A voxel-based morphometric study of age- and sex-related changes in white matter volume in the normal aging brain
Authors Liu H, Wang L, Geng Z, Zhu Q, Song Z, Chang R, Lv H
Received 17 June 2015
Accepted for publication 16 September 2015
Published 24 February 2016 Volume 2016:12 Pages 453—465
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Professor Wai Kwong Tang
Haijing Liu*, Lixin Wang*, Zuojun Geng, Qingfeng Zhu, Zhenhu Song, Ruiting Chang, Huandi Lv
Department of Radiology, Second Hospital of Hebei Medical University, Shijiazhuang, People’s Republic of China
*These authors contributed equally to this work
Objective: To carry out a cross-sectional study of 187 cognitively normal Chinese adults using the voxel-based morphometry (VBM) approach to delineate age-related changes in the white matter volume of regions of interest in the brain and further analyze their correlation with age.
Materials and methods: A total of 187 cognitively normal adults were divided into the young, middle, and old age-groups. Conventional magnetic resonance imaging was performed with the Achieva 3.0 T system. Structural images were processed using VBM8 and statistical parametric mapping 8. Regions of interest were obtained by WFU PickAtlas, and all realigned images were spatially normalized.
Results: Females showed significantly greater total white matter volume than males (t=2.36, P=0.0096, false-discovery rate [FDR] corrected). VBM demonstrated statistically significant age-related differences in white matter volume between the young age-group and the middle age-group (P<0.05, FDR corrected) and between the middle age-group and the old age-group (P<0.05, FDR corrected). No interaction was found between age and sex on white matter volume (P>0.05, FDR corrected). Logistic regression analysis revealed nonlinear correlation between total white matter volume and age (R2=0.124, P<0.001). White matter volume gradually increased before 40 years of age, peaked around 50 years of age, and rapidly declined after 60 years of age.
Conclusion: Significant age-related differences are present in white matter volume across multiple brain regions during aging. The VBM approach may help differentiate underlying normal neurobiological aging changes of specific brain regions from neurodegenerative impairments.
Keywords: brain, aging, magnetic resonance imaging, ROI, white matter volume, voxel-based morphometry
Normal brain aging is a physiological process accompanied by declines in the function of multiple systems in the body, including age-related cognitive decline, which is manifested as a decline in executive function and memory.1 Investigation of age-related brain changes helps in understanding the evolution of degeneration and its mechanisms, and assists in the differentiation of the normal aging brain from neurodegenerative diseases. However, magnetic resonance imaging (MRI) study of brain aging has mostly focused on changes in the gray matter. The white matter is an important component of the human brain, and is responsible for transmitting neural communication between regions in the gray matter. Histopathologic studies reveal that brain aging is marked by loss of myelinated fibers, and bulk-volume loss of white matter is also demonstrated on MRI.2 The distribution of white matter shows regional differences. It has been shown the volume reduction is more apparent in the white matter than in the gray matter, especially in the frontal lobe and corpus callosum. Jernigan et al3 observed a 26% reduction in white matter tissue volume relative to a 14% reduction in gray-matter tissue volume.4
The volume of the white matter is currently mostly determined by voxel-based morphometry (VBM), which shows morphological changes of the white matter by calculating the volume and density of the white matter. Through standardization, segmentation, smoothing, and construction of models from smoothed images and by statistical parametric mapping (SPM), VBM can reveal focal differences in brain regions among people of different ages. VBM using structural brain MRI has been widely used for assessment of the normal aging brain and neurodegenerative diseases, such as Alzheimer’s disease. We hypothesized that age- and sex-related differences are present in white matter volume across multiple brain regions during aging and that VBM helps differentiate underlying normal neurobiological aging changes of specific brain regions from neurodegenerative impairments. In the current study, we carried out a cross-sectional study of 187 cognitively normal Chinese adults of either sex using the VBM approach to delineate age- and sex-related changes in the white matter volume of regions of interest (ROIs) in the brain and further analyzed their correlation with age.
