Skip to main content
Neuroscience Bulletin logoLink to Neuroscience Bulletin
. 2017 Mar 10;33(2):219–237. doi: 10.1007/s12264-017-0118-1

Candidate Biomarkers in Children with Autism Spectrum Disorder: A Review of MRI Studies

Dongyun Li 1, Hans-Otto Karnath 2,3, Xiu Xu 1,
PMCID: PMC5360855  PMID: 28283808

Abstract

Searching for effective biomarkers is one of the most challenging tasks in the research field of Autism Spectrum Disorder (ASD). Magnetic resonance imaging (MRI) provides a non-invasive and powerful tool for investigating changes in the structure, function, maturation, connectivity, and metabolism of the brain of children with ASD. Here, we review the more recent MRI studies in young children with ASD, aiming to provide candidate biomarkers for the diagnosis of childhood ASD. The review covers structural imaging methods, diffusion tensor imaging, resting-state functional MRI, and magnetic resonance spectroscopy. Future advances in neuroimaging techniques, as well as cross-disciplinary studies and large-scale collaborations will be needed for an integrated approach linking neuroimaging, genetics, and phenotypic data to allow the discovery of new, effective biomarkers.

Keywords: Autism spectrum disorder, Biomarker, Neuroimaging, Structural MRI, Diffusion tensor imaging, Resting-state functional MRI, Magnetic resonance spectroscopy, Children, Human

Introduction

Autism spectrum disorder (ASD) is a neurodevelopmental disorder that has a strong genetic basis, a heterogeneous etiology, and various clinical presentations. The core symptoms of ASD include: (1) deficits in social communication and social interaction, and (2) restricted, repetitive patterns of behavior, interests, or activities [1]. The prevalence of ASD has dramatically increased recently from 4 in 10000 to 1 in 68 children [2, 3]. Along with the soaring incidence of ASD, significant financial and emotional costs to the individuals and their families, as well as the numerous pressures on our medical, social, and political lives have been engendered [4]. Hence, determining the causes and making an accurate diagnosis as well as early and effective intervention seem crucial for society [5].

So far, the diagnosis of ASD and the selection criteria for clinical trials have been guided by the Diagnostic and Statistical Manual of Mental Disorders or behavioral diagnostic scales. The apparent disadvantage of symptom-based criteria is that a similar symptom or phenotype may arise from diverse sets of biochemical processes, especially for disorders with numerous genetic or environmental factors like ASD [6]. In the past decade, searching for genetic biomarkers has been one of the hottest spots in ASD research. Numerous related genes have been reported including NRXN1, SHANK3, SHANK2, MECP2, SNC2A, CHD8, DYRKIA, POG2, GRIN2B, KATNAL2, NLGN3, NLGN4, CNTN4, CDH10, CDH9, and SEMA5A [717]. Unfortunately, the genetic underpinnings of ASD are neither simple nor consistent, considering that only 10%–38% of ASD cases have been reported with known genetic deficits [1820]. Because of this heterogeneity and complexity, interest and efforts into searching for more biomarkers and quantifiable parameters are increasing in order to facilitate early and reliable diagnosis, as well as to subgroup patients sharing common pathophysiological underpinnings.

Magnetic resonance imaging (MRI), a non-invasive examination tool, has been widely applied to ASD populations to delineate the developmental trajectory of the brain. Major advances in structural and functional MRI techniques in the past decades have greatly enriched our understanding of neuropathological differences in ASD [19, 21, 22]. Generally, structural MRI has revealed ASD to be a disorder with general and regional brain enlargement, especially in the frontotemporal cortices, while functional MRI studies have highlighted diminished connectivity, especially between frontal-posterior regions [19, 2125].

Here, we review recent MRI studies (since 2000) in young children with ASD, aiming to provide effective biomarkers for the diagnosis of childhood ASD. We focus on studies using structural imaging methods, structural connectivity analyses, diffusion tensor imaging (DTI), neurochemical or metabolic quantification methods, and magnetic resonance spectroscopy (MRS), as well as functional connectivity analyses with resting-state functional MRI (rs-fMRI). We do not consider task-based functional methods, since it is almost impossible to keep a young child awake and still during a functional scan. We place the emphasis on young ASD children because in adolescents and adults the altered brain structures and activities may merely reflect the social deprivation experience elicited by reduced social attention during childhood. Therefore, it is impossible to tell whether observed functional or structural differences are the cause or the result of ASD neuropathology. Another reason is based on brain plasticity. There is growing evidence that the first 3 years of life is a particularly critical developmental period for children with ASD [26, 27]. Thus, the earlier the abnormal neurodevelopmental trajectory (even in infants and toddlers) is identified, the better guided intervention strategies for ASD children can be achieved.

Structural MRI

Structural MRI analysis for neurodevelopmental disorders began to emerge in the 1990s when it focused on the neuroanatomical aspects of brain development. It has been used to measure the total brain volume and volumes of specific structures. Earlier studies used manual delineation for the gray (GM) and white matter (WM) to calculate the volumes of specific regions of interest (ROIs). With technical developments, it is now possible to use program codes to measure the volumes automatically, allowing large data sets to be processed more efficiently [28]. Based on the different analytic methods for structural data, structural MRI studies can be classified into voxel-based morphometry (VBM) and surface-based morphometry (SBM) [29]. VBM targets tissue density and usually focuses on relative GM concentration or volume, or regional volume differences of a certain tissue. SBM addresses topological features, like surface curvature and degree of folding [29, 30]. Notably, brain volume and surface curvature have been hypothesized to have dissociable developmental trajectories with, putatively, different genetic and neurodevelopmental bases [22, 31, 32]. Table 1 summarizes the findings of structural MRI studies in children.

Table 1.

Structural MRI studies of children with ASD.

Reference Age range Brain regions Methods Findings in ASD group
Elia et al. (2000) [57] 5–17 years Corpus callosum; midbrain; cerebellar vermis Area measurements; T-test; regression No abnormalities in the total vermis, vermis lobules VI-VII, pons, and midbrain
Carper et al. (2002) [35] 2–4 years WM and GM volumes ROI; SPSS ↑ WMV in frontal and parietal lobes
↑ GMV in frontal and temporal lobes
Sparks et al. (2002) [36] 3–5 years Cerebrum; cerebellum; amygdala; hippocampus ROI; SPSS; ANCOVA ↑ TBV and amygdala, cerebellar, and hippocampus volume
Herbert et al. (2003) [51] 7–11 years Cerebrum; cerebellum ROI; semi-automated segmentation; SPSS; GLM ↑ TBV and total cerebellar volume
Akshoomoff et al. (2004) [37] 4–6 years Cerebrum; cerebellum; cerebellar vermis; TBV ROI; ANOVA; segmentation Low-functioning autism: ↑ TBV and cerebral volume; ASD: ↑ TBV, cerebral and cerebellar GMV and WMV, anterior and posterior cerebellar vermis area
McAlonan et al. (2005) [56] 10–12 years GM; WM regional density VBM; BAMM; SPSS; GLM; MANCOVA ↓ GM density in frontal and parietal areas; ↓ WM density in cerebellum and left internal capsule and fornices
Hazlett et al. (2006) [38] 1.5–3 years Cerebrum; cerebellum ROI; NLMM; segmentation ↑ GMV and WMV in cerebrum
Hardan et al. (2006) [42] 8–13 years Cortical thickness SBM; Freesurfer Total cerebral sulcal and gyral thickness; no significant difference in frontal and occipital areas
Munson et al. (2006) [62] 3–4 years Cerebrum; amygdala; hippocampus Area measurements; linear modal ↑ Right amygdala volume
Schumann et al. (2010) [39] 1.5–5 years Cerebrum ROI; SPSS; ANCOVA; segmentation ↑ GMV and WMV in cerebrum; notably in frontal, temporal, and cingulate cortices
Jiao et al. (2010) [44] 7–11 years Cortex SBM; T-test; Freesurfer ↑ Thickness in left caudal anterior cingulate cortex and left frontal pole; ↓ thickness in right entorhinal, right lateral orbitofrontal, left lateral orbitofrontal, right medial orbitofrontal, left medial orbitofrontal cortex, and right pars triangularis
Hazlett et al. (2011) [34] 6–7 months Cerebrum; cerebellum ROI; GLM; automatic segmentation; ANOVA No significant difference in TBV, cerebral cortex, cerebellum, or lateral ventricle volumes
Shen et al. (2013) [40] (Longitudinal) 6–9 months; 13–14 months; 19–21 months Cerebrum ROI; LMM; manual segmentation ↑ CSF over frontal lobe at 6–9 mos; ↑ total cerebral volumes at 12–15 mos
Nordahl et al. (2012) [63] 2–4 years Amygdala ROI; ANCOVA ↑ Amygdala volume at both time points
Dierker et al. (2015) [45] 9–12 years Cortex SBM; ANOVA; freesurfer Bilateral differences in sulcal depth in the anterior-insula, frontal-operculum, and temporal-parietal junction
Frazier et al. (2009) [64] 7–12 years Corpus callosum ROI; area measurement ↓ Volume of corpus callosum
Barnea-Goraly et al. (2014) [79] (Longitudinal) 8–12 years; 10–14 years Amygdala; hippocampus Area measurement; rm-ANOVA No difference in hippocampus of both hemispheres

WM, white matter; GM, grey matter; TBV, total brain volume; ROI, region of interest; SBM, surface-based morphometry; VBM, voxel-based morphometry; GLM, general linear models; ANOVA, analysis of variance; ANCOVA, analysis of covariance; rm-ANOVA, repeated measures ANOVA; LMM, linear mixed models; NLMM, non-linear mixed models; SPM, Freesurfer, ad SPSS are data analysis packages.

Cortex

The most consistent observation regarding structural cortical changes in young ASD children versus controls is the increased total volume both in the cortical GM and WM [22, 30, 33, 34]. Increased GM volume (GMV) and WM volume (WMV) have been found in the frontal and temporal lobes and are less pronounced in the parietal and occipital lobes. For example, Carper et al. (2002) revealed increased frontal and temporal GMV and frontal and parietal WMV at young ages (2–4 years old) [35]. Sparks et al. (2002) likewise observed increased cerebral volumes in autistic children aged 4–6 years [36]. Akshoomoff et al. (2004) reported increased total brain volume (TBV), as well as significantly increased WMV and GMV in children of 4–6 years with low-functioning autism compared with high-functioning autism (HFA) [37]. Hazlett et al. (2006) investigated 51 younger autistic children and 25 typically-developing controls (aged 18–35 months). They reported increased cerebral GMV and WMV in the brains of the autistic group [38]. In a group of 1.5–5 year-old autistic children, Schumann et al. (2010) found no changes in the occipital lobe but enlarged cerebral GMV in the frontal, temporal, and parietal lobes, as well as in the cingulate gyrus (located in the limbic lobe) [39]. Hazlett et al. (2011) compared the TBV of 6-month-old high-risk infants with autistic siblings with low-risk infants without autistic family members. They found no significant difference in the cerebrum or lateral ventricle volumes, consistent with the hypothesis that the brain enlargement might be a postnatal event, occurring at ~12 months of age [34]. However, Shen et al. (2013) identified excessive cerebrospinal fluid (CSF) over the frontal lobes at 6–9 months of age but no such difference at 12–15 and 18–24 months [40]. Recently, Gori et al. (2015) extracted features from GM, WM, and CSF measurements to classify autistic and control brains in 4-year-old males. They found that only GM features in different sub-regions showed up to 80% classification performance [41].

SBM studies have only been performed with older autistic children. For instance, Hardan et al. (2006) applied atlas-based SBM to children aged 10 years. They found no changes in the frontal or occipital lobes but increased total cerebral sulcal and gyral thicknesses in the temporal and parietal lobes [42]. Two years later, Hardan et al. (2009) performed follow-up scans on the same group of autistic children, and revealed decreased cortical thickness in the frontal, temporal, and occipital lobes compared to controls [43]. Moreover, another SBM study by Jiao et al. (2010) on 9-year-old autistic children showed decreased thickness in the right entorhinal, right lateral orbitofrontal, left lateral orbitofrontal, right medial orbitofrontal, left medial orbitofrontal cortex, and right pars triangularis, as well as increased thickness in the left caudal anterior cingulate cortex and left frontal pole [44]. More recently, Dierker et al. (2015) found bilateral differences in sulcal depth in the anterior-insula, frontal-operculum, and temporal-parietal junctions [45].

