Anatomical and functional deficits have been studied in patients with amnestic mild cognitive impairment (MCI). However, it is unclear whether and how the anatomical deficits are related to the functional alterations. Present study aims to characterize the association between anatomical and functional deficits in MCI patients.
Seventeen amnestic MCI patients and 18 healthy aging controls were scanned using a T1 Weighted MPRAGE sequence and a gradient-echo echo-planar imaging sequence. Clinical severity of MCI patients was evaluated by using Clinical Dementia Rating, Mini Mental State Examination (MMSE), Clock Drawing Test, Auditory Verbal Learning Test and Activities of Daily Living. VBM with DARTEL was used to characterize the gray matter deficits in MCI. Regional amplitude of low-frequency (0.01–0.08 Hz) fluctuations (ALFF) was used to evaluate regional functional alteration in MCI and fractional ALFF(fALFF) in slow 4 (0.027–0.073 Hz) and slow 5 (0.01–0.027 Hz) were also calculated.
Significantly decreased gray matter volume (GMV) was observed in amnestic MCI group mainly in bilateral prefrontal, left temporal and posterior cingulate cortex. Significant positive correlation was observed between the GMV in left inferior frontal gyrus and MMSE scores. Interestingly, decreased ALFF/fALFF was revealed in MCI group compared to controls mainly in prefrontal, left parietal regions and right fusiform gyrus, while the increased ALFF/fALFF was found in limbic and midbrain. Furthermore, the changes of fALFF in MCI in the slow-5 band were greater than those in the slow-4. No significant correlation was found between the morphometric and functional results.
Findings from the study document that wide spread brain volume reduction accompanied with decreased and increased regional function in MCI, while the anatomical and functional changes were independently. Therefore, the combination of structural and functional MRI methods would provide complementary information and together advance our understanding of the pathophysiology underlying the symptoms of MCI.
Citation: Han Y, Lui S, Kuang W, Lang Q, Zou L, et al. (2012) Anatomical and Functional Deficits in Patients with Amnestic Mild Cognitive Impairment. PLoS ONE 7(2): e28664. doi:10.1371/journal.pone.0028664
Editor: Carlos Soriano-Mas, Institut d'Alta Tecnologia-PRBB, Spain
Received: August 11, 2011; Accepted: November 12, 2011; Published: February 3, 2012
Copyright: © 2011 Han et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by National Natural Science Foundation (Grant Nos. 30970823, 30830045, 30900361), the Distinguished Young Scholars of Sichuan (Grant No. 2011JQ0005), the Programs for New Century Excellent Talents in University (Grant No. NCET-10-0596) and Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20090181120103). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Mild cognitive impairment (MCI) is always being recognized as a transitional state between normal aging and dementia, and revealing the cerebral deficits of MCI would help neurologists in earlier detection and treatment of dementia . Although past morphometry and functional MRI studies – have revealed independent anatomical and functional deficits mainly in frontal, temporal and limbic regions in patients with MCI, one important issue arises recently as to whether and how the anatomical deficits are related to the functional alterations. In patients with dementia, a strict relationship between hypometabolism and gray matter atrophy was observed . However, inconsistent distributions between structural , , – and metabolic changes ,  have been found in patients with MCI by independent studies of anatomy and function. Only a few studies used anatomical and functional methods in combination in MCI, and the results were inconsistent. A previous study  of 21 patients with MCI revealed dissociation of gray matter atrophy and hypometabolism by combination of MRI and positron emission tomography (PET), while our recent resting state fMRI study reported both increased and decreased regional function, which were not significantly influenced by the gray matter loss in the MCI patients . Two recent studies combined anatomic MRI and resting state fMRI in MCI patients, and demonstrated dissociation of gray matter atrophy and altered functional connectivity , . These studies implicated that deficits of MCI arise from systems-level disturbances of both anatomy and function and there is a complicate relationship between the deficits of cerebral anatomy and functional alteration.
In recent years, voxel based morphometry (VBM) is becoming a spatially specific and unbiased method for exploring regional gray matter volume which has already been successfully applied to schizophrenia, , dementia  and MCI . For functional analysis, “resting state” fMRI not only avoids performance confounds  but is easier to implement in the context of clinical studies to assess resting state brain physiology than PET/Single-photon emission computed tomography (SPECT), due to its lower cost, greater availability and non-invasiveness . Spontaneous low-frequency blood-oxygen-level-dependent (BOLD) fluctuations have been observed by fMRI during the “resting” state in both human and animal models. These signals bear numerous similarities to fluctuations in neurophysiological, hemodynamic and metabolic parameters . Both animal  and human studies ,  indicated that the regional amplitude of low-frequency fluctuations (0.01–0.08 Hz; ALFF) reflects spontaneous synchronous neural activity during resting state fMRI studies. Such metric was found reliable and could be used to characterize the regional functional changes in patients . Two kinds of parameters could be used to evaluate the regional amplitude of low-frequency fluctuations, i.e., ALFF and fractional ALFF(fALFF). ALFF measures the total power of a given time course within a specific frequency range , and fALFF measures the power within a specific frequency range divided by the total power in the entire detectable frequency range . Han et al.  had revealed that the changes of ALFF/fALFF in MCI in the slow-5 band (0.01–0.027 Hz) were greater than those in the slow-4 (0.027–0.073 Hz) which suggest the pattern of intrinsic brain activity of MCI is sensitive to specific frequency bands.