Materials and methods
Healthy volunteers were recruited between August 2013 and November 2013. The study protocol was approved by the institutional review board at the Second Hospital of Hebei Medical University. All participants received written and oral information prior to giving written consent, and the study was performed in accordance with the Helsinki II declaration. The inclusion criteria were as follows: 1) right-handedness; 2) native Mandarin speaker; 3) good eyesight and hearing and speaking ability; 4) the Mini-Mental State Examination score >27; 5) no history of nervous system disease or mental illness, such as headache, dizziness, lethargy, seizure, or emotional disturbance; 6) no previous cerebral surgery or trauma, no hypertension (>140/90 mmHg in those aged 60 years and above), diabetes, heart diseases, or other chronic diseases; 7) no alcoholism (defined as consuming more than three alcoholic drinks a day), smoking (defined as three cigarettes per day), long-term medication, or drug addiction; 8) no contraindication for MRI, such as cardiac pacemaker, nerve stimulator, metal artery clip, or metal false tooth; 9) no history of seizure, convulsion, cerebritis, or meningitis; 10) no history of cerebral hypoxia or carbon monoxide or other toxin poisoning; and 11) no abnormality on conventional cerebral MRI, or the presence of hyperintensity signal <2 according to the Wahlund scale,5 or number of scattered degenerative lesions fewer than five. The subjects were divided into a young age-group (20–40 years of age), a middle age-group (41–59 years of age), and an old age-group (60–78 years of age) as previously described.5–7
Conventional MRI was performed with the Achieva 3.0 T system (Philips, Amsterdam, the Netherlands) using an eight-channel head coil, and included T1 fast field echo, axial T1-weighted imaging (T1WI), axial and sagittal T2-weighted imaging (T2WI), and axial T2 fluid-attenuated inversion recovery. The main parameters were as follows: axial T1WI, turbo spin echo (TSE) sequence repetition time (TR) 3,056 ms; echo time (TE) 7.6 ms; inversion time 860 ms; axial T2WI, TSE sequence TR 500 ms; TE 80 ms; axial T2 fluid-attenuated inversion recovery, TR 9,000 ms; TE 140 ms; inversion time 2,600 ms. For these sequences, the slice thickness was 6.0 mm, slice interval 1.0 mm, matrix 512×256, field of view (FOV) 230×220 mm, flip angle 90°, and number of excitations (NEX) 1. The parameters for sagittal T2WI were as follows: TSE sequence, TR 1,707 ms; TE 80 ms; slice thickness 6.0 mm; slice interval 1.0 mm; matrix 328×235, FOV 230×230×121 mm (length × width × height), and NEX 1.
T1W 3-D imaging
The patient was placed in the supine position and kept immobile. Sagittal high-resolution T1W 3-D T1 fast field echo was carried out with the axial scan parallel to the anterior commissure–posterior commissure line. The scan parameters were as follows: TR 7.8 ms, TE 3.8 ms, flip angle 8°, matrix size 252×227, voxel size 1×1×1 mm, FOV 250×250×180 mm, slice thickness 1 mm, slice interval 0 mm, number of slices scanned 180, scan time 2 minutes 58 seconds, and NEX 1.
Structural images were processed using the VBM toolbox (VBM8) (http://dbm.neuro.uni-jena.de/vbm) and statistical parametric mapping (SPM)8 (http://www.fil.ion.ucl.ac.uk/spm; Wellcome Trust Centre for Neuroimaging, London, UK), which combines tissue segmentation, bias correction, and spatial normalization into a unified mode. Individual brains were normalized to tissue probability maps using the International Consortium for Brain Mapping. The voxelization of structural images was 1.5×1.5×1.5 mm. The images were segmented into gray matter, white matter, and cerebrospinal fluid by using the new segmentation in SPM8. The optimally processed images were smoothed with an isotropic Gaussian kernel (full-width half-maximum =8 mm). The total volume of the gray matter, white matter, and cerebrospinal fluid was determined, and the total intracranial volume was calculated from the sum of the volume of the gray matter, white matter, and cerebrospinal fluid. The effects of total gray-matter volume were removed to allow inferences between regional differences in white matter volume.
Measurement of volume using ROIs
ROIs were obtained by WFU PickAtlas,8 and all realigned images were spatially normalized to the Montreal Neurological Institute echo-planar imaging template in SPM8.9 We used the following ROIs (Figure 1): left and right frontal lobe, left and right parietal lobe, left and right temporal lobe, left and right occipital lobe, left and right cerebrum and corpus callosum, midbrain, pons, and medulla oblongata. The significance of group differences in each region was estimated by distributional approximations from the theory of random Gaussian fields.
