general linear model. Additionally, the number of short- and long-range
connections were compared between MS patients and HCs, also with a general linear
modello.
Subsequently, to calculate between-subject correlations, relationships between average
whole-brain SC and FC were quantified in MS and HCs separately using Pearson’s correla-
zioni. Only those frequency bands in which a significant relation between SC and FC was
found in either MS or HCs (or both) were explored further to limit the number of statistical
comparisons.
Then, to calculate between-subject correlations for short- and long-range connections,
Pearson’s correlations between average short-range SC and FC and long-range SC and FC were
performed within identified bands, using the same approach within MS patients and HCs.
Prossimo, the clinical relevance of within-subject coupling, questo è, short- and long-range cou-
pling, was explored by comparing these between HCs, CP, and CI with general linear models,
correcting for age and sex. When significant group effects were found, it was investigated
which groups differed significantly. Coupling measures that significantly differed between
groups were further explored by correlating them with cognitive subdomains and disability,
as well as volumes of lesions, deep and cortical gray matter, using Pearson’s or Spearman’s
(if not normally distributed) correlations.
Finalmente, between-group differences of SC and FC separately in the previously determined fre-
quency bands were assessed with general linear models, correcting for age, sex, and education.
Significance level was set at p < 0.05. Analyses including short- and long-range connec-
tions were Bonferroni corrected for multiple comparisons by dividing the p value by two (p <
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Long-range coupling is related to cognitive impairment in MS
0.025), and group comparisons were Bonferroni corrected by dividing the p value by three
(three group comparisons; p < 0.017).
Post Hoc Analyses
To investigate the specificity of our results, a post hoc analysis was performed calculating
between-subject correlations for both short- and long-range connections in the other fre-
quency bands. Additionally, it was assessed whether relative power of the previously selected
frequency bands was correlated to SC, as the more basic measure of power could confound
the relationship between SC and FC. Furthermore, because the division of tracts into short- and
long-range was previously only performed for structural connections (Meijer et al., 2020), it
was further investigated, in post hoc analyses, whether this division was also applicable to
functional connections. To test the distinctiveness of short- and long-range FC, short-range
FC was correlated with long-range SC, and vice versa. Additionally, whole-brain FC theta
was correlated to both FC theta of short- and long-range connections within the MS patients.
RESULTS
Characteristics of Included Participants
Patients did not differ from HCs with regard to age, sex, and level of education ( p > 0.05).
Tavolo 1 presents an overview of all demographic and clinical variables. The patient cohort
was moderately affected based on disability (median EDSS 3.5), with an average disease dura-
tion of 18 years (range 8.83–37.7). Average cognitive performance was significantly lower in
MS patients compared to HCs (P < 0.001), with 33 (42%) patients displaying cognitive impair-
ment. No significant difference was found in the sparsity of the SC matrices between HCs, CI,
and CP MS patients (F = 0.773, p = 0.464). Also, there was no difference between the number
of short-range (mean: 1,628.9 for HCs, 1,707.2 for MS, F = 3.023, p = 0.085) and long-range
(mean: 1,591.8 for HCs, 1,534.3 for MS, F = 0.193, p = 0.662) connections when comparing
MS patients with HCs.
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Between-Subject Correlations: Relationships Between SC and FC
Within MS, whole-brain SC was significantly related to whole-brain FC in the theta band only
(r = −0.256, p = 0.023; Figure 3), which was not significant in HCs (r = −0.061, p = 0.711).
Whole-brain FC in the alpha bands did not show significant correlations with SC in either
group (MS patients alpha1: r = −0.090, p = 0.429, alpha2: r = −0.097, p = 0.394, HCs alpha1:
r = −0.118, p = 0.467, alpha2: r = −0.012, p = 0.940), thus only the theta band was further
explored.
Correlations between average short-range SC and average short-range FC theta were signif-
icant in MS (r = −0.313, p = 0.005; Figure 3), but not in HCs (r = −0.172, p = 0.290). For long-
range connections there was also a significant relation between average SC and average FC
theta in MS (r = −0.248, p = 0.028, not significant after correcting for two tests performed;
Figure 3), but not in HCs (r = −0.068, p = 0.675). As such, both short- and long-range coupling
in the theta band were evaluated further.
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Within-Subject Correlations: Structure-Function Coupling
A significant effect of group for long-range structure-function coupling (F = 4.04, p = 0.020;
significant after correcting for two tests performed) was found, which was driven by an
increase in CI (M = 0.022, SD = 0.014) compared to HCs (M = −0.033, SD = 0.013) ( p =
0.005; significant after correcting for three group comparisons; Figure 4), but not between
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Figure 3. Between-subject correlations: the relationship between FC theta and SC in MS. (A)
Relation between whole-brain SC and FC (r = −0.256, p = 0.023). (B) Relation between average
long-range SC and FC (r = −0.248, p = 0.028). (C) Relation between average short-range SC and
FC (r = −0.313, p = 0.005). SC = structural connectivity; FC = functional connectivity.
HCs and CP (p = 0.163), or CP and CI (p = 0.109). No significant group effects were seen for
short-range coupling (F = 0.025, p = 0.975), which was not explored further.
