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Advanced Neurology                                         Cortical thickness and regional homogeneity in CSVD



            Monte Carlo simulation correction with a vertex-wise/  for differences in age and education. Bonferroni correction
            cluster-forming threshold of 3 (P < 0.001) and a cluster-  was applied in the GLM for post hoc multiple comparison
            wise  P  <  0.001  (two  tailed).  The  cortical  thicknesses  of   corrections. Partial correlation analysis was conducted to
            significant brain regions were extracted for further study.  explore the relationships between MRI parameters and
                                                               cognitive scale scores, with age and education as covariates.
            2.5. fMRI data                                     P < 0.05 was considered to indicate statistical significance.
            2.5.1. Preprocessing of fMRI                       3. Results

            The fMRI analysis was based on the BOLD sequence.
            DPARSF, a method based on the Resting-State Functional   3.1. Clinical assessments
            MR Imaging Toolkit (http://www.restfmri.net) and   Demographically, there was no difference in sex among
            statistical parametric mapping software package (SPM12;   the CSVD-CI group, CSVD-no-CI group, and NC group.
            www.fil.ion.ucl.ac.uk/spm), was used for the preprocessing   However, both of the CSVD groups were older than the
            of fMRI data. The preprocessing steps included removing   NC group, and the CSVD-CI group had fewer years
            the  first  10 volumes  of  data,  slice  timing  correction,   of education than the other two groups. There was no
            realignment, reorientation, head motion correction (note   significant difference in  Fazekas scores, lacunar infarcts
            that participants with head motion more than 2.0 mm of   count, and microbleeds between the CSVD-CI group and
            displacement in any direction, or 2.0° of rotation in any   the CSVD-no-CI group. In terms of vascular risk factors,
            angular dimension were excluded), image segmentation   there was a significant difference in hypertension, but
            for the high-resolution T1-weighted turbo gradient echo   no significant differences in diabetes, hyperlipidemia,
            sequence and the BOLD sequence by Diffeomorphic    and smoking. In neuropsychological evaluation, there
            Anatomical Registration Through Exponentiated Lie   were significant differences in HAMD and VRIR scores
            algebra,  coregistration  of  T1  images  to  the  functional   between the CSVD-no-CI group and the NC group. Post
            images, normalization using a 12-parameter non-linear   hoc multiple comparisons were performed among the
            transformation to the standard Montreal Neurological   CSVD-CI  group, CSVD-no-CI  group,  and NC  group.
            Institute (MNI) space (3 × 3 × 3 mm ), and band-pass   Detailed information regarding the clinical assessments is
                                            3
            filtering (0.01–0.08 Hz).                          shown in Tables 1-3.
            2.5.2. ReHo analysis                               3.2. Cortical thickness analysis
            The purpose of the fMRI analysis was to explore the   There were significant differences in cortical thickness
            functional changes of certain brain regions that were   among the CSVD-CI group, CSVD-no-CI group, and
            extracted from the structural analysis. The significant brain   NC group in the left insula, right insula, right anterior
            regions in cortical thickness analysis were transferred into   cingulate gyrus (ACG), right cuneus, and right middle
            MNI space and defined as regions of interest (ROIs) in   temporal gyrus (MTG).  Post hoc multiple comparisons
            ReHo analysis. The ReHo analysis using the preprocessed   were performed among the CSVD-CI group, CSVD-
            fMRI data was also performed by DPARSF. The steps for   no-CI group, and NC group, adding age and education as
            acquiring the ReHo value after z-translation and smoothing   covariates. Detailed information for the cortical thickness
            were as follows: (1) Calculating the ReHo value of 27 voxels   analysis is shown in Figure 1, Tables 4 and 5. The CSVD-CI
            and doing a Z-transform, (2) smoothing the ReHo map   group exhibited lower cortical thickness in all five regions
            after Z-transform with a Gaussian kernel of 6 mm FWHM   compared with that in the other two groups, and the
            for noise reduction, and (3) extracting ReHo values of the   CSVD-no-CI group exhibited lower cortical thickness only
            ROIs for further statistical analysis.             in the bilateral insula and the right MTG compared with
                                                               that in the NC group.
            2.6. Statistical analysis
            The demographic data were analyzed using SPSS 16.0   3.3. ReHo analysis
            (SPSS, Chicago, IL, USA). All of the continuous variables   The five brain regions exhibiting group differences in
            were tested for normality before comparison. Analysis of   cortical thickness analysis were targeted as the ROIs
            variance (ANOVA) and the Kruskal–Wallis test were used   in ReHo analysis. ReHo values of ROIs were extracted,
            to compare the variation in age, education, and cognitive   followed by GLM analysis (adding age and education
            scale scores among the three groups according to normality.   as covariates, using  Bonferroni correction for  post hoc
            A  Chi-squared test was used for the comparison of sex   multiple comparisons). There were significant differences
            and vascular risk factors among groups. Changes in ReHo   in ReHo values of the left insula (P = 0.005) and right
            across groups were analyzed using the GLM, controlling   insula (P = 0.024) among the CSVD-CI group, CSVD-


            Volume 1 Issue 1 (2022)                         4                        https://doi.org/10.36922/an.v1i1.48
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