Data were expressed as means ± standard deviation and analyzed using SPSS software version 13.0 (SPSS Inc, Chicago, IL, USA). Sex-related differences in the white matter volume of the whole brain were examined using the t-test for two independent samples, with age and total intracranial volume as covariates. Age-related differences in the white matter volume of the whole brain were examined by two-way analysis of variance. The total intracranial volume was used as the covariate, and absolute voxel values >0.1 mL were included in the analysis. The false-discovery rate (FDR) was used for comparison correction, and P<0.05 was considered statistically significant. The cluster-level statistical threshold was set at 20 for statistically significant difference between brain regions. Correlation of changes in white matter of different brain regions during aging and age was studied by multiple-regression analysis in SPM. Age was an independent variable,2 and the volume of white matter was used as a dependent variable in regression analysis.
Sex-related differences in white matter volume by VBM
A total of 187 subjects – 92 males and 95 females – were included in the study. Their mean age was 47.2 (range 20–78) years. The baseline and demographic data of the study subjects are shown in Table 1. There was no statistical difference in education status (analysis of variance, P=0.077) or sex (χ2 test, P=0.490) among the three groups. Sex-related white matter volume of brain regions are shown in Table 2 and Figure 2. Overall, females showed significantly greater total white matter volume than males (t=2.36, P=0.0096, FDR corrected). Females showed greater white matter volume in the medulla oblongata, pons, bilateral crus cerebri, bilateral medial temporal gyrus, bilateral anterior lobe of the cerebrum, bilateral superior frontal gyrus, orbital gyrus of the left frontal lobe, bilateral parietal lobe, and genu of the cingulate gyrus. Males showed greater white matter volume of the bilateral posterior lobe of the cerebellum, bilateral external capsule of the insular cortex, bilateral straight frontal gyrus, and bilateral parietal lobe.
Table 1 Demographic data of the study subjects
Table 2 Sex-related differences in white matter volume by voxel-based morphometry
Age-related differences in white matter volume by VBM
VBM demonstrated statistically significant age-related differences in white matter volume between the young age-group and the middle age-group (P<0.05, FDR corrected). Age-related white matter volumes of brain regions are shown in Table 3 and Figure 3. Middle-aged subjects showed greater white matter volume than young subjects in the bilateral straight frontal gyrus, bilateral precentral gyrus, bilateral corona radiata, bilateral anterior limb of the internal capsule, right external capsule, right middle cerebellar peduncle, bilateral uncinate gyrus, bilateral lentiform nucleus, and right occipital lobe (P<0.001, uncorrected). Furthermore, the white matter volume of the corpus callosum peaked at the young age and remained stable, and apparent decline was observed after the subjects were 70 years of age (Figure 3C). When uncorrected for multiple comparisons, female and male subjects showed significant difference in the left anterior and posterior lobe of the cerebellum, bilateral corona radiata, pons, left occipital gyrus, and genu of the corpus callosum (Figure 4 and Table 4). No interaction was found between age and sex on white matter volume in young and middle-aged subjects (P>0.05, FDR corrected).
Table 3 Age-related white matter changes in brain regions between young adults and middle-aged adults by voxel-based morphometry
Table 4 Sex-related white matter changes between young and middle-aged adults by voxel-based morphometry
VBM further revealed statistically significant age-related differences in white matter volume between the middle age-group and the old age-group (P<0.05, FDR corrected). Compared to middle-aged subjects, old subjects showed lower white matter volumes in bilateral medial and inferior temporal gyri, bilateral middle frontal gyri, left inferior frontal gyrus, bilateral cerebra, and other brain areas, as shown in Table 5 and Figure 5. No interaction was found between age and sex on white matter volume in middle-aged and old subjects (P>0.05, FDR corrected). Statistically significant age-related differences in white matter volume were also noticed between the young age-group and the old age-group (P<0.05, FDR corrected). Compared to young subjects, old subjects showed lower white matter volumes in the bilateral frontal lobe, bilateral occipital lobe, and other brain areas, as shown in Figure 6 and Table 6. When not corrected for multiple comparison, females showed greater white matter volumes than males, including bilateral corona radiata, left external capsule, right cingulate gyrus, posterior limb of the left internal capsule, bilateral parahippocampal gyrus, and left middle frontal gyrus (Figure 7 and Table 7). No interaction was found between age and sex on white matter volume in young and middle-aged subjects (P>0.05, FDR corrected).
