Lecture 9: Autism Flashcards

1
Q

Name the symptoms and diagnostic criteria for ASD according to DSM-5.

A
  • Persistent deficits in social communication and social interaction across multiple contexts
  • Restricted, repetitive patterns of behavior, interests, or activities
  • Symptoms must be present in the early developmental period
  • Symptoms cause clinically significant impairment in social, occupational, or other important areas of current functioning
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2
Q

Name examples of symptoms of ASD.

A
  • Deficits in social-emotional reciprocity
  • Deficits in non-verbal communicative behaviors
  • Problems with developing and maintaining relationships
  • Stereotyped or repetitive speech or behavior
  • Adherence to routine (difficulties with adaptive functioning)
  • Restricted interests
  • Hyper- or hyporeactivity to sensory input
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3
Q

What is the general prevalence and course of ASD?

A

The worldwide prevalence is about 1-1.5%, with boys being 4 times more often affected. In general, ASD persists into adulthood.

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4
Q

How many patients with ASD also show sensory processing issues?

A

95% show sensory processing issues.

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5
Q

Which comorbidities are common in ASD?

A

ADHD, intellectual disability and epilepsy (very high comorbidity; brain areas important in ASD and epilepsy show overlap).

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6
Q

Name some issues with treating ASD.

A

There are hardly / no treatments for the core symptoms of ASD. Accordingly, only comorbid symptoms are treated. However, the treatments are not biologically informed.

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7
Q

Name some cognitive dysfunctions seen in ASD.

A

Emotional, (selective) attention, adaptive functioning, inhibition and memory.

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8
Q

How did ASD patients score on affective-face processing, go-no-go and set-shifting tasks?

A

ASD patients are significantly slower and make more errors in these tasks.

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9
Q

Regarding genetics, how high is the heritability of ASD?

A

The heritability is about 80%.

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10
Q

Name examples of neural pathology in ASD.

A

In ASD there is a significant cortical overgrowth between 2 and 4 years of age, a reduced area of the corpus callosum, under-connection in a widely distributed set of networks and changes in the neural activity during tasks involving social and affective judgments and differences in the processing of facial and non-facial stimuli.

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11
Q

Name and describe a potential biological mechanism underlying ASD.

A

Imbalance between excitation and inhibition in the brain, in particular in circuits governing sensory processes, memory, and social and emotional behaviors.

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12
Q

What are special aspects of ASD with comorbid epilepsy?

A
  • strong aversive (hypersensitive) reactions to sensory stimuli
  • altered EEGs/ brain rhythms
  • dysfunction of GABAergic transmission
  • i.e. hyperexcitability
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13
Q

Which neurotransmitters are assumed to be involved in the development of ASD? What could be an underlying mechanism?

A

GABA and glutamate. In ASD there is either too few inhibitory GABA or too much excitatory glutamate leading to the excitation-inhibition disbalance seen in ASD.

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14
Q

How could so-called minicolumns be related to the excitation-inhibition disbalance?

A

If minicolumns are densely packed there is a problem with migration leading to less or dysfunctional interneurons (inhibitory). Accordingly, GABA levels go down, inhibition goes down and excitation goes up (e.g. causing seizures).

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15
Q

Which EEG waves are found to be abnormal in ASD?

A

Gamma (during face processing) and alpha waves (increased and earlier peak).

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16
Q

Name some possible E/I treatment options.

A

GABA, glutamate, oxytocin, mTOR, bumetanide and TMS.

17
Q

Name the important brain areas for TMS treatment.

A

DLPFC, IFG, SMA, DMPFC and ACC.