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Andi

09-26-05, 09:17 AM

A good general writeup on the psychoilogy and neurobiology of autism

http://jnnp.bmjjournals.com/cgi/content/full/75/7/945

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The cognitive neuroscience of autism

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S Baron-Cohen


Correspondence to: S Baron-Cohen Autism Research Centre, Departments of Experimental Psychology and Psychiatry, University of Cambridge, Douglas House, Cambridge CB2 2AH, UK; sb205{at}cam.ac.uk<script type="text/javascript"></script>

<HR>The psychology and biology of a complex developmental condition 

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Abbreviations: AS, Asperger syndrome; CC, central coherence; EFT, embedded figures task; E-S, empathising-systemising; HFA, high functioning autism; MRI, magnetic resonance imagingKeywords: autism
Autism is diagnosed when a child or adult has abnormalities in a "triad" of behavioural domains: social development, communication, and repetitive behaviour/obsessive interests.<A HREF="#R1">1,</A><A HREF="#R2">2</A> Autism can occur at any point on the IQ continuum, and IQ is a strong predictor of outcome.<A HREF="#R3">3</A> Autism is also invariably accompanied by language delay (no single words before 2 years old). Asperger syndrome (AS)<A HREF="#R4">4</A> is a subgroup on the autistic spectrum. People with AS share many of the same features as are seen in autism, but with no history of language delay and with an IQ in the average range or above. In this editorial, the main cognitive theories of autism are summarised. These are then followed by a summary of the key neurobiological findings. 

 AUTISM: COGNITIVE ASPECTS 

The mind blindness theory of autism<A HREF="#R5">5</A> proposed that in autism spectrum conditions there are deficits in the normal process of empathy, relative to mental age. These deficits can occur by degrees. The term "empathising" encompasses a range of other terms: "theory of mind", "mind reading", "empathy", and taking the "intentional stance".<A HREF="#R6">6</A> Empathy involves two major elements: (1) the ability to attribute mental states to oneself and others, as a natural way to make sense of agents,<A HREF="#R7">7–</A><A HREF="#R9">9</A> and (2) having an emotional reaction that is appropriate to the other person’s mental state (such as sympathy). 

Since the first test of mind blindness in children with autism,<A HREF="#R10">10</A> there have been more than 30 experimental tests. The vast majority of these have revealed profound impairments in the development of their empathising ability. These are reviewed elsewhere.<A HREF="#R5">5,</A><A HREF="#R11">11</A> Some children and adults with AS only show their empathising deficits on age appropriate adult tests.<A HREF="#R12">12–</A><A HREF="#R14">14</A> This deficit in their empathising is thought to underlie the difficulties such children have in social and communicative development,<A HREF="#R15">15,</A><A HREF="#R16">16</A> and in the imagination of others’ minds.<A HREF="#R17">17,</A><A HREF="#R18">18</A> We can think of these symptoms as the triad of deficits (see fig 1 The triad of impairments in autism). 

http://jnnp.bmjjournals.com/content/vol75/issue7/images/medium/jn18713.f1.gif

Systemising is the drive to analyse systems, in order to understand and predict the behaviour of inanimate events. Systems are all around us in our environment, and include technical systems (such as machines and tools); natural systems (such as biological and geographical phenomena); abstract systems (such as mathematics or computer programs). The way we make sense of any of these systems is in terms of underlying rules and regularities, or specifically an analysis of input-operation-output relations.<A HREF="#R19">19</A> The empathising-systemising (E-S) theory holds that alongside the empathising deficits in autism (see above), systemising is either intact or superior.<A HREF="#R20">20</A> Studies suggest systemising in autism is at least in line with mental age, or superior.<A HREF="#R21">21–</A><A HREF="#R25">25</A> Systemising may relate to a different set of features which we can think of as the triad of strengths (see fig 2 triad of strengths in autism). 

