Tourette’s Disorder

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Tourette’s Disorder

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Tourette’s Disorder. DSM-V Categorization: Neurodevelopmental motor Disorder: Tic Disorders. Characterized with an onset in the developmental period, usually early in development Symptoms of excess as well as deficits/ milestone delays - PowerPoint PPT Presentation

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Tourette’s Disorder

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DSM-V Categorization:Neurodevelopmental motor Disorder: Tic Disorders

Characterized with an onset in the developmental period, usually early in development

Symptoms of excess as well as deficits/ milestone delays

Deficits produce impairments including academic, personal, occupational and social functioning

Frequent co-occurrence with other disorders

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DSM-V Tic Disorders

• Based on the presence of motor and or vocal tics• Duration of symptoms• Age at onset• Absence of any other cause (substance use or

medical condition)• Hierarchical rank:

Tourette’s disorderPersistent motor or vocal tic disorderProvisional tic disorder Specified and unspecified tic disorder

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DSM-V TicsTic: sudden, rapid, recurrent, nonrhythmic motor movement or vocalization (DSM-V)

Motor TicSimple motor ticsComplex motor tics

Vocal TicSimple vocal ticsComplex vocal ticsCoprolalia- obscene inappropriate words or phrasesEcholalia- repeating others’ wordsPalilalia- repeating own words

Video

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DSM-V TS Development/ Course • 4-6 average onset• Severity around 10-12 then a decline in adolescence (small

percentage worsen in adulthood)• Across lifespan tic symptoms manifest/ wax and wane idea • Muscle groups and vocalizations change over time • With age comes a premonitory desire [somatic sensation]

followed by a feeling of relief after expressing the tic• Particular pattern of tics, desire to express “just right”• Vulnerable to co-occurring conditions during “age of risk”

and then followed by decline

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Meeting DSM-V Diagnostic Criteria for TS

• A. Both multiple motor and one or more vocal tics have been present at some time during the illness, although not necessarily concurrently.

• B. The tics may wax and wane in frequency but have persisted for more than 1 year since first tic onset.

• C. Onset is before age 18 years.• D. The disturbance is not attributable to the

physiological effects of a substance or another medical condition.

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DSM-V Prevalence/Cultural influences

• Childhood onset is common, but tics are usually transient

• 3 to 8 per 1,000 school aged children• Males > females (2:1 to 4:1), no gender differences in

kinds of tics• African Americans and Hispanic Americans <

identified cases• Race, ethnicity, and culture: no varying clinical

characteristics, but instead may influence perception and management of disorder (choice of treatment)

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CHARACTERISTICS OF TICS• Mild, moderate or severe- dependent on: frequency,

forcefulness, complexity and daily life impairment• Frequency does not equal impairment: eye blinking 20-30 per

minute vs. loud barking several times an hour• Most individuals experience oscillations in severity over weeks

and months (waxing and waning)• Involuntary but some report “semi-voluntary” based on

suppression ability • Premonitory urges followed by satisfaction after tic is completed• Individuals may disguise tics as purposeful: arm jerk –comb hair

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DSM-V Risk and Prognostic Factors

Temperamental:• Tics are worsened by anxious, excited and exhausted emotions • Tics are better when individual experiences calmness and is focused

Environmental:• Observation of a gesture/sound may result in individual with tic

disorder to imitate (can be perceived incorrectly/purposeful)• Hinders interaction with authority figures

Genetic/Physiological:• Expression and severity influenced• Risk alleles and rare genetic variants have been identified• Obstetrical complications/older paternal age/maternal smoking

during pregnancy and lower birth weight associated with tic severity

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DSM-V Functional Consequences• Many individuals do not experience impairment with their

tics and may even be unaware of their tics• More severe cases usually result in daily living impairments

(not definitive, some severe cases may function just fine)• Co-occurring conditions can lead to greater impairment• Less often tics lead to social isolation, interpersonal

conflict, peer victimization, inability to work/attend school, poor quality of life

