Objective We used diffusion tensor imaging (DTI) to test the following hypotheses: (1) there is decreased white matter (WM) integrity in non-demented Parkinson’s disease (PD), (2) WM integrity is differentially reduced in PD and early Alzheimer’s disease (AD) and (3) DTI changes in non-demented PD are specifically associated with cognitive performance.
Methods This study included 18 non-demented patients with PD, 18 patients with mild cognitive impairment due to incipient AD and 19 healthy elderly normal control (NC) participants in a cross-sectional design. The participants underwent DTI, and tract-based spatial statistics was used to analyse and extract radial diffusivity and fractional anisotropy. Correlations between scores from a battery of neuropsychological tests and DTI were performed in the PD group.
Results Patients with PD had significant differences in DTI in WM underlying the temporal, parietal and occipital cortex as compared with NC. There were no significant differences between the PD and AD groups in the primary region of interest analyses, but compared with NC there was a tendency for more anterior changes in AD in contrast to more posterior changes in PD. In a secondary whole-brain analysis there were frontoparietal areas with significant differences between AD and PD. In patients with PD, there were significant correlations between DTI parameters in WM underlying the prefrontal cortex and executive and visuospatial abilities.
Conclusions In early, non-demented PD we found reduced WM integrity underlying the temporal, parietal and occipital cortices. In addition, WM integrity changes in prefrontal areas were associated with executive and visuospatial ability. These findings support that DTI may be an important biomarker in early PD, and that WM changes are related to cognitive impairment in PD.
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Strengths and limitations of this study
Limitations of our study include lack of postmortem diagnosis. However, in the case of predementia Alzheimer's disease (AD), diagnosis was strengthened by use of cerebrospinal fluid biomarkers, and all patients with Parkinson's disease (PD) had a positive DaTSCAN supporting the clinical diagnosis.
The sample size is relatively low, and thus power issues make it difficult to differentiate between possible AD-specific and PD-specific changes.
Not all patients with PD had measurable cognitive impairment. Thus, it is possible that more pronounced diffusion tensor imaging changes and stronger associations with cognition would have been detected if more PD patients had mild cognitive impairment.
Cognitive impairment is common in Parkinson's disease (PD) and leads to patient suffering, caregiver burden and health-related costs.1
Most imaging studies exploring brain changes associated with cognitive impairment in PD have focused on grey matter atrophy, whereas the importance of white matter (WM) integrity has been less explored. MR diffusion tensor imaging (DTI) may broaden our understanding of WM affection in PD.2 Recently, DTI of anterior and posterior cingulum fibre tracts were found to be more affected in PD dementia (PDD) as compared with controls, and anterior cingulate fibres were more affected in patients with PDD compared with PD without dementia.3 In another recent study it was suggested that WM affection is associated with cognitive impairment in PD, and that brain changes progress in a sequential pattern with hypoperfusion preceding WM damage and grey matter atrophy.4
We and others have previously reported that DTI changes are closely associated with cognitive impairment in Alzheimer's disease (AD).5 To our knowledge, however, analysis of DTI parameters compared with neuropsychological tests in patients with PD and AD has not yet been published. This is important in order to single out PD-specific mechanisms of cognitive impairment. Possibly, these parameters may also be used as biomarkers for PD-driven or AD-driven cognitive impairment. We therefore studied DTI in patients with PD without dementia and compared them with age-matched patients with predementia AD and healthy controls. Our objective was to use DTI to test the following hypotheses: (1) there is decreased WM integrity in non-demented PD, (2) WM integrity in PD is differentially affected from that in early AD and (3) the DTI changes in PD are specifically associated with cognitive performance.
Eighteen patients with PD from a university-hospital-based neurological outpatient clinic were recruited during 2011 and 2012. Twelve patients were included at the time of PD diagnosis and the remaining six were patients diagnosed with PD during 2010 and 2011 and attending regular clinical controls at the outpatient clinic. The inclusion criteria were diagnosis of PD,6 disease duration less than 5 years and either normal cognition, subjective cognitive impairment (SCI) or mild cognitive impairment (MCI) (see table 1 and Cognitive assessment and classification section). The exclusion criteria were dementia (see below), somatic (other than PD), psychiatric or other diseases that might have contributed to cognitive impairment (including drug abuse, moderate or severe depression, solvent exposure, anoxic brain damage and active cancer).