Structure-Function Coupling and Clinical Scores
Within MS, correlations with cognitive subdomains, clinical disability, and MR measures were
only performed for long-range coupling values, as this coupling value significantly differed
between HCs and CI MS patients. All performed correlations were not significant (executive
functioning: r = 0.002, p = 0.884; verbal memory: r = 0.018, p = 0.891; information processing
speed: r = −0.129, p = 0.328; verbal fluency: r = 0.074, p = 0.571; visuospatial memory: r =
−0.012, p = 0.928; disability: r = 0.051, p = 0.660; lesion volume: Rho = −0.007, p = 0.960;
and atrophy: normalized deep gray matter volume: r = −0.009, p = 0.947; normalized cortical
gray matter volume: r = −0.049, p = 0.708).
Comparisons Within Long-Range Connections
Finally, differences in SC and FC theta of long-range connections were separately assessed
between groups. Long-range SC showed a significant effect of group (F = 15.6, p < 0.001),
with CI (M = 0.423, SD = 0.005) showing lower values compared to both CP (M = 0.449,
SD = 0.004, p < 0.001) and HCs (M = 0.461, SD = 0.005, p < 0.001; Figure 5). Conversely,
FC theta of long-range connections showed no effect of group (F = 0.130, p = 0.878; Figure 5).
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Long-range coupling is related to cognitive impairment in MS
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Figure 4. The structure-function coupling for long-range connections within the different groups.
Each dot denotes a participant. Boxplots show the median value per group; *p < 0.05. HC = healthy
controls; CP = cognitively preserved MS patients; CI = cognitively impaired MS patients.
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Figure 5. SC and FC of long-range connections across groups. Each dot denotes a participant. Boxplots show the median value per group. (A)
SC of long-range connections per group. (B) FC of long-range connections per group. *p < 0.05. SC = structural connectivity; FC = functional
connectivity; HC = healthy controls; CP = cognitively preserved MS patients; CI = cognitively impaired MS patients.
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Long-range coupling is related to cognitive impairment in MS
Table 2.
Between-subject correlations for short- and long-range connections
MS
r = −0.271, p = 0.016
r = −0.193, p = 0.089
HC
r = −0.106, p = 0.514
r = 0.041, p = 0.803
r = −0.017, p = 0.880
r = −0.160, p = 0.323
r = −0.096, p = 0.400
r = −0.096, p = 0.554
Short-range alpha1
Short-range alpha2
Long-range alpha1
Long-rang alpha2
Classification Analyses
Receiving operating curve (ROC) analyses showed that structure-function coupling was not a sig-
nificant classifier of cognitive impairment among MS patients, neither for whole-brain (AUC =
0.493, p = 0.913), short-range (AUC = 0.498, p = 0.976), or long-range connections (AUC =
0.611, p = 0.095). Optimal cutoff scores for structure-function coupling was −0.03 for whole-brain
connections (sensitivity = 15%, specificity = 93%), −0.03 for short-range connections (sensitivity =
49%, specificity = 65%), and 0.04 for long-range connections (sensitivity = 46%, specificity = 80%).
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Post Hoc Analyses
To assess the specificity of our results, SC and FC were also correlated in the alpha1 and alpha2
bands, showing a significant correlation between SC and FC of short-range connections in the
alpha1 band for the MS patients (rho = −0.271, p = 0.016, significant after correcting for two tests
performed), but not for HCs (rho = −0.106, p = 0.514). Long-range connections showed no cor-
relations (p < 0.05; see Table 2 for all results). Next, the relative power in the theta band was
correlated to whole-brain SC in MS, yielding nonsignificant results (r = −0.176, p = 0.121),
which indicates that the relationship between SC and FC is not likely to be driven by power.
Furthermore, significant correlations were found between FC theta of short-range connec-
tions and SC of long-range connections: r = −0.280, p = 0.005 (significant after correcting for
two tests performed) and FC theta of long-range connections and SC of short-range connec-
tions: r = −0.330, p = 0.003 (significant after correcting for two tests performed). When further
zooming in on FC, whole-brain FC theta showed a strong correlation to FC theta of both short-
(r = 0.990, p < 0.001, significant after correcting for two tests performed) and long-range (r =
0.986, p < 0.001, significant after correcting for two tests performed) connections within the
MS patients, indicating that short- and long-range connections within the functional network
may not be as distinctive as they are in the structural network.
DISCUSSION
This study aimed to investigate the cognitive relevance of altered coupling between SC and FC
in MS. Significant correlations between SC and FC were only seen in MS but not in HCs, and
only in the theta band. Coupling of FC theta and SC was stronger in CI MS patients compared
to HCs, which was specific for long-range connections.
Between-subject correlations showed that SC was (negatively) related to FC in the theta
band in MS, indicating that patients with more structural damage have higher FC. Previously,
it has been shown that such ‘hyperconnectivity’ is common in neurological diseases as a reac-
tion to structural damage (Hillary et al., 2015; Schoonheim, Meijer, & Geurts, 2015). The theta
band is typically related to relaxed wakefulness (Mari-Acevedo, Yelvington, & Tatum, 2019). In
MS, the theta band has been described before, showing increased power and FC in relation to
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Long-range coupling is related to cognitive impairment in MS
cognitive impairment (Schoonheim et al., 2013; Schoonhoven et al., 2019; Tewarie et al.,
2015; Van der Meer et al., 2013). Why specifically this band would show a relationship
between SC and FC in MS remains unclear. Possibly, structural damage in the form of lesions,
which reduces SC, could result in the previously observed increased FC in the theta band.