According to the above studies, the main differences in the cerebrum of young autistic children are the enlarged total volume of both GM and WM. The most prominent differences were found in the frontal and temporal lobes as well as precentral regions. The growing cerebral volume in early childhood indicates simultaneously decreasing GM and WM density [40]. Interestingly, the changes seem to begin in the autistic cerebrum at the age of ~12 months, i.e., the cerebral enlargement does not occur earlier than 12 months of age [34, 46].

Cerebellum and Subcortical Areas

Cerebellum and Vermis

Cerebellar dysfunction may play a crucial role in the etiology of ASD [47, 48]. The cerebellum is considered to be one of the most consistent sites of abnormality in autism [49, 50]. Most morphometric studies of ASD children have reported increased total cerebellar volume [36, 51, 52] and decreased GMV in some subregions, e.g., crus I and lobules VIII and IX [5355]. However, the results on WMV have been inconsistent. For instance, Courchesne et al. (2001) found a larger cerebellar WMV in 2–3 year-old autistic children [33], while McAlonan et al. (2005) reported decreased WM density in the cerebellum [56]. Regarding the vermis, the results are also contradictory. In older children, Elia et al. (2000) measured the sizes of the cerebellar areas in 22 autistic children and reported no abnormalities in the total vermis, vermis lobules VI–VII, pons, and midbrain [57]. In contrast, Akshoomoff et al. (2004) revealed larger cerebellar WMV and GMV and increased areas of the anterior and posterior cerebellar vermis in 6-year-old autistic children [37].

Amygdala

The amygdala has been the focus of several studies in children with ASD, given its important role in socio-emotional processing [5861]. Sparks et al. (2002) investigated 29 autistic children and typically-developing controls with an average age of 3.9 years and showed bilateral enlargement of the amygdala that was proportional to the overall increase in total cerebral volume [36]. Munson et al. (2006) argued that the enlargement was only found in the right amygdala at the age of 3–4 years [62]. Nordahl et al. (2012) scanned 85 autistic children aged 37 months on average, and re-scanned 45 members of the same group one year later. They found an increased amygdala volume in both cases, confirming that the enlargement starts at ~3 years [63].

Corpus Callosum

A decreased corpus callosum (CC) size in the autistic population has been consistently reported, including reductions localized in the mid-sagittal area, anterior CC, body, and posterior splenium [2, 22, 43, 6469]. A reduced CC has been associated with reduced integration of information and slower processing [2, 68, 69]. However, to our knowledge, CC changes in the early childhood period have not yet been studied. A report by Frazier et al. (2012) investigated 19 autistic children with a mean age of 10.6 years and found consistent reductions in the total CC volume [65].

Basal Ganglia

The basal ganglia play an important role in cognition and motor control via participation in frontostriatal, thalamocortical, and limbic circuits [7073]. In neuroimaging studies of ASD, the basal ganglia have been studied regarding their association with repetitive behaviors [74, 75]. The most consistent finding is an increased caudate volume [76, 77]. Unfortunately, most of the studies were conducted in adults or late adolescence but not in childhood.

Hippocampus

Sparks et al. (2002) found enlarged hippocampi in autistic children at the ages of 3–4 years [36]. Similarly, in 7.5–12.5 year-olds, Schumann et al. (2004) also revealed enlarged hippocampi, especially in an HFA group [78], while in a 10 year-old group, Barnea-Goraly et al. (2014) observed an enlargement only in the right hippocampus [79]. Interestingly, in an older group, Barnea-Goraly et al. (2014) reported no difference in the hippocampus of both hemispheres. These findings indicate that the hippocampus in ASD has an unbalanced growth pattern during early brain development [79].

Conclusions

The most consistent structural MRI finding is the increased growth of total cortical volume in early ASD children. A similar trend has also been demonstrated in some subcortical brain regions (e.g., amygdala and hippocampus) and the cerebellum. Interestingly, studies comparing ASD adolescents or adults with controls did not find such differences and have even reported decreased TBV in ASD patients [35, 80]. Thus, it seems as if brain development during early childhood in ASD is more voluminous than in a typically-developing brain, especially in the frontal and temporal lobes, followed by a possibly reduced volumetric capacity of the brain after adolescence [81, 82].

Diffusion Tensor Imaging (DTI)

Molecular studies have demonstrated dysmaturation of the WM characterized by microstructural changes or disorganization in the brains of autistic populations [83, 84]. It has been reported that synaptogenesis is altered in children with ASD, affecting myelination, and thus compromising WM integrity [85]. DTI, as a non-invasive tool, has been applied in the last decade to developing brains to study both the local connectivity and WM tracts as well as fasciculi that connect regions and lobes [2, 8690]. Metrics such as fractional anisotropy (FA), and mean diffusivity (MD) have been used to measure the directionality and the amount of diffusion, respectively, in a particular ROI or at the level of individual voxels. The most commonly-used DTI methods are tractography, voxel-wise analysis, and tract-based spatial statistics (TBSS). Table 2 summarizes the findings of DTI studies in children.

Table 2.

Diffusion tensor imaging studies of ASD children.

Reference Age range Brain regions Methods Findings in ASD group
Sundaram et al. (2008) [91] 2–7 years Association fibers in frontal lobes DT; ROI; MANCOVA; DTIstudio ↑ MD in short and long-range fibers; ↓ FA in short-range fibers
Hong et al. (2011) [92] 7–11 years Corpus callosum (CC) DT; ROI; WM density and volume; FSL; SPSS ↓ WM density in the anterior third of the CC; ↑ MD in the anterior third of the CC
Nagae et al. (2012) [93] 7–18 years (+/-language impairment) Superior longitudinal fasciculus (SLF); corticospinal tract (CST) DT; GLM; SPSS; DTIstudio ↑ MD in CST (ASD without language impairment); ↑ MD in left SLF (ASD with language impairment)
Wolff et al. (2012) [94] (Longitudinal) 6–7 months; 12–13 months; 23–25 months Global main tracts DT; ROI; DTIprep; SAS ↑ FA in CC body, left fornix, inferior longitudinal fasciculus, uncinate fasciculus (6 mo); no difference in FA (12 mo); ↓ FA in left anterior internal capsule and anterior thalamic radiation (24 mo)
Nair et al. (2013) [95] 9–17 years Cortex; thalamus PT; ROI; FSL; T-test ↑ MD in thalamo-cortical connectivity; negative correlation between fronto-thalamic FA and ADOS score
Joseph et al. (2014) [96] 4–6 years Arcuate fasciculus PT; ANOVA; FSL ↓ RD of arcuate fasciculus
Cheung et al. (2009) [97] 6–14 years Global white matter VBM; SPM; GLM; SPSS ↓ FA in bilateral prefrontal and temporal regions; ↑ FA in SLF and left occipital lobe
Ke et al. (2009) [98] 6–11 years Regional frontal and temporal gyri VBM; SPM ↓ WM density in right frontal and left parietal lobe; ↓ FA in frontal left temporal lobe
Barnea-Goraly et al. (2010) [99] 9–14 years Regional white matter VBM; FSL ↓ FA in frontal, temporal and parietal lobes
Poustka et al. (2012) [100] 8–12 years Fornix; SLF; uncinate fasciculus; CC VBM; DT; SPM ↓ FA in the uncinate fasciculus and right SLF; negative correlation between FA and severity of ASD symptoms
Peterson et al. (2015) [101] 9–12 years Global white matter ROI; ANCOVA; LDDMM ↑ MD through left hemisphere, especially outer-zone of cortical WM
Kumar et al. (2010) [106] 2–9 years Global white matter tracts TBSS; DT; ANOVA; FSL ↓ FA in right uncinate fasciculus, right cingulum, and CC; ↑ MD in right arcuate fasciculus
Weinstein et al. (2011) [107] 2–4 years Global white matter tracts TBSS; DT; FSL ↑ FA in CC, left SLF and bilateral cingulum
Jou et al. (2011) [88] 7–15 years Global white matter tracts TBSS; FSL; SPSS ↓ FA in general association and projection tracts
Shukla et al. (2010) [85] 12–13 years CC; internal capsule; middle cerebellar peduncle TBSS; ROI; VBM; FSL; SPM ↓ FA ↑ MD for global white matter tracts
Walker et al. (2012) [108] 3–7 years Global white matter tracts TBSS; FSL ↓ FA in various areas; ↑ MD in posterior brain regions

WM, white matter; GM, grey matter; RD, radial diffusivity; FA, fractional anisotropy; MD, mean diffusivity; ROI, region of interest; TBSS, tract-based spatial statistics; DT, deterministic tractography; PT, probabilistic tractography; GLM, general linear models; ANOVA, analysis of variances; LDDMM, large deformation diffeomorphic metric mapping; VBM, voxel-based morphometry; SPM, FSL, DTIstudio, DTIprep, SPSS, and SAS are data analysis packages.

Tractography

The majority of tractography studies have found reduced FA and increased MD, indicating more WM microstructural disorganization in the frontal and temporal lobes or dominant tracts. For example, Sundaram et al. (2008) applied deterministic tractography to analyze WM abnormalities in the frontal lobe and checked for short-range connectivity changes in ASD children. They reported higher MD in the whole frontal lobe as well as reduced FA for short-range fibers in ASD children [91]. Hong et al. (2011) also used deterministic tractography to examine connectivity in the CC in HFA children. They revealed decreased WM density in the anterior third of the CC, as well as higher MD and a lower fiber number in the anterior third of the transcallosal fiber tracts [92]. Using deterministic tractography, Nagae et al. (2012) revealed higher MD in the temporal portion of the left superior longitudinal fasciculus in ASD children with language impairment, as well as a significant negative correlation between MD and language score [93]. Wolff et al. (2012) investigated WM fiber tracts in a group of high-risk infants from 6 to 24 months old. Higher FA values were found in the fornix, uncinate fasciculus, and inferior longitudinal fasciculus at 6 months, whereas no such differences were observed at 12 months [94]. Nair et al. (2013) used both fMRI and probabilistic DTI tractography to assess the integrity of thalamo-cortical connectivity in children and adolescents with ASD. They reported increased MD in the thalamo-cortical connections, and decreased functional connectivity in the thalamo-cortical circuitry, as well as a negative correlation between the fronto-thalamic FA and the social and total Autism Diagnostic Observation Schedule score [95]. More recently, Joseph et al. (2014) applied both structural MRI and probabilistic DTI tractography to investigate the anatomo-behavioral relationship addressing language ability in young ASD children. In the ASD children, they found no difference in GM asymmetries but decreased leftward volume and radial diffusivity of the arcuate fasciculus [96].

Voxel-Wise Analysis

Voxel-wise analysis is used to find areas of significant difference and to overcome possible user bias. Cheung et al. (2009) reported reduced FA in bilateral prefrontal and temporal regions as well as the frontal striato-temporal and posterior brain pathways that are associated with communication and social reciprocity impairment and repetitive behavior [97]. Ke et al. (2009) investigated the WM abnormalities in a group of Chinese HFA children. The voxel-wise whole-brain analysis of FA showed decreased WM density in the right frontal lobe, left parietal lobe, and right anterior cingulate [98]. Barnea-Goraly et al. (2010) found reduced FA in age-matched unaffected siblings as compared to children with ASD, suggesting that this may be a potential marker of genetic risk [99]. Poustka et al. (2012) revealed decreased FA values in the uncinate fasciculus and right superior longitudinal fasciculus as well as a negative correlation between the FA values of the affected fiber tracts and the severity of ASD symptoms [100]. A more recent study by Peterson et al. (2015) found widespread increases in MD in many regions of the left hemisphere in children with ASD as compared to typically-developing children [101], supporting the left hemispheric abnormality or atypical hemispheric dominance that has been hypothesized in ASD for the past three decades [102104]. Peterson et al. (2015) used an atlas-based ROI analysis in HFA children and found significantly increased MD of the outer-zone cortical WM, suggesting hypomyelination and increased short-range cortico-cortical connections which might be due to the early WM overgrowth [101].

