Diffusion tensor imaging of the brain in patients with Alzheimer’s disease and cerebrovascular lesions

Diffusion tensor imaging of the brain in patients with Alzheimer’s disease and cerebrovascular lesions 1 first-author †E-mail:csq_q@yahoo.com †E-mail:csq_q@yahoo.com csq_q@yahoo.com 1 2 1 1 Department of Radiology, the Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510630, China Department of Radiology, the Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510630, China Department of Rehabilitation, the Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510630, China Department of Rehabilitation, the Third Affiliated Hospital, Sun Yat-Sen University, Guangzhou 510630, China Background: 2 Recent autopsy study showed a high incidence of cerebrovascular lesions in Alzheimer’s disease (AD). To assess the impact of cerebrovascular pathology in AD, we used diffusion tensor imaging (DTI) to study AD patients with and without cerebrovascular lesions. Materials and Methods: 2 Conventional and DTI scans were obtained from 10 patients with probable AD, 10 AD/V patients (probable AD with cerebrovascular lesions) and ten normal controls. Mean diffusivity ( D ) and fractional anisotropy ( FA ) values of some structures involved with AD pathology were measured. Results: 2 D value was higher in AD patients than in controls in hippocampus and the cingulate gyrus. In AD/V patients, increased D value was found in the same structures and also in the thalamus and basal ganglia compared to controls. There was a significant difference of D value between AD and AD/V patients. FA value reduced in the white matter of left inferior temporal gyrus and in the bilateral middle cingulate gyrus in patients with AD/V compared with controls. The MMSE (mini-mental state examination) score significantly correlated with FA value in the right hippocampus ( r =0.639, P < 0.019), in the right anterior cingulate gyrus ( r =0.587, P < 0.035) and in left parahippocampal gyrus ( r =0.559, P < 0.047). Conclusion: 2 Cerebrovascular pathology had stronger impact on the D value than the AD pathology alone did. Elevated D value in thalamic and basal ganglia may contribute to cognitive decline in AD/V patients. Reduced FA values in AD/V patients may indicate that cerebrovascular pathology induced more severe white matter damage than the AD pathology alone did. Diffusion tensor imaging (DTI) Alzheimer’s disease (AD) Cerebrovascular Magnetic resonance imaging (MRI) INTRODUCTION 1 Diffusion tensor imaging (DTI) is a magnetic resonance imaging (MRI) technique that can be used to characterize the orientational properties of the diffusion process of water molecules (Basser et al., 1994a 1994a ). Application of this technique to the brain has been demonstrated to provide exceptional information on white matter architecture. Usually, the information is conveyed into two types of parameters: mean diffusivity ( D ) which is a measure of the average molecular motion independent of any tissue directionality and is affected by cellular size and integrity (Basser et al., 1994b 1994b ; Pierpaoli et al., 1996 1996 ), and the fractional anisotropy ( FA ), which is one of the most used measures of deviation from isotropy and reflects the degree of alignment of cellular structures within fiber tracts, as well as their structural integrity (Basser and Pierpaoli, 1996 1996 ). Alzheimer’s disease (AD), a progressive neurodegenerative disorder, is the most common cause of dementia in the elderly. Pathological changes originate in the medial temporal region, in the entorhinal cortex and hippocampus, subsequently spreading over the entire limbic cortex and then into neocortical association areas (Braak and Braak, 1998 1998 ). Prior studies showed that there were higher D values in the hippocampi, the temporal stem, the cingulum, the corpus callosum, the centrum semiovale, and the frontal, temperal, occipital and parietal white matter of AD patients than in controls (Kantarci et al., 2001 2001 ; Fellgiebel et al., 2004 2004 ; Bozzali et al., 2002 2002 ; Naggara et al., 2006 2006 ; Xie et al., 2006 2006 ; Muller et al., 2005 2005 ). There were lower FA values in the hippocampus, in the corpus callosum, in the cingulum, in the white matter of the frontal, temporal and parietal lobes of AD patients