Such increased FC in the theta band was also seen in other neurological disorders such as
Alzheimer’s disease, albeit using a different connectivity measure (Briels et al., 2020). Also,
this relationship was found for whole-brain and short-range connections regarding SC and
FC theta, and for short-range connections regarding SC and FC alpha1, whereas in the
long-range connections this relationship did not survive corrections for multiple comparisons.
Additionally, the between-subject correlation between SC and FC was only found in MS
patients and not in HCs. Correlations between SC and FC have previously also been found
in HCs using both MEG and fMRI (Hermundstad et al., 2013; Honey et al., 2009; Meier
et al., 2016; Skudlarski et al., 2008; Tewarie et al., 2019). This specificity to the MS group
could be due to MS pathology itself, either because MS changes the relationship between
SC and FC, or because MS has an effect on SC and FC separately, or both. At the same time,
methodological issues may have obscured correlations between SC and FC in our HCs. As it
has been suggested that different methods to quantify FC lead to different relationships
between SC and FC it seems plausible that using a different imaging modality could lead to
different findings in this relationship (Liegeois, Santos, Matta, Van De Ville, & Sayed, 2020).
Also, perhaps the small control sample that was included in our study might have influenced
the statistical power to determine a significant correlation coefficient within these HCs. As
such, future work remains needed to confirm these specific results.
When investigating CP and CI MS patients separately in comparison to HCs, long-range
coupling (i.e., within-subject coupling) was stronger in CI, indicating a stronger overlap in
structural and functional networks in CI patients compared to HCs. This finding is in line with
previous work where it was shown that a lower overlap between SC and FC is related to better
cognitive performance (Wang et al., 2018), which is further supported by a study in dementia
patients in which also a stronger relationship between SC and FC was found (Cao et al., 2020).
This specific effect in CI could be explained by the higher density of short-range compared to
long-range structural connections in the brain, leading to an increased vulnerability of long-
range connections (Park & Friston, 2013). Thus, alterations to long-range connections may
have larger consequences on the functional network, limiting the repertoire of functional pos-
sibilities when these connections are damaged (van Dam et al., 2021). This limited repertoire
would then result in stronger coupling, which has longitudinally been observed in a previous
MS study (Koubiyr et al., 2020). On the other hand, long-range coupling showing higher
values in CI patients compared to HCs could also be explained by the relationship between
long-range structural connections and cognitive performance only. Moreover, a recent study
found specifically that damage of long-range structural connections was related to cognitive
impairment in MS patients (Meijer et al., 2020). As our analyses indicated that short- and long-
range connections in the functional network may not be similarly distinctive as they are in the
structural network, and because this division is based on structural tracts, it might not be appli-
cable to FC. In fact, the present study did not identify group differences in theta band long-
range FC, while previous research has indicated that theta band whole-brain network topology
is altered in MS using MEG, albeit using a different FC measure (Nauta et al., 2020). In addi-
tion, there was no relation between long-range coupling and individual cognitive domains and
disability. Previous work did find a relationship between whole-brain structure-function cou-
pling and clinical disability (EDSS score) (Koubiyr et al., 2020). Of note, the aforementioned
study used fMRI instead of MEG to calculate FC and only included MS patients in the early
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Long-range coupling is related to cognitive impairment in MS
stages of the disease, whereas patients with a wide range of disease durations were included in
our study. Also, relatively low correlational values (see Figure 3) were obtained between
whole-brain and short- and long-range SC and FC. Previously mentioned technical points
could be the reason why our results indicate that structure-function coupling as operational-
ized here is not a relevant biomarker for cognitive impairment in MS. Although we have
observed interesting between-group differences, our AUC analyses indicate that the biomarker
potential of this quantification of “coupling” remains low, at least when assessing cross-
sectional measures. Future work is needed to investigate whether this measure could be used
to predict subsequent cognitive decline in MS patients. This is supported by recent MEG work
from our group on cognitive functioning in MS, indicating that cross-sectional correlates of
cognition can differ from longitudinal predictors (Nauta et al., 2020). Additionally, it was
recently shown that regional SC-FC coupling might be a more specific and sensitive measure
with regard to its relation with cognitive performance (Gu et al., 2021). Therefore, including
regional information using additional functional modalities might yield more useful biomarkers.
This study does have some limitations. First, more research into the comparison between FA
and the number of streamlines is lacking and newer diffusion sequences and pipelines could
result in improvement in streamline quantifications. Second, the high correlation between
short-range and long-range FC might be related to how FC was quantified. The AECc was
applied to estimate FC and is a measure that has not been applied to MS data before. This
measure was chosen because of its consistency in replicating group differences in other patient
populations (Colclough et al., 2016), and has been utilized in many previous studies (Brookes
et al., 2011; Tewarie et al., 2016). However, it may be insensitive to the specific relevance of
short- and long-range structural connections. Our FC measure may also have been insensitive
due to its pairwise nature. It is now also possible to determine FC by incorporating more than
two brain regions, that is, higher order interactions (Suarez, Markello, Betzel, & Misic, 2020).
Because it is known that SC and FC are not perfectly aligned, models of higher order interac-
tions might contribute to a better understanding of FC (Suarez et al., 2020), and subsequently
of the structure-function relationship. An additional important methodological issue in this
study is that only functional connections with an underlying structural tract were taken into
account. Importantly, the functional connections that were therefore not included in our
analyses could have been involved in cognitive impairment.