http://jnnp.bmjjournals.com/content/vol75/issue7/images/medium/jn18713.f2.gif

People with autism spectrum conditions show unusually strong repetitive behaviour, a strong desire for routines, and a "need for sameness". One cognitive account of this aspect of the syndrome is the executive dysfunction theory.<A HREF="#R26">26–</A><A HREF="#R28">28</A> This assumes that autism involves a form of frontal lobe pathology leading to persevering or inability to shift attention. There is some evidence for such executive deficits.<A HREF="#R29">29</A> But the fact that it is possible for people with AS to exist who have no demonstrable executive dysfunction while still having deficits in empathising and talents in systemising,<A HREF="#R30">30</A> suggests that executive dysfunction is unlikely to be a core feature of autism spectrum conditions. 

The executive account has also traditionally ignored the content of "repetitive behaviour". The E-S theory in contrast draws attention to the fact that much repetitive behaviour involves the child’s "obsessional" or strong interests with mechanical systems (such as light switches or water faucets) or other systems that can be understood in terms of rules and regularities. Rather than these behaviours being a sign of executive dysfunction, these may reflect the child’s intact or even superior interest in systems. One study suggests that autistic obsessions are not random with respect to content (which would be predicted by the content free executive dysfunction theory), but that these test to cluster in the domain of systems.<A HREF="#R31">31</A> 

Weak central coherence (CC)<A HREF="#R32">32,</A><A HREF="#R33">33</A> refers to the individual’s preference for local detail over global processing. This has been demonstrated in terms of an autistic superiority on the embedded figures task (EFT) and the block design subtest.<A HREF="#R25">25,</A><A HREF="#R34">34,</A><A HREF="#R35">35</A> It has also been shown in terms of an autistic deficit in integrating fragments of objects and integrating sentences within a paragraph.<A HREF="#R36">36</A> The faster and more accurate performance on the EFT and block design test have been interpreted as evidence of good segmentation skills, and superior attention to detail. The latter has also been demonstrated on visual search tasks.<A HREF="#R37">37,</A><A HREF="#R38">38</A> 

Systemising requires excellent attention to detail, identifying parameters that may then be tested for their role in the behaviour of the system under examination. So, both the E-S theory and the CC theory predict excellent attention to detail. However, the E-S and CC theories also make opposite predictions when it comes to an individual with autism being able to understand a whole system. The E-S theory predicts that a person with autism, faced with a new system to learn, will show a stronger drive to learn the system compared with someone without autism, so long as there are underlying rules and regularities that can be discovered. Moreover, they will readily grasp that a change of one parameter in one part of the system may have distant effects on another part of the system. In contrast, the CC theory predicts that they should fail to understand whole (global) systems or the relation between parts of a system. This has not yet been tested. 

 AUTISM: NEUROBIOLOGICAL ASPECTS 

Neuroanatomy and neuropathology 

Anatomical abnormalities have been identified in many brain areas in autism. These include the cerebellum,<A HREF="#R39">39–</A><A HREF="#R42">42</A> the brain stem,<A HREF="#R42">42,</A><A HREF="#R43">43</A> frontal lobes,<A HREF="#R44">44–</A><A HREF="#R47">47</A> parietal lobes,<A HREF="#R48">48</A> hippocampus,<A HREF="#R49">49,</A><A HREF="#R50">50</A> and the amygdale.<A HREF="#R49">49</A> Epilepsy also occurs commonly, at least in classic autism.<A HREF="#R51">51</A> In terms of neuropathology, the number of Purkinje cells in the cerebellar cortex is abnormally low.<A HREF="#R52">52–</A><A HREF="#R55">55</A> This has been postulated to lead to disinhibition of the cerebellar deep nuclei and consequent overexcitement of the thalamus and cerebral cortex.<A HREF="#R56">56</A> Abnormalities in the density of packing of neurons in the hippocampus, amygdala, and other parts of the limbic system have also been reported.<A HREF="#R54">54,</A><A HREF="#R55">55,</A><A HREF="#R57">57</A> An abnormally low degree of dendritic branching was also found in a Golgi analysis of the hippocampus of two autistic brains,<A HREF="#R57">57</A> though it remains to be seen if such an abnormality is confirmed in a larger sample. A separate report suggests a reduction in the size of cortical minicolumns and an increase in cell dispersion within these minicolumns. These might indicate an increase in the number of and connectivity between minicolumns.<A HREF="#R58">58,</A><A HREF="#R59">59</A> 