than in controls (Fellgiebel et al., 2004 2004 ; Bozzali et al., 2002 2002 ; Naggara et al., 2006 2006 ; Xie et al., 2006 2006 ; Takahashi et al., 2002 2002 ). Cerebrovascular lesions in AD were not assessed in these prior studies. Recent autopsy studies showed high incidence of cerebrovascular lesions in AD. One study of 730 consecutive cases of AD autopsy reported cerebrovascular pathology in 48% of those AD cases. In particular, minor to moderate cerebrovascular lesions (lacunes, amyloid angiopathy with or without lacunes) were observed in 31.6% of cases and major cerebrovascular lesions (old and recent infarcts and hemorrhages) in 16.7% of cases (Jellinger and Mitter-Ferstl, 2003 2003 ). A population-based longitudinal study on people over 75 also led to the same conclusion (Agüero-Torres et al., 2006 2006 ). In order to clarify whether the elevated D values and reduced FA values were associated with the cerebrovascular pathology in AD, we investigated 20 probable AD (ten AD patients without cerebrovascular lesions and ten AD patients with cerebrovascular lesions) and ten normal controls by using DTI. We focused on the regions involved with the AD pathology (white matter of inferior temporal gyrus; anterior, middle and posterior cingulate gyrus; hippocampus, parahippocampal gyrus and amygdale; lentiform nucleus; caudate nucleus; anterior thalamus and dorsal medial of the thalamus). The D and FA values of those regions were measured. MATERIALS AND METHODS 1 Subject 2 All subjects gave their informed consent prior to their inclusion in this study. We studied 20 patients with probable AD. The patients were divided into two groups: pure AD (AD without cerebrovascular lesions) and AD/V (AD with cerebrovascular lesions). The pure AD group included 6 women and 4 men (mean age 71 years). The AD/V group included 5 women and 5 men (mean age 74 years). The National Institute of Neurological and Communicative Disorders and Stroke/Alzheimer’s Disease and Related Disorders Association (NINCDS/ADRDA) criteria was used for the diagnosis of clinically probable AD. Cases that satisfied criteria for probable AD and have multiple infarcts or lacunes observed on T2 and/or T2 FLAIR (fluid-attenuated inversion recovery) sequence MRI were classified as AD/V. Patients who have no multiple infarcts or lacunes observed were classified as pure AD. Ten healthy controls (6 women, 4 men; mean age 70 years) were recruited. The age difference between controls and patients was not statistically significant. The controls had no complaints of cognitive problems and no evidence of cognitive deficits on formal testing. Major systemic, psychiatric, and other neurological illnesses were carefully investigated and excluded in all subjects. Sudden onset and vascular risk factors were carefully investigated and excluded in the AD/V cases. MRI was normal in all control subjects except aging atrophy of the brain. Neuropsychological tests 2 Mini-mental state examination (MMSE) was used to assess cognitive function for each patient. Three AD and three AD/V patients were severely demented ( MMSE ≤10), five AD and five AD/V patients were moderately demented ( MMSE =11~20), and two AD and two AD/V patients was mildly demented ( MMSE ≥21). All controls were of the normal degree ( MMSE =28~30). MRI acquisition 2 MRI was obtained by using a 1.5-T Vision MRI system (GE Signa Twinspeed, USA). A standard (8HRBRAIN) head coil was used. Prior to DTI, all subjects underwent T2 FLAIR sequence: repetition time ( TR ) 8802 ms, echo time ( TE ) 120 ms, matrix 512×512, field of view (FOV) 240 mm, 5 mm thickness, and 1 mm gap. DTI data were acquired by using a single-shot, diffusion weighted echo-planar imaging sequence ( TR =8000 ms, TE =80 ms). The imaging matrix was 128×128, with a field of view of 246 mm×246 mm. Transverse sections of 3-mm thickness were acquired parallel to the anterior commissure-posterior commissure line. Coronal sections were angulated, perpendicular to the anterior commissure-posterior commissure line. Scan sections covered the entire hemisphere and brainstem without gaps. Diffusion weighting was encoded along 25 independent orientations, and the b value was 1000 s/mm 2 . The acquisition time per dataset was approximately 9 min. The DTI datasets were transferred