To conclude, our results indicate that SC and FC are more strongly related in MS patients
than in HCs, perhaps indicating a loss of the functional repertoire due to structural damage.
Additionally, structure-function coupling of only long-range connections was stronger in CI
MS patients, although the functional relevance of anatomical distance remains unclear. Future
longitudinal work is required to further investigate regional disease stage-specific changes in
structure-function coupling in MS.
ACKNOWLEDGMENTS
We would like to thank all patients and healthy controls for their participation.
AUTHOR CONTRIBUTIONS
Shanna Kulik: Conceptualization; Data curation; Formal analysis; Investigation; Methodology;
Software; Visualization; Writing – original draft; Writing – review & editing. Ilse Nauta: Con-
ceptualization; Data curation; Formal analysis; Investigation; Methodology; Visualization;
Writing – original draft; Writing – review & editing. Prejaas Tewarie: Data curation; Project
administration; Writing – review & editing. Ismail Koubiyr: Conceptualization; Writing –
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Long-range coupling is related to cognitive impairment in MS
review & editing. Edwin van Dellen: Writing – review & editing. Aurelie Ruet: Conceptualiza-
tion; Writing – review & editing. Kim Meijer: Conceptualization; Writing – review & editing.
Brigit de Jong: Funding acquisition; Writing – review & editing. Cornelis Stam: Data curation;
Writing – review & editing. Arjan Hillebrand: Data curation; Software; Writing – review &
editing. Jeroen Geurts: Conceptualization; Funding acquisition; Supervision; Writing – review
& editing. Linda Douw: Conceptualization; Data curation; Investigation; Methodology;
Supervision; Writing – original draft; Writing – review & editing. Menno Schoonheim: Concep-
tualization; Data curation; Funding acquisition; Investigation; Methodology; Supervision;
Writing – original draft; Writing – review & editing.
FUNDING INFORMATION
Brigit de Jong, Stichting MS Research (https://dx.doi.org/10.13039/501100003000), Award ID:
15-911. Jeroen Geurts and Menno Schoonheim, Stichting MS Research (https://dx.doi.org/10
.13039/501100003000), Award ID: 14-358e.
REFERENCES
Aertsen, A. M., Gerstein, G. L., Habib, M. K., & Palm, G. (1989).
Dynamics of neuronal firing correlation: Modulation of “effective
connectivity.” Journal of Neurophysiology, 61(5), 900–917.
https://doi.org/10.1152/jn.1989.61.5.900, PubMed: 2723733
Amato, M. P., Portaccio, E., Goretti, B., Zipoli, V., Ricchiuti, L., De
Caro, M. F., Patti, F., Vecchio, R., Sorbi, S., & Trojano, M. (2006).
The Raoʼs Brief Repeatable Battery and Stroop Test: Normative
values with age, education and gender corrections in an Italian
population. Multiple Scleroris Journal, 12(6), 787–793. https://doi
.org/10.1177/1352458506070933, PubMed: 17263008
Briels, C. T., Schoonhoven, D. N., Stam, C. J., de Waal, H.,
Scheltens, P., & Gouw, A. A. (2020). Reproducibility of EEG
functional connectivity in Alzheimerʼs disease. Alzheimerʼs
Research & Therapy, 12(1), 68. https://doi.org/10.1186/s13195
-020-00632-3, PubMed: 32493476
Brookes, M. J., Woolrich, M., Luckhoo, H., Price, D., Hale, J. R.,
Stephenson, M. C., Barnes, G. R., Smith, S. M., & Morris, P. G.
(2011). Investigating the electrophysiological basis of resting state
networks using magnetoencephalography. Proceedings of the
National Academy of Sciences USA, 108(40), 16783–16788.
https://doi.org/10.1073/pnas.1112685108, PubMed: 21930901
Cao, R., Wang, X., Gao, Y., Li, T., Zhang, H., Hussain, W., Xie, Y.,
Wang, J., Wang, B., & Xiang, J. (2020). Abnormal anatomical
rich-club organization and structural-functional coupling in mild
cognitive impairment and Alzheimerʼs disease. Frontiers in
Neurology, 11, 53. https://doi.org/10.3389/fneur.2020.00053,
PubMed: 32117016
Chard, D. T., Alahmadi, A. A. S., Audoin, B., Charalambous, T.,
Enzinger, C., Hulst, H. E., Rocca, M. A., Rovira, A., Sastre-Garriga,
J., Schoonheim, M. M., Tijms, B., Tur, C., Gandini Wheeler-
Kingshott, C. A. M., Wink, A. M., Ciccarelli, O., Barkhof, F., &
MAGNIMS Study Group. (2021). Mind the gap: From neurons to
networks to outcomes in multiple sclerosis. Nature Reviews
Neurology, 17(3), 173–184. https://doi.org/10.1038/s41582-020
-00439-8, PubMed: 33437067
Chard, D. T., Jackson, J. S., Miller, D. H., & Wheeler-Kingshott,
C. A. (2010). Reducing the impact of white matter lesions on
automated measures of brain gray and white matter volumes.