Thus, the present study was designed to 1) identify regional gray matter deficits and alteration of ALFF/fALFF in drug-naïve patients with MCI; and 2) to investigate the relationship between the deficits of gray matter volume and functional alteration, as well as their association with clinical symptoms.
Compared to the control group, the MCI group showed significantly decreased GMV mainly in bilateral prefrontal, left temporal and posterior cingulate cortex (Table 1, Figure 1). Left middle frontal gyrus survived even after family wised error correction (p = 0.047, corrected with FDR). No significant increase in GMV was found in the MCI group compared to healthy controls. For validating the GMV results, the voxel-wise reproducibility map was generated (Information S1). Overall, our findings exhibited high reproducibility (p<0.01, degree of freedom = 30). Specifically, left inferior frontal gyrus demonstrated the highest reproducibility across validation analyses.
Figure 1. VBM analysis revealed decreased gray matter volume in MCI group compared to controls.
Compared to the control group, the MCI group showed significantly decreased GMV (blue region) in mainly in bilateral prefrontal, left temporal and posterior cingulate cortex.doi:10.1371/journal.pone.0028664.g001
Table 1. VBM analysis revealed decreased gray matter volume in MCI group compared to controls.doi:10.1371/journal.pone.0028664.t001
Significant positive correlation was observed between the GMV in left inferior frontal gyrus and MMSE scores (r = 0.81, p = 0.026). No significant correlation was found between the GMV of the other regions and the clinical symptom severity.
Interestingly, both increased and decreased regional function was revealed in MCI group in relative to controls (Figure 2). The decreased ALFF were observed mainly in bilateral prefrontal, left parietal regions and right fusiform gyrus, while the increased ALFF were mainly found in limbic regions and midbrain (Table 2). ALFF analysis for slow 4 [0.027–0.073 Hz] and slow 5 [0.01–0.027 Hz] band also revealed decreased ALFF in cingulate cortex, prefrontal cortex, occipital regions and the bilateral parietal regions, while increased ALFF was observed in superior temporal gyrus, limbic regions and midbrain (Information S1). Furthermore, the changes of ALFF in MCI in the slow-5 band were greater than those in the slow-4. However, such alteration did not correlated with any of the clinical symptom severity.
Figure 2. ALFF analysis revealed regional functional alteration in MCI group compared to controls.
Compared to the control group, both increased and decreased regional function was revealed in MCI group in relative to controls.doi:10.1371/journal.pone.0028664.g002
Table 2. ALFF analysis revealed both increased and decreased regional function in MCI group compared to controls.doi:10.1371/journal.pone.0028664.t002
Global ALFF for slow 4 and slow 5 between MCI and controls were not significant (p = 0.34 for slow 4, p = 0.12 for slow 5). Leave-one-out reproducibility analysis were also did for all above ALFF analysis and all results showed high reproducibility (p<0.01, degree of freedom = 25), especially for left superior parietal lobule which demonstrated the highest reproducibility across validation analyses (Information S1).
We compared the fALFF between MCI and controls and found that the MCI group showed wide spread decreased fALFF mainly in bilateral medial/dorsallateral prefrontal cortex, cingulate gyrus, occipital regions and left cerebellum. Increased fALFF was revealed only in brain stem regions. Compared with ALFF findings, fALFF revealed more regions with decreased activity, while less regions with increased activity (Information S1). fALFF analysis for slow 4 [0.027–0.073 Hz] and slow 5 [0.01–0.027 Hz] band also revealed decreased fALFF in cingulate cortex, prefrontal cortex, occipital regions and the bilateral parietal regions, while increased fALFF was observed in superior temporal gyrus, limbic regions and midbrain (Information S1). Furthermore, the changes of fALFF in MCI in the slow-5 band were greater than those in the slow-4 (Information S1). However, no overlap nor inter-subject correlation was observed between the fALFF and GMV alternations. Global fALFF for slow 4 and slow 5 between MCI and controls were not significant (p = 0.44 for slow 4, p = 0.27 for slow 5). Leave-one-out reproducibility analysis were also did for all above fALFF analysis and all results showed high reproducibility (p<0.01, degree of freedom = 27), especially for right fusiform gyrus which demonstrated the highest reproducibility across validation analyses (Information S1).
