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. 2017 Mar;38(3):500–506. doi: 10.3174/ajnr.A5036

Lower Magnetization Transfer Ratio in the Forceps Minor Is Associated with Poorer Gait Velocity in Older Adults

S Seiler a, L Pirpamer a, B Gesierich c, E Hofer a,b, M Duering c, D Pinter a, E Jouvent d, F Fazekas a, J-F Mangin e, H Chabriat d, S Ropele a, R Schmidt a,✉
PMCID: PMC7959982  PMID: 27979793

Abstract

BACKGROUND AND PURPOSE:

Gait disturbances in the elderly are disabling and a major public health issue but are poorly understood. In this multimodal MR imaging study, we used 2 voxel-based analysis methods to assess the voxelwise relationship of magnetization transfer ratio and white matter hyperintensity location with gait velocity in older adults.

MATERIALS AND METHODS:

We assessed 230 community-dwelling participants of the Austrian Stroke Prevention Family Study. Every participant underwent 3T MR imaging, including magnetization transfer imaging. Voxel-based magnetization transfer ratio–symptom mapping correlated the white matter magnetization transfer ratio of each voxel with gait velocity. To assess a possible relationship between white matter hyperintensity location and gait velocity, we applied voxel-based lesion-symptom mapping.

RESULTS:

We found a significant association between the magnetization transfer ratio within the forceps minor and gait velocity (β = 0.134; 95% CI, 0.011–0.258; P = .033), independent of demographics, general physical performance, vascular risk factors, and brain volume. White matter hyperintensities did not significantly change this association.

CONCLUSIONS:

Our study provides new evidence for the importance of magnetization transfer ratio changes in gait disturbances at an older age, particularly in the forceps minor. The histopathologic basis of these findings is yet to be determined.

Gait abnormalities in older adults are common.1,2 They are associated with falls3,4 and represent a serious public health issue.1,5 A complex brain network manages supraspinal gait control.6 White matter hyperintensities (WMHs) are common and not necessarily related to clinical symptoms. However on a group level, widespread WMHs have been associated with gait dysfunction, probably as the consequence of disruption of the supraspinal gait network,7–9 and were related to gait performance in several studies,10–13 but results are conflicting.9,14,15 One explanation for conflicting results might be that as reported for cognitive decline,16–18 widespread, invisible, and highly variable microstructural changes in normal-appearing white matter also contribute to gait abnormalities in addition to visible lesions. This hypothesis is supported by 2 DTI studies that reported the higher mean diffusivity and lower fractional anisotropy in the genu of the corpus callosum to be correlated with poorer gait performance independent of visible WMHs.14,19

Complementary information on microstructural brain tissue alterations may come from magnetization transfer imaging (MTI). Other than DTI, which offers information on brain tissue organization,20 MTI offers information on tissue composition.21 Magnetization transfer ratio (MTR) is one of the few MR imaging measures that have been validated postmortem to represent a direct marker of myelin content.22

The only study on MTR and gait found that lower MTR was associated with poorer gait performance, independent of WMHs.23

In this large multimodal MR imaging study, we used voxel-based MTR symptom mapping (VMTRSM) and voxel-based lesion symptom mapping (VLSM) to identify those brain areas in which MTR or WMH-related tissue alterations relate to gait velocity. We hypothesized that alterations, if any, would mainly be located within the frontal white matter because intact fontal subcortical pathways have been reported to be crucial for maintenance of gait performance at a higher level.6,24

