Conclusion
The number of migraine patients is increasing, and need appropriate and effective treatments. Many causes have been implemented to effectively diagnose and treat migraine. Therefore, studying the relationship between white
matter and migraine is necessary to improve the effect of identification of migraine and to avoid wrong examination of the symptoms. This method requires
modern accurate MRI scanners, imaging techniques such as T1- weighted, T2-
weighted, fluid-attenuated inversion recovery MRI (FLAIR), diffusion tensor
imaging (DTI), and voxel-base morphometry (VBM). Age, presence of aura,
nausea, and disability during attack, resistance to treatment, and severity of
headache and duration of migraine are considered a risk factor for development
of WMHs. Based on the studies, migraine is commonly associated with the
change of white matter. However, the association between migraine and structural brain changes and the relationship between properties of migraine attack
and disease condition is complicated by differences in interaction mechanisms,
it is necessary to clarify. There are important limitations of studying such as
the size of patient groups, timing of study, the criteria selection, the control
of potential unpredicted factors and the quality of MRI scanners, which can
effect the accuracy of results.
To elucidate the nature of the relationship between migraine headaches and
white matter changes found, it is able to use DTI for research as DTI is a
powerful support tool at present. It may help people better understand the
progression of migraine and implicate its treatment.
12 trang |
Chia sẻ: hachi492 | Lượt xem: 20 | Lượt tải: 0
Bạn đang xem nội dung tài liệu Overview: Studying the change of white matter associated with migraine desease by magnetic resonance imaging, để tải tài liệu về máy bạn click vào nút DOWNLOAD ở trên
Southeast-Asian J. of Sciences: Vol. 7, No 2 (2019) pp. 178-189
OVERVIEW: STUDYING THE CHANGE OF
WHITE MATTER ASSOCIATED WITH
MIGRAINE DESEASE BY MAGNETIC
RESONANCE IMAGING
Tran Thi Kim Lan∗, Ly Anh Tu∗
and
Nguyen Truong Thanh Hai†
∗Department of Applied Science
University of technology-VNU HCM City, Vietnam
email: kimlantran.bme@gmail.com lyanhtu@hcmut.edu.vn
†University Montpellier, Montpellier city, France
email: thanhhai7486@gmail.com
Abstract
Migraine is a common neurological disorder. It influences the quality
of personal life and also brings economic and social drawbacks. Studies on
the change of white matter associated with migraine disease by magnetic
resonance imaging (MRI) have been investigating in many places around
the world. Early detection of white matter changes in migraine patients
determines its relationship with migraine severity, type and duration[1].
At present, the general method of studying on the change of white
matter associated with migraine disease is using magnetic resonance
imaging. Research groups gathered migraine patients in different ages.
They excluded smokers and patients with hypertension, cardiac disease,
diabetes mellitus, endocrine dysfunction, oncological and hematological
diseases, infectious diseases, demyelinating disorders, and Alzheimer dis-
ease because the repeated attacks of migraine were the only known risk
factors for the change of white matter. Magnetic resonance images of
same patient groups were captured in same MRI scanners and acquisi-
tion protocols in a period of time to investigate functional and structural
abnormalities of white matter due to the effects of the repeated migraines.
Key words: Migraine, brain white matter hyperintensity, quantitative 3.0-Tesla MRI, vol-
umetry, longitudinal analysis
178
T. T. Kim Lan, L. Anh Tu, N. Tr. Thanh Hai 179
The results of studies by magnetic resonance imaging method show
that there are white matter hyperintensities (WMHs) and white matter
lesions (WMLs) associated with migraine and the status of these changes
depend on the frequency of the repeated migraine attacks.
1. Introduction
According to WHO, migraine affects about 15% of world population. This is
the most popular neurological disorder and it ranks 12th in women and 19th
in population for the level of disablement. Normally, migraine is considered
as a benign disorder which does not cause long-term consequences for brain.
Neurologists have usually evaluated that patients suffer migraine to exclude
the secondary causes of headache.