We included two comparison groups: 18 patients with MCI due to AD7 from an ongoing large MCI study in the same university-hospital and who also participated in our recent DTI study.5 These patients were matched in terms of age, gender and level of education to the PD group. To be included, an abnormal score on at least one cerebrospinal fluid (CSF) AD-marker (either CSF-P-τ or CSF AB42) as recommended7 was required. In addition, all patients had memory problems, either subjectively or reported by relatives. CSF extraction was performed by lumbar puncture and analysed according to protocol and as previously described.8 CSF P-τ was considered pathological if ≥80 ng/L, Aß42 if≤550 ng/L and T-τ>if 450 ng/L (age 50–69) or 500 ng/L (age ≥70).9 The inclusion criteria were aged 40–79 years and subjectively impaired cognition for at least 6 months. The exclusion criteria were significantly impaired activities of daily living (ie, dementia), established psychiatric disorder, cancer, drug abuse, solvent exposure and anoxic brain damage including stroke. The included patients did not fulfil any of the core or suggestive criteria for dementia with Lewy bodies (DLB) or criteria consistent with a diagnosis of frontotemporal dementia.
Nineteen healthy, elderly and cognitively normal control (NC) participants were selected from spouses or relatives of the patients with AD-MCI on the basis of a clinical interview by a neurologist and neuropsychological tests administered by a trained neuropsychologist (ie, T-scores≥40 on tests of memory, executive functioning and visuospatial ability). NC was individually matched for age and level of education to the PD and AD-MCI groups.
All patients with PD were examined by a neurologist with training in movement disorders and met the criteria of probable PD (3 of 4 features: asymmetric onset, bradykinesia, rigidity and resting tremor),6 with the exception that the requirement of disease duration more than 3 years was not met by 13 patients (see table 1). To further support the PD diagnosis, all participants had a pathological single photon emission CT using an ioflupane (123I) biomarker (DaTSCAN).10
Standardised rating scales of motor function (Unified Parkinson's Disease Rating Scale (UPDRS) motor subscale)11 and Hoehn and Yahr12 staging were performed by trained research physicians. The mean UPDRS motor and Hoehn and Yahr scores were 12.3±6.8 SD (range 5–31) and 1.7±0.6 SD (range 1.0–2.5), respectively. Fifteen patients with PD used dopaminergic medication, mean total daily levodopa equivalent dose 361±186 SD (range 100–632).13 At inclusion, 10 of 18 patients used levodopa, 5 patients used dopaminagonists and levodopa, 5 patients used only dopaminagonists and 3 patients used no dopaminergic medication. Three patients used antidepressants; no patients used benzodiazepines, antipsychotics or acetylcholinesterase inhibitors.
Depression was assessed using the Geriatric Depression Scale.14 No patients with depressive symptoms above 5/6 cut-off were included, and the mean scores were 2.4±1.3 and 1.2±1.0 SD for the AD and PD groups, respectively, the AD group having slightly more depressive symptoms than the PD group (p=0.043).
Since DTI changes may also relate to cerebrovascular disease, WM lesions (WMLs) in the PD, AD and NC groups were assessed using the method published by Fazekas et al15 by one reviewer with good test–retest reliability (Pearson correlation coefficient 0.83 and 0.92 for periventricular and subcortical WML, respectively). There were no significant differences between the groups (table 1). In addition a composite cerebrovascular risk score in the three groups was made consisting of six items (smoking, diabetes, hypertension, hypercholesterolaemia (ie, total cholesterol above 7 mmol/L or use of anticholesterol agents), hyperhomocysteinaemia (ie, above 15 µmol/L) and known cerebrovascular disease other than stroke and/or known cerebrovascular disease in the family). The total cerebrovascular burden in the individual patient was thus assessed on a scale from 0 to 6, where 0 indicated no burden and 6 indicated maximum burden of disease. There were no significant differences in the mean cerebrovascular burden among the AD, PD and NC groups (table 1).