to a workstation and processed by using functool LX software. D and FA were measured in different region which were carefully selected on the dual echo scans to avoid partial volume averaging from the CSF (cerebrospinal fluid). Regions of interest (ROIs) were range 20~60 mm 2 . The selected areas appeared normal on T2 image and avoided vascular lesions. The following areas were measured bilaterally: the white matter of inferior temporal gyrus; anterior, middle and posterior cingulate gyrus; hippocampus, parahippocampal gyrus and amygdale; lentiform nucleus; caudate nucleus; anterior thalamus and dorsal medial thalamus (Figs. 1a~1c 1a~1c ). ROIs for measurement of D and FA indices: 1=hippocampus; 2=amygdale Statistical analysis 2 Non-parametric Mann-Whitney U tests were used to compare D and FA values measured from patients and healthy controls. The correlations between D values, FA values and the MMSE scores were investigated using Spearman Rank Correlation Coefficient. RESULTS 1 D were significantly higher in the bilateral hippocampus and right posterior cingulate gyrus from pure AD patients than in the corresponding regions from healthy controls (Table 1 1 ). D were also significantly higher in the left hippocampus, in the bilateral dorsal medial thalamus and anterior thalamus, as well as in the right anterior and middle cingulate gyrus, in the right caudate nucleus, in the bilateral lentiform nucleus from patients with AD/V than in the corresponding regions from healthy controls (Table 1 1 ). D values in pure AD patients differ significantly from those in AD/V in the bilateral dorsal medial thalamus and anterior thalamus, as well as in the right anterior and middle cingulate gyrus, in the right caudate nucleus, in the right lentiform nucleus (Table 1 1 ). FA were significantly lower in the white matter of left inferior temporal gyrus and in the bilateral middle cingulate gyrus from patients with AD/V than in the corresponding regions from healthy controls (Table 2 2 ). There were no significant differences in FA between pure AD patients and controls (Table 2 2 ). The MMSE score significantly correlated with FA value in the right hippocampus ( r =0.639, P < 0.019), in the right anterior cingulate gyrus ( r =0.587, P < 0.035) and left parahippocampal gyrus ( r =0.559, P < 0.047). Note: Mann-Whitney U tests for non-parametric data; Co: Controls 2 3 D (m 2 ·s −1 ×10 −10 ) 3 P values Pure AD AD/V Co AD vs Co AD/V vs Co AD vs AD/V Left hippocampus 8.46 (0.88) 9.15 (0.66) 7.76 (0.33) 0.027 0.005 0.079 Right hippocampus 8.55 (0.89) 8.71 (1.15) 7.94 (0.91) 0.046 0.106 0.661 Left dorsal medial thalamus 7.06 (0.38) 8.46 (1.07) 6.87 (0.24) 0.563 0.007 0.008 Right dorsal medial thalamus 7.01 (0.49) 8.01 (0.65) 6.99 (0.24) 0.954 0.019 0.019 Left anterior thalamus 7.05 (0.32) 8.71 (1.49) 7.13 (0.29) 0.372 0.014 0.027 Right anterior thalamus 7.04 (0.27) 7.88 (0.65) 6.98 (0.35) 0.808 0.023 0.014 Right anterior cingulated gyrus 7.52 (0.41) 8.21 (0.55) 7.41 (0.25) 0.529 0.008 0.048 Right middle cingulated gyrus 6.66 (0.27) 7.23 (0.44) 6.63 (0.30) 0.793 0.040 0.023 Right posterior cingulated gyrus 7.25 (0.79) 7.13 (0.54) 6.66 (0.24) 0.046 0.188 0.884 Right audate nucleus 7.00 (0.57) 9.69 (2.39) 7.01 (0.09) 0.862 0.004 0.008 Left lenticular nucleus 6.52 (0.28) 7.85 (0.93) 6.47 (0.24) 0.487 0.042 0.057 Right lenticular nucleus 6.75 (0.67) 8.12 (1.00) 6.46 (0.36) 0.325 0.008 0.027 Note: Mann-Whitney U tests for non-parametric data; Co: Controls 2 3 FA 3 P values Pure AD AD/V Co AD vs Co AD/V vs Co AD vs AD/V Left middle cingulated gyrus 0.505 (0.09) 0.400 (0.06) 0.515 (0.08) 0.753 0.010 0.057 Right middle cingulated gyrus 0.472 (0.06) 0.395 (0.11) 0.515 (0.06) 0.189 0.013 0.143 Left inferior temporal gyrus 0.280 (0.06) 0.245 (0.02) 0.286 (0.04) 0.600 0.048 0.188 In AD/V patients, infarcts and lacunes were detected in the cortical and/or subcortical area of frontal lobe, temperal lobe and parietal lobe, in the basic ganglia, in the centrum semiovale and in the external capsule, and also white matter hyperintensity were detected on T2 FLAIR sequence MRI. DISCUSSION 1 Several studies showed that D value of the hippocampus and posterior cingulate gyrus were significantly higher in patients with AD than in normal control subjects (Kantarci et al., 2001 