Materials and Methods

Study Subjects

The study sample is drawn from the Austrian Stroke Prevention Family Study, a prospective single-center community-based study designed to assess the cerebral effects of vascular risk factors in the healthy elderly population of the City of Graz, Austria. The Austrian Stroke Prevention Family Study represents an extension of the Austrian Stroke Prevention Study, which was established in 1991.25 Between 2006 and 2013, study participants of the Austrian Stroke Prevention Study and their first-degree relatives were invited to enter the Austrian Stroke Prevention Family Study. Individuals were excluded from the study if they had a history of neuropsychiatric disease, including previous cerebrovascular attacks and dementia, or abnormal neurologic examination findings, determined on the basis of a structured clinical interview and a physical and neurologic examination performed by a board-certified neurologist. None of the study participants had a history or MR imaging findings suggestive of normal pressure hydrocephalus. There were also no subjects with a history or signs of heart failure in the study. None of the study participants had uncorrected visual impairment. A total of 381 individuals from 169 families were included in the study. The number of members per family ranged from 2 to 6. All individuals underwent MR imaging, except for 26 who had contraindications. Thus, MTI scans were available in 355 subjects. The participants' ages ranged from 35 to 82 years. We focused on age-related decline in gait velocity and thus included all 230 subjects 60 years of age and older in the current analysis.

The ethics committee of the Medical University of Graz, Austria, approved the study protocol, and written informed consent was obtained from all subjects.

Measurement of Gait Velocity

Study participants were asked to walk a total distance of 8 meters with 3 turns at their usual, self-selected pace on level ground. None of the study participants needed walking aids. Time was measured with a stopwatch. The faster of the 2 trials was used for the subsequent analyses. We chose gait velocity because it can be measured quickly and in a clinical setting without instrumental efforts. It has been shown to be a good measure of mobility in elderly individuals.15

Measurement of Cognition and General Physical Performance

Scores of memory and executive function were assessed as described previously.26

General physical performance was assessed by using the Short Physical Performance Battery (SPPB).27

Vascular Risk Factors

Assessment of vascular risk factors included arterial hypertension, diabetes mellitus, hypercholesterolemia, hypertriglyceridemia, hyperuricemia, cardiac disease, peripheral vascular disease, and venous thrombotic disease and was determined on the basis of history and measurements at the examination as previously described.26

MR Imaging

MR imaging was performed on a 3T whole-body scanner (Magnetom TrioTim; Siemens, Erlangen, Germany) and included conventional imaging and MTI. The MTI sequence was based on a spoiled 3D gradient-echo sequence (TR = 40 ms, TE = 7.38 ms, flip angle = 15°, number of sections = 40, section thickness = 3 mm, in-plane resolution = 0.86 × 0.86 mm) performed with and without a Gaussian-shaped magnetization transfer saturation pulse.

The conventional protocol included an axial FLAIR sequence (TR = 1000 ms, TE = 69 ms, TI = 2500 ms, number of sections = 40, section thickness = 3 mm, no intersection-gap, in-plane resolution = 0.86 × 0.86 mm2) and a high-resolution T1-weighted 3D sequence with magnetization preparation and whole-brain coverage (TR = 1900 ms, TE = 2.19 ms, TI = 900 ms, flip angle = 9°, isotropic resolution = 1 mm).

For assessment of microbleeds, a T2* sequence was used (TR = 35 ms, TE = 14.7 ms, flip angle = 15°, number of sections = 64, section thickness = 2 mm, no intersection-gap, in-plane resolution = 0.90 × 0.90 mm2).

Visual MR Imaging Rating

White matter hyperintensities and silent nonlacunar and lacunar infarcts were recorded on FLAIR images as previously described.26 Microbleeds were recorded on T2*-weighted images following the definition of Greenberg et al.28

Generation of WMH and MTR Maps

WMH maps were generated by using a custom-written Interactive Data Language program (DispImage; Exelis Visual Information Solutions, Boulder, Colorado) as described previously.29 Two highly experienced raters segmented WMHs on FLAIR images by combined region-growing and local thresholding following manual selection.29 The total lesion volume in cubic millimeters was calculated by multiplying the lesion area by the section thickness. WMH volumes in white matter tracts were calculated by overlaying the probabilistic white matter tract atlas (25% probability), provided within the Oxford Centre for fMRI of the Brain Software Library (FSL; http://www.fmrib.ox.ac.uk/fsl),30 on the normalized WMH maps.