• Rare complications include: physical injury, orthopedic injury and neurological injury

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COMORBIDITY

• In addition to tics, many experience co-occurring psychiatric and or neuropsychological difficulties

• Most frequent: ADHD (50%), related learning disorders, OCD (20-60%), anxiety disorders, affective disorders, sensory integration dysfunction and explosive aggressive behaviors

• Not necessarily etiological, many influences possible

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Genetic/ Physiological Mechanisms

<18 onset of motor/vocal tics

Age

Environment

Temperament

Tic severity

Comorbidity:ADHD/OCD

Secondary Features:

Neurological, orthopedic,

physical injuryFunctional impairment

Problems with teachers, parents

and law enforcement

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DO WE HAVE EVIDENCE IN RESEARCH?

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PERSPECTIVE IS KEY

• Some researchers view TS as a discrete single entity with accompanying syndromes

• Others view TS with common causes and varying manifestations more like a spectrum disorder

• When reviewing research regarding TS critical to understand population requirements for TS groups

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ADHD

• More than 50% with TS who come to the attention of physician – ADHD

• 30% with TS experience school difficulties/learning disabilities

• Special care to be taken in medication-stimulants may worsen behaviors/tics

• Relationship between ADHD/TS less understood (O’Rourke et al., 2011)

• Suggested overlapping neurobiology: ADHD/OCD/TS (O’Rourke et al., 2011)

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OCD/anxiety

OCD:• Many with TS may also have obsessive-compulsive symptoms

(OCS)• Disruptive to life and to tics • Need to “even things up”, “feel right”, touching forbidden objects

(hot frying pan)• Complex tic or compulsion• Special care to be taken in medication: antipsychotic vs. SSRIAnxiety:• Unknown if genetically related to TS • Avoidance behavior common: reluctance to go to school or other

activities (sleepovers)

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TEMPERAMENTAL INFLUENCES

• Individuals with TS- higher levels of aggression, hostility and personality disorder (Robertson et al., 1997)

• Tics have been “associated” with increased neuroticism/ additional OCD diagnosis also showed low extraversion (Cath et al., 2001)

• Comorbid ADHD “associated” with emotional instability• Severe OCD symptoms-emotional hypercontrol (Balottin et al., 2009)• Schizotypical personality traits-more common in TS population (Cavanna,

Robertonson, & Critchley, 2007; Comings & Comings, 1987)• TS has been “associated” with significant differences in QofL aspects (home, peer

and family interactions) (Eddy, Rizzo, Gulisano, Agodi, Parchitta, Cali, et al., 2011)• 88% of individuals with TS report tics having an effect on their life-potential to

influence perceptions of abilities and feelings about themselves (Eddy, Rickard, Critchley & Cavanna)

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EXPLOSIVE/AGGRESSIVE BEHAIVOR

• 25-70% of patients with TS report outbursts and anger issues (factor analysis accounting for 62.5% of variance) (Budman, Rockmore, Stokes, & Sossin, 2003)

• Kicking, screaming, threatening others, biting, hitting, fits of anger/rage, punching holes in walls

• Individuals typically afraid of their own behavior• “Run it’s course” nature• Thin barrier between outward expression and

impulses/thoughts• Causes problems with teachers, families, and patients

themselves

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Personality Influenced 25 adult outpatients, TS clinic, all fulfilled DSM-IV-TR criteria for TS

Comprehensive clinical interviews- National Hospital Interview Schedule for TS

Participants completed: Ten Item Personality Index, Beck Depression Inventory, Positive and Negative Affect Schedule, & Yale Global Tic Severity Scale

Group scores were compared: TS patients vs. controls, between-group analysis subgroup of ‘pure TS’ to controls

Results: No significant differences on: BDI, PANAS positive or negative subscales, or the TIPI agreeableness scores