Neurophysiology 

Hyper arousal in response to sensory input, and decreased ability to select between competing sensory inputs, has been reported.<A HREF="#R60">60,</A><A HREF="#R61">61</A> Functional neuroimaging suggests increased activity in sensory areas of the brain normally associated with stimulus driven processing, and decreased activity in areas normally associated with higher cognitive processing. Thus, on the EFT, people with autism show unusually high activation in ventral occipital areas and abnormally low activation in prefrontal and parietal areas.<A HREF="#R62">62</A> In one study they also failed to show normal activity in the fusiform "face area",<A HREF="#R63">63</A> instead showing abnormally high activity in the peristriate cortex and inferior temporal gyrus.<A HREF="#R64">64,</A><A HREF="#R65">65</A> The visual N2 to novel stimuli is also heightened to irrelevant stimuli.<A HREF="#R66">66</A> The P3 in response to auditory stimuli is abnormally generalised to occipital sites in visual cortex.<A HREF="#R67">67</A> 

Regarding EEG results, the P1 evoked potential is either abnormally heightened in response to stimuli that are the target of attention, or abnormally generalised to stimuli that are outside the target of attention.<A HREF="#R68">68</A> Both hemispheres show abnormal activation—indiscriminately—during shifts of attention into either hemifield.<A HREF="#R69">69,</A><A HREF="#R70">70</A> Regarding attention research, a deficit has been found in rapid shifting of attention between modalities,<A HREF="#R39">39</A> between spatial locations<A HREF="#R69">69,</A><A HREF="#R71">71–</A><A HREF="#R76">76</A> and between object features.<A HREF="#R77">77,</A><A HREF="#R78">78</A> 

Morphometry 

Magnetic resonance imaging (MRI) morphometry shows volume deficits in the cerebellum,<A HREF="#R40">40–</A><A HREF="#R42">42,</A><A HREF="#R79">79</A> the brainstem,<A HREF="#R42">42</A> and posterior corpus callosum.<A HREF="#R80">80</A> Regarding the cerebellar abnormalities, a subgroup shows increased cerebellar volume.<A HREF="#R81">81</A> A volume deficit has also been reported in the parietal lobe.<A HREF="#R48">48</A> Neuropsychology suggests this is associated with a narrowed spatial focus of attention.<A HREF="#R68">68</A> 

Longitudinal morphometry 

Using either MRI volumetric analysis, or measures of head circumference, the autistic brain appears to involve transient postnatal macroencephaly.<A HREF="#R82">82</A> Neonates later diagnosed with autism or PDD-NOS (Pervasive Developmental Disorder-Not Otherwise Specified) have normal head circumference, but by 2–4 years of age 90% of these have MRI based brain volumes larger than average.<A HREF="#R44">44–</A><A HREF="#R47">47</A> This reflects an enlargement of cerebellar and cerebral white matter, and cerebral grey matter.<A HREF="#R45">45,</A><A HREF="#R83">83</A> Enlargement of superficial white matter tracts containing cortico-cortical fibres may persist abnormally late into development, while the internal capsule and corpus callosum are smaller.<A HREF="#R84">84</A> Cerebellar and cerebral white matter volumes, and cerebellar vermis size can distinguish 95% of toddlers with autism from normal controls, and predict if the child with autism will be high or low functioning.<A HREF="#R45">45</A> The overgrowth is anterior to posterior (frontal lobes being the largest). This increase in volume of cortical grey matter may reflect a failure of synaptic pruning, or an excess of synaptogenesis.<A HREF="#R56">56</A> 