Association between morphometric and functional findings
No significant correlation was found between the GMV and ALFF/fALFF in patient group. Though the decreased ALFF in the right middle frontal gyrus and left inferior frontal gyrus were found quite near the decreased GMV in the same region (Figure 3.), there was no overlapping between the ALFF/fALFF and GMV results, and the ALFF/fALFF in these regions did not correlate with the GMV.
Figure 3. Overlap between the morphometric (red regions) and functional (blue regions) results.
Though the decreased ALFF in the right middle frontal gyrus and left inferior frontal gyrus (Within red circle) were found quite near the decreased GMV in the same region, the ALFF in these regions did not correlate with the GMV.doi:10.1371/journal.pone.0028664.g003
The present study examined both anatomical and functional abnormalities in a cohort of drug-naïve MCI patients. Reductions in gray matter volume were observed mainly in the prefrontal, left temporal and posterior cingulate cortex (Figure 1), and volume reduction in the left inferior frontal gyrus was related to the severity of symptom. The regional functional alteration included decreased regional functional mainly in prefrontal, left parietal regions and right fusiform gyrus, while the increased regional functional in limbic and midbrain (Figure 2). However, there is no correlation between morphometric and functional deficits, suggesting an independent alteration of morphometry and function at the transitional state between normal aging and dementia.
Consistent with previous studies –, , , , widespread cortical atrophy was found especially in the bilateral frontal lobe, the left temporal gyrus and posterior cingulate cortex. Furthermore, the decreased GMV in the left middle frontal gyrus survived even after family wised error correction (p = 0.047, corrected with FDR). In fact, all these areas are regions typically involved by AD related pathology, as shown by previous MRI , , ,  and PET ,  studies, and the gray matter atrophy in the prefrontal and posterior cingulate cortex were even thought to predict the cognitive decline in MCI patients as revealed by longitudinal VBM studies , . However, we did not find more GMV reduction, especially in the hippocampus which has been the most studied area in MCI cases. In fact, more and more recent studies have shown that structural lesions (eg, neurofibrillary tangles, neuritic plaques) associated with the MCI syndrome are not restricted to hippocampus, but also included the cortical areas . Recent study in patients with mild AD even revealed amyloid deposits in the frontal and parietal lobes instead of the medial temporal lobe structures . Consistent with these findings, our results confirmed the gray matter deficits in the frontal and posterior cingulate cortex in a cohort of drug-naïve MCI patients, suggesting a more diffused cortical deficits than previously thought in MCI.
Furthermore, the decreased volume in the left inferior frontal gyrus was found to be related to the severity of clinical symptom, as measured by the MMSE. The left inferior frontal gyrus has been implicated as an important part in the pathology of MCI, which was thought to be associated with attention and memory processes, including encoding and retrieval and long- and short-term memory –. Increased activation in the left inferior frontal gyrus was associated with improved memory processing in subjects with MCI as revealed in a recent double-blind placebo-controlled fMRI study . However, previous study only has reported positive correlation between the MMSE and the volume of right inferior frontal gyrus . Our results extended previous findings by suggesting that the severity of atrophy in the left inferior frontal gyrus could also be used to evaluate the clinical severity in MCI patients.
Interestingly, resting-state fMRI study revealed both increased and decreased spontaneous activity in MCI group in relative to controls. Abundant previous studies by PET or SPECT have reported hypoactivity in temporal, prefrontal and parietal regions, and decreased glucose metabolism in the temporal and parietal lobes on FDG-PET is recognized as an early imaging marker for the AD pathology , . Consistent with the previous study , decreased ALFF/fALFF was observed in cingulate cortex, medial prefrontal cortex and some parietal regions; while increased ALFF/fALFF was observed in superior temporal gyrus. Furthermore, the changes of ALFF/fALFF in MCI in the slow-5 band were greater than those in the slow-4. However, we also revealed increased ALFF mainly in limbic regions i.e., parahippocampal gyrus, insula and anterior cingulate cortex (Table 2) and midbrain which had been not been found in the previous study and rarely reported by PET or SPECT studies , , , . In fact, task-fMRI studies in MCI have also reported hyperactivation especially in limbic regions during memory encoding –. One possible explanation for this abnormal hyperactivity is a compensatory neural mechanism, i.e., there is a temporary phase of increased activity in areas like parahippocampus along the course of MCI, which may keep the behavioral performance of MCI patients close to the level of cognitively intact elderly subjects. Around the conversion from MCI to clinical AD, such compensatory ability would be lost, which is then seen as poor task performance. This hypothesis was supported by the finding that greater clinical impairment in MCI subjects as related to smaller hippocampal volumes but greater parahippocampal fMRI activation . Another study even found a negative correlation between hippocampal atrophy and left parahippocampal activation only in MCI instead of in the elderly controls or AD patients . However, we did not observed GMV reduction in hippocampus in drug naïve MCI, suggesting such compensatory overactivity in limbic regions occur before the detectable hippocampal atrophy by VBM. Another possibility is the relative small sample size which would low the statistical power.
