Neuropsychiatry

Challenging Phenomenology in Tourette Syndrome and
Obsessive–Compulsive Disorder: The Benefits of Reductionism

Anton Scamvougeras, MBChB, FRCPC
Clinical Associate Professor, Adult Tourette Syndrome Clinic, Neuropsychiatry Unit, Department of Psychiatry, University of British Columbia, Vancouver, British Columbia.



Abstract : This article comments on challenging aspects of the phenomenology of Tourette syndrome and obsessive–compulsive disorder and suggests a reductionistic clinical approach.

Résumé : Remettre en question la phénoménologie du syndrome de la Tourette et du trouble obsessif–compulsif : les avantages du réductionnisme
Cet article commente les aspects controversés de la phénoménologie du syndrome de la Tourette et du trouble obsessifBcompulsif, et propose une approche clinique réductionniste.

Key Words : Tourette syndrome, obsessive–compulsive disorder, phenomenology, reductionism

Psychiatrist: “Are the compulsions like the tics?”
Patient: “Yes”
Psychiatrist: “Are they different?”
Patient: “Yes”

Tourette syndrome (TS) and obsessive–compulsive disorder (OCD) share similar neurobiological mechanisms and, by virtue of that, demonstrate intriguingly interrelated clinical features.

Their etiologies remain unknown. Cooccurrence of the two conditions is common and occurs well beyond what one would expect from chance (1). Association is apparent at the hereditary level in that probands with one condition have a higher incidence of the other condition in family members (2,3). Secondary forms of each condition can independently be caused by neurological disorders of the basal ganglia, such as stroke or tumour (4,5). Functional brain scan studies demonstrate abnormal function of components of corticostriatothalamo-cortical (CSTC) neuronal circuits in both conditions (6,7). Specifically, TS involves the premotor circuit, and OCD involves the lateral orbitofrontal circuit. The CSTC circuits appear to be important as mediators of highly preserved and evolutionarily useful motor and cognitive programs (8). Examples of such programs include those for making common movements (for example, blinking), as well as more complex behaviours such as checking the security of one’s domain, cleaning and grooming the body, cleaning one’s surroundings and, even counting, exploring or collecting objects. Appropriate activity of these circuits allows the individual to perform common actions with maximal efficiency when they are necessary. Dysregulation of these circuits may lead to decreased inhibition of these motor or cognitive programs, with resultant unwanted, senseless, physical and mental overactivity. The symptoms of TS, OCD and related disorders result.

The behaviours, cognitions and affective symptoms seen in these conditions are often complex and difficult to analyze. Distinctions are important because therapeutic direction may depend on them.

In their “pure” forms, the core symptoms of TS and OCD are relatively easily differentiated. A tic is a rapid and nonrhythmic repetitive movement. It is preceded by a physical sensation (a sensory premonitory phenomenon) in more than 80 per cent of patients (9). There is no associated cognition or anxiety. A compulsion, in contrast, is a stereotyped and intentional movement that is performed in response to an obsession (an intrusive thought that is perceived to be senseless to the affected individual). There is a mental anxiety present prior to the compulsion, with temporary relief after the act. There is no associated sensory phenomenon. Patients who suffer both of these pure forms are often eloquent in their ability to differentiate the phenomena as being respectively “physical” and “mental.”

Tics, however, can also consist of coordinated patterns of sequential movements, in which case they are called “complex tics” and may be challenging to differentiate from compulsions. They may appear goalless or may be incorporated into apparently useful actions.

The exact definition of a compulsion still appears to be unclear. Some think that only acts resulting from obsessions should be called compulsions; others, however, only require anxiety or even an urge (10) to call an associated complex movement a compulsion.

Various epiphenomena are associated with the core behaviours, thus each deserves separate consideration.

Sensory phenomena may be localized, as with a sense of building pressure in the shoulder prior to a shoulder elevation tic. Indeed, 75 per cent of individuals with this phenomenon report that resultant tics are voluntary movements that are aimed at relieving this sensation. Other sensory phenomena are nonlocalizable (10) and may be challenging to differentiate from mental dysphoria—more so when they may be coexistent. These symptoms have some features reminiscent of akathisia and likely share neurobiological mechanisms with other causes of that condition.

 

“Just-right phenomena” are actions that have to be performed over and over until something about them is judged to be completed (11). They commonly involve acts such as placing a drinking glass onto a surface. There are no specific associated cognitions. The action usually has to appear right in one of the sensory modalities: it has to feel, look or sound right to achieve the desired endpoint. The exact criteria for the endpoint are often beyond the patient’s descriptive capacities. These repetitive behaviours would be called “compulsions” if they had associated cognitions and “tics” if they did not involve objects outside the body. They are reminiscent of both, but they are neither. They may be labelled “compulsions” by those who only require an urge as the origin of a compulsion.

Other variations confound matters further—in severe forms of OCD, individuals may lose insight into their compulsions, see them as necessary and then technically be suffering delusions. Some patients with comorbid Asperger’s-spectrum syndromes demonstrate unusual thought content that is best characterized as preoccupations but easily confused with obsessions. Some individuals with TS describe urges that may have overlap with sex drive (for instance, the urge to touch a stranger in the genital area). Some behaviours may involve pain as a desired endpoint and may be self injurious. Movements may occur with no specific associated affective state or with mental dysphoria (anxiety or irritability) that may alter once an action is completed.

 



In the clinical setting, a reductionistic approach makes most sense. Describe the action as accurately as possible, calling complex behaviours "intentional repetitive behaviours" (12) if they are not definite pure forms.