The "social brain" 

A neural basis of empathy has built on a model first proposed by Brothers.<A HREF="#R85">85</A> She suggested—from animal lesion studies,<A HREF="#R86">86</A> single cell recording studies,<A HREF="#R87">87</A> and neurological studies—that social intelligence was a function of three regions: the amygdala, the orbitofrontal and medial frontal cortex, and the superior temporal sulcus and gyrus (STG). Together, she called these the "social brain". Abnormalities in autism have been found in the amygdala, the orbito and the medial frontal cortex. 

Regarding the amygdala, there are four lines of evidence for an amygdala deficit in autism.<A HREF="#R88">88</A> Firstly, a neuroanatomical study of autism at postmortem found microscopic pathology (in the form of increased cell density) in the amygdala, in the presence of normal amygdala volume.<A HREF="#R89">89,</A><A HREF="#R90">90</A> Secondly, patients with autism tend to show a similar pattern of deficits to those seen in patients with amygdala lesions.<A HREF="#R91">91</A> Thirdly, a recent structural MRI study of autism reported reduced amygdala volume.<A HREF="#R92">92</A> Finally, in a recent functional magnetic resonance imaging (fMRI) study, adults with high functioning autism (HFA) or Asperger syndrome (AS) showed significantly less amygdala activation during a mentalising task (Reading the Mind in the Eyes task) compared with normal.<A HREF="#R93">93</A> 

Reduced activity has also been found in the left medial frontal cortex,<A HREF="#R94">94</A> during an empathising (theory of mind) task, and also in the orbitofrontal cortex.<A HREF="#R95">95</A> 

 GENETICS OF AUTISM SPECTRUM CONDITIONS 

Ultimately, the cognitive and neural abnormalities in autism spectrum conditions are likely to be caused by genetic factors. The sibling risk rate for autism is approximately 4.5%, or a tenfold increase over general population rates.<A HREF="#R96">96</A> In an epidemiological study of same sex autistic twins, it was found that 60% of monozygotic (MZ) pairs were concordant for autism versus no dizygotic, (DZ) pairs.<A HREF="#R97">97</A> When they considered a broader phenotype (of related cognitive or social abnormalities), 92% of MZ pairs were concordant versus 10% of DZ pairs. The high concordance in MZ twins indicated a high degree of genetic influence, and the risk to a co-MZ twin can be estimated at over 200 times the general population rate. 

Molecular genetic studies are beginning to narrow down candidate regions. There is still little consensus, but two regions have been identified in several (but not all) studies. These are 15q11-13, near the GABAAß3 receptor subunit gene (GABRB3) and a second one on 17q11.2, near the serotonin transporter gene (SLC6A4). The latter is of interest because of reports of increased serotonin (5HT) levels of platelets in autism [204]. Serotonin innervates the limbic system, and so plausibly plays a role in emotion recognition and empathy. Mothers homozygous for GABRB3 knockout fail to engage in normal nurturing behaviour and have epileptiform EEG.<A HREF="#R98">98,</A><A HREF="#R99">99</A> At least four loci on the X chromosome have also been implicated in autism, and are of interest for their power to explain the sex ratio in autism (markedly biased towards males). These are the neuroligin genes (NLGN3, NLGN4), FMR1 (which causes fragile X syndrome), and MECP2. Several reviews of the genetics of autism literature are available, but this is a fast changing field.<A HREF="#R100">100–</A><A HREF="#R102">102</A> 

As of yet, specific genes for autism have not yet been identified, despite the encouraging possibility of candidate regions on chromosomes. The future of research in this field will be not only to isolate the relevant genes but also to understand the function of these genes, and ultimately the relation between these different causal levels in autism. It is hoped that during this research endeavour there will also be evaluations of the most promising treatments. 