Cognitive assessment and classification
All participants performed a cognitive assessment programme, which consisted of three steps. In addition to a clinical interview, Mini-Mental State Examination (MMSE) and domain-specific screening tests were performed by the clinician. As previously described, cognitive staging (in normal, SCI and MCI) according to the Global Deterioration Scale was performed.16
In addition, tests of memory, executive functioning and visuospatial ability were administered by a trained neuropsychologist. The domains selected were chosen as typically impaired in PD and/or AD.17 The Rey Auditory Verbal Learning Test-Delayed Recall (RAVLT-DR) was used to measure episodic verbal memory.18 Visuospatial ability was assessed using the Rey Complex Figure Test (RCFT; reference area 0–36 points).19 In RAVLT-DR and RCFT raw scores were used to analyse correlations to DTI parameters. Aspects of executive functions were assessed by tests measuring divided attention (Trail Making Test-B (TMT-B)),20 response inhibition (Delis-Kaplan Executive Function System (D-KEFS) Color Word, subtest 3)21 and word fluency (Controlled Oral Word Association Test, COWAT).22 The results for the latter tests were converted into T-scores, a normally distributed scale with a mean score of 50 and an SD of 10. T-scores for TMT-B and COWAT were calculated based on normative data provided by Heaton et al,22 and the test of response inhibition was scored according to norms by Delis et al.21 A composite mean T-score was calculated for the executive tests (equal weighting). These tests were used for exploring associations between cognition and DTI.
Selection of WM region of interest
Two region of interests (ROIs) for each cognitive domain (memory, executive functioning and visuospatial ability) were selected a priori on the basis of presumed predilection sites for WM tract changes (figure 1).17
Memory is associated with entorhinal and parahippocampal cortices, and the WM underlying these ROIs were hence selected regarding this domain.
Visuoperceptual abnormalities are associated with posterior cortical dysfunction and cause deficits in visual processing in the temporal, parietal and occipital lobe.23–,26 Occipital hypoperfusion may underlie impairment of visual cognition.27 ,28 Visual information is processed in two parallel pathways, the ventral occipitotemporal pathway and the dorsal occipitoparietal pathway.29 Both extend from the primary visual cortex (V1), but the ventral pathway diverges downwards to visual association areas in the inferior temporal region, and the dorsal pathway diverges upwards to the posterior parietal cortex. Patients with PD are believed to have dysfunction in both.30 The neuroanatomical substrate of visuospatial/visuoperceptual abilities thus involves different cerebral regions, but the occipital lobe is considered to be the most task-specific region concerning visual processing. Based on the presumed anatomical basis of visuospatial function, we hence selected one WM ROI underlying the occipital cortex, that is, the lingual region (adjacent to the parahippocampal cortex) and one WM ROI underlying the posterior parietal cortex, that is, the precuneus region (adjacent to the lingual cortex).
Although dependent on widely distributed networks, neuroimaging studies suggest that executive functions are closely connected to the prefrontal regions of the frontal lobe31 further subdivided into three frontosubcortical circuits, namely the dorsolateral prefrontal cortex (DLPFC; eg, verbal fluency, reasoning and working memory), the orbitofrontal cortex (ie, inhibition) and the anterior cingulate cortex (ie, response conflict and emotional drives).32 According to a narrow definition, the DLPFC is roughly equivalent to Brodmann area 9 and 46, that is, the middle frontal lobe. We therefore selected the WM underlying the middle frontal gyrus (rostral division) and the WM underlying the orbitofrontal cortex (medial division) for further analysis.
Measurements were averaged between hemispheres.
MRI was performed at 1.5 T using a Siemens Espree system (Siemens Healthcare, Erlangen, Germany). Three-dimensional T1-weighted images were acquired using a magnetisation-prepared rapid acquisition gradient echo (MPRAGE) sequence (TR/TE/TI/FA=2400/3.65/1000/8°, matrix=240×192), 160 sagittal slices, thickness=1.2 mm, in-plane resolution of 1 mm×1.2 mm. The protocol also included two-dimensional axial fluid-attenuated inversion recovery images with the following parameters: TR/TE/TI=13420/121/2500, 36 slices, spaced at 3 mm and 3.9 mm thick.
