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Neurology Research International
Volume 2012 (2012), Article ID 517876, 9 pages
DTI and MR Volumetry of Hippocampus-PC/PCC Circuit: In Search of Early Micro- and Macrostructural Signs of Alzheimers's Disease
1Neuroradiology Unit, IRCCS Foundation National Neurological Institute C. Mondino, 27100 Pavia, Italy
2Department of Physics “A. Volta”, University of Pavia, 27100 Pavia, Italy
3Department of Computer Engineering and Systems Science, University of Pavia, 27100 Pavia, Italy
4Neurology Unit, IRCCS Foundation National Neurological Institute C. Mondino, 27100 Pavia, Italy
5Department of Radiology, University of Pavia, 27100 Pavia, Italy
Received 15 March 2011; Accepted 7 April 2011
Academic Editor: Patrice Peran
Copyright © 2012 F. Palesi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Hippocampal damage, by DTI or MR volumetry, and PET hypoperfusion of precuneus/posterior cingulate cortex (PC/PCC) were proposed as biomarkers of conversion from preclinical (MCI) to clinical stage of Alzheimer's disease (AD). This study evaluated structural damage, by DTI and MR volumetry, of hippocampi and tracts connecting hippocampus to PC/PCC (hipp-PC/PCC) in 10 AD, 10 MCI, and 18 healthy controls (CTRL). Normalized volumes, mean diffusivity (MD), and fractional anisotropy (FA) were obtained for grey matter (GM), white matter (WM), hippocampi, PC/PCC, and hipp-PC/PCC tracts. In hippocampi and hipp-PC/PCC tracts, decreased volumes and increased MD were found in AD versus CTRL (). The same results with lower significance () were found in MCI versus CTRL. Verbal memory correlated () in AD with left hippocampal and hipp-PC/PCC tract MD, and in MCI with FA of total WM. Both DTI and MR volumetry of hippocampi and hipp-PC/PCC tracts detect early signs of AD in MCI patients.
Preclinical detection of Alzheimer’s disease (AD) is important to start an early therapeutic treatment, and it will be even more crucial in the next few years, as soon as new drugs will be available. Mild cognitive impairment (MCI) is often the preclinical stage of AD. However, some patients with MCI revert to normal cognitive status, while others, with slow disease progression, remain in this prodromic stage without presenting dementia in their life .
To detect which patients with MCI will convert in AD in the immediate future, an in vivo biomarker is not currently available. CSF tau, phospho-tau, and amyloid measurements are in development [2, 3] but require lumbar puncture; therefore, a noninvasive imaging marker is more appealing for screening outpatients without hospital admission. With this purpose, volumetric MRI measures of mesiotemporal atrophy demonstrated to have some prognostic value [4, 5]. Compared to these volumetric measures of macrostructural damage, diffusion tensor imaging (DTI) indexes of microstructural damage within mesiotemporal lobe have shown to better discriminate MCI from controls [6, 7] and to better detect MCI converters [8–10].
DTI is sensitive to both grey and white matter subtle abnormalities. While in AD degeneration mainly affects grey matter , recent evidences also found an early white matter involvement [12, 13]. It is a matter of debate whether degeneration directly affects the myelin, but a secondary wallerian degeneration certainly drives disconnection of associative cortical areas from the medial temporal lobe. In MCI, the earliest affected area by disconnection seems to be the precuneus/posterior cingulate cortex (PC/PCC), consistently found hypoperfused by many PET studies  and related to the conversion in AD . A recent study combining PET and volumetric MRI showed that PC/PCC hypoperfusion follows medial temporal atrophy through posterior cingulum white matter degeneration . Furthermore, several studies using resting state fMRI showed a functional disconnection between hippocampus and PC/PCC [17, 18].
In this study, to identify sensitive in vivo biomarkers of risk for conversion from MCI to AD, the microstructural damage was measured by DTI in the hippocampus and in the white matter between hippocampus and PC/PCC. The DTI indexes of microstructural damage were compared to volumetric indexes of macrostructural damage in MCI and AD patients, using as control a group of healthy elderly volunteers.
Twenty patients were consecutively recruited through the Memory Clinic of the Neurological Institute C. Mondino, Pavia, Italy, among patients suffering from subjective or objective memory complaint.
Exclusion criteria were age > 80, a history of overt depression  or other psychiatric diseases, significant cerebrovascular disease , and lack of any daily living activity. In this small patients group, exclusion of subjects over 80 years minimizes the contribution of confounding variables of age and of age-related diseases, particularly cerebrovascular disease.