MTR maps were calculated according to the formula MTR = (M0 − MSS)/M0, where M0 represents the signal intensity of a voxel without any radiofrequency saturation and MSS is the signal intensity of the same voxel obtained with the radiofrequency saturation pulse.21

For the subsequent steps, tools from FSL31 were used.

Because we found that MTR provides good contrast in performing tissue segmentation, gray matter, white matter, and CSF partial volume maps were derived from the MTR-weighted scans by using FSL FAST (FMRIB Automated Segmentation Tool; http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/FAST).32

The T1, FLAIR, and MTR-weighted scans were brain-extracted by using the FSL Brain Extraction Tool (http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/BET).33

The resulting skull-stripped T1-weighted images were nonlinearly registered to the Montreal Neurological Institute-152 standard space template (MNI 152) by using FSL FNIRT (FMRIB Nonlinear Image Registration Tool; http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/FNIRT).31

Then, the brain-extracted FLAIR and MTR scans were linearly registered to the corresponding brain-extracted T1-weighted images by using FLIRT (FMRIB Linear Image Registration Tool; http://www.fmrib.ox.ac.uk/).34

We used the transformation matrices from these steps to warp FLAIR and white matter MTR maps to the MNI-152 standard space template. WMH maps were transformed to the MNI-152 standard space template in the same way.

The resulting white matter MTR maps in standard space were eroded by 1 voxel to reduce partial volume effects resulting from “edge” voxels. To produce more normally distributed data, reduce noise, and account for the intersubject and registration variability,35 we smoothed the MTR maps with a 4-mm Gaussian kernel.

A mean white matter MTR mask was created and thresholded to exclude MTR values below 20%.17 We chose this threshold to exclude voxels from CSF and to further reduce the spurious effects of partial volume effects caused by the white matter–gray matter transition zone.

Anatomic structures containing clusters of voxels in which MTR related significantly to gait velocity were localized by overlaying the probabilistic white matter tract atlas (25% probability), provided within FSL,30 on the normalized white matter MTR maps. As in voxelwise analysis, we eroded the segmentations of these tracts by 1 voxel to reduce CSF artifacts at “edge” zones. The resulting “core” white matter mean MTR was used in subsequent analyses.

Statistical Analysis

General Statistical Analysis.

Assumptions of normal distribution were tested with the Kolmogorov-Smirnov test. Normally distributed variables are reported as mean ± SD, and non-normally distributed variables, as median and interquartile range. WMH volume had a skewed distribution containing zero values; therefore, the value 2 was added to the volumes before natural log-transformation. To relate demographic, clinical, and imaging characteristics of the study participants to gait velocity, we categorized subjects into quartiles according to gait velocity distribution. One-way analysis of variance, with quartiles of walking speed as fixed factors and demographic, clinical, and imaging characteristics as outcome variables, and χ2 tests were performed to test significant associations with normally and non-normally distributed variables, respectively. Variables significantly (P < .05) associated with gait speed in these analyses were entered as covariates in the VMTRSM and ROI analyses described in the subsequent paragraphs. Correlations between MTR and gait velocity were calculated by using the Pearson correlation coefficient. Linear multiple regression analysis tested an independent relationship between MTR and gait velocity. To test a possible dose-effect relationship, we used analysis of covariance with MTR quartiles as fixed factors and walking speed as the dependent variable. Age, sex, height, brain volume, general physical performance, presence of vascular risk factors, and MR imaging findings significantly associated with walking speed in the univariate analysis were entered as covariates in the regression analysis and the ANCOVA.

To assess mediating effects of executive function scores on the relationship between MTR and gait velocity, we used bootstrapped models as described by Preacher and Hayes.36

Voxel-Based MTR Symptom Mapping.