However, researchers have recently investigate the brain activation pattern
when migraine attacks and symptoms such as nausea, vomiting, and sensitivity
to light, sound, or smell to find out basic mechanism. There are more evidences
that migraine is unpredictable and the repeated attacks leads to structural and
functional abnormalities, finally chronic headaches.
Using MRI technique has pointed out that migraine is not just a disorder
related to continuous pain or not but a process of the structural and functional
brain changes through time. In the last decade, several ordinary changes were
proved such as gray matter (GM) and white matter (WM). This helps to im-
prove treatments as well as monitor treatment effectiveness in an objective and
non-invasive way.
Migraine is an independent risk factor for brain white matter lesions (WMLs)
and silent posterior circulation territory infarcts [2],[3].Both the disease dura-
tion and the attack frequency have an important role in the lesion evolution,
and the effects of comorbid diseases may also lead to the development of lesions.
While quantitative magnetic resonance imaging (MRI) study of chronic supra-
tentorial white matter hyperintensities (WMHs) in migraine patients demon-
strated tissue damage with axonal loss, decreased glial cell density with im-
paired energy metabolism, an enlarged extracellular space with an increased
extracellular water fraction and decreased blood flow and volume.10 WMHs
could be the consequence of a microvascular ischemic injury in migraine. The
WMHs appeared most frequently in the deep white matter in the anterior circu-
lation territory, mainly in the frontal and parietal lobes, with a similar average
WMH size in all hemispheric lobes [5].
Examination of white matter change associated with migraine patients can
be performed by functional magnetic resonance imaging (fMRI) and diffusion
tensor imaging (DTI) because of its high specification and sensitivity. Com-
monly used to detect changes in brain function and structure in the central
nervous system. Thereby, neuroimaging provides new insights into brain func-
tion and structure that can provide objective signs of the disease.
180 Overview: Studying the change of white matter associated with...
2. Methodology
Method
We searched and review the reference articles studying white matter change
by magnetic resonance imaging in migraineurs, based on title, in the period
2013-2018. The search was limited to English-language publications and studies
of humans. We also reviewed the reference lists of relevant primary articles and
reviews. Diagnostic criteria for migraine were carefully reviewed. Studies used
the International Classification of Headache Disorders for MO and MA. We
included the following imaging techniques: T1- and T2-weighted and fluid-
attenuated inversion recovery MRI, diffusion tensor imaging (DTI), and voxel-
based morphometry (VBM). Studies performed at 1.5 and 3.0 T were included.
All articles were screened for content, methodology, and design carefully.
Patient
Research groups gathered migraine patients in different ages. They excluded
smokers and patients with hypertension, cardiac disease, diabetes mellitus, en-
docrine dysfunction, oncological and hematological diseases, infectious diseases,
demyelinating disorders, and Alzheimer disease because migraine was the only
known risk factor for the change of white matter.
They also divided patients into two major types: migraine without aura and
migraine with aura. Migraine without aura is a clinical syndrome characterized
by headache with specific features and associated symptoms. Migraine with
aura is primarily characterized by the transient focal neurological symptoms
that usually precede or sometimes accompany the headache. Depending on
criteria, all patients were be diagnosed and coded [6].
There were differences about number, age groups, gender, migraine type as
well as the study period (Table 1)
I. Diagnostic criteria of migraine without aura [6]
A. At least five attacks1 fulfilling criteria B-D;
B. Headache attacks lasting 4-72 hours (when untreated or unsuccessfully
treated);
C. Headache has at least two of the following four characteristics:
1. unilateral location;
2. pulsating quality;
3. moderate or severe pain intensity;
4. aggravation by or causing avoidance of routine physical activity (e.g.
walking or climbing stairs).
D. During headache at least one of the following:
1. nausea and/or vomiting;
2. photophobia and phonophobia.