Tract-Based Spatial Statistics (TBSS)

A further innovative method of DTI analysis is TBSS [105]. This method provides advantages over traditional voxel-wise analysis, since it does not require smoothing and allows for a higher spatial comparability. A mean FA skeleton is built and thresholded to exclude areas of high inter-individual variability. Each individual’s FA map is then projected onto the skeleton to collect standard voxel-wise FA statistics across all the individuals. Kumar et al. (2010) combined deterministic tractography and TBSS to investigate the CC region in 5-year-old ASD children. They found lower FA, higher MD, larger numbers of streamlines and voxels, and longer streamlines as well as correlation between macrostructural changes in the uncinate fasciculus and the score on the Gilliam Autism Rating Scale [106]. Weinstein et al. (2011) reported increased FA within the genu and body of the CC, left superior longitudinal fasciculus, and right and left cingulum in a group of very young ASD children using TBSS. The tractography revealed that the increased FA was concentrated in the mid-body of the CC and in the left cingulum [107]. Jou et al. (2011) found reduced FA in the forceps minor, inferior fronto-occipital fasciculus, and superior longitudinal fasciculus [88]. Shukla et al. (2011) demonstrated reduced FA and higher MD in the CC, anterior and posterior limbs of the internal capsule, inferior longitudinal fasciculus, inferior fronto-occipital fasciculus, superior longitudinal fasciculus, cingulum, anterior thalamic radiation, and corticospinal tract [85]. Similarly, Walker et al. (2012) revealed decreased FA values in various brain regions and increased MD in some tracts [108].

Conclusions

Studies using voxel-wise analysis have revealed decreased FA and increased MD in the major WM tracts of ASD children. However, the voxel-wise analysis of DTI has methodological disadvantages such as the dependency on the size of the smoothing kernel and the hindrance of confident conclusions [30]. TBSS overcomes these flaws and has been used in the majority of more recent and on-going tractography studies. Predominantly the latter have revealed reduced FA and higher diffusivity in the main tracts in ASD children, including the uncinate fasciculus, arcuate fasciculus, cingulum bundle, inferior longitudinal fasciculus, and inferior fronto-occipital fasciculus.

Resting-State Functional Magnetic Resonance Imaging

Brain connectomics is a relatively new field of research that maps the brain’s large-scale functional networks “at rest”. Correlated and anti-correlated fMRI signals are measured without performing specific tasks. These signals imply a functional connectivity that reflects structural connectivity [109, 110]. They can be used to explore both the spatial and temporal deviations of the topology of atypical neurodevelopmental processes [111]. Table 3 summarizes the findings of rs-fMRI studies in children.

Table 3.

Resting-state functional MRI studies in ASD children.

Reference Age range (years) Seed brain regions Findings in ASD group
Di Martino et al. (2011) [114] 7–13 Striatal regions (caudate, putamen) ↑ Connectivity in striatal-cortical circuitry
↑ Striatal functional connectivity with the pons
↑ Connectivity of brainstem area, with bilateral insular regions
Lynch et al. (2013) [115] 7–12 Precuneus ↓ Connectivity to cuneus, caudate, and thalamic nuclei
Posterior cingulate cortex ↑ Connectivity to medial and anterolateral temporal cortex, lingual gyrus, posterior parahippocampal gyrus, temporal pole, entorhinal cortex, and perirhinal cortex within the anterior aspect of the medial temporal lobe
Retrosplenial cortex ↑ Connectivity to inferior frontal and middle frontal gyrus, dorsal medial prefrontal cortex, posterior insular cortex, lingual gyrus, posterior parahippocampal gyrus, temporal pole, posterior superior temporal sulcus, and anterior supramarginal gyrus
Uddin et al. (2013) [116] 7–12 Anterior cingulate cortex ↑ Connectivity to superior frontal gyrus, thalamus, and bilateral insular cortex
Precuneus ↑ Connectivity to posterior cingulate cortex and left angular gyrus
Superior temporal gyrus ↑ Connectivity to middle temporal gyrus
Postcentral gyrus ↑ Connectivity to precentral gyrus, left posterior insular cortex, and thalamus
Lateral occipital cortex ↑ Connectivity to intracalcarine cortex, and occipital pole
Wiggins et al. (2011) 119] 10–18 Right superior frontal gyrus ↓ Connectivity to posterior superior frontal gyrus
Rudie et al. (2012) [118] 10–15 (+/-MET mutation) Posterior cingulate cortex ↓ Connectivity of overall default mode network
↓ Connectivity to medial prefrontal cortex in MET-homozygous
↓ Connectivity to medial prefrontal cortex within ASD group
Abrams et al. (2013) [117] 8–12 Posterior superior temporal sulcus ↓ Connectivity of bilateral ventral tegmental area, nucleus accumbens, putamen of basal ganglia, ventromedial prefrontal cortex, left caudate, anterior insular cortex, and orbitofrontal cortex
Nair et al. (2013) [95] 9–17 Right thalamus
Thalamus
↑ Connectivity to temporal areas
↓ Connectivity to prefrontal, parietal-occipital, and somatosensory cortical regions

In an attempt to elucidate putative neurobiological underpinning mechanisms, Just et al. (2004) proposed the “hypoconnectivity theory of ASD”, claiming that the deficit of integration of neuronal information in ASD might be associated with an overall under-functioning of the brain’s integrative circuitry [112]. However, Courchesne and Pierce (2005) suggested that the developmental trajectory for functional brain connectivity in ASD individuals is characterized by both an early local hyperconnectivity and a long-distance hypoconnectivity of the prefrontal cortex based on the findings of an increased short-range (local) connectivity within the frontal lobe but a decreased degree of functional long-range (global) connectivity with the rest of the brain [113]. Di Martino et al. (2011) found only hyperconnectivity in the superior temporal gyrus, insula, and brainstem areas [114]. Moreover, Lynch et al. (2013) and Uddin et al. (2013) both demonstrated increased connectivity in the cingulate cortex and inferior and superior frontal gyri, as well as other specific areas [115, 116]. However, other childhood ASD studies mostly revealed reduced long-range connectivities across different brain regions [95, 117119]. Thus, it has been suggested that the increased local connectivity in ASD children results from overcompensation for the reduced long-range connectivity [95].

1H-MRS Metabolite Spectrum

Neurochemicals are involved in cortical activity as well as in the metabolic processes in the brain. Each metabolite has a unique chemical shift which acts as a signature that is used for the quantification of that specific metabolite. The most common method of metabolite quantification in vivo is through the proton resonance of hydrogen (1H) atoms [120]. 1H-magnetic resonance spectroscopy (1H-MRS) is a non-invasive imaging technique that estimates specific chemical metabolites [121]. Previous studies mainly used 1H-MRS to quantify creatine and phosphocreatine (Cr+PCr), a measure of cellular energy metabolism [122]; N-acetylaspartate (NAA), a marker of neuronal density and activity [123]; choline-containing compounds, a measure primarily reflecting the constituents of cell membranes [122]; and glutamine/glutamate/gamma-aminobutyric acid (GABA) (“Glx”). Recent 1H-MRS studies in ASD patients showed generally decreased NAA [124, 125], Cr+PCr, choline, and Glx [125], as well as increased Glx in adults [126]. However, previous studies also exhibited some inconsistencies, such as decreased [127131], unchanged, or increased NAA in ASD children compared with controls [127, 132135]. In the following, we categorize the recent 1H-MRS studies in young individuals with ASD according to the four main detectable chemical metabolites: Cr+PCr, NAA, choline, and Glx. Table 4 summarizes the findings of MRS studies in children.

Table 4.

MRS studies in ASD children.

Reference Age range (years) Cr+PCr NAA Cho Glx Findings in ASD group
Friedman et al. (2003) [129] 3–4 ↓ Cr+PCr in frontal, parietal, temporal, occipital and thalamus
↓ NAA in bilateral frontal, parietal, and cingulate areas, and in right superior temporal gyrus and left putamen
↓ Cho in cortical areas, temporal lobes, and thalamus
DeVito et al. (2007) [128] 6–17 ↓ Cr+PCr in GM of frontal, temporal, occipital cortices and cerebellum
↓ Cho in cortical areas, temporal lobes, and thalamus
↓ Glx in GM of frontal, occipital, and temporal regions as well as cerebellum
Hardan et al. (2008) [130] 8–15 ↓ Cr+PCr in bilateral thalamus
↓ Cho in cortical areas, temporal lobes, and thalamus
↑ Glx of thalamus is associated with abnormal sensory sensitivity and deficits in body movement modulation
Corrigan et al. (2013) [138] 3–4 ↓ Cr+PCr in GM and WM generally
↓ Cho in cortical areas, temporal lobes, and thalamus generally
Levitt et al. (2003) [131] 5–16 ↓ Cr+PCr in frontal, parietal, temporal, occipital, and thalamus
↓ NAA in bilateral frontal and parietal areas, and in the left caudate
↓ Cho in cortical areas, temporal lobes, and thalamus
↑ Cho in caudate, anterior cingulate cortex and hippocampus-amygdala complex
Friedman et al. (2006) [144] 3–4 ↓ NAA in both GM and WM generally
↓ Cho in cortical areas, temporal lobes, and thalamus
Corrigan et al. (2013) [138] 3–4 ↓ NAA in both GM and WM in cortical regions
↓ Glx in both cortical GM and WM generally
Fujii et al. (2010) [145] 2–13 ↓ NAA/Cr+PCr in anterior cingulate cortex and a deficit in executive functions
Fayed et al. (2005) [178] 2–10 ↓ Cho in both GM and WM of cortical areas, temporal lobes and thalamus
Vasconcelos et al. (2008) [148] 6–10 ↓ Cr+PCr in cerebellum and striatum
↓ NAA in frontal areas
↑ Cho in caudate, anterior cingulate cortex, and hippocampus-amygdala complex
Gabis et al. (2008) [146] 8–14 ↓ NAA in Hippocampus-amygdala complex
↑ Cho in caudate, anterior cingulate cortex, and hippocampus-amygdala complex
Doyle-Thomas et al. (2014) [151] 7–18 ↓ Glx/Cr+PCr in cerebellum and ↑ Glx/Cr+PCr in putamen
↓ NAA/Cr+PCr in thalamus and ↑ NAA/Cr+PCr in caudate

Cho, Choline; Cr+PCr, creatine and phosphocreatine; Glx, glutamine,glutamate and GABA; GM, grey matter; NAA, N-acetylaspartate; WM, white matter.

Creatine and Phosphocreatine

In 1H-MRS, Cr and PCr are quantified together [136]. They play a crucial role in the adenosine triphosphate (ATP) and adenosine diphosphate (ADP) energy-transfer process. ATP results from oxidative phosphorylation in neuronal and glial mitochondria and glycolysis in the cytosol. A phosphate bond is released from ATP through the enzyme creatine kinase to store energy. The free phosphate bond then binds with Cr to form PCr. When cellular mitochondria require energy, ADP and a third phosphate bond are resynthesized to ATP via oxidative phosphorylation [122, 136, 137]. Cr is highly-expressed in the mitochondria of neurons and is crucial for cellular energy production and in the maintenance of cortical homeostasis [122, 137].

In children with ASD, reduced Cr+PCr levels have been reported across the cortical regions [128130, 138]. Turner and Gant (2014) reviewed the biochemistry of Cr and revealed an association between reduced Cr+PCr and ASD-like behaviors, such as abnormal learning skills, intellectual disability, and repetitive and compulsive behaviors. This correlation could be due to delayed or impaired axon growth during brain development, in which Cr+PCr are crucial elements [139]. However, no correlation between Cr+PCr levels and autistic symptom severity has been found in children with ASD [140]. Moreover, cortical Cr+PCr is commonly considered to be stable and has been extensively used as a reference for other metabolites [120, 122, 127, 136].

N-Acetylaspartate (NAA)

NAA is synthesized in the mitochondria of neurons and is catabolized in glial cells and oligodendrocytes, acting as a precursor of fatty-acids to form the myelin around axons [137]. Quantified by 1H-MRS, the NAA level is considered to reflect neuronal density, integrity, and metabolism [104, 131, 136, 141]. It is well accepted that NAA is comparable across both GM and WM, while it is more abundant in WM than in GM, due to its role in transmission of action potentials [142, 143].