To find associations between MTR values within a voxel and gait velocity, we used the permutation-based statistical interference tool for nonparametric testing (FSL Randomize tool; http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/Randomise/UserGuide).31 Five thousand permutations were performed to build the null distribution, and significant associations were determined by selecting the threshold-free cluster-enhancement option. To correct for multiple comparisons, a family-wise error–adjusted P value < .05 was considered statistically significant because voxel-based analyses test thousands of voxels separately. If we controlled the family-wise error, the chance of ≥1 false-positive across all voxels was lower than 5%. Age, sex, height, brain volume, general physical performance, and variables that were univariatey associated with walking speed were entered as covariates.

ROI Analysis.

To identify white matter tracts in which mean MTR correlates with gait velocity, we overlaid the probabilistic white matter tract atlas30 provided within FSL on significant voxels from the VMTRSM analysis.

The mean MTR within identified tracts was calculated in standard space by using FSLMATHS (http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/Fslutils). We eroded identified tracts by 1 voxel to reduce possible CSF contamination and partial volume effects from “edge” voxels. The mean MTR in the resulting “skeletonized” tracts was used in the subsequent linear multiple regression analysis.

A possible dose-effect relation of MTR within identified tracts and gait velocity was investigated by means of analysis of covariance with MTR in quartiles.

Age, sex, height, general physical performance, brain volume, and variables univariate-associated with walking speed were entered as covariates in the linear multiple regression analysis and the analysis of covariance. A P value < .05 was considered statistically significant.

Voxel-Based Lesion Symptom Mapping.

Nonparametric mapping was used to relate WMH location to gait velocity.37 One thousand permutations were performed to build the null distribution, and the Brunner-Munzel test was applied for statistical significance.38 Briefly, permutation testing is a procedure that compares a test statistic to a null distribution derived from the dataset of interest itself. Permuting how the dependent and independent variables are paired typically derives the permutation null distribution. When the null hypothesis is true (no effect), the observed pairings should be no more likely to generate an extreme test statistic than any other.39 Voxels affected in <7 subjects were not considered for analysis. Correction for multiple testing was achieved by permutation-generated family-wise error thresholds. Age, sex, height, and brain volume were entered as covariates. To identify the localization of significant voxels within major white matter tracts, we used the probabilistic white matter tract atlas30 provided within FSL.

Results

Characteristics of the Study Population

Demographic, clinical, and imaging characteristics of the study participants are summarized in the On-line Table. Individuals who walked slower were significantly older and shorter, their general physical performance was worse, and they more often had diabetes compared with their faster counterparts. Slower participants performed worse on executive function tasks and had more microbleeds on brain imaging. WMHs and cardiac disease did not relate to gait velocity.

Imaging Data

In the voxel-based MTR symptom-mapping analysis, we found significant clusters of MTR voxels that were positively correlated with gait velocity bilaterally within the frontal white matter (Fig 1A). The association remained significant after correction for multiple comparisons and adjustment for age, sex, height, brain volume, general physical performance, microbleeds, diabetes, and hyperuricemia. To examine the spatial relationship between these clusters and major white matter tracts, we projected significant clusters from the VMTRSM analysis on the probabilistic white matter tract atlas in MNI space. As shown in Fig 1B, there was substantial overlap with the forceps minor.

Fig 1.

Fig 1.

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Result of voxel-based MTR symptom-mapping analysis. A, Yellow/orange represents MTR voxels positively related to gait velocity. The statistical map is superimposed on the MNI-152 standard space template and is family-wise error–corrected for multiple comparisons (P < .05). The result is independent of age, sex, height, the presence of microbleeds, SPPB total score, diabetes, hyperuricemia, and brain volume. B, The statistical map shown in A (MTR voxels positively related to gait velocity) is now superimposed on the Johns Hopkins University DTI-based white matter tract atlas. Shades of green indicate different white matter tracts, as defined by the atlas. Most of the MTR voxels positively related to gait velocity (yellow/orange) are located within the forceps minor (light green frontal tract, indicated by black arrows).