Neuropsychology examination by a standardised battery evaluated different cognitive domain . In this study, we only considered the global measure of cognitive impairment as expressed by MMSE , and verbal memory as expressed by short story recall .
After clinical and neuropsychological examinations, 10 patients were diagnosed with amnestic mild cognitive impairment  and 10 with mild probable Alzheimer's disease (NINCDS2-ARDA criteria ) (Table 1).
Twenty elderly subjects were recruited on a volunteer base through a local recreational association (“Argento Vivo,” i.e., “Live silver,” Bereguardo, PV). After clinical and neuropsychological examinations, two volunteers affected by vascular cognitive impairment were excluded. The remaining 18 healthy volunteers were included as control group (CTRL) and underwent the MRI session.
2.2. MRI Acquisition
All data were acquired on a 1.5 Tesla MRI scanner (Intera, Philips Gyroscan, Koninklijke, The Netherlands) using an eight-channel head (SENSE) third-party coil.
All subjects were scanned with a structural MRI protocol, including a dual turbo spin echo (TSE) sequence (proton density and T2), a volumetric T1-weighted sequence, and diffusion tensor imaging (DTI) data. Functional MRI data during resting state are not considered in this study. Additional FLAIR images were acquired only in patients with some punctuate lesions on PD-T2 images. While most patients and volunteers showed some punctuate lesions, only few showed confluent lesions, in any case never involving more than a third of total white matter. Although subtle cerebrovascular disease may be a factor concurring to cognitive impairment in MCI and AD, for the purpose of this study the total lesion load was not assessed.
Diffusion tensor imaging (DTI) data were acquired using a single-shot EPI spin echo sequence (TR/TE = 11800/70 ms) with a b-value of 900 s/mm2, applying diffusion gradients along 15 directions. Sixty axial slices with no slice gap were acquired (FOV = 224 mm, acquisition matrix = 88 × 90, reconstruction matrix = 96 × 96, 2.5 mm isotropic voxel, number of averages = 3).
Volumetric T1-weighted data was collected using a fast field echo sequence (TR/TE = 8.6/4 ms, flip angle 8°) and one hundred seventy sagittal slices with a thickness of 1.2 mm (FOV = 240 mm, matrix = 192 × 192, in-plane resolution 1.25 × 1.25 mm, reconstruction matrix = 256 × 256).
2.3. MR Imaging Analysis
Image analysis was performed on a workstation with Linux Ubuntu 9.10, running SPM8 (Wellcome Department of Cognitive Neurology, http://www.fil.ion.ucl.ac.uk/) on MATLAB 7.9 (The MathWorks, Natick, Mass, USA http://www.mathworks.com/), FreeSurfer (http://surfer.nmr.mgh.harvard.edu/), and FSL (FMRIB Software Library, http://www.fmrib.ox.ac.uk/fsl/) software (Figure 1).
A nonparametric nonuniformity intensity normalization was applied on volumetric T1-weighted images [24, 25] using FreeSurfer. Then using FSL , the following tools were applied sequentially: brain extraction by the BET  tool to clear noncerebral voxels; segmentation by the FAST  tool into grey matter (GM), white matter (WM), and cerebrospinal fluid (CSF); segmentation by the FIRST tool of left and right hippocampi . Left and right precuneus (PC) and posterior cingulate cortex (PCC) were obtained by an inversion of the nonlinear transformation between the volumetric images and the MNI152 template, on which the AAL template was superimposed.
Diffusion-weighted images were corrected for motion and eddy current distortion by the FDT tool. After brain extraction, diffusion tensor was reconstructed using an iterative least square algorithm (Marquardt-Levenberg nonlinear fit) to calculate mean diffusivity (MD) and fractional anisotropy (FA) maps.
A probabilistic tractography of the tract connecting the hippocampus with PC/PCC (Hipp-PC/PCC) was performed on each hemisphere by the FDT tool [30, 31]; first, volumetric T1-weighted image, ROIs of hippocampi, and PC/PCC were coregistered onto diffusion-weighted images, then coregistered hippocampi were used as seed ROI, and coregistered PC/PCC were used as target ROI. Reconstructed tracts were thresholded at 30.
B0 images were normalized onto the EPI template in stereotaxic MNI152 space for each subject. Normalization transformation was applied to all reconstructed tracts. Normalized nonthresholded tracts were binarized, averaged for the three different groups (CTRL, MCI, and AD patients), and then smoothed with a 5 mm Gaussian kernel.