 

 ACKNOWLEDGEMENTS 

The author was supported by the MRC during the period of this work. I am grateful to Matthew Belmonte for discussions of the neuroscience of autism literature. This editorial has benefited from a preview of Belmonte et al (in press).

stanzen

09-26-05, 10:28 AM

Due to the controversies surrounding autism, several scientific journals are releasing some of their review articles on the topic. This one below, also provides a lengthy abstract.

As a companion to the above, here's an great review article about the genetics of autism, published in Pediatrics:

http://pediatrics.aappublications.org/cgi/content/full/113/5/e472

<table bgcolor="#e1e1e1" cellpadding="0" cellspacing="0" width="100%"> <tbody><tr><td align="left" bgcolor="#ffffff" valign="middle" width="5%">
</td> <th align="left" valign="middle" width="95%"> ABSTRACT </th></tr></tbody> </table> <table align="right" border="1" cellpadding="5"> <tbody><tr><th align="left"> http://pediatrics.aappublications.org/icons/toc/uarrow.gifTOP
(http://pediatrics.aappublications.org/cgi/content/full/113/5/e472#top) http://pediatrics.aappublications.org/icons/toc/dot.gifABSTRACT
http://pediatrics.aappublications.org/icons/toc/darrow.gifMETHODS
(http://pediatrics.aappublications.org/cgi/content/full/113/5/e472#SEC1) http://pediatrics.aappublications.org/icons/toc/darrow.gifRESULTS
(http://pediatrics.aappublications.org/cgi/content/full/113/5/e472#SEC2) http://pediatrics.aappublications.org/icons/toc/darrow.gifDISCUSSION
(http://pediatrics.aappublications.org/cgi/content/full/113/5/e472#SEC3) http://pediatrics.aappublications.org/icons/toc/darrow.gifCONCLUSION
(http://pediatrics.aappublications.org/cgi/content/full/113/5/e472#SEC4) http://pediatrics.aappublications.org/icons/toc/darrow.gifREFERENCES
(http://pediatrics.aappublications.org/cgi/content/full/113/5/e472#BIBL) </th></tr></tbody> </table>
Autism is a complex, behaviorally defined, static disorder of the immature brain that is of great concern to the practicing pediatrician because of an astonishing 556% reported increase in pediatric prevalence between 1991 and 1997, to a prevalence higher than that of spina bifida, cancer, or Down syndrome. This jump is probably attributable to heightened awareness and changing diagnostic criteria rather than to new environmental influences. Autism is not a disease but a syndrome with multiple nongenetic and genetic causes. By autism (the autistic spectrum disorders [ASDs]), we mean the wide spectrum of developmental disorders characterized by impairments in 3 behavioral domains: 1) social interaction; 2) language, communication, and imaginative play; and 3) range of interests and activities. Autism corresponds in this article to pervasive developmental disorder (PDD) of the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition and International Classification of Diseases, Tenth Revision. Except for Rett syndrome—attributable in most affected individuals to mutations of the methyl-CpG-binding protein 2 (MeCP2) gene—the other PDD subtypes (autistic disorder, Asperger disorder, disintegrative disorder, and PDD Not Otherwise Specified [PDD-NOS]) are not linked to any particular genetic or nongenetic cause. Review of 2 major textbooks on autism and of papers published between 1961 and 2003 yields convincing evidence for multiple interacting genetic factors as the main causative determinants of autism. Epidemiologic studies indicate that environmental factors such as toxic exposures, teratogens, perinatal insults, and prenatal infections such as rubella and cytomegalovirus account for few cases. These studies fail to confirm that immunizations with the measles-mumps-rubella vaccine are responsible for the surge in autism. Epilepsy, the medical condition most highly associated with autism, has equally complex genetic/nongenetic (but mostly unknown) causes. Autism is frequent in tuberous sclerosis complex and fragile X syndrome, but these 2 disorders account for but a small minority of cases. Currently, diagnosable medical conditions, cytogenetic abnormalities, and single-gene defects (eg, tuberous sclerosis complex, fragile X syndrome, and other rare diseases) together account for <10% of cases. There is convincing evidence that "idiopathic" autism is a heritable disorder. Epidemiologic studies report an ASD prevalence of http://pediatrics.aappublications.org/math/sim.gif3 