Given the prominent association of MTR voxels and walking speed within the forceps minor, we assessed the mean MTR of the forceps minor in standard space and used a linear regression model, adjusted for age, sex, height, brain volume, general physical performance, microbleeds, diabetes, and hyperuricemia to determine the association between forceps minor MTR and gait velocity. Higher mean MTR within the forceps minor was positively related to gait velocity (β = 0.134; 95% CI, 0.011–0.258; P = .033) (Fig 2). This association remained virtually unchanged when global WMH volume or WMH volume within the forceps minor was added to the analysis (β = 0.162; 95% CI, 0.024–0.307; P = .029; and β = 0.136; 95% CI, 0.013–0.261; P = .030, respectively). Because the correlation between MTR and walking speed seemed to be dependent on a few outliers who walked quite fast, we repeated the regression analysis and excluded participants with walking speeds ±1.5 SDs from the population mean. This step did not substantially alter the direction or strength of the association (β = 0.117; 95% CI, −0.012–0.248; P = .076).

Fig 2.

Fig 2.

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Correlation (r = 0.20; 95% CI, 0.08–0.32; P = .002) between walking speed (x-axis, meters/second) and MTR within the forceps minor (y-axis, percentage). r indicates the Pearson correlation coefficient.

We examined executive function as a confounder because it related significantly to gait velocity in the univariate analysis. Indeed, executive function attenuated the effect of forceps minor MTR on gait speed, and there remained only a nonsignificant trend (β = 0.123; 95% CI, −0.002–0.243; P = .054). A Preacher and Hayes36 bootstrap method showed that executive dysfunction had no significant mediation effect on the association between MTR and gait velocity (indirect effect, 0.016; bootstrapped standard error, 0.013; bootstrapped 95% CI, −0.0047–0.0460).

Figure 3 illustrates the associations between quartiles of mean MTR distribution in the forceps minor and gait velocity. Analysis of covariance, which we corrected for age, sex, height, brain volume, general physical performance, microbleeds, diabetes, and hyperuricemia, showed an independent linear dose-effect relationship between forceps minor-MTR quartiles and gait velocity (P for linear trend = .031).

Fig 3.

Fig 3.

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Analysis of covariance results. The mean MTR (percentage) of the forceps minor was divided into quartiles (x-axis). The first quartile was the lowest. Ranges of the MTR quartiles are as follows: quartile 1, 24.18–26.79; quartile 2, 26.80–27.43; quartile 3, 27.44–28.08; quartile 4, 28.09–30.00. Values on the y-axis represent the estimated mean walking speed in meters/second of subjects within each quartile, adjusted for age, sex, height, SPPB total score, the presence of microbleeds, diabetes, hyperuricemia, and brain volume. Increasing MTR values within the forceps minor are related to higher gait velocity in a dose-dependent manner (P for linear trend = .031).

VLSM identified no voxel clusters in which WMHs related significantly to slower gait speed.

Discussion

In this study of older adults free of stroke, dementia, and other neurologic diseases, we used 2 observer-independent methods to identify micro- and macrostructural determinants of gait velocity. We found a dose-dependent association between MTR values in the forceps minor and gait velocity, independent of age, sex, height, general physical performance, diabetes, hyperuricemia, brain volume, microbleeds, and WMH volume. Lower MTR, suspected of representing decreased myelin content,17,22 related to slower gait velocity. VLSM showed no voxel clusters in which WMHs were significantly related to a slower gait velocity. Different results of MTR and WMH analysis in the current study are not surprising in light of the work of Wong et al,40 who reported no significant relationship among MTR, WMH, and cerebrovascular risk factors, suggesting an independent pathophysiology for each measure.

