ASD (Autism Spectrum Disorders) Flashcards

1
Q

What are some basic characteristics of ASD?

A
  1. neurodevelopmental disorder with complex etiology (cause)
  2. genetic factors play a central role and so does interaction with non-genetic factors
  3. clinical and etiologic diversity
  4. characterized by impairments in reciprocal social interaction, verbal and non verbal communication and a preference for repetitive activity
  5. it is on a spectrum
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2
Q

what is the prevalence of ASD?

A

1 in 68 and a recurrence risk estimated at 8-18%

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3
Q

How common is ASD in Canada?

A

1 in 135 kids in K to grade 11 in montreal

1 in 150 in 3 to 10 yo in alberta

1 in 95 across 6 regions

1 in 94 in gr 1 to 12 in calgary

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4
Q

What is the epidemiololgy of ASD?

A
  • more common in boys than girls (4:1 sex ratio)
  • genetic and environmental factors play a big role in biological vulnerability
  • rates of ASD are consistant across international studies and ethnic and socioeconomic groups (except in the US diagnosis is less in minorities because theres not much access to healthcare)
  • prevalence estimates steadily increasing over past 40 years
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5
Q

What is ASD?

A

it is a developmental disorder like autism
- it changes with development in terms of clinical expression and it affects development like affects social experience, learning/cognition..etc..

it is heterogenous (clinically and etiologically diverse in terms of clinical and biological ways)

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6
Q

According to the DSM-5 what are the requirements to be diagnosed with ASD? copy in notes

A
  1. persistent deficits in social communication and interactions (need 3 out of 3 on that list)
  2. restricted, repetitive patterns of behavior, interests and activities (need 2/4 on the list)

therefore a total of 5/7 and higher is needed to be diagnosed with ASD

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7
Q

How do people with ASD show deficits in social-emotional reciprocity?

A
  • One of the deficits in social communication and interaction across multiple contexts in DSM-5
    it ranges from abnormal social approach to failure of normal back and forth conversation, to reduced sharing interestes, emotions or affect; to failure to initiate or respond to social interactions

difficulty reading people and their motivations and intentions in a conversation and show either disengagement or TOO much engagement in their own topics and ideas

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8
Q

How do individuals with ASD show nonverbal communicative behaviors?

A
  • One of the deficits in social communication and interaction across multiple contexts in DSM-5
  • used for social interaction ranging for example:
  • from poorly integrated verbal and nonverbal communication; to abnormalities making eye contact and body language; to deficits in understanding and use of gestures; to a total lack of facial expressions and nonverbal communications

in little kids it shows as lacking joint attention skills like looking at something when they want it and then looking at the adult and then looking back at the object

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9
Q

How do individuals with ASD show deficits in developing, maintaining and understanding relationships?

A
  • One of the deficits in social communication and interaction across multiple contexts in DSM-5
  • ranges from:
  • difficulties adjusting behavior to suit various social contexts; to difficulties in sharing imaginative play or making friends; to absence of interest in peers
  • ranges bascially from completely disengaged to somewhat having friends but in a very small circle
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10
Q

How are restricted, repetitive patterns of behavior, interests, or activities shown in ASD according to DSM-5?

A
  1. sterotyped or repetitive motor movements, use of objects or speech shown in ASD –> for example: simple motor stereoypes include lining up toys or flipping objects, echolalia (echoing what u say) and idisyncratic phases (innapropriate word use)
  2. insistence on sameness, inflexible adherence to routines, or ritualized patterns of verbal/nonverbal behavior (i.e. showing extreme distress at small changes, difficulty transitioning, ridgid thinking patterns, greeting rituals, need to take same route or eat same food everyday) do not feel comfortable with unpredictability
  3. highly restricted and fixated interests that are abnormal in intensity or focus (i.e. strong attachment to or preoccupation with unusual objects, excessively circumscribed or preservative interest) [i.e. public transportation]
  4. Hyper- or hypo-sensitivity to sensory input or unusual interests in sensory aspects of the environment (i.e. apparent indifference to pain/temperature, adverse response to specific sounds or textures, excessive smelling or touching of objects, visual fascination with lights or movement)
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11
Q

What are 6 major differences between DSM-5 and DSM-4 in defining ASD?

A
  1. in DSM-5 theres two rather than 3 symptom domains
  2. fewer permutations of symptoms for diagnosis (fewer ordering of the symptoms) therefore more on a spectrum
  3. diagnostic qualifiers rather than subtypes
  4. severity in each symptom domain relates to level of support required
  5. age of onset is early but may not be evident until demands overwhelm capacity (in adult diagnosis)
  6. boundaries are recast –> if you are diagnosed w ASD in DSM - 4 then u for sure are in DSM-5)
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12
Q

What is the early signs of ASD findings in high risk infants?

A
  1. social communication
  2. play interests and behavior
  3. motor skills and behavior
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13
Q

How does social communication deficits manifest in high-risk infants?

A

manifests through:

  1. delayed words and gestures
  2. atypical eye gaze
  3. reduced social smiling
  4. reduced joint attention behaviors
  5. reduced expression of positive affect (lack of ability to enagage even with familiar people) and lack of showing positive emotions
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14
Q

How does Play deficit manifest in high risk infants?