to 6/1000, with a male to female ratio of 3:1. This skewed ratio remains unexplained: despite the contribution of a few well characterized X-linked disorders, male-to-male transmission in a number of families rules out X-linkage as the prevailing mode of inheritance. The recurrence rate in siblings of affected children is http://pediatrics.aappublications.org/math/sim.gif2% to 8%, much higher than the prevalence rate in the general population but much lower than in single-gene diseases. Twin studies reported 60% concordance for classic autism in monozygotic (MZ) twins versus 0 in dizygotic (DZ) twins, the higher MZ concordance attesting to genetic inheritance as the predominant causative agent. Reevaluation for a broader autistic phenotype that included communication and social disorders increased concordance remarkably from 60% to 92% in MZ twins and from 0% to 10% in DZ pairs. This suggests that interactions between multiple genes cause "idiopathic" autism but that epigenetic factors and exposure to environmental modifiers may contribute to variable expression of autism-related traits. The identity and number of genes involved remain unknown. The wide phenotypic variability of the ASDs likely reflects the interaction of multiple genes within an individual's genome and the existence of distinct genes and gene combinations among those affected. There are 3 main approaches to identifying genetic loci, chromosomal regions likely to contain relevant genes: 1) whole genome screens, searching for linkage of autism to shared genetic markers in populations of multiplex families (families with >1 affected family member); 2) cytogenetic studies that may guide molecular studies by pointing to relevant inherited or de novo chromosomal abnormalities in affected individuals and their families; and 3) evaluation of candidate genes known to affect brain development in these significantly linked regions or, alternatively, linkage of candidate genes selected a priori because of their presumptive contribution to the pathogenesis of autism. Data from whole-genome screens in multiplex families suggest interactions of at least 10 genes in the causation of autism. Thus far, a putative speech and language region at 7q31-q33 seems most strongly linked to autism, with linkages to multiple other loci under investigation. Cytogenetic abnormalities at the 15q11-q13 locus are fairly frequent in people with autism, and a "chromosome 15 phenotype" was described in individuals with chromosome 15 duplications. Among other candidate genes are the FOXP2, RAY1/ST7, IMMP2L, and RELN genes at 7q22-q33 and the GABAA receptor subunit and UBE3A genes on chromosome 15q11-q13. Variant alleles of the serotonin transporter gene (5-HTT) on 17q11-q12 are more frequent in individuals with autism than in nonautistic populations. In addition, animal models and linkage data from genome screens implicate the oxytocin receptor at 3p25-p26. Most pediatricians will have 1 or more children with this disorder in their practices. They must diagnose ASD expeditiously because early intervention increases its effectiveness. Children with dysmorphic features, congenital anomalies, mental retardation, or family members with developmental disorders are those most likely to benefit from extensive medical testing and genetic consultation. The yield of testing is much less in high-functioning children with a normal appearance and IQ and moderate social and language impairments. Genetic counseling justifies testing, but until autism genes are identified and their functions are understood, prenatal diagnosis will exist only for the rare cases ascribable to single-gene defects or overt chromosomal abnormalities. Parents who wish to have more children must be told of their increased statistical risk. It is crucial for pediatricians to try to involve families with multiple affected members in formal research projects, as family studies are key to unraveling the causes and pathogenesis of autism. Parents need to understand that they and their affected children are the only available sources for identifying and studying the elusive genes responsible for autism. Future clinically useful insights and potential medications depend on identifying these genes and elucidating the influences of their products on brain development and physiology. 

<hr> Key Words: autism • genetic • chromosome • review