Contradictory to our hypothesis, there is no overlap between the morphometric and functional results, or any correlations between the altered regional GMV and ALFF, though the decreased ALFF in the right middle frontal gyrus and left inferior frontal gyrus were found quite near the decreased GMV in the same gyrus (Figure 3). By now, only a few studies used anatomical and functional methods in combination in MCI or AD patients. The results from combination of brain volumetrics and PET ,  showed that hypometabolism largely exceeds gray matter atrophy in most brain regions of AD patients . Another study even observed dissociated effect of atrophy and hypometabolism on episodic memory in MCI patients using the same method . Only two recent studies combine VBM and resting state fMRI in MCI patients, and they also found no overlap between regions with gray matter atrophy and regions with altered functional connectivity , . These results altogether with our findings support that brain volume and function may change independently and act different role in the earliest cognitive symptoms of MCI. The altered regional function may represent effects of early neurodegeneration .
Several methodological issues should be considered when interpreting the present results. First, although DARTEL-VBM was employed in the current study, which minimizes the contamination of brain tissue with non-brain voxels compared to standard VBM  , the use of a Chinese sample may affect the accuracy of normalization because the generic MNI template differs structurally from the brains of non-Caucasian populations . However, as both patients and controls were from a similar ethnic background, the groups differences observed seem unlikely to have been affected by ethnic factors. Second, though we temporally bandpass filtered all fMRI data (0.01–0.08 Hz), and removed components with high correlation to CSF or white matter or with low correlation to gray matter, we cannot completely rule out the influence of physiological noise on our findings due to its variation over time and across subjects. Simultaneous recording of heart rate and respiratory rate and depth during fMRI scanning might help further reduce physiological noise artifacts . Nevertheless, the consistency among the resting state connectivity patterns evidenced by the present data and other studies ,  does reduce the concern about the magnitude of such potential artifacts. Finally, there is a lack of consensus about the exact physiological nature of ALFF. Though ALFF is thought to reflect spontaneous neural activity , its exact basis remains to be fully characterized.
Taken together, current study combines anatomical and functional MRI to examine their relationship in a cohort of drug-naïve MCI patients. Findings from the study document that wide spread brain volume reduction accompanied with decreased and increased regional function in MCI, while the anatomical and functional changes were independently. Therefore, the combination of structural and functional MRI methods would provide complementary information and together advance our understanding of the pathophysiology underlying the symptoms of MCI.
Materials and Methods
A total of 35 right-handed subjects were recruited in the present study including 17 drug-naïve MCI and 18 healthy aging controls (Table 3). All patients and healthy controls were recruited at the Mental Health Centre of West China Hospital. This study was approved by the West China Hospital Medical Ethics Committee, and all patients and controls gave written informed consent to their participation. Diagnosis of MCI was determined by consensus of two experienced neurologists according to the criteria for amnestic MCI –, which included (a) memory complaint, preferably confirmed by an informant; (b) objective memory impairment, adjusted for age and education; (c) normal or near-normal performance on general cognitive functioning and no or minimum impairment of daily life activities; (d) the Clinical Dementia Rating (CDR) score of 0.5; and (e) not meeting the criteria for dementia according to the DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, 4rd edition, revised). Healthy controls were recruited from the local area by poster advertisement and screened using Structured Interview for DSM-IV Non-Patient Edition to confirm the lifetime absence of psychiatric and neurological illness. Information about age, sex, height, weight, handedness (based on the Annett handedness scale ), years of education, duration of illness and clinical symptom ratings were obtained by two experienced clinical neurologists prior to MR examinations. All subjects were evaluated using the Mini Mental State Examination (MMSE), Clock Drawing Test (CDT), Auditory Verbal Learning Test (AVLT), Activity of Daily Living (ADL), Hachinski Ischemic Scaling (HIS), Hamilton Depression Scale (HAMD), and Clinical Dementia Rating Scale (CDR). Age, sex, height, weight and years of education were matched between the MCI and control subjects (Table 3). The following exclusion criteria applied to all subjects: the existence of neurological disorder, alcohol or drug abuse, any physical illness such as hepatitis, brain tumor, or epilepsy as assessed based on clinical evaluations and medical records. Brain MR images (i.e., T1 weighted and T2 weighted images) were inspected by an experienced neuroradiologist, and no gross abnormalities was observed for any subject.