2001 ; Fellgiebel et al., 2004 2004 ; Rose et al., 2000 2000 ). Our findings are in agreement with those in prior studies. It was postulated that this increase in D value reflects loss of neural cell, decreased fiber density, including the disruption and loss of axonal membranes or myelin (Kantarci et al., 2001 2001 ). In the prior DTI studies on AD patients, impact of cerebrovascular pathology was not discussed. Our data showed D value differs not only between patients with AD/V and controls, but also between AD group and AD/V group. The different D value of these two groups is not caused by the severity of the disease because the patients in AD and AD/V groups are chosen in proportion according to the severity of their cognitive dysfunction. The significant elevated D values in AD/V patients might be due to the synergistic impact of AD pathology and cerebrovascular pathology. Autopsy study showed AD with vascular lesions cases had less severe AD pathology than those with AD alone (Riekse et al., 2004 2004 ). Recent studies showed lower density of plaques and tangles in brains with cerebrovascular lesions (Jellinger, 2002 2002 ). Thus in AD/V patients elevated D would be due to other changes than those associated to AD pathology. D value from AD/V patients is significantly higher than that from pure AD patients, which may indicate cerebrovascular pathology had stronger impact on D value than AD pathology alone did. Primary infarct and lacunes could demonstrate large elevated D values and reduced FA values that would confound the results, so we avoided these areas when we measure D value and FA value. Nevertheless infarct in AD/V could cause anterograde degeneration of the fibre pathways. Neuropathological studies indicated lacunes and demyelination often co-exist (95% of cases with lacunes had white matter demyelination) (Gold et al., 2005 2005 ). The disruption of myelin and axons might be expected to increase the mean diffusivity of water molecules. In addition, the microvascular change might also contribute to higher D values. Microvascular changes with decreased density and structural abnormalities causing regional metabolic and blood-brain barrier dysfunctions with ensuing neuronal damage would lead to increased diffusion of water molecules. Morphological substrates of cognitive decline associated with cerebrovascular disease are still strongly debated. In the cardiovascular health study, 23% of individuals older than age 65 had MRI evidence of lacunes; however, 89% were essentially clinically silent from a cognitive point of view. However, neuropathological studies indicated that small macroinfarcts and even microscopic ischemic lesions can lead to dementia. In a recent autopsy study of 72 cases, the researchers found thalamic and basal ganglia but not deep white matter lacunes are independent predictors of cognitive decline. They suggested the importance of location in defining the cognitive impact of lacunes (Gold et al., 2005 2005 ). In the present data, the elevated D value in the thalamic and basal ganglia in AD/V patients may contribute to dementia progress. Reduced FA value found in the white matter of left inferior temporal gyrus, in the bilateral middle cingulate gyrus from patients with AD/V indicated disturbed integrity of white matter tracts in this region. This alteration might be due to the breakdown of the myelin sheath and disintegration of axonal microfilaments caused by Wallerian degeneration. In pure AD patients FA did not differ from that in controls. Prior studies showed decreased FA in various regions of the brain in AD patients (Fellgiebel et al., 2004 2004 ; Bozzali et al., 2002 2002 ; Naggara et al., 2006 2006 ; Xie et al., 2006 2006 ; Takahashi et al., 2002 2002 ), but the regions detected with decreased FA were different in different studies. There are some reasons for the discrepancy between findings in the prior studies and our study. One reason is that we did not measure D and FA in some structures such as the corpus callosum and the frontal and parietal white matter. Second, the small group size of our data and prior studies might cause different results. Third, the figures in some of those studies showed multiple infarcts, lacunar, as well as white matter hyperintensity and even the selected