Significant difference between groups for four other TIPI scores (extraversion: MWU = 170.5, p = 0.005; conscientiousness: MWU = 204, p = 0.033; emotional stability: MWU = 130.5, p<0.001; openness: MWU = 196.5, p = 0.022)

Correlations: significance for emotional stability scores negatively related to BDI (SR= -0.501, p = 0.011, PANAS negative subscale scores (SR = -0.482, p = 0.015) and positively related to PANAS positive subscale scores (Sr = 0.682, p<0.001). TIPI emotional stability negatively related to BDI scores (Sr = -0.891, p<0.001) and positively related to PANAS positive subscale scores (Sr = 0.619,

p = 0.014)

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Behavioral Influences

• Self-Injurious Behaviors (deliberate/repetitive infliction of self-harm)

• Skin/scab picking, hair pulling, pinching oneself, self-biting• Study focused on the relationship between SIB and other

behavioral features that commonly co-occur with TS (Mathews et al., 2004) ~300 subjects with TS participating in three genetic studies

• Analyzed SIB, obsessions, compulsions, tic severity, attention deficit hyperactivity disorder related impulsivity, risk taking behaviors, and rages

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Stress Related INFLUENCES• Life events are commonly used for the purpose of measuring stress

• Stressful life events and TS relationship is unclear• Tic expression may be involved (Meidinger et al., 2005; Woods &

Himle, 2004)

• Impact of stressful life events and tic severity is best predicted by parental report (Lin et al., 2007)

• Comorbid OCD: more stressful life events than controls (Findley et al., 2003)

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ENVIRONMENTAL INFLUENCES

• Literature review • Antecedent vs. Consequence Factors• Fatigue and social activities- exacerbate tics• Concentration, studying, relaxation- attenuate tics• Limited to applying these findings to population or even other clinical

samples because of self-report issues and reported in aggregate form• Negative consequences reported to have negative or neutral outcomes• Positive consequences resulting in positive outcomes• Consequences were parent reported• Generalizability unclear, overall however, stressful frustrating or

anxiety provoking events reported to exacerbate tics

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ENVIRONMENTAL INFLUENCES

• ‘tic-talk’ condition found to increase frequency of vocal but not motor tics (Woods, Watson, Wolfe, Twohig, & Friman, 2001)

• Tics found to increase in presence of certain people (teacher, custodian, father, mother, examiner) (Malatesta, 1990)

• Videotaping of children watching emotional video- most severe tics at specific emotional states, least severe in anger/happiness

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LIMITATIONS IN UNDERSTANDING CONTEXTUFAL FACTORS

• The studies reviewed examined the relationship in experimental settings

• Isolating certain variables would be most helpful in applying these findings to treatment interventions

• Little information about the premonitory ‘urge’ in the development of the disorders

• Most interesting but still unknown: Is it tics themselves that are impacted by contextual factors or is it the suppression/inhibitory behaviors that are being changed?

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GENETIC INFLUENCES

• Previous studies have sought to identify several chromosomal regions associated with the susceptibility loci for TS

• TS and Chronic motor tics among first-degree relatives 2.0% and 12.0% (respectively)

• Morbid risk for TS among relatives: 9.8%-15%• When replicated, results typically do not hold• Difficult to extract out comorbid ADHD in findings, unable to

conclude TS specific findings (< 10% of patients account for ‘pure’ TS population (Ozonoff et al., 1998; Mahone et al., 2002)

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Neurological influences

• Suggested involvement of the frontal cortex connections to subcortical regions including basal ganglia through the frontal cortico-striatal-thalamo-cortico circuits (Mink, 2001; Singer, 2005; Albin and Mink, 2006)

• Suggested abnormality in brain systems that effect neural transmission from limbic to motor systems deficit in regions involved with motivation and action (Jeffries et al., 2002)

• Involvement with frontal cortex including response inhibition and selective attention (Bornstein et al., 1991; Johannes et al., 2001; Channon et al., 2003)

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GENETIC/ PHYSIOLOGICAL INFLUENCES

• rs-fcMRI used to explore the possible disruption of brain systems in patients with TS (Fair et al., 2007a, 2008; Fransson et al., 2007)

• Defects in neural circuits from the cerebral cortex through the structures constituting the basal ganglia and back to the cerebrum (Olson, 2004).