Table 5 Age-related white matter changes between middle-aged and old persons by voxel-based morphometry
Figure 5 Age-related white matter volume changes between middle-aged adults and old adults.
Table 6 Age-related white matter changes between young and old persons by voxel-based morphometry
Table 7 Sex-related white matter changes between young and old persons by voxel-based morphometry
Correlation of white matter volume and age
Logistic regression analysis use age2 as an independent variable and total white matter volume as a dependent variable and total intracranial volume as a covariate revealed nonlinear correlation between total white matter volume and age (R2=0.124, P<0.001) (Figure 8). White matter volume gradually increased before 40 years of age, peaked around 50 years of age, and rapidly declined after 60 years of age. When age or age2 were used as an independent variable and the white matter volume of each ROI used as a dependent variable, logistic regression analysis showed a nonlinear squared correlation between the white matter volume of most ROIs and age, particularly the white matter volume of the frontal lobe (R2=0.13, P<0.001) (Table 8 and Figure 9). No significant correlation was observed between the white matter volume of bilateral cerebri, midbrain, pons, and medulla oblongata and age.
Figure 8 Scatter plots and simple nonlinear regressions (quadratic, cubic) of white matter volume (WMV) on age for the whole white matter.
Table 8 Correlation of age and white matter volume by region of interest (ROI) and sex
Figure 9 Plots of white matter volume (WMV) versus age (including best-fit regression lines).
Structural changes may occur in multiple regions of the aging brain, leading to decline in neurocognitive function, which is manifested as decline in memory and executive function. Imaging studies by MRI and other techniques show that degenerative changes in the white matter are an important contributor to brain aging. It has been shown that compared to younger persons, elderly persons show apparent reduction in brain volume, with a 3% decrease in gray-matter volume and an 11% reduction in white matter volume, mainly in the frontal lobe and corpus callosum.10 White matter volume increases before the age of 50 years, and significantly declines after the age of 60 years.11,12 Changes in white matter volume differ by brain regions during aging. Schmidt et al13 found that white matter changes occur prior to reduction in brain volume in cognitively normal elderly persons. The current study used the VBM approach to delineate age-related changes in white matter volume in cognitively normal adults, and demonstrates widespread age-related differences in multiple regions of the human brain. Compared to young subjects, old subjects had markedly lower white matter volumes in multiple ROIs of the brain, such as the frontal lobe, the internal capsule, the splenium of the corpus callosum, the occipital lobe, and the left temporal lobe. This is partially consistent with findings by Giorgio et al,14 who demonstrated a linear negative association of white matter volume with advancing age in various brain regions like the internal capsule. We further demonstrated that changes in white matter volume occur early in the process, as middle-aged subjects showed significantly higher white matter volume than young subjects in multiple regions of the brain.
It remains inconclusive whether white matter volume correlates with age, though studies have demonstrated brain atrophy in the aging brain.15,16 Our findings were that white matter volume of multiple ROIs of the brain changes with age and correlates with age, showing an inverse U-shaped curve. Our study reveals that white matter volume peaks around 50 years of age and starts a gradual decline thereafter. The reduction in white matter volume is accelerated in a squared equation, which is consistent with findings by other investigators.15,17 Unlike the correlation of gray-matter volume and age, there have been controversies in reports on the correlation of white matter volume and age. One study indicated that white matter volume in persons 70 years of age was only reduced by approximately 6% compared to persons 30 years of age, but declined by as much as 25% in persons 80 years of age.18 Shankar19 found that white matter volume was on the rise before the age of 40 years and thereafter declined at an annual rate of 0.5%, which was accelerated after 70 years of age. Another study showed a peak of white matter volume around the age of 40 years, which started to decline in a squared equation after 50 years of age.20 Some other studies, however, found no apparent correlation between white matter volume and age,21 a negative correlation between white matter volume and age,22 or focal reduction of white matter volume with age.23
Our VBM revealed that the bilateral frontal lobe and bilateral temporal lobe were the earliest brain regions to manifest reduction in white matter volume, while the occipital lobe was the last brain region to show changes in white matter volume. This is consistent with the asynchrony of white matter development. The white matter in humans exhibits spatiotemporal heterogeneity in its development, and myelination differs temporally across brain regions. Myelination occurs last in the frontal lobe, while it starts earlier in the occipital lobe. In the frontal lobe, the myelin sheath is thinner and the repair mechanism less efficient, and oligodendrocytes are prone to metabolic insults. Therefore, the bilateral frontal lobe is the most vulnerable region in the brain, while the occipital lobe shows slower decline in white matter volume. We also found that the white matter volume of the corpus callosum peaked at young age and remained stable until 70 years of age, when it started apparent decline. The splenium and genu of the corpus callosum showed noticeable reductions in white matter volume in old persons. Our findings indicate that different brain regions show uneven changes in white matter volume. Future studies tracking white matter volume changes over time may be required to delineate the spatiotemporal pattern of white matter volume changes.