Research on NAA has revealed a consistent phenomenon, i.e., it is generally reduced in children with ASD. In a group of 3–4 year-old ASD children, Friedman et al. (2003) reported NAA reduction in the frontal, parietal, and cingulate areas of both hemispheres, as well as in the right superior temporal gyrus and left putamen, compared with typically-developing children [129]. In an older group of ASD children with a mean age of 10.4 years, Levitt et al. (2003) revealed similar findings of reduced NAA in both left and right frontal and parietal areas, as well as in the left caudate. They also claimed that reduced parietal axon density, marked by reduced WM NAA, is associated with deficits in eye gaze, spatial perception, and memory [131]. Comparing children with ASD and those with pervasive developmental disorder, Friedman et al. (2006) found an extensively decreased NAA level in the ASD group across both GM and WM [144]. Similarly, Corrigan et al. (2013) found a general NAA reduction across most cortical regions in both GM and WM [138]. Interestingly, Fujii et al. (2010) reported a relationship between a reduced NAA/Cr+PCr ratio in the anterior cingulate cortex and a deficit in executive functions. Moreover, they also found a correlation between decreased NAA/Cr+PCr and social and communication disabilities [145].

Choline

Choline is synthesized in the liver and is essential for the synthesis of the neurotransmitter acetylcholine. Choline-containing compounds along with membrane phospholipids make up 40% of myelin. In 1H-MRS, the choline level is highest in the WM [120]. The cortical choline levels indicate the equilibrium of neuronal cellular membrane phospholipid metabolism [120, 137, 146, 147].

In children with ASD, choline-containing compounds are generally decreased in cortical areas, the temporal lobes, and thalamus [128131, 138], indicating a deficit in membrane phospholipid turnover. However, studies have also reported increased choline levels in ASD children in different brain regions, e.g. caudate, anterior cingulate cortex, and hippocampus-amygdala complex [131, 146, 148]. Even though the findings are contradictory, they revealed a similar phenomenon, that ASD children have neural maturation different from typically-developing children.

Glx (Glutamate, Glutamine, and GABA)

Glx are the most abundant neurotransmitters (90% in synapses), taking up to 60%–80% of the glucose oxidation and energy consumption in cortical neurons [149, 150]. They are most concentrated in GM and play essential roles in neural migration, differentiation, and plasticity [125, 132, 136, 140]. In ASD children, De Vito et al. (2007) reported extensive reduction of Glx in the GM of frontal, occipital, and temporal regions as well as the cerebellum [128]. Corrigan et al. (2013) reported a general decrease in Glx in both cortical GM and WM [138]. Harden et al. (2008) pointed out that abnormal sensory sensitivity and deficits in body movement modulation are associated with increased thalamic Glx [130]. In addition, Doyle-Thomas et al. (2014) demonstrated that an increased thalamic Glx level is associated with disabled social interaction [151].

MRI and Genetics

As outlined in the introduction, ASD has a strong genetic basis. Biological studies have revealed that many ASD-related genes influence the formation of neuronal circuits [21, 152, 153]. However, little is known about how these genes affect brain structure and function. As reviewed above, altered brain structures and functions have continuously been reported in ASD with a satisfying amount of consistency. Since brain structure and function are heritable [21, 154156], gene-related imaging may serve to demonstrate the possible neural mechanisms through which phenotypic heterogeneity arises from genetic heterogeneity in ASD [21].

One innovative gene-related imaging study has compared ASD children carrying positively testable ASD-related gene(s) with typically-developing controls [118]. In particular, the authors were interested in the MET (Met Receptor Tyrosine) gene. They combined fMRI, rs-fMRI, and DTI in a large sample of ASD children (n = 164) with MET gene classification and controls. Indeed, the presence of risk alleles in ASD children had a significantly larger impact on functional connectivity than controls. In the ASD risk-allele group, the fMRI showed reduced functional connectivity from posterior cingulate to medial prefrontal cortex. DTI exhibited decreased FA in the splenium portion of the CC that connects to the posterior cingulate. Moreover, group-by-genotype interactions revealed more deactivation of the posterior cingulate, medial prefrontal, and primary auditory cortices, lower functional connectivity of these regions, and lower WM integrity in tracts connecting these regions (splenium, cingulum, and superior and inferior longitudinal fasciculus). Investigating the impact of another ASD-related gene (CNTNAP2; contactin-associated protein-like 2), Scott-Van Zeeland et al. (2010) revealed that risk-allele-carrying ASD children showed a pattern of diffusely increased functional connectivity between the frontal cortex and temporal lobes, while typically-developing controls exhibited a clear connectivity between frontal cortex- and language-related cortical regions [157].

According to these limited findings, we can only speculate that ASD-related genes may contribute to atypical connectivity and development. More studies combining genetic information and multimodal neuroimaging data are needed to understand the relationship between heterogeneous neuropathological phenotypes and the clinical manifestations of ASD, as well as to improve diagnostic tools and treatment strategies [158].

Support Vector Machine Technologies

The findings of MRI studies have substantially advanced our understanding of the neural mechanisms underpinning ASDs. However, the integration of neuroimaging tools into clinical practice has so far been limited, partly because it is unclear which information revealed by these tools is relevant to diagnosis and treatment decisions. Support Vector Machine (SVM) technology is a specific type of supervised machine learning that aims to classify data points by maximizing the margin between classes in a high-dimensional space [159, 160]. The optimal SVM algorithm is developed through a “training” phase in which training data are used to develop an algorithm able to discriminate between groups previously defined by the operator (e.g. patients versus controls). Once a so-called “decision function” or “hyperplane” is learned from the training data, it can be used to predict the class of a new test example. The interesting aspect of the SVM is that it is multivariate and takes into account inter-regional correlations. Therefore, it is extremely well-suited to take into account and test subtle differences in intra-regional correlations of brain metabolism, function, and anatomy [161, 162]. This may be of particular relevance to ASD, in which the abnormalities are usually in the development of the whole neural system rather than isolated regions.

SVMs have been widely used to aid the diagnosis of neurological disorders, such as Alzheimer’s disease [163166] and Parkinson’s disease [167, 168], as well as to identify those brain areas in stroke patients that are involved in a particular (cognitive) function [169, 170]. Among ASD patients, the SVM was first applied in adults. Singh et al. developed a diagnostic model generated by the LPboost-based algorithm to distinguish autistic children from controls, based on voxel-wise cortical thickness and ~40,000 points for each individual; they reported 89% classification accuracy based on cross-validation [171]. Ecker et al. (2010) applied SVM classifiers to investigate the predictive value of whole-brain structural volumetric changes in ASD, and obtained 81% classification accuracy based on cross-validation [172]. More recently, Ecker et al. (2013) pooled regional WM and GM volumes in ASD patients using SVMs and classified ASD patients with a high true positive rate [173]. As for ASD children, the number of reports is relatively limited. In a group of ASD children (mean age 9.2 ± 2.1 years), Jiao et al. (2010) used 4 different machine-learning techniques (including SVMs) to generate diagnostic models from both the VBM and SBM results. They reported a better classification performance for the thickness-based data than those based on regional volumes [44]. Lately, Jin et al. (2015) used an SVM classifier to identify high-risk ASD infants from WM tracts and whole-brain connectivity. Their proposed function achieved an accuracy of 76% and an area of 0.8 under the receiver operating characteristic curve [174].

To conclude, SVM technology is extremely promising in its contribution to an accurate and valid diagnosis of ASD. However, for ASD in children, the application of SVM is still at the beginning. More studies are needed to produce reliable diagnostic models based on imaging data.

Summary and Future Direction

The main findings of MRI studies in children are summarized in Table 5.

Table 5.

Summary of main MRI findings.

MRI approaches Findings
Structural MRI Cortex
Increased total GM and WM volumes
Increased GM and WM volumes in frontal and temporal areas
Increased cingulate cortex
Atypical variation of cortical thickness in frontal, temporal, and parietal lobes
Cerebellum and subcortical areas
Cerebellum
Increased total volume
Increased GM volume
Decreased WM density
Amygdala
Increased volumes in younger children bilaterally
Trajectory of development of amygdala follows overall trajectory of TBV
Corpus callosum
Decreased overall size
Increased regional volume
Basal ganglia
Increased caudate volume
Atypical shapes of the structures
Hippocampus
Increased size of hippocampi in young children
Enlargement located especially on the right side
No difference between sides in older children
Diffusion tensor imaging Decreased FA in the whole brain, frontal lobe, arcuate fasciculus, across the entire CC, and in anterior thalamic radiation
Increased FA in arcuate fasciculus and in CC in young children
Increased MD in whole brain, frontal and temporal lobes, and across the entire CC
Resting-state fMRI Altered functional connectivity in the default mode network
Hyper-connectivity in striatal-cortical circuitry, precuneus, cingulate cortex, and temporal-frontal circuity
Under-connectivity in anterior-posterior connections
Magnetic resonance spectroscopy Decreased NAA levels in general GM and WM, especially in frontal, temporal, cingulate, and caudate areas
Decreased Cr+PCr levels in general GM and WM, especially in frontal, parietal, temporal, occipital cortex, and thalamus
Decreased choline levels in cortical areas, temporal lobes, and thalamus
Increased choline levels in caudate, anterior cingulate cortex, and hippocampus-amygdala complex
Decreased Glx in GM of frontal, occipital, temporal cortex, and cerebellar regions
Increased Glx in thalamus and putamen

Young ASD children exhibit differences in brain morphometry, neurochemical components, and structural and functional connectivity. So far, a diverse set of potential biomarkers including genetic, biochemical, morphological, hormonal, immunological, neuropathological, neuropsychological, and behavioral biomarkers have been identified. However, for most of these markers it is not yet clear if they are contributing factors to the development of ASD or are a result of another underlying abnormality. Longitudinal studies − especially covering very young children with ASD − may help answer this question.

It should be kept in mind that MRI techniques are limited to a certain level of spatial and temporal resolution. If this level is not precise enough to visualize the synaptic or neuronal abnormalities where the core features or heterogeneity of ASD arises neuroimaging may ultimately not be the best tool for parsing these differences. However, in combination with post-mortem tissue analysis or animal models, neuroimaging studies have the potential to provide a critical intermediate step between the genetic basis and the phenotype. Such approaches allow us to deconstruct the conceptions of ASD deeply to where they can be grounded in biology [87, 175].

While most of the studies reviewed here are still characterized by methodological variability and relatively small sample sizes, studies with pooled data samples and homogeneous analytical approaches are needed. Large-scale collaboration networks of that type are ABIDE (“Autism Brain Imaging Data Exchange”) [114, 176, 177] and NDAR (“National Database for Autism Research”). They combine imaging data from multiple sites and integrate both genetic and behavioral data. These projects will allow researchers to achieve sufficient power to detect true brain-gene-behavior relationships [21]. In general, multi-site and multi-modal studies based on large patient groups is one of the key strategies to increase the probability of the discovery of new effective biomarkers in ASD and to comprehensively characterize the clinical, behavioral, and cognitive symptoms of this disorder.

Along with the growing numbers of gene-related MRI studies, the application of multimodal MRI scanning and collaboration networks, as well as advanced analytical methods are needed. Techniques, such as a machine learning classifier or prediction, may serve to identify patterns of biomarkers across different modalities, relevant to clinical diagnosis and genotype, severity rating, prognosis, and/or response to treatment. Last but not least, further large-sample studies on ASD children are needed to search for reliable biomarker patterns and diagnostic models based on imaging data.