Table 3. Demographic information for treatment naïve MCI patients and the healthy controls.doi:10.1371/journal.pone.0028664.t003
High resolution T1-weighted images were acquired using a 3T MR imaging system (Siemens, Trio) with a volumetric T1 Weighted MPRAGE sequence (TR = 8.5 msec, TE = 3.4 msec, Flip angle = 12°, slice thickness = 1 mm) using an 12 channel phase array head coil. A Field of View (FOV) of 240×240 mm2 was used with an acquisition matrix comprising 256 readings of 128 phase encoding steps, producing 156 contiguous coronal slices with slice thickness of 1.0 mm. The final matrix of T1-weighted images was automatically interpolated in-plane to 512×512 which yields an in-plane resolution of 0.47×0.47 mm2. MR images sensitized to changes in BOLD signal levels (TR/TE = 2,000/30 ms; flip angle = 90°) were obtained by a gradient-echo echo-planar imaging (EPI) sequence. During the MR examination, subjects were instructed to relax with their eyes closed, keeping awake (confirmed by subjects immediately after the experiment). There were five dummy scans collected before fMRI scans and the first two volumes of fMRI time series were discarded for magnetization stabilization. The slice thickness was 5 mm (no slice gap) with a matrix size of 64×64 and FOV of 240×240 mm2, resulting in a voxel size of 3.75×3.75×5 mm3. Each brain volume comprised 30 axial slices and each functional run contained 200 image volumes. A traditional T2 weighted image with 20 contiguous axial slices was also acquired to rule out gross brain abnormalities for all subjects.
Voxel-based morphometry with DARTEL was performed using SPM8 (Welcome Trust Center for Neuroimaging, London, UK, http://www.filion.ucl.ac.uk/spm/software/spm8/). The procedure included 5 steps : (1) checking for scanner artifacts and gross anatomical abnormalities for each subject; (2) setting the image origin to the anterior commissure; (3) segmenting the images into the GM and WM images in SPM8 toolbox; (4) using the DARTEL toolbox on SPM8 to produce a high-dimensional normalization protocol, following John Ashburner's chapter in its standard version including the Montreal Neurological Institute (MNI) space transformation ; (5) The segmented images were modulated with the Jacobian determinants derived from the spatial normalization . Checking for homogeneity across the sample and using standard smoothing by a Gaussian kernel with a full width of half maximum of 8 mm.
Regional function analysis
Preprocessing and statistical analysis of functional images were carried out using SPM8. For each subject, EPI images were slice-time corrected and realigned to the middle image in the first series, and were subsequently unwraped to correct for susceptibility-by-movement interaction. Individual mean functional images were first coregistered to structural images (3D T1-weighted anatomical images) using a linear transformation, and the parameters were used for coregistration of all the realigned images. All the coregistered images were spatially normalized to the MNI template with the parameters from VBM and each voxel was re-sampled to 3×3×3 mm3.
Regional amplitude of low-frequency fluctuations, which are thought to reflect spontaneous neural activity in non-human ,  and human ,  subjects during resting state, was used to evaluate regional functional alteration in MCI. The ALFF was calculated using REST  with a procedure similar to that used in our earlier study , , . In brief, after bandpass filtering (0.01–0.08 Hz)  and linear-trend removing, the time series was transformed to the frequency domain using fast Fourier transform (FFT) (parameters: taper percent = 0, FFT length = shortest) and the power spectrum was obtained. Then, the power spectrum obtained by FFT was square root transformed and then averaged across 0.01–0.08 Hz at each voxel. This averaged square root was taken as the ALFF. Fractional ALFF (fALFF) is the fraction of ALFF in a given frequency band to the ALFF over the entire frequency range detectable in the given signal . As fALFF may be more robust against physiological noises, the low-frequency range for BOLD signal were further decomposed into slow 4 [0.027–0.073 Hz] and slow 5 [0.01–0.027 Hz] band . Finally, the fALFF for slow 4 and slow 5 band were calculated. For standardization purposes, the ALFF/fALFF of each voxel was divided by the global mean ALFF/fALFF value , . Finally, all the ALFF/fALFF images was smoothed by a Gaussian kernel with a full width of half maximum of 8 mm.
Voxel-by-voxel based comparisons of gray matter volume (GMV) were performed between groups using two sample t-tests with age, sex and year of education as covariates. The significance of group differences was set at p<0.05 corrected with FDR. To identify the association between structural abnormalities and clinical symptom severity, the average GMV values of all voxels in abnormal areas revealed by VBM were extracted and correlated with Hachinski, CDT, AVLT, MMSE and ADL scores using partial correlation analysis with age, disease duration, sex and year of education as covariates.