E. Not better accounted for by another ICHD-3 diagnosis.
II. Diagnostic criteria of migraine with aura [4].
A. At least two attacks fulfilling criteria B and C;
T. T. Kim Lan, L. Anh Tu, N. Tr. Thanh Hai 181
B. One or more of the following fully reversible aura symptoms:
1. visual;
2. sensory;
3. speech and/or language;
4. motor;
5. brainstem;
6. retinal;
C. At least three of the following six characteristics:
1. at least one aura symptom spreads gradually over 5 minutes;
2. two or more aura symptoms occur in succession;
3. each individual aura symptom lasts 5-60 minutes;
4. at least one aura symptom is unilateral [2];
5. at least one aura symptom is positive [3];
6. the aura is accompanied, or followed within 60 minutes, by headache;
D. Not better accounted for by another ICHD-3 diagnosis.
There were differences about number, age groups, gender, migraine type as
well as the study period (Table 1)
Table 1. Studies of white matter changes on migraine patients.[5][7][8]
182 Overview: Studying the change of white matter associated with...
MR Scanning Protocol
Experiments were carried out in brain MRI techniques such as T1- weighted,
T2-weighted, fluid-attenuated inversion recovery MRI (FLAIR), diffusion ten-
sor imaging (DTI), and voxel-base morphometry (VBM). The most common
MRI sequences are T1-weighted and T2-weighted scans. T1-weighted images
are produced by using short TE and TR times. The contrast and brightness
of the image are predominately determined by T1 properties of tissue. Con-
versely, T2-weighted images are produced by using longer TE and TR times.
In these images, the contrast and brightness are predominately determined by
the T2 properties of tissue. In general, T1- and T2-weighted images can be
easily differentiated by looking the CSF. CSF is dark on T1-weighted imaging
and bright on T2-weighted imaging. A third commonly used sequence is the
Fluid Attenuated Inversion Recovery (Flair). The Flair sequence is similar to a
T2-weighted image except that the TE and TR times are very long. By doing
so, abnormalities remain bright but normal CSF fluid is attenuated and made
dark. This sequence is very sensitive to pathology and makes the differentiation
between CSF and an abnormality much easier.
Studies performed at 1,5 to 3T MRI scanners with 8 to 12 channel phased
array head coil for MR measurements. To capture high resolution images, the
sequence parameters were used for different performances. For each brain MRI
techniques, sequences were done with the following parameters: Repetition
time (TR), Echo time (TE), Slice thickness, Field of view, Matrix or diffusion
weighted (DW) images with the b value.
Imagine Analysis
Original images were transferred to a work station. Data were fed to a
computer and analyzed by software of analysis tools for FMRI, MRI and DTI
brain imaging data. There are many different steps involved in a neuroimaging
analysis and there is not just one order in which to perform them. Depend-
ing on the researcher, the paradigm at hand, or the modality analyzed (sMRI,
fMRI, dMRI), the order can differ. Some steps may occur earlier or later or
may be left out entirely. Nonetheless, the general procedure for analysis can
be divided into the following three steps: preprocessing, model specification
and estimation, statistical inference. Preprocessing is the term used to for all
the steps taken to improve our data and prepare it for statistical analysis such
as slice timing correction, motion correction, artifact detection, coregistration,
normalization, smoothing, segmentation. Model specification and estimation is
to test our hypothesis on our data we first need to specify a model that incor-
porates this hypothesis and accounts for multiple factors. Statistical inference
making inferences about the estimated parameters using appropriate statistical
methods.
Szilvia et al used Matlab software’s curve fitting toolbox and a self-written
program code (The MathWorks Inc., Natick, MA, USA) software to analyze T1,
T. T. Kim Lan, L. Anh Tu, N. Tr. Thanh Hai 183
T2, and diffusion data processing while perfusion analysis was carried out by the
Siemens Perfusion software (Siemens Medical Solutions, Erlangen, Germany).
The arterial input function was determined by an experienced radiologist. The
free-hand ROIs were drawn on hyperintense lesions on T2∗ images by referring
to T2-weighted and FLAIR images [5].