areas measured for D values and FA value showed hyperintensity on T2 image (Fellgiebel et al., 2004 2004 ; Bozzali et al., 2002 2002 ; Rose et al., 2000 2000 ). We speculate that the results of these reports might reflect mixing changes due to cerebrovascular and pure AD pathology. The cerebrovascular damage might cause the differences, because cerebrovascular lesions are usually sporadic and asymmetric. Our results may suggest that AD with cerebrovascular pathology have more severe white matter damage. The correlations found between the MMSE score and FA value in the right hippocampus, in the left parahippocampal gyrus and in the right anterior cingulate gyrus suggested that damage of these structures contribute to the cognitive impairment of AD. These findings are consistent with prior observations (Petrella et al., 2003 2003 ). In conclusion, cerebrovascular pathology had stronger impact on the D value than the AD pathology alone did. Elevated D value in thalamic and basal ganglia may contribute to cognitive decline in AD/V patients. Reduced FA values in AD/V patients may indicate that cerebrovascular pathology induced more severe white matter damage than the AD pathology alone did. Damage of the right hippocampus, the left parahippocampal gyrus and the right anterior cingulate gyrus may contribute to the cognitive impairment of AD patients. This conclusion is limited by the small number of enrolled patients and controls. Future studies of largescale sample have to be done to examine the relationship of DTI changes to pathology of AD. References H Agüero-Torres , M Kivipelto , E von Strauss . Rethinking the dementia diagnoses in a population-based study: what is Alzheimer’s disease and what is vascular dementia? A study from the Kungsholmen Project . Dement Geriatr Cogn Disord , 2006 . 22 ( 3 ): 244 - 249 . 16902279 DOI: 10.1159/000094973 http://doi.org/10.1159/000094973 . Rethinking the dementia diagnoses in a population-based study: what is Alzheimer’s disease and what is vascular dementia? A study from the Kungsholmen Project PJ Basser , C Pierpaoli . Microstructural features measured using diffusion tensor imaging . J Magn Reson B , 1996 . 111 ( 3 ): 209 - 219 . 8661285 DOI: 10.1006/jmrb.1996.0086 http://doi.org/10.1006/jmrb.1996.0086 . Microstructural features measured using diffusion tensor imaging PJ Basser , J Mattiello , D Le Bihan . MR diffusion tensor spectroscopy and imaging . Biophys J , 1994 . 66 ( 1 ): 259 - 267 . 8130344 . MR diffusion tensor spectroscopy and imaging PJ Basser , J Mattiello , D Le Bihan . Estimation of the effective self-diffusion tensor from the NMR spin-echo . J Magn Reson B , 1994 . 103 ( 3 ): 247 - 254 . 8019776 DOI: 10.1006/jmrb.1994.1037 http://doi.org/10.1006/jmrb.1994.1037 . Estimation of the effective self-diffusion tensor from the NMR spin-echo M Bozzali , A Falini , M Franceschi , M Cercignani , M Zuffi , G Scotti , G Comi , M Filippi . White matter damage in Alzheimer’s disease assessed in vivo using diffusion tensor magnetic resonance imaging . J Neurol Neurosurg Psychiatry , 2002 . 72 ( 6 ): 742 - 746 . 12023417 DOI: 10.1136/jnnp.72.6.742 http://doi.org/10.1136/jnnp.72.6.742 . White matter damage in Alzheimer’s disease assessed in vivo using diffusion tensor magnetic resonance imaging H Braak , E Braak . Evolution of neuronal changes in the course of Alzheimer’s disease . J Neural Transm Suppl , 1998 . 53 127 - 140 . 9700651 . Evolution of neuronal changes in the course of Alzheimer’s disease A Fellgiebel , P Wille , MJ Müller , G Winterer , A Scheurich , G Vucurevic , LG Schmidt , P Stoeter . Ultrastructural hippocampal and white matter alterations in mild cognitive impairment: a diffusion tensor imaging study . Dement Geriatr Cogn Disord , 2004 . 18 ( 1 ): 101 - 108 . 15087585 DOI: 10.1159/000077817 http://doi.org/10.1159/000077817 . Ultrastructural hippocampal and white matter alterations in mild cognitive impairment: a diffusion tensor imaging study G Gold , E Kovari , FR Herrmann , A Canuto , PR Hof , JP Michel , C Bouras , P Giannakopoulos . Cognitive consequences of thalamic, basal ganglia, and deep white matter lacunes in brain aging and dementia . Stroke , 2005 . 36 ( 6 ): 1184 - 1188 . 