Journal of Magnetic Resonance Imaging, 32(1), 223–228.
https://doi.org/10.1002/jmri.22214, PubMed: 20575080
Chiaravalloti, N. D., & DeLuca, J. (2008). Cognitive impairment in
multiple sclerosis. Lancet Neurology, 7(12), 1139–1151. https://
doi.org/10.1016/S1474-4422(08)70259-X
Colclough, G. L., Woolrich, M. W., Tewarie, P. K., Brookes, M. J.,
Quinn, A. J., & Smith, S. M. (2016). How reliable are MEG
resting-state connectivity metrics? NeuroImage, 138, 284–293.
https://doi.org/10.1016/j.neuroimage.2016.05.070, PubMed:
27262239
Derks, J., Wesseling, P., Carbo, E. W. S., Hillebrand, A., van Dellen,
E., de Witt Hamer, P. C., Klein, M., Schenk, G. J., Geurts, J. J. G.,
Reijneveld, J. C., & Douw, L. (2018). Oscillatory brain activity
associates with neuroligin-3 expression and predicts progression
free survival in patients with diffuse glioma. Journal of Neuro-
oncology, 140(2), 403–412. https://doi.org/10.1007/s11060-018
-2967-5, PubMed: 30094719
Eijlers, A. J. C., Meijer, K. A., van Geest, Q., Geurts, J. J. G., &
Schoonheim, M. M. (2018a). Determinants of cognitive impair-
ment in patients with multiple sclerosis with and without atrophy.
Radiology, 288(2), 544–551. https://doi.org/10.1148/radiol
.2018172808, PubMed: 29786489
Eijlers, A. J. C., van Geest, Q., Dekker, I., Steenwijk, M. D., Meijer,
K. A., Hulst, H. E., Barkhof, F., Uitdehaag, B. M. J., Schoonheim,
M. M., & Geurts, J. J. G. (2018b). Predicting cognitive decline in
multiple sclerosis: A 5-year follow-up study. Brain, 141(9),
2605–2618. https://doi.org/10.1093/ brain/awy202, PubMed:
30169585
Faivre, A., Robinet, E., Guye, M., Rousseau, C., Maarouf, A., Le
Troter, A., Zaaraoui, W., Rico, A., Crespy, L., Soulier, E., Confort-
Gouny, S., Pelletier, J., Achard, S., Ranjeva, J. P., & Audoin, B.
(2016). Depletion of brain functional connectivity enhancement
Network Neuroscience
353
l
D
o
w
n
o
a
d
e
d
f
r
o
m
h
t
t
p
:
/
/
d
i
r
e
c
t
.
m
i
t
.
/
/
t
e
d
u
n
e
n
a
r
t
i
c
e
-
p
d
l
f
/
/
/
/
/
6
2
3
3
9
2
0
2
8
1
7
0
n
e
n
_
a
_
0
0
2
2
6
p
d
t
.
f
b
y
g
u
e
s
t
t
o
n
0
7
S
e
p
e
m
b
e
r
2
0
2
3
Long-range coupling is related to cognitive impairment in MS
leads to disability progression in multiple sclerosis: A longitudi-
nal resting-state fMRI study. Multiple Sclerosis Journal, 22(13),
1695–1708. https://doi.org/10.1177/1352458516628657,
PubMed: 26838014
Fleischer, V., Radetz, A., Ciolac, D., Muthuraman, M., Gonzalez-
Escamilla, G., Zipp, F., & Groppa, S. (2019). Graph theoretical
framework of brain networks in multiple sclerosis: A review of
concepts. Neuroscience, 403, 35–53. https://doi.org/10.1016/j
.neuroscience.2017.10.033, PubMed: 29101079
Gong, G., He, Y., Concha, L., Lebel, C., Gross, D. W., Evans, A. C.,
& Beaulieu, C. (2009). Mapping anatomical connectivity patterns
of human cerebral cortex using in vivo diffusion tensor imaging
tractography. Cerebral Cortex, 19(3), 524–536. https://doi.org/10
.1093/cercor/bhn102, PubMed: 18567609
Gu, Z., Jamison, K. W., Sabuncu, M. R., & Kuceyeski, A. (2021).
Heritability and interindividual variability of regional
structure-function coupling. Nature Communications, 12(1),
4894. https://doi.org/10.1038/s41467-021-25184-4, PubMed:
34385454
Hermundstad, A. M., Bassett, D. S., Brown, K. S., Aminoff, E. M.,
Clewett, D., Freeman, S., Frithsen, A., Johnson, A., Tipper, C. M.,
Miller, M. B., Grafton, S. T., & Carlson, J. M. (2013). Structural
foundations of resting-state and task-based functional connectivity
in the human brain. Proceedings of the National Academy of
Sciences USA, 110(15), 6169–6174. https://doi.org/10.1073
/pnas.1219562110, PubMed: 23530246
Hillary, F. G., Roman, C. A., Venkatesan, U., Rajtmajer, S. M., Bajo,
R., & Castellanos, N. D. (2015). Hyperconnectivity is a funda-
mental response to neurological disruption. Neuropsychology,
29(1), 59–75. https://doi.org/10.1037/neu0000110, PubMed:
24933491
Hillebrand, A., Barnes, G. R., Bosboom, J. L., Berendse, H. W., &
Stam, C. J. (2012). Frequency-dependent functional connectivity
within resting-state networks: An atlas-based MEG beamformer
solution. NeuroImage, 59(4), 3909–3921. https://doi.org/10
.1016/j.neuroimage.2011.11.005, PubMed: 22122866
Hillebrand, A., Tewarie, P., van Dellen, E., Yu, M., Carbo, E. W.,
Douw, L., Gouw, A. A., van Straaten, E. C., & Stam, C. J.