 

As if these descriptive issues were not enough, there are also purely semantic challenges. Words such as “compulsive” and “obsessive” are widely used in the English language in ways that differ from their clinical definitions. Someone may be labelled a “compulsive” shopper or an “obsessive” gardener. In a related sense, most psychiatrists will eventually have the experience of being referred a patient for assessment of OCD, only to find that the individual is someone who has a degree of neatness and organization about their lives that is substantially more prominent than that of the referring clinician. Thus, obsessiveness has been mistaken for obsessions and compulsions, the distinguishing feature being that the former is not seen as senseless by the patient.

In the clinical setting, a reductionistic approach makes most sense. Describe the action as accurately as possible, calling complex behaviours “intentional repetitive behaviours” (12) if they are not definite pure forms. Describe all epiphenomena including sensory phenomena, cognitions, affective state, changes with the completion of the action, how endpoint is judged, senselessness and so on. Treatment, therefore, focuses on the most disabling symptoms, with the aim to improve overall quality of life rather than to eliminate all symptoms. Medication choice is based on knowledge of how parsed phenomena best respond to specific current therapies. For the purpose of diagnosis, certain labels may be applied (“OCD” or “Tourette”), but the therapeutic path will more closely relate to the pattern of phenomena than will the broad labels which, by nature, will lose resolution when it comes to understanding the individual’s unique situation.

Faced with related phenomenology dilemmas, the TS Classification Study Group (13) used a reductionistic approach when it said of its numerous tic syndromes, “Although some of these separate entities may ultimately be shown to be caused by the same etiology (or even the same gene), until that is established it is considered best to divide the condition into distinct entities.” “(This classification) can both expand and consolidate, as (etiological factors) are identified (13).” One promise of reductionism is that accurate description of the variations of phenotype will lead to the best chance of correlating such variation with neurobiological underpinnings, as the latter become elucidated. We may find that phonic tics are simply motor tics of noise-making musculature; however, we may find that they are somehow neurobiologically distinct from other tics. We do not yet know, and until we do, we should continue to subdivide them. An approach such as this one has already led to the description of two likely biologically distinct types of OCD (10).

 



References

1. Apter A, Pauls DL, Bleich A, Zohar AH, Kron S, Ratzoni G. In: Chase TN, Friedhoff AJ, Cohen DJ, editors. 1992. A population-based epidemiological study of Tourette syndrome among adolescents in Israel. Advances in neurology; Tourette syndrome: genetics, neurobiology and treatment. Volume 58. New York: Raven Press. p 61–5.

2. Pauls DL, Leckman JF. Genetics of Tourette syndrome. In: Cohen DJ, Bruun R, Leckman JF, editors. Tourette syndrome and tic disorders: clinical understanding and treatment. New York: J Wiley; 1988. p 91–102.

3. Pauls DL, Alsobrook JP, Goodman W, Rasmussen S, Leckman JF. A family study of obsessive-compulsive disorder. Am J Psychiatry 1995;152:76–84.

4. Sacks O. Acquired tourettism in adult life. In: Friedhoff AJ, Chase T, editors. Gilles de la Tourette syndrome. New York: Raven Press; 1982. p 89–92.

5. Swoboda KL, Jenicke MA. Frontal abnormalities in a patient with obsessive-compulsive disorder: the role of structural lesions in obsessive-compulsive behaviour. Neurology 1995;45:2130–4.

6. Wolf SS, Jones DW, Knable MB, Gorey JG, Lee KS, Hyde TM. Tourette syndrome: prediction of phenotypic variation in monozygotic twins by caudate nucleus D2 receptor binding. Science 1996;273:1225–7.

7. Saxena S, Rauch SL. Functional neuroimaging and the neuroanatomy of obsessive-compulsive disorder. Psychiatr Clin North Am 2000;23:563–86.

8. Middleton FA, Strick PL. A revised neuroanatomy of frontal-subcortical circuits. In: Lichter DG, Cummings JL, editors. Frontal-subcortical circuits in psychiatric and neurological disorders. New York: The Guilford Press; 2001. p 44–55.

9. Cohen AJ, Leckman JF. Sensory phenomena associated with Gilles de la Tourette syndrome. J Clin Psychiatry 1992;53:319–23.

10. Miguel EC, Rosario-Campos MC, Shavitt RG, Hounie AG, Mercadante MT. In: Cohen DJ, Goetz CG, Jankovic J, editors. 2001. The tic related obsessive-compulsive disorder phenotype and treatment implications. Advances in neurology. Volume 85. Tourette Syndrome. Philadelphia: Lippincott Williams and Wilkins. p 43–55.

11. Leckman JF, Walker DE, Goodman WK, Pauls DL, Cohen DJ. “Just-right” perceptions associated with compulsive behaviour in Tourette syndrome. Am J Psychiatry 1994;151:675–80.

12. Miguel EC, Coffey BJ, Baer L, Savage CR, Rauch SL, Jenicke MA. Phenomenology of intentional repetitive behaviours in obsessive compulsive disorder and Tourette disorder. J Clin Psychiatry 1995;56:246–55.

13. Tourette Syndrome Classification Study Group. Definitions and classification of tic disorders. Arch Neurol 1993;50:1013–6.


Bulletin Archives in English | Archives du Bulletin en français
Information for Contributors | Information à l'intention des auteurs
Subscription Rates | Prix d'abonnements
Advertising Rates | Tarifs publicitaires
CPA Publications | Publications de l'APC
CPA Home | Page d'accueil