Our results are in line with MTR and DTI findings in normal aging and in patients with cerebral small-vessel disease.14,19,24 The only MTR study in healthy, older adults described a relationship between whole-brain MTR and gait velocity.23 The authors of this investigation quantified MTR changes globally by using histogram-based metrics. This is a very robust approach, but it fails to provide information on the location of MTR changes that relate to gait. Our voxelwise approach overcomes this limitation and thus extended previous results by identifying MTR alterations within the forceps minor as important determinants of walking speed. de Laat et al24 studied 429 individuals 50–85 years of age with cerebral small-vessel disease. These authors found loss of white matter integrity in the corpus callosum, particularly the genu where the forceps minor crosses. Similar results were reported by Della Nave et al14 and Bhadelia et al,19 who also showed that participants with abnormal gait had lower fractional anisotropy in the genu of the corpus callosum. Even though DTI probes brain tissue organization rather than brain tissue composition like MTI, previous DTI results largely resemble our MTR findings.20,21 Microstructural brain tissue changes in the forceps minor were consistently linked with gait disturbances both in normal aging and in patients with cerebral small-vessel disease.14,19

The forceps minor is a large fiber bundle that connects the bilateral prefrontal cortices of the hemispheres,8,41 which play an important role in motor control, especially in older adults.42 Intact interhemispheric connections may be important for maintaining motor control at a high level.43 We observed no significant relationship between WMHs or lacunes and gait performance in our community-dwelling sample. Conversely, individuals with a higher number of microbleeds had slower gait velocity. This is partly in line with 1 recent study that reported an association between microbleeds, but not WMHs and gait velocity, in community-dwelling adults.44 Microbleeds occur in the wake of cerebral small-vessel disease, and their presence relates to microstructural brain tissue changes.45 However, neither the inclusion of WMHs nor of lacunes or microbleeds in the regression analysis changed the association between MTR of the forceps minor and gait velocity significantly.

The 2 previous DTI studies14,19 also found that DTI measures in the genu of the corpus callosum remained significantly associated with poorer gait performance after adding WMH volume to the analysis. Considering that more widespread WMHs seen in elderly individuals are a marker of coexisting cerebral small-vessel disease, previous results and the results of the current study indicate that factors other than cerebral small-vessel disease may also play an important role in the development of gait disturbances during aging. Postmortem studies that correlate MTR and DTI measures with brain tissue alterations are thus likely to improve our pathophysiologic understanding of age-related gait abnormalities.

The current study has several strengths. It is the largest cohort study on gait performance using voxel-based MTR mapping to date. The study is community-based, with prospectively planned radiologic and clinical protocols. With MTI, images with a much higher spatial resolution and signal-to-noise ratio can be produced than is possible with DTI acquisitions. There are also no echo-planar imaging–induced artifacts. The high scan resolution allowed accurate registration of scans and segmentation of tissue types and WMHs. A thorough postprocessing procedure and rigorous quality control of segmentations reduced the effects of coregistration errors and CSF contamination to a minimum.

There are also limitations. The study has a cross-sectional design. Other potential underlying mechanisms for our findings, beyond a direct causal relationship between microstructural damage and disturbances in gait velocity, are possible. Among them are peripheral neuromuscular disease, the presence of hip and joint disease, or visual disturbances or cognitive dysfunction. We had expected peripheral neuromuscular disease and hip and joint diseases to be reflected in the SPPB total score, which was considered a confounder in our regression model. Inclusion of the SPPB total score did not significantly alter our results, arguing against a large effect of general physical performance on the relationship between forceps minor MTR and gait velocity.

When we added executive function scores to the regression analysis, the relationship between MTR of the forceps minor and walking speed was attenuated. There remained only a nonsignificant trend. In contrast to authors in previous studies who reported executive functions exerting mediating effects on the relationship between structural brain changes and gait,46,47 we were unable to confirm that executive function is a mediator in the association between forceps minor MTR and gait speed in the current investigation. It is likely that the effect of MTR on gait became nonsignificant when the executive function score was introduced simply because a trivial amount of variance was explained in addition to the model without inclusion of results of executive function testing. Participants were directed to walk at their “usual pace,” allowing them to make a personal choice between a range of gait speeds. This could have biased our results. However, usual gait speed correlated well with the SPPB score in our study and was shown to relate significantly to disability in previous work.27 Previous data even suggest that usual gait speed alone is nearly as good a predictor of disability outcome as extensive physical testing.27