ALFF maps in the MCI and control groups were compared on a voxel-wise basis using a two sample t-test in SPM8 with age, sex and year of education as covariates and p<0.05 corrected with FDR was used. Global ALFF between MCI and controls were also compared using a two sample t-test with age, sex and year of education as covariates. To identify the association of regional ALFF with GMV abnormalities, a full voxel-to-voxel correlation of ALFF and GMV images was made using Bivariate correlation analysis in SPM8 and p<0.05 corrected for multiple comparisons was used. To get that, the average ALFF values and the average GMV values of all voxels in abnormal areas revealed by voxel-wise analysis were extracted, respectively. Then the averaged ALFF or GMV values were correlated with the GMV or the ALFF images. To identify the association of regional ALFF with clinical symptom severity, the average ALFF values of all voxels in abnormal areas revealed by voxel-wise analysis were extracted and correlated with the Hachinski, CDT, AVLT, MMSE and ADL scores using partial correlation analysis with age, disease duration, sex and year of education as covariates.
To validate the reproducibility of each region showing changes, leave-one-out cross validation analysis for both structural (VBM) and functional (ALFF/FALFF) analyses was conducted. Specifically, we randomly leave one patient out and performed patient-control comparisons (leading total 17 group comparisons). For each voxel, the ratio of showing significant difference in the measure (i.e., the number of comparisons exhibiting group difference in this voxel divides the total 17 comparisons) was computed as the finding reproducibility of this voxel. The mean reproducibility across all voxels within each region was calculated to measure this region's reproducibility.
Includes the methods, results and discussion for fractional ALFF analysis and leave-one-out analysis. ALFF/fALFF maps for slow 4 [0.027–0.073 Hz] and slow 5 [0.01–0.027 Hz] band in the MCI and control groups were compared on a voxel-wise basis using a two sample t-test in SPM8 with age, sex and year of education as covariates and p<0.05 corrected with FDR was used. Leave-one-out reproducibility analysis were also did for all above ALFF/fALFF analysis and all results showed high reproducibility (p<0.01 FDR corrrected).
Conceived and designed the experiments: YH SL. Performed the experiments: YH SL LZ QL. Analyzed the data: YH SL. Contributed reagents/materials/analysis tools: WK JJ. Wrote the paper: YH SL WK JJ.
- 1. Petersen RC, Roberts RO, Knopman DS, Boeve BF, Geda YE, et al. (2009) Mild cognitive impairment: ten years later. Arch Neurol 66: 1447–1455.
- 2. Pihlajamaki M, Jauhiainen AM, Soininen H (2009) Structural and functional MRI in mild cognitive impairment. Curr Alzheimer Res 6: 179–185.
- 3. Bozzali M, Filippi M, Magnani G, Cercignani M, Franceschi M, et al. (2006) The contribution of voxel-based morphometry in staging patients with mild cognitive impairment. Neurology 67: 453–460.
- 4. Gili T, Cercignani M, Serra L, Perri R, Giove F, et al. (2011) Regional brain atrophy and functional disconnection across Alzheimer's disease evolution. J Neurol Neurosurg Psychiatry 82: 58–66.
- 5. Kinkingnehun S, Sarazin M, Lehericy S, Guichart-Gomez E, Hergueta T, et al. (2008) VBM anticipates the rate of progression of Alzheimer disease: a 3-year longitudinal study. Neurology 70: 2201–2211.
- 6. Petrella JR, Sheldon FC, Prince SE, Calhoun VD, Doraiswamy PM (2011) Default mode network connectivity in stable vs progressive mild cognitive impairment. Neurology 76: 511–517.
- 7. Villain N, Desgranges B, Viader F, de la Sayette V, Mezenge F, et al. (2008) Relationships between hippocampal atrophy, white matter disruption, and gray matter hypometabolism in Alzheimer's disease. J Neurosci 28: 6174–6181.
- 8. Sorg C, Riedl V, Muhlau M, Calhoun VD, Eichele T, et al. (2007) Selective changes of resting-state networks in individuals at risk for Alzheimer's disease. Proc Natl Acad Sci U S A 104: 18760–18765.
- 9. Baron JC, Chetelat G, Desgranges B, Perchey G, Landeau B, et al. (2001) In vivo mapping of gray matter loss with voxel-based morphometry in mild Alzheimer's disease. Neuroimage 14: 298–309.
- 10. Matsuda H, Kitayama N, Ohnishi T, Asada T, Nakano S, et al. (2002) Longitudinal evaluation of both morphologic and functional changes in the same individuals with Alzheimer's disease. J Nucl Med 43: 304–311.
- 11. Borroni B, Anchisi D, Paghera B, Vicini B, Kerrouche N, et al. (2006) Combined 99mTc-ECD SPECT and neuropsychological studies in MCI for the assessment of conversion to AD. Neurobiol Aging 27: 24–31.
- 12. Ibanez V, Pietrini P, Alexander GE, Furey ML, Teichberg D, et al. (1998) Regional glucose metabolic abnormalities are not the result of atrophy in Alzheimer's disease. Neurology 50: 1585–1593.
