OBJECTIVE: To perform a quantitative analysis of the brain volume of elderly individuals in a population-based sample. MATERIALS AND METHODS: This was a radiological assessment and voxel-based quantitative analysis, with surface alignment, of 525 magnetic resonance imaging scans of individuals between 60 and 103 years of age who participated in the Saúde, Bem-estar e Envelhecimento (Health, Well-being, and Aging) study in the city of São Paulo, Brazil. RESULTS: We noted a median rate of reduction in total brain volume of 2.4% per decade after 60 years of age. Gray and white matter both showed volume reductions with age. The total brain volume/intracranial brain volume ratio differed between males and females. CONCLUSION: We have corroborated the findings of studies conducted in the United States and Europe. The total brain volume/intracranial brain volume ratio is higher in men, representing a potential bias for the conventional radiological assessment of atrophy, which is typically based on the evaluation of the cerebrospinal fluid spaces.
OBJECTIVE: To perform a quantitative analysis of the brain volume of elderly individuals in a population-based sample. MATERIALS AND METHODS: This was a radiological assessment and voxel-based quantitative analysis, with surface alignment, of 525 magnetic resonance imaging scans of individuals between 60 and 103 years of age who participated in the Saúde, Bem-estar e Envelhecimento (Health, Well-being, and Aging) study in the city of São Paulo, Brazil. RESULTS: We noted a median rate of reduction in total brain volume of 2.4% per decade after 60 years of age. Gray and white matter both showed volume reductions with age. The total brain volume/intracranial brain volume ratio differed between males and females. CONCLUSION: We have corroborated the findings of studies conducted in the United States and Europe. The total brain volume/intracranial brain volume ratio is higher in men, representing a potential bias for the conventional radiological assessment of atrophy, which is typically based on the evaluation of the cerebrospinal fluid spaces.
Entities:
Keywords:
Aging; Brain; Image interpretation, computer-assisted/methods; Magnetic resonance imaging; Neuroimaging
Normal aging is associated with gradual brain atrophy([1]). Almost all of the
studies conducted to date, regardless of the methodology employed, have confirmed
the basic observation that as adults age, their brains become smaller and the sulci
increase in size and depth([2]). However, cerebral atrophy is a complex phenomena
that is only partially related to a reduction in the number of neurons, which varies
less than 10% from 20 to 90 years of age; it also occurs as a consequence of myelin
loss-apparently preceding the neuronal loss([3]). Although the neocortex shows milder
changes, neuron loss in other areas, the hippocampus in particular, remains quite
stable over a lifetime([4]). Other factors, including intercellular space loss,
water reduction, and vascular changes, may also play a role in the reduction in
brain volume during the normal aging process([5]).The use of high-resolution magnetic resonance imaging (MRI) has enabled the detailed
assessment of aging-related changes in brain morphometry([6]). Although estimates
typically indicate that brain tissue volume is smaller in older adults than in
younger individuals, data regarding the effects of aging on gray matter versus white
matter are not consistent([7]) and continue to constitute a topic of investigation.
The contradictory findings might be attributable to the relatively small sample
sizes. Most studies of the topic have analyzed samples comprising ≤ 200
subjects-Allen et al.([8]) included 87 subjects, Giorgio et
al.([1]) included 66 subjects, and Raz et
al.([2]) included 200 participants-and have not recruited
subjects using epidemiological sampling. Another technical aspect that could result
in variations across studies is the method of analysis, which rarely takes factors
such as race and ethnicity into account. Therefore, normalization of morphometric
analyses by intracranial volume (ICV) is used in order to correct the head size data
and is believed to be fundamental to reducing false statistical interpretation of
brain volume and provides the basis for between-patient
comparisons([9]).The recent literature on dementia is densely populated by quantitative MRI
studies([10]). It is not only relevant to measure overall brain
atrophy but also useful to describe regional reductions in brain volume. For
instance, atrophy of the hippocampus has been found to correlate strongly with the
severity of Alzheimer's disease, as determined by pathology at autopsy. Accurate
quantification of the region-specific effects of aging is important for establishing
a structural paradigm to identify age-related regional cortical changes and
disease-specific regional cortical volume changes such as those that occur in
Alzheimer's disease([11]). However, in the clinical setting, quantitative
volumetric analysis of the brain is not always possible, because of financial
constraints (especially in public health care systems), poor MRI technique, or
limited operator knowledge for quality evaluation of the automated results. In this
context, most radiology reports are based only on subjective assessment of
intracranial structures. In addition, the majority of medical residency training
programs have yet to incorporate quantitative biomarker evaluation methods. Most of
the training is conventional, mostly reflecting self-experience based on individual
learning and exposure to relevant cases.There have been attempts to improve the visual assessment of brain MRI via the use of
predefined atrophy scores, as a means of reducing interindividual variation.