References

  • 1.American Psychiatric Publishing . Autism spectrum disorder fact sheet. Bethesda, MD: NINDS; 2016. [Google Scholar]
  • 2.Alexander AL, Lee JE, Lazar M, Boudos R, DuBray MB, Oakes TR, et al. Diffusion tensor imaging of the corpus callosum in Autism. Neuroimage. 2007;34:61–73. doi: 10.1016/j.neuroimage.2006.08.032. [DOI] [PubMed] [Google Scholar]
  • 3.Christensen DL, Baio J, Van Naarden Braun K, Bilder D, Charles J, Constantino JN, et al. Prevalence and characteristics of autism spectrum disorder among children aged 8 years-autism and developmental disabilities monitoring network, 11 sites, United States, 2012. MMWR Surveill Summ. 2016;65:1–23. doi: 10.15585/mmwr.ss6503a1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Buescher AV, Cidav Z, Knapp M, Mandell DS. Costs of autism spectrum disorders in the United Kingdom and the United States. JAMA Pediatr. 2014;168:721–728. doi: 10.1001/jamapediatrics.2014.210. [DOI] [PubMed] [Google Scholar]
  • 5.Fein D, Barton M, Eigsti IM, Kelley E, Naigles L, Schultz RT, et al. Optimal outcome in individuals with a history of autism. J Child Psychol Psychiatry. 2013;54:195–205. doi: 10.1111/jcpp.12037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Goldani AA, Downs SR, Widjaja F, Lawton B, Hendren RL. Biomarkers in autism. Front. Psychiatry. 2014;5:100. doi: 10.3389/fpsyt.2014.00100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.El-Fishawy P, State MW. The genetics of autism: key issues, recent findings, and clinical implications. Psychiatr Clin North Am. 2010;33:83–105. doi: 10.1016/j.psc.2009.12.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, et al. Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways. Hum Mol Genet 2012, 21: 3513–3523. [DOI] [PMC free article] [PubMed]
  • 9.Iossifov I, Ronemus M, Levy D, Wang Z, Hakker I, Rosenbaum J, et al. De novo gene disruptions in children on the autistic spectrum. Neuron. 2012;74:285–299. doi: 10.1016/j.neuron.2012.04.009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Lee TL, Raygada MJ, Rennert OM. Integrative gene network analysis provides novel regulatory relationships, genetic contributions and susceptible targets in autism spectrum disorders. Gene. 2012;496:88–96. doi: 10.1016/j.gene.2012.01.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, et al. A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. Ann Hum Genet. 2009;73:263–273. doi: 10.1111/j.1469-1809.2009.00523.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Murdoch JD, State MW. Recent developments in the genetics of autism spectrum disorders. Curr Opin Genet Dev. 2013;23:310–315. doi: 10.1016/j.gde.2013.02.003. [DOI] [PubMed] [Google Scholar]
  • 13.Ronald A, Butcher LM, Docherty S, Davis OS, Schalkwyk LC, Craig IW, et al. A genome-wide association study of social and non-social autistic-like traits in the general population using pooled DNA, 500 K SNP microarrays and both community and diagnosed autism replication samples. Behav Genet. 2010;40:31–45. doi: 10.1007/s10519-009-9308-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, et al. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 2012;485:237–241. doi: 10.1038/nature10945. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.State MW, Levitt P. The conundrums of understanding genetic risks for autism spectrum disorders. Nat Neurosci. 2011;14:1499–1506. doi: 10.1038/nn.2924. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Wang K, Zhang H, Ma D, Bucan M, Glessner JT, Abrahams BS, et al. Common genetic variants on 5p14.1 associate with autism spectrum disorders. Nature. 2009;459:528–533. doi: 10.1038/nature07999. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Weiss LA, Arking DE, Gene Discovery Project of Johns Hopkins & the Autism Consortium. Daly MJ, Chakravarti A. A genome-wide linkage and association scan reveals novel loci for autism. Nature. 2009;461:802–808. doi: 10.1038/nature08490. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Persico AM, Napolioni V. Autism genetics. Behav Brain Res. 2013;251:95–112. doi: 10.1016/j.bbr.2013.06.012. [DOI] [PubMed] [Google Scholar]
  • 19.Ruggeri B, Sarkans U, Schumann G, Persico AM. Biomarkers in autism spectrum disorder: the old and the new. Psychopharmacology (Berl) 2014;231:1201–1216. doi: 10.1007/s00213-013-3290-7. [DOI] [PubMed] [Google Scholar]
  • 20.Zafeiriou DI, Ververi A, Dafoulis V, Kalyva E, Vargiami E. Autism spectrum disorders: the quest for genetic syndromes. Am J Med Genet B Neuropsychiatr Genet. 2013;162B:327–366. doi: 10.1002/ajmg.b.32152. [DOI] [PubMed] [Google Scholar]
  • 21.Hernandez LM, Rudie JD, Green SA, Bookheimer S, Dapretto M. Neural signatures of autism spectrum disorders: insights into brain network dynamics. Neuropsychopharmacology. 2015;40:171–189. doi: 10.1038/npp.2014.172. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Mahajan R, Mostofsky SH. Neuroimaging endophenotypes in autism spectrum disorder. CNS Spectr. 2015;20:412–426. doi: 10.1017/S1092852915000371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Lenroot RK, Yeung PK. Heterogeneity within Autism Spectrum Disorders: What have We Learned from Neuroimaging Studies? Front Hum Neurosci. 2013;7:733. doi: 10.3389/fnhum.2013.00733. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Ha S, Sohn IJ, Kim N, Sim HJ, Cheon KA. Characteristics of brains in autism spectrum disorder: structure, function and connectivity across the lifespan. Experimental Neurobiology. 2015;24:273–284. doi: 10.5607/en.2015.24.4.273. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Yerys BE, Herrington JD. Multimodal imaging in autism: an early review of comprehensive neural circuit characterization. Curr Psychiatry Rep. 2014;16:496. doi: 10.1007/s11920-014-0496-2. [DOI] [PubMed] [Google Scholar]
  • 26.Sacrey LA, Bennett JA, Zwaigenbaum L. Early infant development and intervention for autism spectrum disorder. J Child Neurol. 2015;30:1921–1929. doi: 10.1177/0883073815601500. [DOI] [PubMed] [Google Scholar]
  • 27.Zwaigenbaum L, Bauman ML, Stone WL, Yirmiya N, Estes A, Hansen RL, et al. Early identification of autism spectrum disorder: recommendations for practice and research. Pediatrics. 2015;136(Suppl 1):S10–S40. doi: 10.1542/peds.2014-3667C. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Hernandez-Garcia L, Buschkuehl M. Advances in longitudinal MRI diagnostic tests. Expert Opin Med Diagn. 2012;6:309–321. doi: 10.1517/17530059.2012.686995. [DOI] [PubMed] [Google Scholar]
  • 29.Chen R, Jiao Y, Herskovits EH. Structural MRI in autism spectrum disorder. Pediatr Res. 2011;69:63R–68R. doi: 10.1203/PDR.0b013e318212c2b3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Ismail MM, Keynton RS, Mostapha MM, ElTanboly AH, Casanova MF, Gimel’farb GL, et al. Studying autism spectrum disorder with structural and diffusion magnetic resonance imaging: a survey. Front Hum Neurosci. 2016;10:211. doi: 10.3389/fnhum.2016.00211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Goldman-Rakic PS. Development of cortical circuitry and cognitive function. Child Dev. 1987;58:601–622. doi: 10.2307/1130201. [DOI] [PubMed] [Google Scholar]
  • 32.Panizzon MS, Fennema-Notestine C, Eyler LT, Jernigan TL, Prom-Wormley E, Neale M, et al. Distinct genetic influences on cortical surface area and cortical thickness. Cereb Cortex. 2009;19:2728–2735. doi: 10.1093/cercor/bhp026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Courchesne E, Karns CM, Davis HR, Ziccardi R, Carper RA, Tigue ZD, et al. Unusual brain growth patterns in early life in patients with autistic disorder: an MRI study. Neurology. 2001;57:245–254. doi: 10.1212/WNL.57.2.245. [DOI] [PubMed] [Google Scholar]
  • 34.Hazlett HC, Poe MD, Gerig G, Styner M, Chappell C, Smith RG, et al. Early brain overgrowth in autism associated with an increase in cortical surface area before age 2 years. Arch Gen Psychiatry. 2011;68:467–476. doi: 10.1001/archgenpsychiatry.2011.39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Carper RA, Moses P, Tigue ZD, Courchesne E. Cerebral lobes in autism: early hyperplasia and abnormal age effects. Neuroimage. 2002;16:1038–1051. doi: 10.1006/nimg.2002.1099. [DOI] [PubMed] [Google Scholar]
  • 36.Sparks BF, Friedman SD, Shaw DW, Aylward EH, Echelard D, Artru AA, et al. Brain structural abnormalities in young children with autism spectrum disorder. Neurology. 2002;59:184–192. doi: 10.1212/WNL.59.2.184. [DOI] [PubMed] [Google Scholar]
  • 37.Akshoomoff N, Lord C, Lincoln AJ, Courchesne RY, Carper RA, Townsend J, et al. Outcome classification of preschool children with autism spectrum disorders using MRI brain measures. J Am Acad Child Adolesc Psychiatry. 2004;43:349–357. doi: 10.1097/00004583-200403000-00018. [DOI] [PubMed] [Google Scholar]
  • 38.Hazlett HC, Poe MD, Gerig G, Smith RG, Piven J. Cortical gray and white brain tissue volume in adolescents and adults with autism. Biol Psychiatry. 2006;59:1–6. doi: 10.1016/j.biopsych.2005.06.015. [DOI] [PubMed] [Google Scholar]
  • 39.Schumann CM, Bloss CS, Barnes CC, Wideman GM, Carper RA, Akshoomoff N, et al. Longitudinal magnetic resonance imaging study of cortical development through early childhood in autism. J Neurosci. 2010;30:4419–4427. doi: 10.1523/JNEUROSCI.5714-09.2010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Shen MD, Nordahl CW, Young GS, Wootton-Gorges SL, Lee A, Liston SE, et al. Early brain enlargement and elevated extra-axial fluid in infants who develop autism spectrum disorder. Brain. 2013;136:2825–2835. doi: 10.1093/brain/awt166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Gori I, Giuliano A, Muratori F, Saviozzi I, Oliva P, Tancredi R, et al. Gray matter alterations in young children with autism spectrum disorders: comparing morphometry at the voxel and regional level. J Neuroimaging. 2015;25:866–874. doi: 10.1111/jon.12280. [DOI] [PubMed] [Google Scholar]
  • 42.Hardan AY, Muddasani S, Vemulapalli M, Keshavan MS, Minshew NJ. An MRI study of increased cortical thickness in autism. Am J Psychiatry. 2006;163:1290–1292. doi: 10.1176/ajp.2006.163.7.1290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43.Hardan AY, Libove RA, Keshavan MS, Melhem NM, Minshew NJ. A preliminary longitudinal magnetic resonance imaging study of brain volume and cortical thickness in autism. Biol Psychiatry. 2009;66:320–326. doi: 10.1016/j.biopsych.2009.04.024. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Jiao Y, Chen R, Ke X, Chu K, Lu Z, Herskovits EH. Predictive models of autism spectrum disorder based on brain regional cortical thickness. Neuroimage. 2010;50:589–599. doi: 10.1016/j.neuroimage.2009.12.047. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Dierker DL, Feczko E, Pruett JR, Jr, Petersen SE, Schlaggar BL, Constantino JN, et al. Analysis of cortical shape in children with simplex autism. Cereb Cortex. 2015;25:1042–1051. doi: 10.1093/cercor/bht294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Chenn A, Walsh CA. Regulation of cerebral cortical size by control of cell cycle exit in neural precursors. Science. 2002;297:365–369. doi: 10.1126/science.1074192. [DOI] [PubMed] [Google Scholar]
  • 47.Becker EB, Stoodley CJ. Autism spectrum disorder and the cerebellum. Int Rev Neurobiol. 2013;113:1–34. doi: 10.1016/B978-0-12-418700-9.00001-0. [DOI] [PubMed] [Google Scholar]