- 13. Chetelat G, Desgranges B, de la Sayette V, Viader F, Berkouk K, et al. (2003) Dissociating atrophy and hypometabolism impact on episodic memory in mild cognitive impairment. Brain 126: 1955–1967.
- 14. Han Y, Wang J, Zhao Z, Min B, Lu J, et al. (2011) Frequency-dependent changes in the amplitude of low-frequency fluctuations in amnestic mild cognitive impairment: a resting-state fMRI study. Neuroimage 55: 287–295.
- 15. Lui S, Deng W, Huang X, Jiang L, Ma X, et al. (2009) Association of cerebral deficits with clinical symptoms in antipsychotic-naive first-episode schizophrenia: an optimized voxel-based morphometry and resting state functional connectivity study. Am J Psychiatry 166: 196–205.
- 16. Lui S, Deng W, Huang X, Jiang L, Ouyang L, et al. (2009) Neuroanatomical differences between familial and sporadic schizophrenia and their parents: an optimized voxel-based morphometry study. Psychiatry Res 171: 71–81.
- 17. Callicott JH, Mattay VS, Verchinski BA, Marenco S, Egan MF, et al. (2003) Complexity of prefrontal cortical dysfunction in schizophrenia: more than up or down. Am J Psychiatry 160: 2209–2215.
- 18. Lui S, Ouyang L, Chen Q, Huang X, Tang H, et al. (2008) Differential interictal activity of the precuneus/posterior cingulate cortex revealed by resting state functional MRI at 3T in generalized vs. Partial seizure. J Magn Reson Imaging 27: 1214–1220.
- 19. Karas GB, Scheltens P, Rombouts SA, Visser PJ, van Schijndel RA, et al. (2004) Global and local gray matter loss in mild cognitive impairment and Alzheimer's disease. Neuroimage 23: 708–716.
- 20. Shmuel A, Leopold DA (2008) Neuronal correlates of spontaneous fluctuations in fMRI signals in monkey visual cortex: Implications for functional connectivity at rest. Hum Brain Mapp 29: 751–761.
- 21. Laufs H, Krakow K, Sterzer P, Eger E, Beyerle A, et al. (2003) Electroencephalographic signatures of attentional and cognitive default modes in spontaneous brain activity fluctuations at rest. Proc Natl Acad Sci U S A 100: 11053–11058.
- 22. Goncalves SI, de Munck JC, Pouwels PJ, Schoonhoven R, Kuijer JP, et al. (2006) Correlating the alpha rhythm to BOLD using simultaneous EEG/fMRI: inter-subject variability. Neuroimage 30: 203–213.
- 23. Zuo XN, Di Martino A, Kelly C, Shehzad ZE, Gee DG, et al. (2010) The oscillating brain: complex and reliable. Neuroimage 49: 1432–1445.
- 24. Zang YF, He Y, Zhu CZ, Cao QJ, Sui MQ, et al. (2007) Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI. Brain Dev 29: 83–91.
- 25. Zou QH, Zhu CZ, Yang Y, Zuo XN, Long XY, et al. (2008) An improved approach to detection of amplitude of low-frequency fluctuation (ALFF) for resting-state fMRI: fractional ALFF. J Neurosci Methods 172: 137–141.
- 26. Tisserand DJ, van Boxtel MP, Pruessner JC, Hofman P, Evans AC, et al. (2004) A voxel-based morphometric study to determine individual differences in gray matter density associated with age and cognitive change over time. Cereb Cortex 14: 966–973.
- 27. Price JL, Morris JC (1999) Tangles and plaques in nondemented aging and “preclinical” Alzheimer's disease. Ann Neurol 45: 358–368.
- 28. Klunk WE, Engler H, Nordberg A, Wang Y, Blomqvist G, et al. (2004) Imaging brain amyloid in Alzheimer's disease with Pittsburgh Compound-B. Ann Neurol 55: 306–319.
- 29. Prince SE, Daselaar SM, Cabeza R (2005) Neural correlates of relational memory: successful encoding and retrieval of semantic and perceptual associations. J Neurosci 25: 1203–1210.
- 30. Prince SE, Tsukiura T, Cabeza R (2007) Distinguishing the neural correlates of episodic memory encoding and semantic memory retrieval. Psychol Sci 18: 144–151.
- 31. Wagner AD, Pare-Blagoev EJ, Clark J, Poldrack RA (2001) Recovering meaning: left prefrontal cortex guides controlled semantic retrieval. Neuron 31: 329–338.
- 32. Petrella JR, Prince SE, Krishnan S, Husn H, Kelley L, et al. (2009) Effects of donepezil on cortical activation in mild cognitive impairment: a pilot double-blind placebo-controlled trial using functional MR imaging. AJNR Am J Neuroradiol 30: 411–416.
- 33. Bell-McGinty S, Lopez OL, Meltzer CC, Scanlon JM, Whyte EM, et al. (2005) Differential cortical atrophy in subgroups of mild cognitive impairment. Arch Neurol 62: 1393–1397.