A voxelwise statistical analysis was performed using the general linear model framework implemented in SPM8 . The resulting t-statistic maps, after family-wise error (FWE) correction for multiple comparisons, were thresholded at .
The FA and MD maps were co-registered (with a full affine transformation, FLIRT tool ) on volumetric brain-extracted images, then this affine transformation was applied to reconstructed thresholded tracts.
Eventually, average FA and MD were calculated for brain tissue (BT), white matter (WM), grey matter (GM), hippocampi, PC/PCC, and tracts connecting hippocampi with PC/PCC. Absolute volume (mm3) and relative volume, expressed as ratio between absolute volume (mm3) and intracranial volume (mm3), were calculated for BT, WM, GM, hippocampi, PC/PCC, and tracts connecting hippocampi with PC/PCC.
2.4. Statistical Analysis
Statistical analysis was performed using SPSS. Average FA values, average MD, values and volumetric values were statistically compared using a Student t-test for nonpaired (independent) data between AD and CTRL, between MCI and CTRL, and between MCI and AD. The significant level was set at for each test. Finally, a Pearson’s correlation analysis was performed between MRI data and cognitive scores (MMSE and verbal memory).
3.1. Volumetry Analysis
Average group values, with respective standard deviations, were reported in Table 2 for relative volumes of each investigated structure. In AD compared to CTRL, volumes of total BT, total GM, and left PC/PCC were significantly decreased (), but even more significantly ( or less) at the level of both hippocampi and tracts connecting hippocampi with PC/PCC. In MCI compared to CTRL, volumes of both hippocampi and tract connecting right hippocampus with PC/PCC were significantly decreased () compared to CTRL. In AD compared to MCI, volumes of left PC/PCC and tract connecting left hippocampus with PC/PCC were significantly decreased () (Figure 2(b)).
3.2. DTI Analysis
Average group values, with respective standard deviations, were reported in Table 3 for MD of each investigated structure. In AD compared to CTRL, MD of total BT, total WM, and right PC/PCC were significantly increased (), but more significantly increased () were MD of total GM, left PC/PCC, both hippocampi and both tracts connecting hippocampi with PC/PCC. In MCI compared to CTRL, MD of both hippocampi and both tracts connecting hippocampi with PC/PCC were significantly increased (). In AD compared to MCI, MD of total BT, total GM, and left hippocampus were significantly increased () (Figure 2(a)).
Average group values, with respective standard deviations, were reported in Table 4 for FA of each investigated structure. In AD compared to CTRL, FA of right hippocampus and tract connecting right hippocampus with PC/PCC were significantly decreased (), but more significantly decreased ( or less) were FA of left hippocampus and tract connecting left hippocampus with PC/PCC. In MCI compared to CTRL, FA of left hippocampus was the only significantly decreased () compared to CTRL. In AD compared to MCI, FA of tract connecting left hippocampus with PC/PCC was the only significantly decreased ().
Results of group analysis for tract connecting each hippocampus with homologous PC/PCC are reported in Figures 3 and 4. Figure 3 shows reconstructed tracts in CTRL, MCI, and AD patients. Variability maps for these tracts show progressive decrease of volume and consistency from CTRL to AD patients.
In Figure 4 are shown the results of voxelwise analysis on probability distribution of the tract connecting each hippocampus with homologous PC/PCC in MCI and AD patients compared with CTRL (, FWE correction). In AD (red blobs) patients, probability of connection between hippocampus and PC/PCC was decreased in the whole parahippocampal WM, symmetrically in the two hemispheres. In MCI (blue blobs), probability of connection between hippocampus and PC/PCC was decreased in restricted areas of anterior parahippocampal WM, asymmetrically in the two hemispheres.
3.3. Correlation between Volumetric and Diffusion MR Indexes (Table 5)
Volume and MD of total BT and total GM were correlated in CTRL and in MCI, not in AD.
Volume and MD, of hippocampi and PC/PCC were correlated in MCI, not in CTRL, and in AD only of the left hippocampus and the right PC/PCC.
Volume, MD and FA of hipp-PC/PCC tracts were correlated in CTRL and in MCI, but in AD, only volume and MD of the left tract.
3.4. Correlation with Cognitive Scores (Table 6)
In AD, volumes of total BT, volumes of total WM, MD of left hippocampus, and MD of left tract connecting hippocampus with PC/PCC correlate significantly () with verbal memory scores. MD of left tract connecting hippocampus with PC/PCC was the only parameter correlating also with MMSE score. In MCI, FA of total WM was the only parameter correlating significantly () with verbal memory. No correlation was found between volumetric or DTI parameters and cognitive scores in CTRL.