  • 48.Wang SS, Kloth AD, Badura A. The cerebellum, sensitive periods, and autism. Neuron. 2014;83:518–532. doi: 10.1016/j.neuron.2014.07.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Allen G. The cerebellum in autism. Clin. Neuropsychiatry. 2005;2:321–337. [Google Scholar]
  • 50.Fatemi SH, Aldinger KA, Ashwood P, Bauman ML, Blaha CD, Blatt GJ, et al. Consensus paper: pathological role of the cerebellum in autism. Cerebellum. 2012;11:777–807. doi: 10.1007/s12311-012-0355-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Herbert MR, Ziegler DA, Deutsch CK, O’Brien LM, Lange N, Bakardjiev A, et al. Dissociations of cerebral cortex, subcortical and cerebral white matter volumes in autistic boys. Brain. 2003;126:1182–1192. doi: 10.1093/brain/awg110. [DOI] [PubMed] [Google Scholar]
  • 52.Stanfield AC, McIntosh AM, Spencer MD, Philip R, Gaur S, Lawrie SM. Towards a neuroanatomy of autism: a systematic review and meta-analysis of structural magnetic resonance imaging studies. Eur Psychiatry. 2008;23:289–299. doi: 10.1016/j.eurpsy.2007.05.006. [DOI] [PubMed] [Google Scholar]
  • 53.Duerden EG, Mak-Fan KM, Taylor MJ, Roberts SW. Regional differences in grey and white matter in children and adults with autism spectrum disorders: an activation likelihood estimate (ALE) meta-analysis. Autism Res. 2012;5:49–66. doi: 10.1002/aur.235. [DOI] [PubMed] [Google Scholar]
  • 54.Stoodley CJ. Distinct regions of the cerebellum show gray matter decreases in autism, ADHD, and developmental dyslexia. Front Syst Neurosci. 2014;8:92. doi: 10.3389/fnsys.2014.00092. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Yu KK, Cheung C, Chua SE, McAlonan GM. Can Asperger syndrome be distinguished from autism? An anatomic likelihood meta-analysis of MRI studies. J Psychiatry Neurosci. 2011;36:412–421. doi: 10.1503/jpn.100138. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.McAlonan GM, Cheung V, Cheung C, Suckling J, Lam GY, Tai KS, et al. Mapping the brain in autism. A voxel-based MRI study of volumetric differences and intercorrelations in autism. Brain. 2005;128:268–276. doi: 10.1093/brain/awh332. [DOI] [PubMed] [Google Scholar]
  • 57.Elia M, Ferri R, Musumeci SA, Panerai S, Bottitta M, Scuderi C. Clinical correlates of brain morphometric features of subjects with low-functioning autistic disorder. J Child Neurol. 2000;15:504–508. doi: 10.1177/088307380001500802. [DOI] [PubMed] [Google Scholar]
  • 58.Baron-Cohen S, Ring HA, Bullmore ET, Wheelwright S, Ashwin C, Williams SC. The amygdala theory of autism. Neurosci Biobehav Rev. 2000;24:355–364. doi: 10.1016/S0149-7634(00)00011-7. [DOI] [PubMed] [Google Scholar]
  • 59.Howard MA, Cowell PE, Boucher J, Broks P, Mayes A, Farrant A, et al. Convergent neuroanatomical and behavioural evidence of an amygdala hypothesis of autism. Neuroreport. 2000;11:2931–2935. doi: 10.1097/00001756-200009110-00020. [DOI] [PubMed] [Google Scholar]
  • 60.Schultz RT. Developmental deficits in social perception in autism: the role of the amygdala and fusiform face area. Int J Dev Neurosci. 2005;23:125–141. doi: 10.1016/j.ijdevneu.2004.12.012. [DOI] [PubMed] [Google Scholar]
  • 61.Sweeten TL, Posey DJ, Shekhar A, McDougle CJ. The amygdala and related structures in the pathophysiology of autism. Pharmacol Biochem Behav. 2002;71:449–455. doi: 10.1016/S0091-3057(01)00697-9. [DOI] [PubMed] [Google Scholar]
  • 62.Munson J, Dawson G, Abbott R, Faja S, Webb SJ, Friedman SD, et al. Amygdalar volume and behavioral development in autism. Arch Gen Psychiatry. 2006;63:686–693. doi: 10.1001/archpsyc.63.6.686. [DOI] [PubMed] [Google Scholar]
  • 63.Nordahl CW, Scholz R, Yang X, Buonocore MH, Simon T, Rogers S, et al. Increased rate of amygdala growth in children aged 2 to 4 years with autism spectrum disorders: a longitudinal study. Arch Gen Psychiatry. 2012;69:53–61. doi: 10.1001/archgenpsychiatry.2011.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 64.Frazier TW, Hardan AY. A meta-analysis of the corpus callosum in autism. Biological Psychiatry. 2009;66:935–941. doi: 10.1016/j.biopsych.2009.07.022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Frazier TW, Keshavan MS, Minshew NJ, Hardan AY. A two-year longitudinal MRI study of the corpus callosum in autism. J Autism Dev Disord. 2012;42:2312–2322. doi: 10.1007/s10803-012-1478-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 66.Freitag CM, Luders E, Hulst HE, Narr KL, Thompson PM, Toga AW, et al. Total brain volume and corpus callosum size in medication-naive adolescents and young adults with autism spectrum disorder. Biol Psychiatry. 2009;66:316–319. doi: 10.1016/j.biopsych.2009.03.011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Hardan AY, Minshew NJ, Keshavan MS. Corpus callosum size in autism. Neurology. 2000;55:1033–1036. doi: 10.1212/WNL.55.7.1033. [DOI] [PubMed] [Google Scholar]
  • 68.Just MA, Cherkassky VL, Keller TA, Kana RK, Minshew NJ. Functional and anatomical cortical underconnectivity in autism: evidence from an FMRI study of an executive function task and corpus callosum morphometry. Cereb Cortex. 2007;17:951–961. doi: 10.1093/cercor/bhl006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Mason RA, Williams DL, Kana RK, Minshew N, Just MA. Theory of Mind disruption and recruitment of the right hemisphere during narrative comprehension in autism. Neuropsychologia. 2008;46:269–280. doi: 10.1016/j.neuropsychologia.2007.07.018. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Bostan AC, Dum RP, Strick PL. Cerebellar networks with the cerebral cortex and basal ganglia. Trends Cogn Sci. 2013;17:241–254. doi: 10.1016/j.tics.2013.03.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Middleton FA, Strick PL. Basal ganglia and cerebellar loops: motor and cognitive circuits. Brain Res Brain Res Rev. 2000;31:236–250. doi: 10.1016/S0165-0173(99)00040-5. [DOI] [PubMed] [Google Scholar]
  • 72.Middleton FA, Strick PL. Basal ganglia output and cognition: evidence from anatomical, behavioral, and clinical studies. Brain Cogn. 2000;42:183–200. doi: 10.1006/brcg.1999.1099. [DOI] [PubMed] [Google Scholar]
  • 73.Utter AA, Basso MA. The basal ganglia: an overview of circuits and function. Neurosci Biobehav Rev. 2008;32:333–342. doi: 10.1016/j.neubiorev.2006.11.003. [DOI] [PubMed] [Google Scholar]
  • 74.Estes A, Shaw DW, Sparks BF, Friedman S, Giedd JN, Dawson G, et al. Basal ganglia morphometry and repetitive behavior in young children with autism spectrum disorder. Autism Res. 2011;4:212–220. doi: 10.1002/aur.193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Hollander E, Anagnostou E, Chaplin W, Esposito K, Haznedar MM, Licalzi E, et al. Striatal volume on magnetic resonance imaging and repetitive behaviors in autism. Biol Psychiatry. 2005;58:226–232. doi: 10.1016/j.biopsych.2005.03.040. [DOI] [PubMed] [Google Scholar]
  • 76.Sears LL, Vest C, Mohamed S, Bailey J, Ranson BJ, Piven J. An MRI study of the basal ganglia in autism. Prog Neuropsychopharmacol Biol Psychiatry. 1999;23:613–624. doi: 10.1016/S0278-5846(99)00020-2. [DOI] [PubMed] [Google Scholar]
  • 77.Williams CA, Dagli A, Battaglia A. Genetic disorders associated with macrocephaly. Am J Med Genet A. 2008;146A:2023–2037. doi: 10.1002/ajmg.a.32434. [DOI] [PubMed] [Google Scholar]
  • 78.Schumann CM, Hamstra J, Goodlin-Jones BL, Lotspeich LJ, Kwon H, Buonocore MH, et al. The amygdala is enlarged in children but not adolescents with autism; the hippocampus is enlarged at all ages. J Neurosci. 2004;24:6392–6401. doi: 10.1523/JNEUROSCI.1297-04.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 79.Barnea-Goraly N, Frazier TW, Piacenza L, Minshew NJ, Keshavan MS, Reiss AL, et al. A preliminary longitudinal volumetric MRI study of amygdala and hippocampal volumes in autism. Prog Neuropsychopharmacol Biol Psychiatry. 2014;48:124–128. doi: 10.1016/j.pnpbp.2013.09.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Nordahl CW, Lange N, Li DD, Barnett LA, Lee A, Buonocore MH, et al. Brain enlargement is associated with regression in preschool-age boys with autism spectrum disorders. Proc Natl Acad Sci USA. 2011;108:20195–20200. doi: 10.1073/pnas.1107560108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81.Courchesne E, Campbell K, Solso S. Brain growth across the life span in autism: age-specific changes in anatomical pathology. Brain Res. 2011;1380:138–145. doi: 10.1016/j.brainres.2010.09.101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Lange N, Travers BG, Bigler ED, Prigge MB, Froehlich AL, Nielsen JA, et al. Longitudinal volumetric brain changes in autism spectrum disorder ages 6–35 years. Autism Res. 2015;8:82–93. doi: 10.1002/aur.1427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Casanova MF, Buxhoeveden DP, Brown C. Clinical and macroscopic correlates of minicolumnar pathology in autism. J Child Neurol. 2002;17:692–695. doi: 10.1177/088307380201700908. [DOI] [PubMed] [Google Scholar]
  • 84.Casanova MF, van Kooten IA, Switala AE, van Engeland H, Heinsen H, Steinbusch HW, et al. Minicolumnar abnormalities in autism. Acta Neuropathol. 2006;112:287–303. doi: 10.1007/s00401-006-0085-5. [DOI] [PubMed] [Google Scholar]
  • 85.Shukla DK, Keehn B, Muller RA. Tract-specific analyses of diffusion tensor imaging show widespread white matter compromise in autism spectrum disorder. J Child Psychol Psychiatry. 2011;52:286–295. doi: 10.1111/j.1469-7610.2010.02342.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 86.Catani M. Diffusion tensor magnetic resonance imaging tractography in cognitive disorders. Curr Opin Neurol. 2006;19:599–606. doi: 10.1097/01.wco.0000247610.44106.3f. [DOI] [PubMed] [Google Scholar]
  • 87.Chanraud S, Zahr N, Sullivan EV, Pfefferbaum A. MR diffusion tensor imaging: a window into white matter integrity of the working brain. Neuropsychol Rev. 2010;20:209–225. doi: 10.1007/s11065-010-9129-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 88.Jou RJ, Jackowski AP, Papademetris X, Rajeevan N, Staib LH, Volkmar FR. Diffusion tensor imaging in autism spectrum disorders: preliminary evidence of abnormal neural connectivity. Aust NZ J Psychiatry. 2011;45:153–162. doi: 10.3109/00048674.2010.534069. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Mukherjee P, McKinstry RC. Diffusion tensor imaging and tractography of human brain development. Neuroimaging Clin N Am. 2006;16:19–43. doi: 10.1016/j.nic.2005.11.004. [DOI] [PubMed] [Google Scholar]
  • 90.White T, Nelson M, Lim KO. Diffusion tensor imaging in psychiatric disorders. Top Magn Reson Imaging. 2008;19:97–109. doi: 10.1097/RMR.0b013e3181809f1e. [DOI] [PubMed] [Google Scholar]
  • 91.Sundaram SK, Kumar A, Makki MI, Behen ME, Chugani HT, Chugani DC. Diffusion tensor imaging of frontal lobe in autism spectrum disorder. Cereb Cortex. 2008;18:2659–2665. doi: 10.1093/cercor/bhn031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Hong S, Ke X, Tang T, Hang Y, Chu K, Huang H, et al. Detecting abnormalities of corpus callosum connectivity in autism using magnetic resonance imaging and diffusion tensor tractography. Psychiatry Res. 2011;194:333–339. doi: 10.1016/j.pscychresns.2011.03.009. [DOI] [PubMed] [Google Scholar]