Sex-related white matter changes associated with aging remain ill defined. Several studies have shown that changes in white matter volume did not correlate with sex.24,25 Allen et al15 found that males showed greater correlation of total white matter volume with age than females. Another study revealed that females had apparently higher total white matter volume than males, while males had higher white matter volume in focal regions compared to females.21 The current study found that females showed markedly higher white matter volume in multiple brain regions, including the parietal lobe, bilateral medial temporal gyri, left occipital lobe, and bilateral anterior lobes of the cerebrum. Our findings are not consistent with Voineskos et al, who found that females had greater reduction in white matter volume of the parietal lobe.26 It was found that males had more marked atrophy of the temporal lobe than females during aging.27 Brain metabolism shows sex-related difference in certain brain regions, such as the temporal lobe, the parietal lobe, and the cerebrum,28 but no study has been done to characterize sex-related differences in white matter volume during aging. It remains undefined if sex plays a role in white matter volume changes during aging.
Age-related white matter changes first occur in the frontal lobe and the precentral and postcentral sulci. These brain areas are associated with memory, cognition, and sensation. As one ages, the temporal lobe, especially the hippocampus, begins to show age-related changes, leading to impaired memory. Deeper brain structures like the brain stem that are related to basic life activities do not exhibit apparent age-related changes, or age-related changes develop much later in life. The relation between white matter changes and neuropsychiatric disorders has been pursued by investigators. For example, white matter changes have been documented during transition of the prodromal phase of schizophrenia.29 Wright et al investigated 50 schizophrenia patients by diffusion tensor imaging, and observed a significant age-related decline in white matter blood perfusion.30 Reppermund studied 381 subjects aged between 72 and 92 years, and found that reduced white matter integrity was associated with late-life depression.31 They showed that white matter changes in the superior frontal gyrus, posterior thalamic radiation, superior longitudinal fasciculus, and body of the corpus callosum predicted depression at follow-up. Our current study also demonstrated age-related changes in these brain regions. It is worthwhile to explore the relation between age-related white matter changes and the risk of neuropsychiatric disorders in future studies.
Studying changes in white matter volume that occur in the normal brain with aging is important for understanding the mechanisms leading to these changes, and for better characterization of neurodegenerative disorders whose risk increases with advancing age. However, there are apparent limitations for the use of VBM for studying white matter volume changes. The white matter lacks features to yield consistency in registration, and there is also a lack of uniform standards for measuring white matter volume, rendering comparison across studies difficult. The findings of the current study may also differ from those of earlier studies, because these studies may have used different methods, such as diffusion tensor imaging or (because of the differences in segmentation) smoothing and construction of models from smoothed images. Nevertheless, cerebral aging is a complex and heterogeneous process that is associated with a high degree of interindividual variability. Moreover, our population was highly selected, and may not represent the typical aging population, and the conclusions of the study should be interpreted with caution. Our study of a large cohort of cognitively normal subjects aged 20–78 years provided SPM of changes in white matter volume of ROIs of the brain and characterized the pattern of loss and preservation of brain regions during aging. We demonstrated significant age-related differences in changes in white matter volume across multiple brain regions during aging. These data suggest that the VBM approach may provide an emerging paradigm in the normal aging brain that may help in differentiating underlying normal neurobiological aging changes of specific brain regions from neurodegenerative impairments.
The authors report no conflicts of interest in this work.
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