The aim of the study was to identify sensitive in vivo biomarkers of Alzheimer's disease, to be employed in clinical setting in single patients and to predict the risk for conversion from MCI to AD. The DTI indexes of microstructural damage showed to be at least as sensitive as volumetric indexes of structural damage to identify mesiotemporal damage in differentiating AD and MCI patients from CTRL. The poor correlation between volume and DTI indexes in AD group suggests that macrostructural and microstructural damage may occur in different times in the course of the disease thus may be differently sensitive.
In AD, and to less extent in MCI, atrophy and MD increases were found not only in both hippocampi, but also very significant in white matter tracts connecting hippocampi with precuneus/posterior cingulate cortex. To our knowledge, no study assessed simultaneously atrophy and diffusivity in both hippocampus and parahippocampal-posterior cingulum tract.
We observed also a significant decrease of FA in the hipp-PC/PCC tracts in AD the left tract significantly more than in MCI. The volume of this left hipp-PC/PCC tract, and the volume of left PC/PCC were also found more significantly decreased in AD than in MCI. These results could be explained by a degenerative damage in hipp-PC/PCC tracts, secondary to hippocampal damage. This degenerative damage in hipp-PC/PCC tracts, in agreement with the Villain model, could drive the PC/PCC dysconnection, thus causing in these cortical areas first hypoperfusion in MCI (as found commonly by PET studies, included Villain et al.) and later MD increase and atrophy in AD (as found in the present study, mainly in the left hemisphere). The portion of cingulate tract identified by Villain is included in the tract connecting hippocampi with precuneus/posterior cingulate cortex in our study.
These significant DTI differences between MCI and CTRL groups are not consistently found in literature. Among several DTI studies in MCI, hippocampal MD increase in MCI was found only by few authors [6, 7, 10]. Some studies also found that hippocampal MD detects MCI converters better than hippocampal atrophy [8, 10]. Compared to Muller and Scola, our approach uses a more precise segmentation, specifically of the whole hippocampus as performed in Ray, 2006. While Ray, 2006, used a manual segmentation, our approach with automatic segmentation, still capable to detect early abnormalities in hippocampus of MCI patients, may be more feasible in a clinical setting. Among DTI studies in MCI focusing on white matter tracts, an MD increase in parahippocampal-posterior cingulum was found by few recent studies [34, 35].
It is not known whether damage of parahippocampal-posterior cingulum is the crucial abnormality in MCI converting to AD or not. In the present study, although MD of total BT and total GM differentiated AD from MCI, other significant differences between AD and MCI were found in MD of left hippocampus, FA and volume of left hipp-PC/PCC tract, and volume of left PC/PCC. Therefore, the hippocampus-PC/PCC circuit seems to be specifically involved in AD. While a study using a voxelwise approach  failed to find significant MD increase in any white matter region in MCI, the main white matter region with MD increase in early AD was the parahippocampal tract. Another study of the same group, using an ROI-based approach, found that the occipital white matter was found to be the region differentiating better MCI converters from MCI non converters . In that study, however, posterior cingulum and parahippocampal tract were not investigated.
About clinical relevance of volumetric and DTI abnormalities, we looked at correlations with cognitive variables, verbal memory, and MMSE scores. Verbal memory impairment is the earlier crucial deficit in MCI and AD. In this study, in AD the verbal memory score correlated with indexes of global atrophy (total BT, total WM) and at mesiotemporal level only with MD increase, not with atrophy, of left hippocampus and tract connecting left hippocampus with PC/PCC. The clinical relevance of MD increases is also supported by the finding that MD of the tract connecting left hippocampus with PC/PCC was the only variable correlating also with scale of global cognitive status, as expressed by MMSE. In this study, in MCI the verbal memory score correlated only with FA of total WM. Because all MCI patients in this cohort were amnestic MCI, verbal memory was affected in them all, but only few are likely to develop AD in the next years. Therefore, in MCI the correlation of verbal memory score with FA of total WM may reflect a pathological mechanism not specifically related to the Alzheimer's pathology, for instance, to a generic WM damage due to a subtle cerebrovascular disease.
Both MR volumetric measure of macrostructural damage and DTI measure of microstructural damage, both in grey and white matter, are candidates to be sensitive in vivo biomarkers of mesiotemporal damage predicting conversion from MCI to AD.
DTI abnormalities, especially MD increase, seem to be more clinically relevant than atrophy.