Examples include the visual rating system for medial temporal atrophy and the
entorhinal cortex atrophy score([10][12]). The overall severity of atrophy in
the medial temporal lobe, as well as in the hippocampus, entorhinal cortex, and
perirhinal cortex, can be scored with the visual rating system for medial temporal
atrophy, as proposed by Shen et al.([13]), which apparently has better discriminatory
power than do volumetric methods and shows a strong correlation with memory scores.
However, these scores can be calculated only from coronal images intersecting the
mammillary bodies, which require correct image plane acquisition, a condition that
is not always met in clinical settings.The purpose of this epidemiological MRI study was to describe the profile of elderly
individuals living in a megacity in South America, in terms of brain volume, by age
and gender; to compare our findings with those of similar studies conducted in other
regions of the world; and to describe the MRI appearance of the median-volume brains
in each age group. We believe that this approach could inform future quantitative
volumetric analyses, as well as helping clinical radiologists by providing normative
information and serving as a proxy for an atlas to support daily practice.
MATERIALS AND METHODS
Volunteers were recruited, through the use of an epidemiological sampling method, in
the city of São Paulo, Brazil, throughout the year of 2013. All participants
gave written informed consent. Of the 525 volunteers participating on this studied,
331 (63.0%) were women. The distribution of the participants by age group was as
follows: 60-64 years, 89 (17.0%); 65-69 years, 118 (22.5%); 70-74 years, 79 (15.0%);
75-79 years, 70 (13.3%); 80-84 years, 78 (14.8%); 85-89 years, 59 (11.2%); 90-94
years, 25 (4.8%); and 95-103 years, 7 (1.3%).All MRI examinations were performed in the same 3.0 T scanner (Tim Trio; Siemens
Healthcare, Erlangen, Germany), with a 32-channel head coil, and the same
examination protocol. A T1-weighted volumetric sequence, based on the Alzheimer's
Disease Neuroimaging Initiative 2 protocol([14]), was acquired with the following
parameters: T1-weighted, three-dimensional magnetization-prepared rapid-acquisition
gradient echo imaging; 1-mm isotropic voxels; repetition time: 2500 ms; echo time:
3.45 ms; inversion time: 1100 ms; and flip angle: 7°. Four trained neuroradiologists
analyzed the images to exclude visible abnormalities and head movement
artifacts.Images were processed and analyzed with FreeSurfer software, version 5.3.0 (Athinoula
A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Boston,
MA, USA), on a high-performance computer, to construct models of the cortical
surface. These well-validated and fully automated procedures were described in
detail by Fischl et al.([15]). In brief, after intensity normalization, skull
stripping, and image segmentation, we generated a single filled white-matter volume
was for each hemisphere, using a connected component algorithm. We then generated a
surface tessellation for each white-matter volume by fitting a deformable template.
This process resulted in a triangular cortical mesh for the gray- and white-matter
surfaces consisting of approximately 150,000 vertices (i.e., points) per hemisphere.
Measures of cortical thickness were computed as the closest distance from the gray-
and white-matter boundaries to the gray matter and cerebrospinal fluid boundary at
each vertex on the tessellated surface. Thickness data were smoothed using a 10-mm
surface-based smoothing kernel. The quantitative results were grouped into age
groups of 5 years each and were compared by gender.
