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Obsessive-Compulsive Disorder and


-Compulsive Spectrum Disorders:
Diagnostic and Dimensional Issues
By Eric Hollander, MD, Suah Kim, BA, Sumant Khanna, MD, PhD,
and Stefano Pallanti, MD, PhD

ABSTRACT
FOCUS POINTS
Although obsessive-compulsive disorder (OCD) Key findings support the validity of separating
is classified as an anxiety disorder in the DSM-IV, obsessive-compulsive disorder (OCD) from the
anxiety disorders.
recent considerations for a reclassification into an
A new category of obsessive compulsive spectrum
obsessive-compulsive spectrum disorders (OCSDs) disorders (OCSDs) is proposed.
cluster are gaining prominence. Similarities in Determining which disorders to include in this cat-
egory deserves further discussion.
symptomatology, course of illness, patient popu-
lation, and neurocircuitry of OCD and OCSD are
supported by comorbidity, family, and neurological Despite efforts in this field, there are several funda-
studies, which also offer a critical re-evaluation of mental unresolved issues, including the question of
the relationship between OCD and anxiety disor- which disorders should be grouped together in this
ders. This review examines potential classifications category and which characteristics to include as
of OCD among the wider spectrum of affective their shared common features. A reclassification of
disorders and at the interface between affective OCD among the OCSDs would allow for better scru-
disorders and addiction. In addition, it has been tiny of distinct obsessive-compulsive symptoms,
suggested that the categorical diagnostic approach as currently this disorder often goes undetected
would be enhanced by an additional dimensional in patients who complain of a broad symptom of
approach, including parameters such as stability anxiety. Advantages and disadvantages of estab-
of mood and ability to sustain attention. With fur- lishing OCSDs and its implications for diagnosis,
ther studies, it is ultimately the goal to define OCD treatment, and research are discussed.
and related disorders based on endophenotypes. CNSSpectr. 2007;12:2(Suppl 3):5-13

Dr. Hollander is Esther and Joseph Klingenstein professor and chair of psychiatry, and director of the Seaver and NY Autism Center
of Excellence at the Mount Sinai School of Medicine in New York City. Ms. Kim is research coordinator in the Compulsive, Impulsive,
and Anxiety Disorders Program at the Mount Sinai School of Medicine. Dr. Khanna is a psychiatrist at The Psychiatric Clinic, Vasant
Vihar, in New Delhi, India. Dr. Pallanti is associate professor of psychiatry at the Institute of Neuroscience at the University of Florence
in Italy, and adjunct associate professor at the Mount Sinai School of Medicine in New York City.
Disclosures: Dr. Hollander has been a speaker for Abbott, Lundbeck, Pfizer, and Wyeth; is on the advisory boards of Abbott, Neuropharm,
Somaxon, and Wyeth; has received grants/honoraria from Abbott, Eli Lilly, Forest, and Pfizer; and has a financial interest in Neuropharm.
Ms. Kim reports no financial, academic, or other interest in any organization that may pose a conflict of interest. Dr. Khanna has been
a speaker for and on the advisory board of Johnson & Johnson; and has received grants/honoraria from Pfizer. Dr. Pallanti has been a
speaker for and on the advisory boards of Eli Lilly, GlaxoSmithKline, and Pfizer; and has received grants/honoraria from Abbott, Eli Lilly,
GlaxoSmithKline, Innovapharma, Lundbeck, and Pfizer.
Submitted for publication: June 12, 2006; Accepted January 4, 2007.
Please direct all correspondence to: Eric Hollander, MD, Department of Psychiatry, One Gustave Levy Place, Box 1230, New York,
NY 10029; Tel: 212-659-8287; Fax: 212-987-4031; E-mail: eric.hollander@mssm.edu.
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E. Hollander, S. Kim, S. Khanna, S. Pollanti