(2016). Direction of information flow in large-scale resting-state
networks is frequency-dependent. Proceedings of the National
Academy of Sciences USA, 113(14), 3867–3872. https://doi.org
/10.1073/pnas.1515657113, PubMed: 27001844
Hipp, J. F., Hawellek, D. J., Corbetta, M., Siegel, M., & Engel, A. K.
(2012). Large-scale cortical correlation structure of spontaneous
oscillatory activity. Nature Neuroscience, 15(6), 884–890. https://
doi.org/10.1038/nn.3101, PubMed: 22561454
Honey, C. J., Sporns, O., Cammoun, L., Gigandet, X., Thiran, J. P.,
Meuli, R., & Hagmann, P. (2009). Predicting human resting-state
functional connectivity from structural connectivity. Proceedings
of the National Academy of Sciences USA, 106(6), 2035–2040.
https://doi.org/10.1073/pnas.0811168106, PubMed: 19188601
Honey, C. J., Thivierge, J. P., & Sporns, O. (2010). Can structure
predict
function in the human brain? NeuroImage, 52(3),
766–776. https://doi.org/10.1016/j.neuroimage.2010.01.071,
PubMed: 20116438
Koubiyr, I., Deloire, M., Brochet, B., Besson, P., Charre-Morin, J.,
Saubusse, A., Tourdias, T., & Ruet, A. (2020). Structural
constraints of functional connectivity drive cognitive impairment
in the early stages of multiple sclerosis. Multiple Scleroris Journal,
1352458520971807. https://doi.org/10.1177/1352458520971807,
PubMed: 33283582
Kurtzke, J. F. (1983). Rating neurologic impairment in multiple
sclerosis: An expanded disability status scale (EDSS). Neurology,
33(11), 1444–1452. https://doi.org/10.1212/wnl.33.11.1444,
PubMed: 6685237
Liegeois, R., Santos, A., Matta, V., Van De Ville, D., & Sayed, A. H.
(2020). Revisiting correlation-based functional connectivity and
its relationship with structural connectivity. Network Neurosci-
ence, 4(4), 1235–1251. https://doi.org/10.1162/netn_a_00166,
PubMed: 33409438
Lipp, I., Parker, G. D., Tallantyre, E. C., Goodall, A., Grama, S.,
Patitucci, E., Heveron, P., Tomassini, V., & Jones, D. K. (2020).
Tractography in the presence of multiple sclerosis lesions. Neuro-
Image, 209, 116471. https://doi.org/10.1016/j.neuroimage.2019
.116471, PubMed: 31877372
Liuzzi, L., Gascoyne, L. E., Tewarie, P. K., Barratt, E. L., Boto, E., &
Brookes, M. J. (2017). Optimising experimental design for MEG
resting state functional connectivity measurement. NeuroImage,
155, 565–576. https://doi.org/10.1016/j.neuroimage.2016.11
.064, PubMed: 27903441
Lopez-Soley, E., Solana, E., Martinez-Heras, E., Andorra, M.,
Radua, J., Prats-Uribe, A., Montejo, C., Sola-Valls, N., Sepulveda,
M., Pulido-Valdeolivas, I., Blanco, Y., Martinez-Lapiscina, E. H.,
Saiz, A., & Llufriu, S. (2020). Impact of cognitive reserve and
structural connectivity on cognitive performance in multiple
sclerosis. Frontiers in Neurology, 11, 581700. https://doi.org/10
.3389/fneur.2020.581700, PubMed: 33193039
Mari-Acevedo, J., Yelvington, K., & Tatum, W. O. (2019). Normal EEG
variants. Handbook of Clinical Neurology, 160, 143–160. https://doi
.org/10.1016/B978-0-444-64032-1.00009-6, PubMed: 31277844
Meier, J., Tewarie, P., Hillebrand, A., Douw, L., van Dijk, B. W.,
Stufflebeam, S. M., & Van Mieghem, P. (2016). A mapping
between structural and functional brain networks. Brain Connec-
tivity, 6(4), 298–311. https://doi.org/10.1089/brain.2015.0408,
PubMed: 26860437
Meijer, K. A., Steenwijk, M. D., Douw, L., Schoonheim, M. M., &
Geurts, J. J. G. (2020). Long-range connections are more severely
damaged and relevant for cognition in multiple sclerosis. Brain,
143(1), 150–160. https://doi.org/10.1093/ brain/awz355,
PubMed: 31730165
Messaritaki, E., Foley, S., Schiavi, S., Magazzini, L., Routley, B.,
Jones, D. K., & Singh, K. D.
(2021). Predicting MEG
resting-state functional connectivity from microstructural infor-
mation. Network Neuroscience, 5(2), 477–504. https://doi.org
/10.1162/netn_a_00187, PubMed: 34189374
Nauta, I. M., Kulik, S. D., Breedt, L. C., Eijlers, A. J., Strijbis, E. M.,
Bertens, D., Tewarie, P., Hillebrand, A., Stam, C. J., Uitdehaag,
B. M., Geurts, J. J., Douw, L., de Jong, B. A., & Schoonheim,
M. M. (2020). Functional brain network organization measured
with magnetoencephalography predicts cognitive decline in
multiple sclerosis. Multiple Sclerosis Journal, 1352458520977160.
https://doi.org/10.1177/1352458520977160, PubMed: 33295249
Pardini, M., Yaldizli, O., Sethi, V., Muhlert, N., Liu, Z., Samson,
R. S., Altmann, D. R., Ron, M. A., Wheeler-Kingshott, C. A.,
Miller, D. H., & Chard, D. T. (2015). Motor network efficiency and
disability in multiple sclerosis. Neurology, 85(13), 1115–1122.