Jixin et al used the Brain (FMRIB)’s Diffusion Toolbox (FDT) 2.0 and parts
of the FMRIB Software Library (FSL) 4.1.9 (Oxford Centre for Functional Mag-
netic Resonance Imaging of the Brain Software Library, www.fmrib.ox.ac.uk/fsl/).
FSL is a comprehensive library of analysis tools for FMRI, MRI and DTI brain
imaging data. It runs on Apple and PCs (both Linux, and Windows via a
Virtual Machine), and is very easy to install. Most of the tools can be run
both from the command line and as GUIs (”point-and-click” graphical user
interfaces) [7,9,10].
Mohamed Negm et al transferred all original DICOM images to Philips
workstation. Data were analyzed by the same radiology consultant. He de-
tected white matter hyperintensities through high-signal-intensity punctate foci
on T2WI and FLAIR images [8].
Statistical analysis
Data were usually analyzed by the IBM SPSS Software version 20. They
used different tests such as Mann- Whitney test (for abnormally distributed
quantitative variables, to compare between two studied groups with and with-
out aura to each other), Wilcoxon’s test (to compare the baseline and follow-up
values), Kruskal Wallis test (for abnormally distributed quantitative variables,
to compare between more than two studied groups, and Post Hoc ”Dunn’s mul-
tiple comparisons test” for pairwise comparisons) Spearman’s correlation (to
investigate the relationship between the number of migraine attacks and the
hyperintensity number) and Pearson’s chi-square test ( to evaluate changes of
size of hyperintensity categories)., the Bonferroni correction was used to reduce
type 1 error [5,8].
3. Result
The study of Szilvia et al.1 included 17 patients with migraine. Their age
ranged from 22 to 68 years. 15 patients (88.24%) were females, and 2 patients
(11.76%) were males. 10 patients (58.82%) of the patients had migraine without
aura and 7 patients (41.18%) had migraine with aura. 17.65% of the studied
patients had migraine for less than 20 years, and 8 (47.06%) patients had
migraine for 20-30 years, while 4 patients (23.53%) had migraine for 30-40
years, and 2 patients (11.76%) had migraine for more than 15 years. The
average of attack frequency per month was 3.35 in both 2009 and 2012 and
the highest was 10 times. There were 4 patients attacked less, just one case
attacked more while the rest was unchanged.
184 Overview: Studying the change of white matter associated with...
Changes in Number of WMHs
From 2009 to 2010, almost patients experienced an increase of the number
of WMHs, the only exception was a forty-three years old patient. It can be
seen that the number of WMHs of two male patients were higher than those of
female. The average number of WMHs was 22 in the year 2009 and was 29 in
the year 2012. The proportion of patients whose number of WMHs were about
20-40 and over 40 grew from 35.29% and 17.65% to 47.05% and 23.25% while
the percentage of patients having less than 20 WMHs fell for 17.61%.
Changes in Size of WMHs
Most of the WMHs became larger after the 3-year long follow-up period.
All patients had at least 1 WMH with an increased volume (Table 1). Only
the minority of WMHs had the same size at baseline and 3 years later. A total
of 91 WMHs had a smaller volume at follow-up and all patients had at least 1
WMH that became smaller.
Changes in Prevalence of WMHs
The number of newly developed hyperintensities (n = 130) was higher than
the number of disappeared ones (n = 22), (Tables 1). Whereas 16 patients had
at least 1 newly developed WMH, only 6 patients who had at least 1 disappeared
WMH were identified (Table 1). The age of patients having disappeared WMHs
ranged from 35-68 years (Table 2) Figure 1 shows the changes of size, the
presence of hyperintensities through tree-year period from 2009 to 2012. Axial
fluid-attenuated inversion recovery brain MRI images of 2 migraine patients
show changes between the baseline and the follow-up studies regarding the
white matter hyperintensities. These include unchanged right frontal and larger
left fronto-parietal bright signal intensities and appearance of a new frontal
hyperintensity (A), and a disappeared frontal hyperintense lesion (B). Images
are presented in radiological convention (left = right).