RESULTS
As expected, we noted a reduction in brain volume in the older age groups (Figure 1). The median rate of brain volume
reduction was 2.4% per decade after 60 years of age. Among the 5-year intervals
(from 60 to 105 years), the rate varied from 0.2% to 4.6%, although the differences
were not statistically significant. We also observed no significant difference
between the gray and white matter in terms of the rate of volumetric reduction
(Figure 2).
Figure 1
Brain volume, ICV/total brain volume ratio, and standard deviation, by
age group and gender.
Figure 2
Gray- and white-matter volume distribution, by age group.
Brain volume, ICV/total brain volume ratio, and standard deviation, by
age group and gender.Gray- and white-matter volume distribution, by age group.In each of the age groups studied, the total (uncorrected) brain volume was higher in
the men than in the women (Figure 1). However,
the ICV-corrected brain volumes were higher in the women (Figure 3).
Figure 3
MRI scans of median-volume brains, by age group.
MRI scans of median-volume brains, by age group.Qualitative analysis (visual assessment) of the brain images showed enlargement of
the intracranial cerebrospinal fluid spaces with aging. Sulci enlargement was
consistent with aging and was more related to the age groups than to the changes in
ventricular size (Figure 3).
DISCUSSION
Aging-related reductions in overall brain volume have been widely explored in the
literature and have been observed for gray and white matter alike. Walhovd et
al.[16] assessed the
heterogeneous age responses of various brain volumes and found that age led to a
decline in white-matter structures, as well as in all gray-matter and subcortical
structures, with the exception of the globus pallidus. Conversely, Giorgio et
al.([1])
reported specific brain areas for which they found linear or nonlinear correlations
between volume and age. In the present study, we evaluated the entire brain,
assessed the white- and gray-matter volumes independently. The qualitative
evaluation of the entire brain remains accepted as an important first impression and
plays an important role in clinical practice.A population-based approach to recruiting the participants in our study likely
yielded results different from those obtained when convenience samples are
employed([6]). In a one-year longitudinal study, Resnick et
al.([7])
studied the ventricle-brain ratio and found consistent data, revealing a small but
significant increase over the study period. In the present cross-sectional study, we
assessed ventricle size by age group but could not prove that it increases with age,
the visual analysis showing that the size of the sulci increased more
consistently.In the present study, the total (uncorrected) brain volumes were typically larger in
the men than in the women, in all of the age groups studied, whereas the
ICV-corrected brain volumes were lower in the men. This result is in line with those
of the majority of studies. For instance, Resnick et al.([7]) also found higher
uncorrected brain volumes in men. However, the authors did not find any changes when
brain volume was corrected for height. This last finding is in apparent contrast to
those of our study. However, we used a different type of volumetric acquisition and
evaluated data obtained through voxel-based volumetry (with and without ICV
correction). In fact, when we compared our results with those of Salgorzaei et
al.([9]),
there were even more similarities. Those authors found that the values for brain
volume and ICV were higher in women than in men. In addition, the median rate of
reduction in brain volume over time in the present study was approximately 2.4% per
decade after age 60, which is comparable to the rates reported in previous studies.
Miller et al.([17]) posited that the rate of volume loss in the brain
as a whole is 2% per decade, similar to the approximately 1.9% posited by Seshadri
et al.([18]).
