Impact of scale space search on age-and gender-related changes in MRIbased cortical morphometry
McConnell Brain Imaging Center, Montréal Neurological Institute, McGill University, Montréal, Québec, Canada. Human Brain Mapping
(Impact Factor: 5.97).
In magnetic resonance imaging based brain morphometry, Gaussian smoothing is often applied to increase the signal-to-noise ratio and to increase the detection power of statistical parametric maps. However, most existing studies used a single smoothing filter without adequately justifying their choices. In this article, we want to determine the extent for which performing a morphometry analysis using multiple smoothing filters, namely conducting a scale space search, improves or decreases the detection power. We first compared scale space search with single-filter analysis through a simulated population study. The multiple comparisons in our four-dimensional scale space searches were corrected for using a unified P-value approach. Our results illustrate that, compared with a single-filter analysis, a scale space search analysis can properly capture the variations in analysis results caused by variations in smoothing, and more importantly, it can obviously increase the sensitivity for detecting brain morphometric changes. We also show that the cost of an increased critical threshold for conducting a scale space search is very small. In the second experiment, we investigated age and gender effects on cortical volume, thickness, and surface area in 104 normal subjects using scale space search. The obtained results provide a perspective of scale space theory on the morphological changes with age and gender. These results suggest that, in exploratory studies of aging, gender, and disease, conducting a scale space search is essential, if we are to produce a complete description of the structural changes or abnormalities associated with these dimensions. Hum Brain Mapp, 2012. © 2012 Wiley Periodicals, Inc.
Available from: Lu Zhao
- "To address this issue, we used the scale space search based brain morphometric analysis algorithm [Zhao et al., 2013] to obtain a relatively complete description of the structural changes at different scale levels (different smoothing filter sizes). Compared with conventional single-filter analyses, the scale space search method can properly capture the variations in analysis results caused by variations in smoothing, and it can obviously increase the detection sensitivity (for more details, please read [Zhao et al., 2013]). The scale space search analysis was implemented using our Scale Space Cortical Morphometry toolbox (http:// www.bic.mni.mcgill.ca/users/zhao/softwares.html) and the SurfStat toolbox (http://www.math.mcgill.ca/keith/ "
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ABSTRACT: Functional neuroimaging studies have revealed abnormal brain dynamics of male sexual arousal (SA) in psychogenic erectile dysfunction (pED). However, the neuroanatomical correlates of pED are still unclear. In this work, we obtained cortical thickness (CTh) measurements from structural magnetic resonance images of 40 pED patients and 39 healthy control subjects. Abnormalities in CTh related to pED were explored using a scale space search based brain morphometric analysis. Organizations of brain structural covariance networks were analyzed as well. Compared with healthy men, pED patients showed significantly decreased CTh in widespread cortical regions, most of which were previously reported to show abnormal dynamics of male SA in pED, such as the medial prefrontal, orbitofrontal, cingulate, inferotemporal, and insular cortices. CTh reductions in these areas were found to be significantly correlated with male sexual functioning degradation. Moreover, pED patients showed decreased interregional CTh correlations from the right lateral orbitofrontal cortex to the right supramarginal gyrus and the left angular cortex, implying disassociations between the cognitive, motivational, and inhibitory networks of male SA in pED. This work provides structural insights on the complex phenomenon of psychogenic sexual dysfunction in men, and suggests a specific vulnerability factor, possibly as an extra "organic" factor, that may play an important role in pED. Hum Brain Mapp, 2015. © 2015 Wiley Periodicals, Inc.
© 2015 Wiley Periodicals, Inc.
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ABSTRACT: Many large-scale longitudinal imaging studies have been or are being widely conducted to better understand the progress of neuropsychiatric and neurodegenerative disorders and normal brain development. The goal of this article is to develop a multiscale adaptive generalized estimation equation (MAGEE) method for spatial and adaptive analysis of neuroimaging data from longitudinal studies. MAGEE is applicable to making statistical inference on regression coefficients in both balanced and unbalanced longitudinal designs and even twin and familial studies, whereas standard software platforms have several major limitations in handling these complex studies. Specifically, conventional voxel-based analyses in these software platforms involve Gaussian smoothing imaging data and then independently fitting a statistical model at each voxel. However, the conventional smoothing methods suffer from the lack of spatial adaptivity to the shape and spatial extent of region of interest and the arbitrary choice of smoothing extent, while independently fitting statistical models across voxels does not account for the spatial properties of imaging observations and noise distribution. To address such drawbacks, we adapt a powerful propagation-separation (PS) procedure to sequentially incorporate the neighboring information of each voxel and develop a new novel strategy to solely update a set of parameters of interest, while fixing other nuisance parameters at their initial estimators. Simulation studies and real data analysis show that MAGEE significantly outperforms voxel-based analysis.
Available from: Hongtu Zhu
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ABSTRACT: The aim of this paper is to develop a spatial Gaussian predictive process (SGPP) framework for accurately predicting neuroimaging data by using a set of covariates of interest, such as age and diagnostic status, and an existing neuroimaging data set. To achieve better prediction, we not only delineate spatial association between neuroimaging data and covariates, but also explicitly model spatial dependence in neuroimaging data. The SGPP model uses a functional principal component model to capture medium-to-long-range (or global) spatial dependence, while SGPP uses a multivariate simultaneous autoregressive model to capture short-range (or local) spatial dependence as well as cross-correlations of different imaging modalities. We propose a three-stage estimation procedure to simultaneously estimate varying regression coefficients across voxels and the global and local spatial dependence structures. Furthermore, we develop a predictive method to use the spatial correlations as well as the cross-correlations by employing a cokriging technique, which can be useful for the imputation of missing imaging data. Simulation studies and real data analysis are used to evaluate the prediction accuracy of SGPP and show that SGPP significantly outperforms several competing methods, such as voxel-wise linear model, in prediction. Although we focus on the morphometric variation of lateral ventricle surfaces in a clinical study of neurodevelopment, it is expected that SGPP is applicable to other imaging modalities and features.
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