15891000 DOI: 10.1161/01.STR.0000166052.89772.b5 http://doi.org/10.1161/01.STR.0000166052.89772.b5 . Cognitive consequences of thalamic, basal ganglia, and deep white matter lacunes in brain aging and dementia KA Jellinger . Alzheimer disease and cerebrovascular pathology: an update . J Neural Transm , 2002 . 109 ( 5-6 ): 813 - 836 . 12111471 DOI: 10.1007/s007020200068 http://doi.org/10.1007/s007020200068 . Alzheimer disease and cerebrovascular pathology: an update KA Jellinger , E Mitter-Ferstl . The impact of cerebrovascular lesions in Alzheimer disease—a comparative autopsy study . J Neurol , 2003 . 250 ( 9 ): 1050 - 1055 . 14504965 DOI: 10.1007/s00415-003-0142-0 http://doi.org/10.1007/s00415-003-0142-0 . The impact of cerebrovascular lesions in Alzheimer disease—a comparative autopsy study K Kantarci , CRJr Jack , YC Xu , NG Campeau , PC O′Brien , GE Smith , RJ Ivnik , BF Boeve , E Kokmen , EG Tangalos , 等 . Mild cognitive impairment and Alzheimer disease: regional diffusivity of water . Radiology , 2001 . 219 ( 1 ): 101 - 107 . 11274543 . Mild cognitive impairment and Alzheimer disease: regional diffusivity of water MJ Muller , D Greverus , PR Dellani , C Weibrich , PR Wille , A Scheurich , P Stoeter , A Fellgiebel . Functional implications of hippocampal volume and diffusivity in mild cognitive impairment . Neuroimage , 2005 . 28 ( 4 ): 1033 - 1042 . 16084115 DOI: 10.1016/j.neuroimage.2005.06.029 http://doi.org/10.1016/j.neuroimage.2005.06.029 . Functional implications of hippocampal volume and diffusivity in mild cognitive impairment O Naggara , C Oppenheim , D Rieu , N Raoux , S Rodrigo , G Dalla Barba , JF Meder . Diffusion tensor imaging in early Alzheimer’s disease . Psychiatry Res , 2006 . 146 ( 3 ): 243 - 249 . 16520023 . Diffusion tensor imaging in early Alzheimer’s disease JR Petrella , RE Coleman , PM Doraiswamy . Neuroimaging and early diagnosis of Alzheimer disease: a look to the future . Radiology , 2003 . 226 ( 2 ): 315 - 336 . 12563122 . Neuroimaging and early diagnosis of Alzheimer disease: a look to the future C Pierpaoli , P Jezzard , PJ Basser , A Blarnett , G Di Chiro . Diffusion tensor MR imaging of the human brain . Radiology , 1996 . 201 ( 3 ): 637 - 648 . 8939209 . Diffusion tensor MR imaging of the human brain RG Riekse , JB Leverenz , W McCormick , JD Bowen , L Teri , D Nochlin , K Simpson , C Eugenio , EB Larson , D Tsuang . Effect of vascular lesions on cognition in Alzheimer’s disease: a community-based study . J Am Geriatr Soc , 2004 . 52 ( 9 ): 1442 - 1448 . 15341544 DOI: 10.1111/j.1532-5415.2004.52405.x http://doi.org/10.1111/j.1532-5415.2004.52405.x . Effect of vascular lesions on cognition in Alzheimer’s disease: a community-based study SE Rose , F Chen , JB Chalk , FO Zelaya , WE Strugnell , M Benson , J Semple , DM Doddrell . Loss of connectivity in Alzheimer’s disease: an evaluation of white matter tract integrity with colour coded MR diffusion tensor imaging . J Neurol Neurosurg Psychiatry , 2000 . 69 ( 4 ): 528 - 530 . 10990518 DOI: 10.1136/jnnp.69.4.528 http://doi.org/10.1136/jnnp.69.4.528 . Loss of connectivity in Alzheimer’s disease: an evaluation of white matter tract integrity with colour coded MR diffusion tensor imaging S Takahashi , H Yonezawa , J Takahashi , M Kudo , T Inoue , H Tohgi . Selective reduction of diffusion anisotropy in white matter of Alzheimer disease brains measured by 3.0 Tesla magnetic resonance imaging . Neurosci Lett , 2002 . 332 ( 1 ): 45 - 48 . 12377381 DOI: 10.1016/S0304-3940(02)00914-X http://doi.org/10.1016/S0304-3940(02)00914-X . Selective reduction of diffusion anisotropy in white matter of Alzheimer disease brains measured by 3.0 Tesla magnetic resonance imaging S Xie , JX Xiao , GL Gong , YF Zang , YH Wang , HK Wu , XX Jiang . Voxel-based detection of white matter abnormalities in mild Alzheimer disease . Neurology , 2006 . 66 ( 12 ): 1845 - 1849 . 16801648 DOI: 10.1212/01.wnl.0000219625.77625.aa http://doi.org/10.1212/01.wnl.0000219625.77625.aa . Voxel-based detection of white matter abnormalities in mild Alzheimer disease This work complies with the current laws of the People’s Republic of China. The work has got the approval of the Ethics Committee. 10.1631/jzus.2007.B0242 2006-05-28 2006-10-30 2022-01-05 Copyright © 2007, Journal of Zhejiang University Science 2007 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 04 08