INTRODUCTION sive-compulsive features, comorbidities, lifetime


Obsessive-compulsive disorder (OCD) is a course, neurocircuitry, patient demographics, life-
chronic and debilitating disorder marked by time course, and treatment response, OCD may be
recurrent obsessions and/or compulsive behav- conceptualized as an OCSD alongside body dys-
iors often performed to alleviate distress caused morphic disorder (BDD), pathological gambling,
by the pervasive thoughts. The most common eating disorders, and autism.43
obsessions involve contamination, sexual imag- Leckman and colleagues 9 determined four
ery, aggression, doubting, order, and symmetry. dimensions of OCD: (1) obsessions/checking; (2)
Obsessions also have an egodystonic quality in symmetry/ordering; (3) contamination/cleaning;
that many OCD sufferers describe their intrusive and (4) hoarding. The first dimension is character-
thoughts as alien to themselves and not derived ized by obsessions of aggression, sex, religion,
from their mind but extrinsically imposed. or about the body, and checking behaviors; the
Compulsions are most often counting, washing, second dimension involves preoccupations with
checking, ordering, and hoarding. The obsessions order, symmetry, or exactness, and/or compul-
and compulsions associated with OCD are time sions of counting, rearranging, or ritualistic rep-
consuming and contribute to psychosocial impair- etitions; the third dimension involves obsessions
ments and significant distress. There is also an about contamination and compulsive washing and
avoidance quality to OCD as many sufferers try cleaning; and the fourth dimension includes hoard-
to evade situations and things that will trigger ing obsessions and compulsions. Correlates have
OCD symptoms. Although OCD is currently clas- been found between symmetry/hoarding factors
sified as an anxiety disorder in the Diagnostic and comorbid chronic tics and obsessive-compul-
and Statistical Manual of Mental Disorders, sive personality disorder.10 Individuals diagnosed
Fourth Edition (DS/W-/1/),1 recent considerations withTourette's syndrome or chronic tic disorder
for a reclassification into an obsessive compul- scored significantly higher on obsessions/check-
sive spectrum disorder (OCSD) cluster is gain- ing and symmetry/ordering factors.9 Furthermore,
ing prominence. Similarities in symptomatology, hoarding was also associated with pathological
course of illness, patient population and neurocir- grooming behaviors seen in trichotillomania, skin-
cuitry of OCD and OCSD are supported by comor- picking, and nail-biting.11 This model reflects the
bidity, family, and neurological studies, which heterogeneous phenotype of OCD.12 Other inves-
also offer a critical reevaluation into the relation- tigators argue for subtyping of OCD,13 specifically
ship between OCD and anxiety disorders. OCD with tics, as those patients who suffer from
comorbid tics show different symptomatology,
tend to be male, and are less responsive to sero-
NOSOLOGY OF OBSESSIVE- tonin reuptake inhibitors (SRIs) compared to those
COMPULSIVE DISORDfR without comorbid tics.14
Under the current DSM-IV classification, OCD
is categorized as an anxiety disorder together with Alternatively, OCD may be conceptualized as
agoraphobia, panic disorder, generalized anxiety existing within a broad spectrum of affective dis-
disorder (GAD) and posttraumatic stress disorder orders (Figure 1) or one may consider it a group
(PTSD).The primary reason for this classification of disorders lying midway between affective dis-
is anxiety's principal role in OCD. The obsessions orders and addiction disorders (Figure 2). From
associated with OCD contribute to escalating a dimensional viewpoint, these problems may
anxiety, and the compulsive behaviors are often be visualized as lying along a phenomenological
performed to try to reduce this anxiety.2 Anxiety dimension of compulsivity and impulsivity (Figure
disorder and OCD sufferers also exhibit an urge to 3). Furthermore, by incorporating a more dimen-
escape provoking stimuli with subsequent avoid- sional approach with the categorical methodol-
ance behaviors.3The fault in this comparison is that ogy, patients must have sufficient severity of both
anxiety is a rather broad symptom that is apparent obsessions and compulsions to have a diagnosis
in several other psychiatric disorders including of OCD wherein this OCD may be classified with
depression, schizophrenia, and bipolar disorder. associated symptom domains of varying sever-
Classifying OCD as an anxiety disorder contrib- ity (Figure 4). OCSDs can also be sub-divided
utes little to understanding both the etiology of into three clusters: (A) body image and somatic
this heterogeneous disorder and in development disorder; (B) impulse-control disorders; and (C)
of effective treatment. Because of shared obses- neurological disorders With repetitive behaviors.5

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February 2007
Obsessive-Compulsive Disorder and Obsessive-Compulsive
Spectrum Disorders: Diagnostic and Dimensional Issues