Network Neuroscience
354
l
D
o
w
n
o
a
d
e
d
f
r
o
m
h
t
t
p
:
/
/
d
i
r
e
c
t
.
m
i
t
.
t
/
/
e
d
u
n
e
n
a
r
t
i
c
e
-
p
d
l
f
/
/
/
/
/
6
2
3
3
9
2
0
2
8
1
7
0
n
e
n
_
a
_
0
0
2
2
6
p
d
.
t
f
b
y
g
u
e
s
t
t
o
n
0
7
S
e
p
e
m
b
e
r
2
0
2
3
Long-range coupling is related to cognitive impairment in MS
https://doi.org/10.1212/ WNL.0000000000001970, PubMed:
26320199
Park, H. J., & Friston, K. (2013). Structural and functional brain net-
works: From connections to cognition. Science, 342(6158),
1238411. https://doi.org/10.1126/science.1238411, PubMed:
24179229
Robinson, P. A. (2012). Interrelating anatomical, effective, and
functional brain connectivity using propagators and neural field
theory. Physical Review E: Statistical, Nonlinear, and Soft Matter
Physics, 85(1 Pt 1), 011912. https://doi.org/10.1103/PhysRevE.85
.011912, PubMed: 22400596
Schoonheim, M. M., Geurts, J. J., Landi, D., Douw, L., van der
Meer, M. L., Vrenken, H., Polman, C. H., Barkhof, F., & Stam,
C. J. (2013). Functional connectivity changes in multiple sclerosis
patients: A graph analytical study of MEG resting state data.
Human Brain Mapping, 34(1), 52–61. https://doi.org/10.1002
/hbm.21424, PubMed: 21954106
Schoonheim, M. M., Meijer, K. A., & Geurts, J. J. (2015). Network
collapse and cognitive impairment in multiple sclerosis. Frontiers
in Neuroscience, 6, 82. https://doi.org/10.3389/fneur.2015
.00082, PubMed: 25926813
Schoonhoven, D. N., Fraschini, M., Tewarie, P., Uitdehaag, B. M.,
Eijlers, A. J., Geurts, J. J., Hillebrand, A., Schoonheim, M. M.,
Stam, C. J., & Strijbis, E. M. (2019). Resting-state MEG measure-
ment of functional activation as a biomarker for cognitive decline
in MS. Multiple Sclerosis Journal, 25(14), 1896–1906. https://doi
.org/10.1177/1352458518810260, PubMed: 30465461
Skudlarski, P., Jagannathan, K., Calhoun, V. D., Hampson, M.,
Skudlarska, B. A., & Pearlson, G. (2008). Measuring brain
connectivity: Diffusion tensor imaging validates resting state
temporal correlations. NeuroImage, 43(3), 554–561. https://
doi.org/10.1016/j.neuroimage.2008.07.063, PubMed:
18771736
Stam, C. J., Nolte, G., & Daffertshofer, A. (2007). Phase lag index:
Assessment of functional connectivity from multi channel EEG
and MEG with diminished bias from common sources. Human
Brain Mapping, 28(11), 1178–1193. https://doi.org/10.1002
/hbm.20346, PubMed: 17266107
Steenwijk, M. D., Pouwels, P. J., Daams, M., van Dalen, J. W.,
Caan, M. W., Richard, E., Barkhof, F., & Vrenken, H. (2013).
Accurate white matter lesion segmentation by k nearest neighbor
classification with tissue type priors (kNN-TTPs). NeuroImage
Clinical, 3, 462–469. https://doi.org/10.1016/j.nicl.2013.10
.003, PubMed: 24273728
Suarez, L. E., Markello, R. D., Betzel, R. F., & Misic, B. (2020).
Linking structure and function in macroscale brain networks.
Trends in Cognitive Sciences, 24(4), 302–315. https://doi.org/10
.1016/j.tics.2020.01.008, PubMed: 32160567
Taulu, S., & Simola, J. (2006). Spatiotemporal signal space separa-
tion method for rejecting nearby interference in MEG measure-
ments. Physics in Medicine & Biology, 51(7), 1759–1768. https://
doi.org/10.1088/0031-9155/51/7/008, PubMed: 16552102
Tewarie, P., Abeysuriya, R., Byrne, A., OʼNeill, G. C., Sotiropoulos,
S. N., Brookes, M. J., & Coombes, S. (2019). How do spatially
distinct frequency specific MEG networks emerge from one
underlying structural connectome? The role of the structural
eigenmodes. NeuroImage, 186, 211–220. https://doi.org/10
.1016/j.neuroimage.2018.10.079, PubMed: 30399418
Tewarie, P., Hillebrand, A., Schoonheim, M. M., van Dijk, B. W.,
Geurts, J. J., Barkhof, F., Polman, C. H., & Stam, C. J. (2014a).