• Cingulo-opercular network: maintenance of tasks sets across events within task period

• Fronto-parietal network: rapidly adaptive online control• TD: strength of correlation coefficients ‘between’ differences in control networks

seem to be stronger in children and decline with age (Fair et al., 2007)• Consideration of TS behaviors lead to theory of 3 suggested possibilities (Church et

al., 2009) : 1. Abnormal connectivity within and between cingulo-opercular network2. Altered connectivity with and within fronto-parietal network3. More widespread set of differences could affect both networks and relations between

them

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GENTIC/ PHYSIOLOGICAL INFLUENCES

• Largest off-curve differences found mostly in fronto-parietal network (adaptive control-/ controlling settings from one event to the next)

• Immaturity in connections may be related to adaptive control network being more vulnerable to distraction while cingulo-opercular network (set-maintenance) stable and resistant

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GENTIC/ PHYSIOLOGICAL INFLUENCES

• Results for TS showed underdevelopment in 10-15 year olds, instead reflecting 7-9 year old

• Groups of adolescents TD and with TS: 34 functional connections (p < 0.05) but after Benjamini and Hochberg False Discovery Rate correction, no emphasis produced

• Connections examined using rs-fcMRI show weaker functional connections

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WHAT DO These DIFFERENCES MEAN?

• As mentioned, fronto-parietal network is associated with supporting online task-control while allowing for adaptive change from one event to the next (disruption here might make sense for the increase in severity in different environments that produce a change in emotion (going from calm to excitement, > frequency and severity of tics)

• The fronto-parietal network has also been hypothesized as being more susceptible to distraction which would make transient control impaired

• Adolescents with TS (10-15) may have less functional communication between distant areas of cortex and over communication between closer regions (similar to young children)

• Lack of long range communication could explain inability to supress unwanted behaviors in TS

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Genetic influences

• 6 family studies have previously looked into familial related conditions in TS (5- US & Europe, 1-Japan)

• Interviews from first degree family members• Found morbid risk of 9.8-15% among relatives• 15-20% for other tics• Age correct rates among first degree relatives 2.0-12%• More recently, researchers suggest inheritance patterns

are more complex than originally thought and are seeking association and linkage studies (Pauls, 2003)

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Problems with Genetic association/linkage studies

ASSOCIATION:• Case control or family based• Limited by many irrelevant markers appearing

to be disease associated• High rates of false positives• Population stratification- cases and controls

differ not only with phenotype of interests but overall population genetic ancestry

• Difficult to find appropriate control group

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Problems with Genetic association/linkage studies

• LINKAGE (Pauls, 2003):• Members of the Tourette Syndrome Association International

Consortium on Genetics (TSAICG) conducted all initial linkage studies• 31 multigenerational families were studied • > 800 genetic marker loci were screened• No strong positive evidence found for linkage with TS• Re-conducted by TSAICG in sib-pair study of 76 families• 64 had only two affected siblings• 10 had three effected siblings • 2 had 4 and 5 affected siblings• Candidate genes such as the dopamine D4 receptor DRD4 have been

suggested but fail to be replicated (Pauls, 2003)

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Review• Temperament, environment, & genetics/physiology in relation

to TS commonly produced inconclusive research findings• Tic severity may to be influenced by awareness, context, age,

& comorbidity• Immature connectivity throughout neurological regions have

been measured and may influence the inability to inhibit unwanted behaviors

• Research findings of TS struggle to be generalizable to entire population because of high comorbidity rates

• As earlier stated, perspective of disorder is important in approaching targets of treatment intervention

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Neuroanatomical/Genetic

Substrates

Motor Tics/ (simple or complex)Vocal Tics

Age

Comorbidity ADHD/OCD

Awareness of Behaviors

Tic Severity

Self-InjuryInattentiveness

AggressionFunctional ImpairmentDeficits in relationships

Stress/Anxiety/Fatigue/

InattentionInhibitory deficits

Academic/Behavioral Functioning

Socialization/Peer- acceptance/

Quality of relationships

Cunningham TS Model 2013

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REFERENCES

American Psychiatric Association. (2013). Diagnostic and

statistical manual of mental disorders (5th ed.). Arlington, VA: American Psychiatric Publishing.