Figure 1. The changes of white matter hyperintensities through tree-year
period from 2009 to 2012 [5]]
T. T. Kim Lan, L. Anh Tu, N. Tr. Thanh Hai 185
The study of Mohamed Negm et al. [8] showed that white matter hy-
perintensities are detected as high-signal-intensity punctate foci on T2WI and
FLAIR images and the most common areas of white matter was the centrum
semiovale while the converse of deep white matter was seen like small high-
signal-intensity lesions due to ischemic brain changes. There were two patients
groups: those with white matter hyperintense punctate foci and those without
any lesions. There were about the haft of migraine patients who had white
matter hyperintense punctate foci (43.1%). 9.2% of them had one lesion (fig-
ure 2), 13.8%) patients had 2 lesions (figure 3) and the rest had more than
186 Overview: Studying the change of white matter associated with...
2 lesions. Figure 2 illustrates Axial FLAIR MRI image of 50-year-old female
patient, not known to have any chronic illness, presented with migraine with
aura for 10-year duration of grade III severity. It shows small single bright focus
at the right centrum semiovale (arrow) while Axial FLAIR MRI image of 25-
year-old female patient, not known to have any chronic illness, presented with
migraine without aura for 6-year duration of grade II severity, not responding
to medical treatment shows two left frontal white matter hyperintense lesions
(arrows) (figure 3).
Figure 2. Axial FLAIR MRI image shows small single bright focus at the
right centrum semiovale (arrow)[8]
Figure 3. Axial FLAIR MRI image shows two left frontal white matter
hyperintense lesions (arrows)[8]
The study of Szilvia et al compared between data in 2009 (the baseline
study) and data in 2012 (follow-up study), A significantly higher number of
WMHs was detected than in the baseline study (498 vs 370, P < .001). In all
locations, the hyperintensity number was higher in the deep white matter (P <
.001), the subcortical (P = .012), and the periventricular (P = .021) locations.
Large hyperintensities significantly increased in size more often than medium-
T. T. Kim Lan, L. Anh Tu, N. Tr. Thanh Hai 187
sized or small hyperintensities (P < .002), while size decrease was most common
in small hyperintensities (P < .002). The number of increased or decreased-
sized hyperintensities did not correlate with age, the disease duration, or the
frequency of migraine attacks (correlation coefficients: 0.160, 0.360 and -0.470,
P > .05, respectively). The number of newly developed hyperintensities did not
correlate with age, the disease duration, or the frequency of migraine attacks
(correlation coefficients: 0.196, 0.261, and -0.286, P > .05, respectively). While
the number of disappeared hyperintensities did not correlate with the age and
disease duration (correlation coefficients: -0.014 and 0.158, P > .05), the num-
ber of disappeared WMHs negatively correlated with the attack frequency at
baseline (coefficient: -0.517, P = .034). Meanwhile, according to multivariate
analysis of the study of Mohamed Negm et al , neither gender nor duration of
attack had statistically difference, but age, migraine severity grade, pain inten-
sity during attack, nausea, disability, and tolerability had a highly statistically
significant difference, while migraine duration and resistance to treatment had
a statistically significant difference.
4. Discussion
In these studies, scientists investigated a studied migraine group with brain
WMHs performing the same quantitative MRI measurements for a period time.
The only known risk factors were the recurrent headache attacks, which could
be the cause of progression in the tissue impairment inside the WMHs or could
lead to the volume change of hyperintensities and the formation of new hyper-
intensities. The size of WMHs did not remain constant. The majority of them
increased in size while the proportion of the decrease was lower. The quantity
of new WMHs formation were higher than the disappearance. As a result, the
number of WMHs rose. As a result, migraine may be a risk factor for struc-
tural brain changes including white matter abnormalities, infarct-like lesions,
and volumetric changes in the white matter regions. The higher hyperintensity
number associated with higher cerebral and lobar hyperintensity volumes. A
higher number of newly developed hyperintensities were detected than disap-
peared hyperintensities. The repeated headache attacks with different attack
frequency and attack intensity may have a different impact on changes of white
matter hyperintensities. Based on these findings, patients with disappeared hy-
perintensities had a low migraine attack frequency at baseline.