  • 93.Nagae LM, Zarnow DM, Blaskey L, Dell J, Khan SY, Qasmieh S, et al. Elevated mean diffusivity in the left hemisphere superior longitudinal fasciculus in autism spectrum disorders increases with more profound language impairment. AJNR Am J Neuroradiol. 2012;33:1720–1725. doi: 10.3174/ajnr.A3037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 94.Wolff JJ, Gu H, Gerig G, Elison JT, Styner M, Gouttard S, et al. Differences in white matter fiber tract development present from 6 to 24 months in infants with autism. Am J Psychiatry. 2012;169:589–600. doi: 10.1176/appi.ajp.2011.11091447. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Nair A, Treiber JM, Shukla DK, Shih P, Muller RA. Impaired thalamocortical connectivity in autism spectrum disorder: a study of functional and anatomical connectivity. Brain. 2013;136:1942–1955. doi: 10.1093/brain/awt079. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Joseph RM, Fricker Z, Fenoglio A, Lindgren KA, Knaus TA, Tager-Flusberg H. Structural asymmetries of language-related gray and white matter and their relationship to language function in young children with ASD. Brain Imaging Behav. 2014;8:60–72. doi: 10.1007/s11682-013-9245-0. [DOI] [PubMed] [Google Scholar]
  • 97.Cheung C, Chua SE, Cheung V, Khong PL, Tai KS, Wong TK, et al. White matter fractional anisotrophy differences and correlates of diagnostic symptoms in autism. J Child Psychol Psychiatry. 2009;50:1102–1112. doi: 10.1111/j.1469-7610.2009.02086.x. [DOI] [PubMed] [Google Scholar]
  • 98.Ke X, Tang T, Hong S, Hang Y, Zou B, Li H, et al. White matter impairments in autism, evidence from voxel-based morphometry and diffusion tensor imaging. Brain Res. 2009;1265:171–177. doi: 10.1016/j.brainres.2009.02.013. [DOI] [PubMed] [Google Scholar]
  • 99.Barnea-Goraly N, Lotspeich LJ, Reiss AL. Similar white matter aberrations in children with autism and their unaffected siblings: a diffusion tensor imaging study using tract-based spatial statistics. Arch Gen Psychiatry. 2010;67:1052–1060. doi: 10.1001/archgenpsychiatry.2010.123. [DOI] [PubMed] [Google Scholar]
  • 100.Poustka L, Jennen-Steinmetz C, Henze R, Vomstein K, Haffner J, Sieltjes B. Fronto-temporal disconnectivity and symptom severity in children with autism spectrum disorder. World J Biol Psychiatry. 2012;13:269–280. doi: 10.3109/15622975.2011.591824. [DOI] [PubMed] [Google Scholar]
  • 101.Peterson D, Mahajan R, Crocetti D, Mejia A, Mostofsky S. Left-hemispheric microstructural abnormalities in children with high-functioning autism spectrum disorder. Autism Res. 2015;8:61–72. doi: 10.1002/aur.1413. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Dawson G, Meltzoff AN, Osterling J, Rinaldi J. Neuropsychological correlates of early symptoms of autism. Child Dev. 1998;69:1276–1285. doi: 10.2307/1132265. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Escalante-Mead PR, Minshew NJ, Sweeney JA. Abnormal brain lateralization in high-functioning autism. J Autism Dev Disord. 2003;33:539–543. doi: 10.1023/A:1025887713788. [DOI] [PubMed] [Google Scholar]
  • 104.Kleinhans NM, Muller RA, Cohen DN, Courchesne E. Atypical functional lateralization of language in autism spectrum disorders. Brain Res. 2008;1221:115–125. doi: 10.1016/j.brainres.2008.04.080. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Smith SM, Jenkinson M, Johansen-Berg H, Rueckert D, Nichols TE, Mackay CE, et al. Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data. Neuroimage. 2006;31:1487–1505. doi: 10.1016/j.neuroimage.2006.02.024. [DOI] [PubMed] [Google Scholar]
  • 106.Kumar A, Sundaram SK, Sivaswamy L, Behen ME, Makki MI, Ager J, et al. Alterations in frontal lobe tracts and corpus callosum in young children with autism spectrum disorder. Cereb Cortex. 2010;20:2103–2113. doi: 10.1093/cercor/bhp278. [DOI] [PubMed] [Google Scholar]
  • 107.Weinstein M, Ben-Sira L, Levy Y, Zachor DA, Ben Itzhak E, Artzi M, et al. Abnormal white matter integrity in young children with autism. Hum Brain Mapp. 2011;32:534–543. doi: 10.1002/hbm.21042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108.Walker L, Gozzi M, Lenroot R, Thurm A, Behseta B, Swedo S, et al. Diffusion tensor imaging in young children with autism: biological effects and potential confounds. Biol Psychiatry. 2012;72:1043–1051. doi: 10.1016/j.biopsych.2012.08.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.Mevel K, Fransson P. The functional brain connectome of the child and autism spectrum disorders. Acta Paediatr. 2016;105:1024–1035. doi: 10.1111/apa.13484. [DOI] [PubMed] [Google Scholar]
  • 110.Rane P, Cochran D, Hodge SM, Haselgrove C, Kennedy DN, Frazier JA. Connectivity in autism: a review of MRI connectivity studies. Harv Rev Psychiatry. 2015;23:223–244. doi: 10.1097/HRP.0000000000000072. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 111.Fox PT, Friston KJ. Distributed processing; distributed functions? Neuroimage. 2012;61:407–426. doi: 10.1016/j.neuroimage.2011.12.051. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Just MA, Cherkassky VL, Keller TA, Minshew NJ. Cortical activation and synchronization during sentence comprehension in high-functioning autism: evidence of underconnectivity. Brain. 2004;127:1811–1821. doi: 10.1093/brain/awh199. [DOI] [PubMed] [Google Scholar]
  • 113.Courchesne E, Pierce K. Brain overgrowth in autism during a critical time in development: implications for frontal pyramidal neuron and interneuron development and connectivity. Int J Dev Neurosci. 2005;23:153–170. doi: 10.1016/j.ijdevneu.2005.01.003. [DOI] [PubMed] [Google Scholar]
  • 114.Di Martino A, Kelly C, Grzadzinski R, Zuo XN, Mennes M, Mairena MA, et al. Aberrant striatal functional connectivity in children with autism. Biol Psychiatry. 2011;69:847–856. doi: 10.1016/j.biopsych.2010.10.029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 115.Lynch CJ, Uddin LQ, Supekar K, Khouzam A, Phillips J, Menon V. Default mode network in childhood autism: posteromedial cortex heterogeneity and relationship with social deficits. Biol Psychiatry. 2013;74:212–219. doi: 10.1016/j.biopsych.2012.12.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Uddin LQ, Supekar K, Lynch CJ, Khouzam A, Phillips J, Feinstein C, et al. Salience network-based classification and prediction of symptom severity in children with autism. JAMA Psychiatry. 2013;70:869–879. doi: 10.1001/jamapsychiatry.2013.104. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117.Abrams DA, Lynch CJ, Cheng KM, Phillips J, Supekar K, Ryali S, et al. Underconnectivity between voice-selective cortex and reward circuitry in children with autism. Proc Natl Acad Sci USA. 2013;110:12060–12065. doi: 10.1073/pnas.1302982110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 118.Rudie JD, Hernandez LM, Brown JA, Beck-Pancer D, Colich NL, Gorrindo P, et al. Autism-associated promoter variant in MET impacts functional and structural brain networks. Neuron. 2012;75:904–915. doi: 10.1016/j.neuron.2012.07.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 119.Wiggins JL, Peltier SJ, Ashinoff S, Weng SJ, Carrasco M, Welsh RC, et al. Using a self-organizing map algorithm to detect age-related changes in functional connectivity during rest in autism spectrum disorders. Brain Res. 2011;1380:187–197. doi: 10.1016/j.brainres.2010.10.102. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 120.Bertholdo D, Watcharakorn A, Castillo M. Brain proton magnetic resonance spectroscopy: introduction and overview. Neuroimaging Clin N Am. 2013;23:359–380. doi: 10.1016/j.nic.2012.10.002. [DOI] [PubMed] [Google Scholar]
  • 121.Kato T, Inubushi T, Kato N. Magnetic resonance spectroscopy in affective disorders. J Neuropsychiatry Clin Neurosci. 1998;10:133–147. doi: 10.1176/jnp.10.2.133. [DOI] [PubMed] [Google Scholar]
  • 122.Ross B, Bluml S. Magnetic resonance spectroscopy of the human brain. Anat Rec. 2001;265:54–84. doi: 10.1002/ar.1058. [DOI] [PubMed] [Google Scholar]
  • 123.Clarke CE, Lowry M, Horsman A. Unchanged basal ganglia N-acetylaspartate and glutamate in idiopathic Parkinson’s disease measured by proton magnetic resonance spectroscopy. Mov Disord. 1997;12:297–301. doi: 10.1002/mds.870120306. [DOI] [PubMed] [Google Scholar]
  • 124.Aoki Y, Kasai K, Yamasue H. Age-related change in brain metabolite abnormalities in autism: a meta-analysis of proton magnetic resonance spectroscopy studies. Transl Psychiatry. 2012;2:e69. doi: 10.1038/tp.2011.65. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 125.Baruth JM, Wall CA, Patterson MC, Port JD. Proton magnetic resonance spectroscopy as a probe into the pathophysiology of autism spectrum disorders (ASD): a review. Autism Res. 2013;6:119–133. doi: 10.1002/aur.1273. [DOI] [PubMed] [Google Scholar]
  • 126.Naaijen J, Lythgoe DJ, Amiri H, Buitelaar JK, Glennon JC. Fronto-striatal glutamatergic compounds in compulsive and impulsive syndromes: a review of magnetic resonance spectroscopy studies. Neurosci Biobehav Rev. 2015;52:74–88. doi: 10.1016/j.neubiorev.2015.02.009. [DOI] [PubMed] [Google Scholar]
  • 127.Brown MS, Singel D, Hepburn S, Rojas DC. Increased glutamate concentration in the auditory cortex of persons with autism and first-degree relatives: a (1)H-MRS study. Autism Res. 2013;6:1–10. doi: 10.1002/aur.1260. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 128.DeVito TJ, Drost DJ, Neufeld RW, Rajakumar N, Pavlosky W, Williamson P, et al. Evidence for cortical dysfunction in autism: a proton magnetic resonance spectroscopic imaging study. Biol Psychiatry. 2007;61:465–473. doi: 10.1016/j.biopsych.2006.07.022. [DOI] [PubMed] [Google Scholar]
  • 129.Friedman SD, Shaw DW, Artru AA, Richards TL, Gardner J, Dawson G, et al. Regional brain chemical alterations in young children with autism spectrum disorder. Neurology. 2003;60:100–107. doi: 10.1212/WNL.60.1.100. [DOI] [PubMed] [Google Scholar]
  • 130.Hardan AY, Minshew NJ, Melhem NM, Srihari S, Jo B, Bansal R, et al. An MRI and proton spectroscopy study of the thalamus in children with autism. Psychiatry Res. 2008;163:97–105. doi: 10.1016/j.pscychresns.2007.12.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Levitt JG, O’Neill J, Blanton RE, Smalley S, Fadale D, McCracken JT, et al. Proton magnetic resonance spectroscopic imaging of the brain in childhood autism. Biol Psychiatry. 2003;54:1355–1366. doi: 10.1016/S0006-3223(03)00688-7. [DOI] [PubMed] [Google Scholar]
  • 132.Bejjani A, O’Neill J, Kim JA, Frew AJ, Yee VW, Ly R, et al. Elevated glutamatergic compounds in pregenual anterior cingulate in pediatric autism spectrum disorder demonstrated by 1H MRS and 1H MRSI. PLoS One. 2012;7:e38786. doi: 10.1371/journal.pone.0038786. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 133.Murphy DG, Critchley HD, Schmitz N, McAlonan G, Van Amelsvoort T, Robertson D, et al. Asperger syndrome: a proton magnetic resonance spectroscopy study of brain. Arch Gen Psychiatry. 2002;59:885–891. doi: 10.1001/archpsyc.59.10.885. [DOI] [PubMed] [Google Scholar]
  • 134.O’Brien FM, Page L, O’Gorman RL, Bolton P, Sharma A, Baird G, et al. Maturation of limbic regions in Asperger syndrome: a preliminary study using proton magnetic resonance spectroscopy and structural magnetic resonance imaging. Psychiatry Res. 2010;184:77–85. doi: 10.1016/j.pscychresns.2010.08.007. [DOI] [PubMed] [Google Scholar]