Functional brain network analysis using minimum spanning trees
in multiple sclerosis: An MEG source-space study. NeuroImage,
88, 308–318. https://doi.org/10.1016/j.neuroimage.2013.10
.022, PubMed: 24161625
Tewarie, P., Hillebrand, A., van Dijk, B. W., Stam, C. J., OʼNeill, G. C.,
Van Mieghem, P., Meier, J. M., Woolrich, M. W., Morris, P. G., &
Brookes, M. J. (2016). Integrating cross-frequency and within band
functional networks in resting-state MEG: A multi-layer network
approach. NeuroImage, 142, 324–336. https://doi.org/10.1016/j
.neuroimage.2016.07.057, PubMed: 27498371
Tewarie, P., Schoonheim, M. M., Schouten, D. I., Polman, C. H.,
Balk, L. J., Uitdehaag, B. M., Geurts, J. J., Hillebrand, A., Barkhof,
F., & Stam, C. J. (2015). Functional brain networks: Linking
thalamic atrophy to clinical disability in multiple sclerosis, a
multimodal fMRI and MEG study. Human Brain Mapping,
36(2), 603–618. https://doi.org/10.1002/hbm.22650, PubMed:
25293505
Tewarie, P., Steenwijk, M. D., Tijms, B. M., Daams, M., Balk, L. J.,
Stam, C. J., Uitdehaag, B. M., Polman, C. H., Geurts, J. J., Barkhof,
F., Pouwels, P. J., Vrenken, H., & Hillebrand, A. (2014b). Disruption
of structural and functional networks in long-standing multiple
sclerosis. Human Brain Mapping, 35(12), 5946–5961. https://doi
.org/10.1002/hbm.22596, PubMed: 25053254
Tournier, J. D., Calamante, F., & Connelly, A. (2007). Robust deter-
mination of the fibre orientation distribution in diffusion MRI:
Non-negativity constrained super-resolved spherical deconvolu-
tion. NeuroImage, 35(4), 1459–1472. https://doi.org/10.1016/j
.neuroimage.2007.02.016, PubMed: 17379540
Tournier, J. D., Calamante, F., & Connelly, A. (2012). MRtrix:
Diffusion tractography in crossing fiber regions. International
Journal of Imaging Systems and Technology, 22(1), 53–66.
https://doi.org/10.1002/ima.22005
Tzourio-Mazoyer, N., Landeau, B., Papathanassiou, D., Crivello, F.,
Etard, O., Delcroix, N., Mazoyer, B., & Joliot, M. (2002). Auto-
mated anatomical labeling of activations in SPM using a macro-
scopic anatomical parcellation of the MNI MRI single-subject
brain. NeuroImage, 15(1), 273–289. https://doi.org/10.1006
/nimg.2001.0978, PubMed: 11771995
van Dam, M., Hulst, H. E., & Schoonheim, M. M. (2021). Coupling
structure and function in early MS: How a less diverse repertoire
of brain function could lead to clinical progression. Multiple
Sclerosis Journal, 27(4), 491–493. https://doi.org/10.1177
/1352458520987798, PubMed: 33719745
van den Heuvel, M. P., Sporns, O., Collin, G., Scheewe, T., Mandl,
R. C., Cahn, W., Goni, J., Hulshoff Pol, H. E., & Kahn, R. S. (2013).
Abnormal rich club organization and functional brain dynamics in
schizophrenia. JAMA Psychiatry, 70(8), 783–792. https://doi.org
/10.1001/jamapsychiatry.2013.1328, PubMed: 23739835
Van der Meer, M. L., Tewarie, P., Schoonheim, M. M., Douw, L.,
Barkhof, F., Polman, C. H., Stam, C. J., & Hillebrand, A.
(2013). Cognition in MS correlates with resting-state oscillatory
brain activity: An explorative MEG source-space study. Neuro-
Image Clinical, 2, 727–734. https://doi.org/10.1016/j.nicl.2013
.05.003, PubMed: 24179824
van Klink, N., van Rosmalen, F., Nenonen, J., Burnos, S., Helle, L.,
Taulu, S., Furlong, P. L., Zijlmans, M., & Hillebrand, A. (2017).
Network Neuroscience
355
l
D
o
w
n
o
a
d
e
d
f
r
o
m
h
t
t
p
:
/
/
d
i
r
e
c
t
.
m
i
t
.
/
t
/
e
d
u
n
e
n
a
r
t
i
c
e
-
p
d
l
f
/
/
/
/
/
6
2
3
3
9
2
0
2
8
1
7
0
n
e
n
_
a
_
0
0
2
2
6
p
d
t
.
f
b
y
g
u
e
s
t
t
o
n
0
7
S
e
p
e
m
b
e
r
2
0
2
3
Long-range coupling is related to cognitive impairment in MS
Automatic detection and visualisation of MEG ripple oscillations
in epilepsy. NeuroImage Clinical, 15, 689–701. https://doi.org/10
.1016/j.nicl.2017.06.024, PubMed: 28702346
Verhage, F. (1964). Intelligentie en leeftijd onderzoek bij Nederlan-
ders van twaalf tot zevenenzeventig jaar. [Intelligence and age:
Research study in Dutch individual aged twelve to seventy-
seven]. Assen, the Netherlands: Van Gorcum.
Wang, J., Khosrowabadi, R., Ng, K. K., Hong, Z., Chong, J. S. X.,
Wang, Y., Chen, C. Y., Hilal, S., Venketasubramanian, N., Wong,
T. Y., Chen, C. L., Ikram, M. K., & Zhou, J. (2018). Alterations in
brain network topology and structural-functional connectome
coupling relate to cognitive impairment. Frontiers in Aging Neu-
roscience, 10, 404. https://doi.org/10.3389/fnagi.2018.00404,
PubMed: 30618711
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