Only the clinical followup of MCI patients will show which is the most sensitive parameter to be employed to predict the conversion rate on single patients in a clinical setting.
The authors thank Federica Negri and all volunteers of the local recreational association “Argento Vivo” (i.e., “Live silver”) in Bereguardo, PV, Italy, particularly their president, Rampi Teresita, for the enthusiastic support to this study.
- R. C. Petersen, G. E. Smith, S. C. Waring, R. J. Ivnik, E. G. Tangalos, and E. Kokmen, “Mild cognitive impairment: clinical characterization and outcome,” Archives of Neurology, vol. 56, no. 3, pp. 303–308, 1999.
- B. Palumbo, D. Siepi, I. Sabalich, C. Tranfaglia, and L. Parnetti, “Cerebrospinal fluid neuron-specific enolase: a further marker of Alzheimer's disease?” Functional Neurology, vol. 23, no. 2, pp. 93–96, 2008.
- A. Caroli and G. B. Frisoni, “The dynamics of Alzheimer's disease biomarkers in the Alzheimer's disease neuroimaging initiative cohort,” Neurobiology of Aging, vol. 31, no. 8, pp. 1263–1274, 2010.
- P. Calvini, A. Chincarini, G. Gemme et al., “Automatic analysis of medial temporal lobe atrophy from structural MRIs for the early assessment of Alzheimer disease,” Medical Physics, vol. 36, no. 8, pp. 3737–3747, 2009.
- L. K. McEvoy, C. Fennema-Notestine, J. C. Roddey et al., “Alzheimer disease: quantitative structural neuroimaging for detection and prediction of clinical and structural changes in mild cognitive impairment,” Radiology, vol. 251, no. 1, pp. 195–205, 2009.
- M. J. Müller, D. Greverus, C. Weibrich et al., “Diagnostic utility of hippocampal size and mean diffusivity in amnestic MCI,” Neurobiology of Aging, vol. 28, no. 3, pp. 398–403, 2007.
- K. M. Ray, H. Wang, Y. Chu et al., “Mild cognitive impairment: apparent diffusion coefficient in regional gray matter and white matter structures,” Radiology, vol. 241, no. 1, pp. 197–205, 2006.
- A. Fellgiebel, P. R. Dellani, D. Greverus, A. Scheurich, P. Stoeter, and M. J. Müller, “Predicting conversion to dementia in mild cognitive impairment by volumetric and diffusivity measurements of the hippocampus,” Psychiatry Research—Neuroimaging, vol. 146, no. 3, pp. 283–287, 2006.
- K. Kantarci, R. C. Petersen, B. F. Boeve et al., “DWI predicts future progression to Alzheimer disease in amnestic mild cognitive impairment,” Neurology, vol. 64, no. 5, pp. 902–904, 2005.
- E. Scola, M. Bozzali, F. Agosta et al., “A diffusion tensor MRI study of patients with MCI and AD with a 2-year clinical follow-up,” Journal of Neurology, Neurosurgery and Psychiatry, vol. 81, no. 7, pp. 798–805, 2010.
- H. Braak and E. Braak, “Diagnostic criteria for neuropathologic assessment of Alzheimer's disease,” Neurobiology of Aging, vol. 18, no. 4, pp. S85–S88, 1997.
- G. Bartzokis, “Age-related myelin breakdown: a developmental model of cognitive decline and Alzheimer's disease,” Neurobiology of Aging, vol. 25, no. 1, pp. 5–18, 2004.
- X. J. Sun, Q. C. Lu, and Y. Cai, “Effect of cholecystokinin on experimental neuronal aging,” World Journal of Gastroenterology, vol. 11, no. 4, pp. 551–556, 2005.
- K. Herholz, S. F. Carter, and M. Jones, “Positron emission tomography imaging in dementia,” British Journal of Radiology, vol. 80, no. 2, pp. S160–S167, 2007.
- S. Morbelli, A. Piccardo, G. Villavecchia et al., “Mapping brain morphological and functional conversion patterns in amnestic MCI: a voxel-based MRI and FDG-PET study,” European Journal of Nuclear Medicine and Molecular Imaging, vol. 37, no. 1, pp. 36–45, 2010.
- N. Villain, M. Fouquet, J. C. Baron et al., “Sequential relationships between grey matter and white matter atrophy and brain metabolic abnormalities in early Alzheimer's disease,” Brain, vol. 133, no. 11, pp. 3301–3314, 2010.