Balottin, U., Rossi, M., Rossi, G., Vigano, L., Salini, S., Lanzi, G, et al. The rorscharch test and gilles de la tourette’s syndrome: A

pilot case control study. Brain Development, 31, 657-665.

Bloch, M. H., & Leckman, J. F. (2009). Clinical course of tourette syndrome. Journal of Psychosomatic Research, 67, 497-501.

Brito, G. N. O. (1997). A neurobiological model for tourette syndrome centered on the nucleus accumbens.

Medical Hypotheses, 49, 133-142.

Budman, C. L., Rockmore, L., Stoke, J., & Sossin, M. (2003). Clinical phenomenology of episodic rage in children with

tourette syndrome. Journal of Psychosomatic Research, 55, 59-65.

Cath, D. C., Spinhoven, P., Landman, A. D., & van Kempen, G. M. J. (2001). Psychopathology and personality characteristics in

relation to blood serotonin in tourette’s synfrome and obsessive-compulsive disorder. Journal of

Psychopharmochology, 15, 111-119.

Church, J. A., Fair, D. A., Dosenbach, N. U. F., Cohen, A. L., Miezin, F. M., Peterson, S. E., & Schlaggar, B. L.

(2009). Control networks in paediatric tourette syndrome show immature and anomalous patterns of

functional connectivity. Brain, A Journal of Neurology, 132, 225-238.

Conelea, C. A., & Woods. D. W. (2008). The influence of contextual factors on tic expression in tourette’s syndrome:

A review. Journal of Psychosomatic Research, 65, 487-496.

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Eddy, C. M., Rickards, H. E., Critchley, H. D., & Cavanna, A. E. (2013). A controlled study of personality and

affect in tourette syndrome. Comprehensive Psychiatry, 54, 105-110.

Findley, D. B., Leckman, J. F., Katsovich, L., Lin, H., Zhang, H., Grantz, H. et al. (2003). Development of the yale

children’s global stress index (YCGSI) and its application in children and adolescents with tourette

syndrome and obsessive-compulsive disorder. Journal of American Academy of Child Adolescent Psychiatry, 42,

450-457.

Jeffries, K. J., Schooler, C., Schoenbach, C., Herscovitch, P., Chase, T. N., & Braun, A. R. (2002). The functional

neuroanatomy of tourette’s syndrome: An fdg pet study III: Functional coupling of regional

cerebral metabolic rates. Neuropsychopharmacology, 27, 92-104.

Leckman, J. F. (2002). Tourette’s syndrome. The Lancet, 360, 1577-1586.

Lin, H., Katsovich, L., Ghebremichael, M., Findley, D. B., Grantz, H., Lombroso, P. J., et al. (2007). Psychosocial stress predicts future symptom

severities in children and adolecents with tourette synfrome and/or obsessive compulsive disoder. Journal of Child Psychology and Psychiatry, 48, 157-166.

Pauls, D. L. (2003). An update on the genetics of gilles de la tourette syndrome. Journal of Psychosomatic

Research, 55, 7-12.

Robertson, M. M., Banerjee, S., Hiley, P.J. F., & Tannock, C. (1997). Personality disorder and psychopathology

in tourette’s syndrome: A controlled study. Br J Psychiatry, 171, 283-286.

Steinberg, T., Shmuel-Baruch, S., Horesh, N., & Apter, A. (2013). Life events and tourette syndrome.

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