The lack of an association between heart disease and walking speed might have been caused by the rather short walking distance (8 m) and the possibility of walking at a normal pace in our study. It was described previously that the presence of heart disease rather affects long-distance walking tests.48 We realize that we tested the association between voxel values and walking speed in a far larger number of voxels in MTR analysis that compose the whole white matter than in the lesion-based analysis. Consequently, the risk of finding associations due to chance alone is probably higher in the MTR analyses, and by contrast, the risk of missing associations that actually exist is probably higher in the lesion-based analysis. In this study, besides family-wise error control, the symmetry of our findings in both hemispheres is a strong argument against findings due to chance alone.

The variance of the VMTRSM analyses was substantial. The reason for this large variability of results, which hampers the utility of findings, is unclear. It remains to be seen whether other methods of image analysis such as Tract-Based Spatial Statistics (TBSS; http://fsl.fmrib.ox.ac.uk/fsl/fslwiki/TBSS)49 might resolve this problem.

Some subjects originated from the same families. This might lead to correlated errors in the statistical models. FSL includes no regular option to correct voxelwise analyses for family structure. Including, for instance, random effects would be very difficult to interpret. However, we consider this a minor issue here, given the small number of subjects per family.

Our voxelwise approach is neither useful nor intended to diagnose a single subject. However, our results broaden the pathophysiologic understanding of MTR and gait disturbances in aging. Future longitudinal studies might use high-resolution, 3D MTR scans to tailor reliable predictors for gait disturbances in older age.

Conclusions

Our study provides new evidence for the importance of MTR changes in gait disturbances at an older age, particularly in the forceps minor. Identification of the causes and the histopathologic origin of these MR imaging–detected tissue alterations is important because therapeutic measures may be derived.

Supplementary Material

16-00118.pdf
16-00118.pdf (31.5KB, pdf)

ABBREVIATIONS:

MNI

Montreal Neurological Institute

MTI

magnetization transfer imaging

MTR

magnetization transfer ratio

SPPB

Short Physical Performance Battery

VLSM

voxel-based lesion symptom mapping

VMTRSM

voxel-based MTR symptom mapping

WMH

white matter hyperintensity

Footnotes

Disclosures: Stephan Seiler—RELATED: Grant: Comments: This work was supported by FP6 ERA-NET NEURON grant (01EW1207) and by the Austrian Science Fund project I904*; Support for Travel to Meetings for the Study or Other Purposes: Comments: Travel costs for a study group meeting I attended (at Zuers, Austria) were covered by the grants indicated above.* Marco Duering—RELATED: Grant: European Union FP6 ERA-NET NEURON Grant*; Support for Travel to Meetings for the Study or Other Purposes: European Union FP6 ERA-NET NEURON Grant*; UNRELATED: Grants/Grants Pending: German Center for Neurodegenerative Diseases Inter-Site Project Else Kröner-Fresenius-Stiftung*; Payment Lectures including Service on Speakers Bureaus: Bayer Vital GmbH, Comments: lectures. Jean-Francois Mangin—RELATED: Grant: Mechanisms of Small Vessel Related Brain Damage and Cognitive Impairment*. Hugues Chabriat—UNRELATED: Board Membership: Servier, Comments: clinical trial preparation*; Consultancy: Johnson & Johnson, Comments: Data and Safety Monitoring Board. Reinhold Schmidt—RELATED: Grant: FP6 ERA-NET NEURON grant (01EW1207) and the Austrian Science Fund project I904.* *Money paid to the institution.

This work was supported by the FP6 ERA-NET NEURON grant (01 EW1207/Mechanisms of Small Vessel Related Brain Damage and Cognitive Impairment) and by the Austrian Science Fund project I904.

Parts of the data were presented at the Annual Meeting of the Austrian Alzheimer Society, October 24–25, 2014; Villach, Austria.

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