  • 135.Oner O, Devrimci-Ozguven H, Oktem F, Yagmurlu B, Baskak B, Munir KM. Proton MR spectroscopy: higher right anterior cingulate N-acetylaspartate/choline ratio in Asperger syndrome compared with healthy controls. AJNR Am J Neuroradiol. 2007;28:1494–1498. doi: 10.3174/ajnr.A0625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 136.Kousi E, Tsougos I, Eftychia K. Proton magnetic resonance spectroscopy of the central nervous system. In: Fountas K (Ed.). Novel Frontiers of Advanced Neuroimaging. InTech, 2013, pp 19–50.
  • 137.Rae CD. A guide to the metabolic pathways and function of metabolites observed in human brain 1H magnetic resonance spectra. Neurochem Res. 2014;39:1–36. doi: 10.1007/s11064-013-1199-5. [DOI] [PubMed] [Google Scholar]
  • 138.Corrigan NM, Shaw DW, Estes AM, Richards TL, Munson J, Friedman SD, et al. Atypical developmental patterns of brain chemistry in children with autism spectrum disorder. JAMA Psychiatry. 2013;70:964–974. doi: 10.1001/jamapsychiatry.2013.1388. [DOI] [PubMed] [Google Scholar]
  • 139. Turner CE, Gant N. Chapter 2.2—the biochemistry of creatine. Mag Reson Spectrosc 2014: 91–103.
  • 140.Page LA, Daly E, Schmitz N, Simmons A, Toal F, Deeley Q, et al. In vivo 1H-magnetic resonance spectroscopy study of amygdala-hippocampal and parietal regions in autism. Am J Psychiatry. 2006;163:2189–2192. doi: 10.1176/ajp.2006.163.12.2189. [DOI] [PubMed] [Google Scholar]
  • 141.Chugani DC, Sundram BS, Behen M, Lee ML, Moore GJ. Evidence of altered energy metabolism in autistic children. Prog Neuropsychopharmacol Biol Psychiatry. 1999;23:635–641. doi: 10.1016/S0278-5846(99)00022-6. [DOI] [PubMed] [Google Scholar]
  • 142.Ford TC, Crewther DP. A comprehensive review of the (1)H-MRS metabolite spectrum in autism spectrum disorder. Front Mol Neurosci. 2016;9:14. doi: 10.3389/fnmol.2016.00014. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 143.Pouwels PJ, Frahm J. Regional metabolite concentrations in human brain as determined by quantitative localized proton MRS. Magn Reson Med. 1998;39:53–60. doi: 10.1002/mrm.1910390110. [DOI] [PubMed] [Google Scholar]
  • 144.Friedman SD, Shaw DW, Artru AA, Dawson G, Petropoulos H, Dager SR. Gray and white matter brain chemistry in young children with autism. Arch Gen Psychiatry. 2006;63:786–794. doi: 10.1001/archpsyc.63.7.786. [DOI] [PubMed] [Google Scholar]
  • 145.Fujii E, Mori K, Miyazaki M, Hashimoto T, Harada M, Kagami S. Function of the frontal lobe in autistic individuals: a proton magnetic resonance spectroscopic study. J Med Invest. 2010;57:35–44. doi: 10.2152/jmi.57.35. [DOI] [PubMed] [Google Scholar]
  • 146.Gabis L, Wei H, Azizian A, DeVincent C, Tudorica A, Kesner-Baruch Y, et al. 1H-magnetic resonance spectroscopy markers of cognitive and language ability in clinical subtypes of autism spectrum disorders. J Child Neurol. 2008;23:766–774. doi: 10.1177/0883073808315423. [DOI] [PubMed] [Google Scholar]
  • 147.Suzuki K, Nishimura K, Sugihara G, Nakamura K, Tsuchiya KJ, Matsumoto K, et al. Metabolite alterations in the hippocampus of high-functioning adult subjects with autism. Int J Neuropsychopharmacol. 2010;13:529–534. doi: 10.1017/S1461145709990952. [DOI] [PubMed] [Google Scholar]
  • 148.Vasconcelos MM, Brito AR, Domingues RC, da Cruz LC, Jr, Gasparetto EL, Werner J, Jr, et al. Proton magnetic resonance spectroscopy in school-aged autistic children. J Neuroimaging. 2008;18:288–295. doi: 10.1111/j.1552-6569.2007.00200.x. [DOI] [PubMed] [Google Scholar]
  • 149.Brady STSGJ, Albers RW, et al. Basic Neurochemistry: Principles of Molecular. Cellular and Medical Neurobiology: Elsevier Academic Press; 2011. [Google Scholar]
  • 150.Rothman DL, Behar KL, Hyder F, Shulman RG. In vivo NMR studies of the glutamate neurotransmitter flux and neuroenergetics: implications for brain function. Annu Rev Physiol. 2003;65:401–427. doi: 10.1146/annurev.physiol.65.092101.142131. [DOI] [PubMed] [Google Scholar]
  • 151.Doyle-Thomas KA, Card D, Soorya LV, Wang AT, Fan J, Anagnostou E. Metabolic mapping of deep brain structures and associations with symptomatology in autism spectrum disorders. Res Autism Spectr Disord. 2014;8:44–51. doi: 10.1016/j.rasd.2013.10.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 152.Parikshak NN, Luo R, Zhang A, Won H, Lowe JK, Chandran V, et al. Integrative functional genomic analyses implicate specific molecular pathways and circuits in autism. Cell. 2013;155:1008–1021. doi: 10.1016/j.cell.2013.10.031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 153.Won H, Mah W, Kim E. Autism spectrum disorder causes, mechanisms, and treatments: focus on neuronal synapses. Front Mol Neurosci. 2013;6:19. doi: 10.3389/fnmol.2013.00019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 154.Chiang MC, McMahon KL, de Zubicaray GI, Martin NG, Hickie I, Toga AW, et al. Genetics of white matter development: a DTI study of 705 twins and their siblings aged 12 to 29. Neuroimage. 2011;54:2308–2317. doi: 10.1016/j.neuroimage.2010.10.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 155.Fornito A, Zalesky A, Bassett DS, Meunier D, Ellison-Wright I, Yucel M, et al. Genetic influences on cost-efficient organization of human cortical functional networks. J Neurosci. 2011;31:3261–3270. doi: 10.1523/JNEUROSCI.4858-10.2011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 156.Glahn DC, Winkler AM, Kochunov P, Almasy L, Duggirala R, Carless MA, et al. Genetic control over the resting brain. Proc Natl Acad Sci U S A. 2010;107:1223–1228. doi: 10.1073/pnas.0909969107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 157.Scott-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, et al. Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2. Sci Transl Med. 2010;2:56. doi: 10.1126/scitranslmed.3001344. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 158.Fox MD, Greicius M. Clinical applications of resting state functional connectivity. Front Syst Neurosci. 2010;4:19. doi: 10.3389/fnsys.2010.00019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 159.Pereira F, Mitchell T, Botvinick M. Machine learning classifiers and fMRI: a tutorial overview. Neuroimage. 2009;45:S199–S209. doi: 10.1016/j.neuroimage.2008.11.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 160.Vapnik VN. The Nature of Statistical Learning Theory. New York: Springer-Verlag; 1995. [Google Scholar]
  • 161.Koshino H, Carpenter PA, Minshew NJ, Cherkassky VL, Keller TA, Just MA. Functional connectivity in an fMRI working memory task in high-functioning autism. Neuroimage. 2005;24:810–821. doi: 10.1016/j.neuroimage.2004.09.028. [DOI] [PubMed] [Google Scholar]
  • 162.McAlonan GM, Daly E, Kumari V, Critchley HD, van Amelsvoort T, Suckling J, et al. Brain anatomy and sensorimotor gating in Asperger’s syndrome. Brain. 2002;125:1594–1606. doi: 10.1093/brain/awf150. [DOI] [PubMed] [Google Scholar]
  • 163.Davatzikos C, Fan Y, Wu X, Shen D, Resnick SM. Detection of prodromal Alzheimer’s disease via pattern classification of magnetic resonance imaging. Neurobiol Aging. 2008;29:514–523. doi: 10.1016/j.neurobiolaging.2006.11.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 164.Guo Y, Wu G, Commander LA, Szary S, Jewells V, Lin W, et al. Segmenting hippocampus from infant brains by sparse patch matching with deep-learned features. Med Image Comput Comput Assist Interv. 2014;17:308–315. doi: 10.1007/978-3-319-10470-6_39. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 165.Zhang D, Wang Y, Zhou L, Yuan H, Shen D. Alzheimer’s Disease Neuroimaging I. Multimodal classification of Alzheimer’s disease and mild cognitive impairment. Neuroimage. 2011;55:856–867. doi: 10.1016/j.neuroimage.2011.01.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 166.Zhu D, Li K, Terry DP, Puente AN, Wang L, Shen D, et al. Connectome-scale assessments of structural and functional connectivity in MCI. Hum Brain Mapp. 2014;35:2911–2923. doi: 10.1002/hbm.22373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 167.Haller S, Badoud S, Nguyen D, Garibotto V, Lovblad KO, Burkhard PR. Individual detection of patients with Parkinson disease using support vector machine analysis of diffusion tensor imaging data: initial results. AJNR Am J Neuroradiol. 2012;33:2123–2128. doi: 10.3174/ajnr.A3126. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 168.Pan SIS, Warwick K, Aziz TZ. Parkinson’s Disease tremor classification – a comparison between support vector machines and neural networks. Expert Syst Appl. 2012;39:10764–10771. doi: 10.1016/j.eswa.2012.02.189. [DOI] [Google Scholar]
  • 169.Smith DV, Clithero JA, Rorden C, Karnath HO. Decoding the anatomical network of spatial attention. Proc Natl Acad Sci U S A. 2013;110:1518–1523. doi: 10.1073/pnas.1210126110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 170.Zhang Y, Kimberg DY, Coslett HB, Schwartz MF, Wang Z. Multivariate lesion-symptom mapping using support vector regression. Hum Brain Mapp. 2014;35:5861–5876. doi: 10.1002/hbm.22590. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 171.Singh V, Mukherjee L, Chung MK. Cortical surface thickness as a classifier: boosting for autism classification. Med Image Comput Comput Assist Interv. 2008;11:999–1007. doi: 10.1007/978-3-540-85988-8_119. [DOI] [PubMed] [Google Scholar]
  • 172.Ecker C, Rocha-Rego V, Johnston P, Mourao-Miranda J, Marquand A, Daly EM, et al. Investigating the predictive value of whole-brain structural MR scans in autism: a pattern classification approach. Neuroimage. 2010;49:44–56. doi: 10.1016/j.neuroimage.2009.08.024. [DOI] [PubMed] [Google Scholar]
  • 173.Ecker C, Ginestet C, Feng Y, Johnston P, Lombardo MV, Lai MC, et al. Brain surface anatomy in adults with autism: the relationship between surface area, cortical thickness, and autistic symptoms. JAMA Psychiatry. 2013;70:59–70. doi: 10.1001/jamapsychiatry.2013.265. [DOI] [PubMed] [Google Scholar]
  • 174.Jin Y, Wee CY, Shi F, Thung KH, Ni D, Yap PT, et al. Identification of infants at high-risk for autism spectrum disorder using multiparameter multiscale white matter connectivity networks. Hum Brain Mapp. 2015;36:4880–4896. doi: 10.1002/hbm.22957. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 175.Georgiades SSP, Boyle M. Importance of studying heterogeneity in autism. Neuropsychiatry. 2013;3:123–125. doi: 10.2217/npy.13.8. [DOI] [Google Scholar]
  • 176.Di Martino A, Yan CG, Li Q, Denio E, Castellanos FX, Alaerts K, et al. The autism brain imaging data exchange: towards a large-scale evaluation of the intrinsic brain architecture in autism. Mol Psychiatry. 2014;19:659–667. doi: 10.1038/mp.2013.78. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 177.Di Martino A, Castellanos FX, Anderson J, Alaerts K, Assaf M, Behrmann Deen D, et al. The Autism Brain Imaging Data Exchange (ABIDE) Consortium: Open Sharing of Autism Resting State fMRI Data. Beijing: Human Brain Mapping Edition:18, 2012.
  • 178.Fayed N, Modrego PJ. Comparative study of cerebral white matter in autism and attention-deficit/hyperactivity disorder by means of magnetic resonance spectroscopy. Acad Radiol. 2005;12:566–569. doi: 10.1016/j.acra.2005.01.016. [DOI] [PubMed] [Google Scholar]

Articles from Neuroscience Bulletin are provided here courtesy of Springer

RESOURCES