Since these studies varied in sample size, participant selection, headache
characteristics, test methodology, timing of study, and data interpretation,
the authors suggested additional longitudinal studies with a broad range of
attack frequency and severity for better understanding the association between
migraine and structural brain changes and to clarify the association to attack
frequency and disease duration and the difference led to the increase of the
cerebral hyperintensity count.
188 Overview: Studying the change of white matter associated with...
There still were study limitations such as the size of patient groups, the
criteria selection, the control of potential unpredicted factors and the quality of
MRI scanners. The small sample size is a consequence of the longitudinal design
and strict selection criteria. Unfortunately, small sample size did not allow
extensive correlation of WMH characteristics with clinical headache parameters
including investigation of differences amongmigraine subgroups, neither control
for potential confounding factors.
5. Conclusion
The number of migraine patients is increasing, and need appropriate and ef-
fective treatments. Many causes have been implemented to effectively diag-
nose and treat migraine. Therefore, studying the relationship between white
matter and migraine is necessary to improve the effect of identification of mi-
graine and to avoid wrong examination of the symptoms. This method requires
modern accurate MRI scanners, imaging techniques such as T1- weighted, T2-
weighted, fluid-attenuated inversion recovery MRI (FLAIR), diffusion tensor
imaging (DTI), and voxel-base morphometry (VBM). Age, presence of aura,
nausea, and disability during attack, resistance to treatment, and severity of
headache and duration of migraine are considered a risk factor for development
of WMHs. Based on the studies, migraine is commonly associated with the
change of white matter. However, the association between migraine and struc-
tural brain changes and the relationship between properties of migraine attack
and disease condition is complicated by differences in interaction mechanisms,
it is necessary to clarify. There are important limitations of studying such as
the size of patient groups, timing of study, the criteria selection, the control
of potential unpredicted factors and the quality of MRI scanners, which can
effect the accuracy of results.
To elucidate the nature of the relationship between migraine headaches and
white matter changes found, it is able to use DTI for research as DTI is a
powerful support tool at present. It may help people better understand the
progression of migraine and implicate its treatment.
References
[1] T.J Schwedt et al., Advanced neuroimaging of migraine, Lancet Neurol, vol. 8 (2009),
560-568.
[2] A. Bashir et al., Migraine and structural changes in the brain: A systematic review and
meta-analysis, Neurology, vol. 81 (2013), 1260-1268.
[3] M.C. Kruit et al., Migraine is a risk factor for subclinical brain lesions, JAMA, vol. 291
(2004), 427-434.
[4] M. Aradi et al., Quantitative MRI studies of chronic brain white matter hyperintensities
in migraine patients, Headache, vol. 53 (2013),752-763.
[5] E. Szilvia et al., Changes of Migraine-Related White Matter Hyperintensities After 3
Years: A Longitudinal MRI Study, Headache, Wiley Periodicals, pp. 55-70, Jan. 2015.
T. T. Kim Lan, L. Anh Tu, N. Tr. Thanh Hai 189
[6] “Headache Classification Committee of the International Headache Society”, The Inter-
national Classification of Headache Disorders, 2nd edn. Cephalalgia, 2014.
[7] L. Jixin et al., Migraine-Related Gray Matter and White Matter Changes at a 1-Year
Follow-Up Evaluation, The Journal of Pain, 14 (12) (Dec 2013), 1703-1708.
[8] N. Mohamed et al., Relation between migraine pattern and white matter hyperintensities
in brain magnetic resonance imaging, The Egyptian Journal of Neurology, Psychiatry
and Neurosurgery, 2018.
[9] S.M. Smith et al., Advances in functional and structural MR image analysis and imple-
mentation as FSL, NeuroImage, 23(S1) (2004), 208-219.
[10] M. Jenkinson et al., FSL, NeuroImage, 62(2012), 782-90.
Các file đính kèm theo tài liệu này:
overview_studying_the_change_of_white_matter_associated_with.pdf