DTI was acquired using a single shot echo planar imaging sequence with the following parameters: b=750 s/mm2; 12 diffusion directions repeated five times; 5 b0-values per slice, TR=6100 ms, TE=117 ms, number of slices: 30, slice thickness: 3 mm (gap 1.9 mm), in-plane resolution: 1.2×1.2 mm2, bandwidth: 840 Hz/pixel.
MRI segmentations and analyses
The Oxford Centre for Functional MRI of the Brain (FMRIB) Software Library (FSL) V.4.133 was used for DTI analyses and calculations. Initially, FMRIB’s Linear Image Registration Tool23 was used for affine registrations of each DTI volume to the low-b (b=0) image.
Fractional anisotropy (FA) and eigenvalue maps were created. Radial diffusivity (DR) is defined as the mean of eigenvalue 2 and 3. Tract-Based Spatial Statistics34 was used for voxel-wise statistical analysis of the DTI variables (FA and DR). FMRIB's Diffusion Toolbox was used to create DTI by fitting a tensor model to the raw diffusion data, and FSL's Brain Extraction Tool was used for subsequent brain extraction. All participants’ FA data were then aligned into a common space using a non-linear registration tool (FMRIB) which uses a B-spline representation of the registration warp field.35 Further, the mean FA image was created and thinned to create a mean FA skeleton that represents the centres of all tracts common to the group. Each participant's aligned FA data were then projected onto this skeleton and the resulting data fed into voxel-wise cross-subject statistics. DR data were then extracted from each participant according to the skeletonised FA map. Moreover, WM ROIs based on the FreeSurfer WM parcellations were extracted for FA and DR—the FSL FMRIB FA template (to which every participant's FA volume initially was registered) was co-registered to the standard space T1 volume MNI152, which subsequently went through the FreeSurfer processing stream to create a volume with WM parcellations. The processing stream includes segmentation of the subcortical WM and deep grey matter volumetric structures36 and parcellation of the cortical surface37 according to a previously published parcellation scheme.38 This labels cortical sulci and gyri, and thickness values are calculated in the ROIs. Based on the cortical parcellation, WM in the gyrus underneath each cortical label was identified. Each WM voxel within a gyrus was labelled according to the label of the nearest cortical voxel. Deep WM was not assigned to a particular cortical area, with a 5 mm distance limit. The registration between the FA template and the MNI152 volume was applied to the volume with the WM parcellations, and the resulting volume was used to extract the skeletonised DR data from each WM ROI.
SPSS/PASW statistics V.18 was used for statistical analyses and p≤0.05 was considered statistically significant. Comparisons among the three groups (PD, AD and NC) were made using one-way analysis of variance (ANOVA), Kruskal-Wallis test, Student t test, Mann-Whitney test or χ2 test as appropriate (table 1). The DTI WM ROI variables were normally distributed (after the effects of age and sex had been corrected by regression analysis), and hence one-way ANOVA (with a priori planned contrast AD vs NC and PD vs NC including polynomial linear trends) was used to compare the three groups. Unbiased, voxel-based whole-brain analysis was also performed. However, due to the small sample sizes resulting in low statistical power to detect expected small differences between AD and PD, ROI analyses were chosen as the primary analyses.
The relationship between cognition and DTI in PD was assessed as follows:
Primarily, Pearson correlations between each of the three cognitive domains with the two a priori selected brain regions were determined. In secondary analyses, we determined Pearson correlations between all six ROIs and the three cognitive domains. Finally, the specific executive tests were correlated with the two frontal regions.
The effects of sex and age on the DTI DR parameters were corrected by linear regression before correlations were determined.
Demographics and clinical characteristics (age, gender, disease duration, education and Fazekas score) did not differ among the groups (table 1). The mean MMSE score was lower in the AD and PD groups than NC (p < 0.001), and the MMSE scores in AD (27.3±1.8 SD) were slightly lower than that in PD (28.8±1.4 SD; p=0.009). The locations of the selected ROI's are illustrated in figure 1.
DTI changes in PD compared with AD and NC subjects
The ANOVA-analysis revealed significant between-group differences in all preplanned DTI ROIs.