- 34. Mosconi L, Tsui WH, Herholz K, Pupi A, Drzezga A, et al. (2008) Multicenter standardized 18F-FDG PET diagnosis of mild cognitive impairment, Alzheimer's disease, and other dementias. J Nucl Med 49: 390–398.
- 35. Mosconi L, Tsui WH, Pupi A, De Santi S, Drzezga A, et al. (2007) (18)F-FDG PET database of longitudinally confirmed healthy elderly individuals improves detection of mild cognitive impairment and Alzheimer's disease. J Nucl Med 48: 1129–1134.
- 36. Dickerson BC, Salat DH, Bates JF, Atiya M, Killiany RJ, et al. (2004) Medial temporal lobe function and structure in mild cognitive impairment. Ann Neurol 56: 27–35.
- 37. Dickerson BC, Salat DH, Greve DN, Chua EF, Rand-Giovannetti E, et al. (2005) Increased hippocampal activation in mild cognitive impairment compared to normal aging and AD. Neurology 65: 404–411.
- 38. Hamalainen A, Pihlajamaki M, Tanila H, Hanninen T, Niskanen E, et al. (2007) Increased fMRI responses during encoding in mild cognitive impairment. Neurobiol Aging 28: 1889–1903.
- 39. Chetelat G, Desgranges B, Landeau B, Mezenge F, Poline JB, et al. (2008) Direct voxel-based comparison between grey matter hypometabolism and atrophy in Alzheimer's disease. Brain 131: 60–71.
- 40. Good CD, Johnsrude IS, Ashburner J, Henson RN, Friston KJ, et al. (2001) A voxel-based morphometric study of ageing in 465 normal adult human brains. Neuroimage 14: 21–36.
- 41. Katura T, Tanaka N, Obata A, Sato H, Maki A (2006) Quantitative evaluation of interrelations between spontaneous low-frequency oscillations in cerebral hemodynamics and systemic cardiovascular dynamics. Neuroimage 31: 1592–1600.
- 42. Birn RM, Diamond JB, Smith MA, Bandettini PA (2006) Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI. Neuroimage 31: 1536–1548.
- 43. Harrison BJ, Pujol J, Lopez-Sola M, Hernandez-Ribas R, Deus J, et al. (2008) Consistency and functional specialization in the default mode brain network. Proc Natl Acad Sci U S A 105: 9781–9786.
- 44. Petersen RC, Doody R, Kurz A, Mohs RC, Morris JC, et al. (2001) Current concepts in mild cognitive impairment. Arch Neurol 58: 1985–1992.
- 45. Petersen RC, Smith GE, Waring SC, Ivnik RJ, Tangalos EG, et al. (1999) Mild cognitive impairment: clinical characterization and outcome. Arch Neurol 56: 303–308.
- 46. Petersen RC, Stevens JC, Ganguli M, Tangalos EG, Cummings JL, et al. (2001) Practice parameter: early detection of dementia: mild cognitive impairment (an evidence-based review). Report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology 56: 1133–1142.
- 47. Bergouignan L, Chupin M, Czechowska Y, Kinkingnehun S, Lemogne C, et al. (2009) Can voxel based morphometry, manual segmentation and automated segmentation equally detect hippocampal volume differences in acute depression? Neuroimage 45: 29–37.
- 48. Ashburner J (2007) A fast diffeomorphic image registration algorithm. Neuroimage 38: 95–113.
- 49. Leopold DA, Murayama Y, Logothetis NK (2003) Very slow activity fluctuations in monkey visual cortex: implications for functional brain imaging. Cereb Cortex 13: 422–433.
- 50. Song XW, Dong ZY, Long XY, Li SF, Zuo XN, et al. (2011) REST: a toolkit for resting-state functional magnetic resonance imaging data processing. PLoS One 6: e25031.
- 51. Lui S, Huang X, Chen L, Tang H, Zhang T, et al. (2009) High-field MRI reveals an acute impact on brain function in survivors of the magnitude 8.0 earthquake in China. Proc Natl Acad Sci U S A 106: 15412–15417.
- 52. Yang H, Long XY, Yang YH, Yan H, Zhu CZ, et al. (2007) Amplitude of low frequency fluctuation within visual areas revealed by resting-state functional MRI. NeuroImage 36: 144–152.
- 53. Cordes D, Haughton VM, Arfanakis K, Carew JD, Turski PA, et al. (2001) Frequencies contributing to functional connectivity in the cerebral cortex in “resting-state” data. AJNR Am J Neuroradiol 22: 1326–1333.
- 54. Zang Y, Jiang T, Lu Y, He Y, Tian L (2004) Regional homogeneity approach to fMRI data analysis. Neuroimage 22: 394–400.