A
  • reduced imitation of actions
  • reduced interest in social play
  • repetititive actions with toys like spinning and rolling
  • prolonged/intense visual examination of toys and other objects
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15
Q

How does atypical motor skills and behavior manifest in high risk infants?

A
  • delayed fine and gross motor skills
  • reduced motor control
  • repetitive/atypical motor behaviors and postures (waving arms up and down)
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16
Q

What are 3 methods of assessment in order for clinical settings of ASD?

A
  1. structured developmental and medical history (know their history) like initial concerns, developmental course, ASD symptoms, medical ROS (sleep, feeding and other med problems), and family + psychological history
  2. structured observation of social, communication, and play-related behaviors
  3. Developmental context –> assessment of language, cognitive and adaptive skills (developmental delays etc..)
17
Q

What are some signs of atypical brain development in ASD? (6)

A
  1. abnormal acceleration in brain growth to age 2-3
  2. abnormal neural connectivity
  3. neuropahtologic abnormalities
  4. abnormal brain activation with social perceptual tasks (decreased activation of FFA during face recgonition, and less amygdala activation and poorer preformance on tasks requiring subjects w ASD to judge facial emotion)
  5. increased head circumference and brain volume among the most consistently replicated findings in ASD (20-30% macrocephaly) related to larger surface area rather than more thickness in cortical membrane
  6. recent studies indicate post-natal onset of macrocephaly (average or below head size at birth)
18
Q

How is white matter abnormal in ASD?

A

white matter is disproportionately enlarged relative to gray matter

  • white matter volume increase is found in subcortical areas and in origins and terminatios of projection and sensory fibers
  • corpus callosum is abnormally small relative to brain volume
  • structural and functional neuroimagining studies are consistence with the increased local and reduced distal connectivity (i.e. thats why they’re better at focusing on more detail oriented tasks rather than ones that require u to see the larger picture due to lack of distal connections)

their local connectivity is good for example between the same areas
distal: between larger areas and hemispheres

19
Q

What do neuropathological studies show in terms of ASD?

A
  1. limbic system abnormalities: reduced number of cerebellar purkinje cells, small and densely packed neurons in limbic regions like amygdala, hippocampus and entorhinal cortex
  2. abnormalities in brain stem, cranial nerve nucleii suggesting even earlier prenatal orgin
  3. neuroinflammation –> micgroglia (role in synaptic pruning releases pro inflam. cytokines when activated; evidence of microglial activation in ASD in selected brain regions like dosolateral prefrontal cortex; cortical minicolumns are narrower and more numerous (immature) with greater cell dispersion; note associations between ASD and autoimmune disorders in family members like MS, diabetes..etc..
20
Q

What is the genetics of ASD?

A
  • ASD is a strongly genetic disorder (90% heritibility) with MZ rates of 36-95%
  • recent processes of genetics include: central role of rare de novo and inherited rare genetic varients like CNV’s
  • atypical synaptic plasticity as a common functional mechanism
21
Q

What is the relation between ASD genes and synaptic plasticity?

A

ASD genes are ‘meeting at the synapse’
- meaning that many asd genes identified make proteins involved in regulating and maintaining neuronal synapse development and plasticity

22
Q

What has whole genome sequencing (WGS) show in terms of ASD?

A

shows that 16/32 families with deletrious genetic variants tat may have implications for clinical management and counseling
- de novo mutations identified in 19% and x-linked or autosomal inherited alterations linked in 30% of asd probands

23
Q

What was the significant finding in multiplex study?

A

that siblings with ASD may carry different pathogenic mutations; one sibling may have autism or ASD and the other kid might have another ID

therefore theres no single gene that accounts for autism/ASD

24
Q

What are the 3 routine recommended investigations of ASD patients?

A
  1. audiology (to see if hearing isnt an issue in social understanding and response)
  2. clinical microarray (array CGH) genetics testing
  3. molecular testing for FraX (particularily for boys)
25
Q

what are other selective recommended invesitgations for ASD?

A
  1. ferritin, TSH, CK, lead (iron levels testing)
  2. metabolic testing for things like PKU
  3. EEG
  4. neuroimaging
26
Q

What do the EEG’s indicate in ASD?

A

EEG is not justified in children with ASD and ‘regression’ and does not predict subclinical epilepsy and does not alter management

27
Q

What does neuroimaging indicate for ASD?

A

some studies indicated relatively high rates of mostly minor CNS structural abnormalities in ASD
- other studies found low rates

summary: only indicated with specific comorbid diagnosis like TS or localizing findings

28
Q

What are some novel therapeutics for ASD?

A
  • moving to an era of pharmacogenomics and tailored intervention
  • identification of gene defects is the first step towards understanding the molecular pathophysiology and has yielded new treatments like for fragX and rett’s syndrome
  • oxytocin has also been shown to increase levels of social interactions in individuals with ASD
29
Q

How is autism described as neurodiversity among the individuals who have it?

A

neurodiversity movement looks at ASD as a way of being

autistic adults view autisic as being a part of that person and a different way seeing the world (view it as being unique)