In (temporal ROIs) WM underlying the entorhinal cortex (ERC-WM), DR was higher compared with NC in AD (p=0.002), but did not reach significance in PD (p=0.059; figure 2). DR in ERC-WM increased from NC to PD to AD (linear trend p=0.002). Similar findings emerged for WM underlying the parahippocampal cortex, that is, AD (p<0.001) and PD (p=0.030) as compared with NC, with a gradient NC<PD<AD (linear trend p<0.001).
In the occipital ROI, higher DR (as compared with NC) was found in WM underlying the lingual gyrus in PD (p=0.034), but not in AD (p=0.071) with a gradient NC<AD<PD (linear trend p=0.034); figure 3).
In the parietal ROI (WM underlying the precuneus cortex), higher DR (as compared with NC) was found in PD (p=0.020) and AD (p=0.003), with a gradient NC<AD<PD (linear trend p=0.007).
The AD-MCI and PD group did not differ regarding the disease duration.
In (frontal ROIs) WM underlying the rostral middle frontal cortex (RMFC-WM) had higher DR in AD (p=0.019), but not in PD (p=0.213) as compared with NC (gradient NC<PD<AD).
Similar findings were found for WM underlying the medial orbitofrontal cortex, that is, higher DR in AD (p=0.005), but not in PD (p=0.102), with a gradient NC<PD<AD (linear trend p=0.020).
There were no significant differences in DR in any of the WM ROIs between the PD and AD groups. In a secondary analysis we found similar between group differences for FA (data not shown).
The voxel-based analyses were generally consistent with the findings from the ROI analyses.
In addition to the expected findings between AD versus NC (DR; figure 4) and PD versus NC (FA; figure 5), there were significant differences in DTI parameters (DR) between AD and PD, with higher DR in AD compared with PD in frontoparietal regions on the left side (corrected for multiple comparisons using threshold-free cluster enhancement; figure 6). However, no significant changes were found for FA in AD versus NC or AD versus PD, and similarly for DR between PD versus NC.
Associations between DTI and cognition in PD
T-scores for the different neuropsychological tests in the PD group showed the following (mean and SD): TMT-B (36.7±21.1), response inhibition (46.6±14.3), word fluency (46.0±9.6) and composite score for executive tests (43.1±12.0). The mean and SD for raw scores on RAVLT and RCFT were 7.1±3.2 and 28.5±9.2, respectively.
No correlations were found between memory (RAVLT-DR) and prespecified DTI variables. Complex figure reproduction did not correlate with the occipital ROI, but in the secondary analyses a correlation with DR in the RMFC-WM was found (r=−0.57; p=0.014).
When using the composite score for executive functions, we found a significant correlation to DR in RMFC-WM (r=−0.49; p=0.041). Analysing subtests of executive functioning (raw scores), we found a correlation between DR in RMFC-WM and time to complete the color-word interference test (r=0.51; p=0.030) and TMT-B (r=0.55: p=0.019).
Voxel-based whole-brain analyses revealed no significant correlations between DTI parameters (DR and FA), memory and composite score for executive functions. Similarly, there were no correlations between DR and performance on RCFT. We found, however, significant correlations between FA and visuoconstruction (RCFT) in corpus callosum (figure 7).
The main finding in this study was that patients with PD without dementia had significant differences in WM DTI-derived metrics in WM underlying the temporal, parietal and occipital cortex as compared with NC. Thus, our findings support the first hypothesis, that WM integrity is disturbed even in early PD.
Our second hypothesis was that there would be differences in DTI parameters between AD and PD. Although we did not find significant differences between the two groups in the primary ROI-based analysis, patients with PD and AD differed from NC in the hypothesised direction (DR in the temporal ROIs NC<PD<AD and in the parietal and occipital ROIs NC<AD<PD). In voxel-wise whole-brain analysis we found, however, significant changes between AD and PD (DR) in mainly frontoparietal regions including parts of the corticospinal tracts, that is, higher DR for AD. In addition, the voxel-wise whole-brain analyses showed significant DTI associations in corpus callosum with visuoconstruction.
Our final hypothesis, that DTI changes in PD are associated with cognitive ability, was also at least partly supported. Although we did not find any significant correlations between performance on memory tasks and DTI DR, there were moderately strong correlations between DR in WM underlying the prefrontal cortex and executive tests as well as visuospatial ability.