- M. D. Greicius, G. Srivastava, A. L. Reiss, and V. Menon, “Default-mode network activity distinguishes Alzheimer's disease from healthy aging: evidence from functional MRI,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 13, pp. 4637–4642, 2004.
- C. Sorg, V. Riedl, R. Perneczky, A. Kurz, and A. M. Wohlschläger, “Impact of Alzheimer's disease on the functional connectivity of spontaneous brain activity,” Current Alzheimer Research, vol. 6, no. 6, pp. 541–553, 2009.
- M. Hamilton, “Development of a rating scale for primary depressive illness,” The British Journal of Social and Clinical Psychology, vol. 6, no. 4, pp. 278–296, 1967.
- V. C. Hachinski, L. D. Iliff, and E. Zilhka, “Cerebral blood flow in dementia,” Archives of Neurology, vol. 32, no. 9, pp. 632–637, 1975.
- H. Spinnler and G. Tognoni, “Taratura e standardizzazione italiana di test neuropsicologici,” Italian Journal of Neurological Sciences, supplement 8, pp. 1–120, 1987.
- M. F. Folstein, S. E. Folstein, and P. R. McHugh, ““Mini mental state”. A practical method for grading the cognitive state of patients for the clinician,” Journal of Psychiatric Research, vol. 12, no. 3, pp. 189–198, 1975.
- G. McKhann, D. Drachman, and M. Folstein, “Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA work group under the auspices of department of health and human services task force on alzheimer's disease,” Neurology, vol. 34, no. 7, pp. 939–944, 1984.
- J. G. Sled, A. P. Zijdenbos, and A. C. Evans, “A nonparametric method for automatic correction of intensity nonuniformity in mri data,” IEEE Transactions on Medical Imaging, vol. 17, no. 1, pp. 87–97, 1998.
- W. Zheng, M. W. L. Chee, and V. Zagorodnov, “Improvement of brain segmentation accuracy by optimizing non-uniformity correction using N3,” NeuroImage, vol. 48, no. 1, pp. 73–83, 2009.
- S. M. Smith, M. Jenkinson, M. W. Woolrich et al., “Advances in functional and structural MR image analysis and implementation as FSL,” NeuroImage, vol. 23, supplement 1, pp. S208–S219, 2004.
- S. M. Smith, “Fast robust automated brain extraction,” Human Brain Mapping, vol. 17, no. 3, pp. 143–155, 2002.
- Y. Zhang, M. Brady, and S. Smith, “Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm,” IEEE Transactions on Medical Imaging, vol. 20, no. 1, pp. 45–57, 2001.
- B. Patenaude, S. M. Smith, D. N. Kennedy, and M. Jenkinson, “A Bayesian model of shape and appearance for subcortical brain segmentation,” NeuroImage. In press.
- T. E. J. Behrens, H. J. Berg, S. Jbabdi, M. F. S. Rushworth, and M. W. Woolrich, “Probabilistic diffusion tractography with multiple fibre orientations: what can we gain?” NeuroImage, vol. 34, no. 1, pp. 144–155, 2007.
- T. E. J. Behrens, M. W. Woolrich, M. Jenkinson et al., “Characterization and propagation of uncertainty in diffusion-weighted MR imaging,” Magnetic Resonance in Medicine, vol. 50, no. 5, pp. 1077–1088, 2003.
- O. Ciccarelli, A. T. Toosy, G. J. M. Parker et al., “Diffusion tractography based group mapping of major white-matter pathways in the human brain,” NeuroImage, vol. 19, no. 4, pp. 1545–1555, 2003.
- M. Jenkinson and S. Smith, “A global optimisation method for robust affine registration of brain images,” Medical Image Analysis, vol. 5, no. 2, pp. 143–156, 2001.
- I. L. H. Choo, D. Y. Lee, J. S. Oh et al., “Posterior cingulate cortex atrophy and regional cingulum disruption in mild cognitive impairment and Alzheimer's disease,” Neurobiology of Aging, vol. 31, no. 5, pp. 772–779, 2010.
- K. Kiuchi, M. Morikawa, T. Taoka et al., “Abnormalities of the uncinate fasciculus and posterior cingulate fasciculus in mild cognitive impairment and early Alzheimer's disease: a diffusion tensor tractography study,” Brain Research, vol. 1287, pp. 184–191, 2009.
- F. Agosta, M. Pievani, S. Sala et al., “White matter damage in Alzheimer disease and its relationship to gray matter atrophy,” Radiology, vol. 258, no. 3, pp. 853–863, 2011.