As previously mentioned, the rates observed for the various age groups evaluated in
the present study ranged from 0.2% to 4.6%. That variation may reflect the
population-based nature of our evaluation, the MRI parameters evaluated, or simply
the analysis methods employed. Radiological interpretation based on visual
assessment, even when a comprehensive rating scale is used, has a higher rate of
interobserver variation than does the evaluation of age-related brain volume
reduction([19]). We suspect that the overall effect observed for
the median rate of total (uncorrected) brain volume reduction is not sufficient to
be detected by conventional (non-quantitative) radiological evaluation in clinical
practice.Another important aspect of our study is the epidemiological sampling method. Most
studies of this topic employ conventional recruiting methods. Volunteers respond to
announcements or are part of the hard-to-reach populations. However, the selection
of “super-normal” volunteers as control subjects in investigations of disease
mechanisms, especially those related to the aging process, does not constitute a
valid means of creating a group of controls that are representative of the typical
patients seen in clinical practice. The selection of obviously “successfully aging
subjects” is not equivalent to that of “asymptomatic” healthy individuals and
constitutes a potential source of bias([8]). Our data sample was derived from the
Saúde, Bem-estar e Envelhecimento (Health, Well-being,
and Aging) study([20]), funded by the Pan American Health Organization and
conducted in major cities in South America, which was designed to provide the best
possible representation of the target population. Population-based study designs are
likely to reduce selection biases by ensuring that all individuals enrolled in the
study have levels of exposure to environmental factors similar to those of the
general population([6]). Considering the median brain volume loss in a more
comprehensive scenario helps extrapolate these results to daily practice, because
the neuropsychological history is usually incomplete as well as because there are a
substantial number of conditions, including vascular diseases, dementia,
medications, traumas, and infectious diseases, of varying intensities, all acting
together.One previous study found good agreement between a radiologist and neurosurgeons in
terms of the overall interpretation of computed tomography scans of the brain,
although the level of agreement was found to be poor for assessments of
leukoaraiosis and reduced brain volume([21]). Subtle MRI findings tend to result in
poor inter-rater reliability, although there are divergent results in the literature
regarding the exact degree of inter-rater reliability for each finding or medical
specialty. That underscores the need for automated methods of obtaining quantitative
data on brain volume loss-especially given the rapidly evolving aging process among
city dwellers in South America. We believe that an approach such as the one we have
adopted herein may help improve understanding of this phenomena.Specifically in routine radiological practice, normative imaging data are an
important source of comparison, such data also being used with regularity in
residency and subspecialty training programs. Although the images presented in our
study were not acquired to that end, they provide a source of visual comparison that
could be useful in cases of inconclusive findings regarding volumetric changes in
the brain, especially when quantitative data are not available.One interesting finding of the present study is that the ratio between the ICV and
total brain volume differed between men and women. The men tended to have a smaller
brain volume relative to the ICV than did the women. A possible consequence is that
reports of MRI brain evaluations might be more likely to mention atrophy (or related
terms) when the subject is male, given that the radiological interpretation is
comparative; that is, if the enlarged cerebrospinal fluid spaces are visually more
prominent (as they are in men), the degree of brain reduction might be
overestimated.
CONCLUSION
The determination of brain volume is an important tool for radiologists in clinical
practice. The comparison with peers from the same region, gender, and age group is
crucial. Previous studies have reported that men have bigger brains than do women,
although the ratio of brain matter to ICV is higher in women. The rate of brain
volume reduction observed in our sample is in agreement with that reported in
previous studies. The MRI scans of the median-volume brains, by age group, presented
in this population-based study could be helpful in clinical practice. There is a
need for further studies, involving a more in-depth investigation of this topic, in
order to promote earlier, more accurate diagnosis of a wide variety of diseases that
are prevalent among the elderly.
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Authors: Giovanni B Frisoni; Nick C Fox; Clifford R Jack; Philip Scheltens; Paul M Thompson Journal: Nat Rev Neurol Date: 2010-02 Impact factor: 42.937
Authors: Jae-Won Jang; So Young Park; Young Ho Park; Min Jae Baek; Jae-Sung Lim; Young Chul Youn; SangYun Kim Journal: J Alzheimers Dis Date: 2015 Impact factor: 4.472
Authors: Ana V Oliveira-Pinto; Carlos H Andrade-Moraes; Lays M Oliveira; Danielle R Parente-Bruno; Raquel M Santos; Renan A Coutinho; Ana T L Alho; Renata E P Leite; Claudia K Suemoto; Lea T Grinberg; Carlos A Pasqualucci; Wilson Jacob-Filho; Roberto Lent Journal: Brain Struct Funct Date: 2015-09-28 Impact factor: 3.270
Authors: Débora Terribilli; Maristela S Schaufelberger; Fábio L S Duran; Marcus V Zanetti; Pedro K Curiati; Paulo R Menezes; Márcia Scazufca; Edson Amaro; Cláudia C Leite; Geraldo F Busatto Journal: Neurobiol Aging Date: 2009-03-12 Impact factor: 4.673