Our results are consistent with the recent findings that patients with PD, PDD and DLB have more pronounced WM affection than NC.3 ,4 ,39–,41 Patients with PD with significant DTI changes in these studies had, however, more severe cognitive impairment (lower mean MMSE scores) than in our PD group. Of note, Hattori et al4 found no significant DTI changes in the PD cognitively normal group as compared with NC. In contrast we found significant WM tract changes in a mixed group of patients with PD with and without MCI. However, in a recent study by Meltzer et al42 mean diffusivity differences (but not FA) were also found in PD cognitively normal participants (relative to NC) confined to corpus callosum, but not in other brain regions. Despite a cross-sectional design, the same study also suggested that microstructural WM integrity loss increases with cognitive deterioration. In another recent study, WM abnormalities were not found in PD cognitively normal participants, in contrast to a distributed pattern of WM changes (reduced FA), mainly in frontal areas, in patients with PD with MCI.43 Taken together, these findings lend support to the idea that WM tract changes evolve in parallel to cognitive decline in PD.
We did not find correlations between loss of (presumably) visual-tract WM integrity in parieto-occipital regions and tests of visuoconstruction. In the study by Watson et al40 the widespread correlations found between executive functions and parameters of DTI in DLB could be explained by the more advanced disease stage or the potentially different disease progression in DLB and PD. Our study found associations between prefrontal DTI changes and executive functioning in a similar pattern as described by Meltzer et al.42 Although there were numerical differences in DTI parameters in prefrontal cortex between PD and NC, they were not statistically significant. This may be due to the small sample size, and stronger associations might have been found if other prefrontal ROIs had been selected. In addition, the complexity of neuronal networks and different brain areas involved in neuropsychological testing make it difficult to exactly localise neuroanatomical substrates of disease. The few DTI studies available in Lewy body disease also suggest that WM changes are rather widespread even at an early disease stage.
Of note, in our study AD and PD cases had different mean MMSE scores, which might have influenced the findings. This is not surprising since per definition all patients with AD had MCI, whereas some of the patients with PD were cognitively intact, and the MMSE emphasises language and memory items and thus is more sensitive to the changes in early AD than in PD. Although significant, the differences in depression scores between patients with AD and PD were minor and below cut-off for possible depression, and we do not think this had any major influence on the results. Yet, we cannot entirely exclude the possibility that minor differences in overall cognition affected the comparison between AD and PD.
However, regardless of the complexity of neuronal disease, the clinical correlates to DTI changes in Lewy body disease suggest that DTI may be a useful biomarker for this type of neurodegeneration.
Limitations of our study include lack of postmortem diagnosis. However, in the case of predementia AD, diagnosis was strengthened by use of CSF biomarkers and all patients with PD had a positive DaTSCAN supporting the clinical diagnosis.
The sample size is relatively low, and thus power issues make it difficult to reach statistical significance and differentiate between AD and PD-specific changes.
Not all patients with PD had measurable cognitive impairment. Thus, it is possible that more pronounced changes and stronger associations with cognition would have been detected if we had focused on patients with PD with established MCI.
Only FA and DR were evaluated, whereas other parameters, such as mean diffusivity, axial diffusivity, were not explored.
Contributors DA and TF planned and supervised the study. EA, VKK, PS and AH collected the data. EA and VKK performed the statistical analysis. EA wrote the first draft and all the authors critically reviewed and revised the manuscript. AB was responsible for set-up and quality control of the MRI protocol. PS was responsible for processing of MRI data and voxel-wise statistical analyses. EH was responsible for the implementation of neuropsychological tests in cooperation with DA and TF. AE was responsible for coordination and interpretation of DaTSCAN.
Funding Southern and Eastern Norway Regional Health Authority (grant number 2011093) and Akershus University Hospital.
Competing interests DA has received honoraria or research support from Lundbeck, Inc, Novartis, GE Healthcare, and GlaxoSmithKline; serves on the editorial boards of International Psychogeriatrics, Movement Disorders, and the Journal of Neurology, Neurosurgery, and Psychiatry.
Patient consent Obtained.
Ethics approval South-Eastern Norway ethical committee for medical research.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement No additional data are available.
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