The first cluster is characterized by obsessions Pathological gamblers, for example, exhibit higher
with the body, which includes hypochondriasis, levels of obsessionality than healthy controls.16
binge-eating disorder, anorexia nervosa, BDD, The third cluster of OCSD involves neurologically
and depersonalization disorder.These disorders based disorders such asTS, Sydenham's chorea,
are similar to OCD in that they involve disrupting and autism, which all display repetitive behav-
preoccupations often coupled with ritualistic or iors. In these disorders, compulsions are repetitive
repetitive behavior such as repetitive visits to the motor behaviors and are usually without obses-
doctor, mirror checking, and multiple plastic sur- sions. It is thought that anomalies in the basal gan-
geries intended to reduce the anxiety caused by glia seen in these disorders are involved in the
the intrusive obsessions. Moreover, the obses- displayed repetitive behaviors and stereotypies.1719
sions can be similar to those observed in OCD in The content of the compulsions and obsessions
that they may involve symmetry, health issues, of these neurological disorders are also differ-
or overblown ideas.The second cluster includes ent from those seen in OCD.TS typically displays
impulse-control disorders such as sexual disorders echophenomena, touching, mental play, and self-
often involving obsessions, compulsions or para- injurious behaviors.20 Autistic characteristics usu-
philias, pathological gambling, trichotillomania, ally involve hoarding, telling and asking, touching,
compulsive shopping disorder, Internet usage dis- and repetitive ordering. Concerns about contami-
order, and pathological excoriation (skin-picking). nation, symmetry, aggression, and somatic, reli-
Although the impulsive behaviors characteristic gious, and sexual obsessions are less common in
of these disorders offer short-term pleasure not this disorder. Cleaning, checking and counting are
present in OCD, these impulse-control disorders also uncommon compulsions.21
are similar to OCD in that sufferers experience ten-
sion and arousal associated with their behaviors.7 EPIDEMIOLOGY OF OBSESSIVE-
Even though these disorders are characterized by COMPULSIVE DISORDER
impulsiveness, they share the compulsiveness While OCD is categorized as an anxiety disorder
aspect of OCD as the behaviors displayed often under the DSM-IV, it is listed independently as a dis-
act to reduce distress from the obsessions that order but also within a grouping alongside neurotic,
are also prevalent in impulse-control disorders.15 stress-related, and somatoform disorders in the

FIGURE 1 . FIGURE 2 .
Conceptualization of OCD Existence Conceptualization of OCD as Existing
Within a Spectrum of Affective Disorders Between Affective and Addiction
Disorders
Affective spectrum disorders

depressive
disorders

Obsessive-compulsive
disorders Obsessive-compulsive
disorders
anxiety disorders

OCD=obsessive-compulsive disorder; ICDs=impulse control disorders;


OCD=obsessive-compulsive disorder; ICDs=impulse control disorders; BDD=body dysmorphic disorder;TS=Tourette's syndrome; PG=pathological
BDD=body dysmorphic disorder; TS=Tourette's syndrome. gambling.

Hollander E, Kim S, Khanna S, Pallanti S. CNS Spectr. Vol 12, No 2 (Suppl Hollander E, Kim S, Khanna S, Pallanti S. CNS Spectr. Vol 12, No 2 {Suppl
3). 2007. 3). 2007.

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E. Hollander, S. Kim, S. Khanna, S. Pallanti

International Classification of Diseases,Jenth Edition that very few OCD sufferers sought treatment at
{ICD-10).22 Research in the epidemiology of OCD has all3637 or were receiving inadequate, episodic treat-
gained interest in the past two decades amounting ment.38 Furthermore, the majority of OCD patients
to disparate findings that further exemplify both in worldwide phenomenological clinical studies
the fundamental differences in the patient popula- were thought to display both obsessions and com-
tion and in diagnostic assessment.The most com- pulsions simultaneously,39 but the obsessive type
monly used instruments to assess prevalence of appears in more epidemiological studies. Following
OCD are the Diagnostic Interview Schedule (DIS),2324 these mixed results, Fontenelle and colleagues32
the Composite International Diagnostic Instrument suggest determining a global assessment tool for
(CIDI)2626 the Schedule for Affective Disorders and OCD, producing more culturally applicable research
Schizophrenia (SADS)27 and the Clinical Interview instruments, and conducting multinational studies
Schedule-Revised (CIS-R).28The DIS was adapted
of the sociodemographic, clinical, and predictive
from the DSM-III and later, the DSM-III-R. Although
aspects of OCD to attain a better understanding of
its implementation yielded higher prevalence rates
the descriptive epidemiology of OCD.
across seven countries than previously reported
(from 1.9% to 2.5% for lifetime prevalence and
from 1.1% to 1.8% annual prevalence29), many have METHODS OF COMPARISONS
argued that the too-lenient severity criteria in this INTO OCD, ANXIETY DISORDERS,
assessment may falsely inflate figures for OCD.The AND OCSD
CIDI was adapted from both /CD and DSM criteria.
Prevalence rates based on this instrument varied Comorbidity Studies
from 0.3%30 to 3.1 %31 across studies. Some sug- A complication with relating two different dis-
gest that the CIDI also allows for overdiagnoses of orders via comorbidity studies is in determin-
OCD by lay interviewers as seen in the DIS. Also, ing if the comorbid disorder may actually be a
the variability in the results offered by the CIDI could long-term complication to the primary disorder.
be a reflection of DSM and ICD differences as prev- Comorbidities of mood and anxiety disorders in
alence rates using the ICD is typically lower than
OCD were investigated in several studies. The
when using DSM criteria across OCD studies.32 The
SADS adapted from the DSM-IVoffered a preva-
lence rate of 1.8% which was considered more real- FIGURE 4 .
istic.33There are also divergent findings in treatment Conceptualization that OCD Consists
seeking samples. While some studies showed OCD of Obsessions, Compulsions, and
patients were utilizing health services more fre- Symptom Domains of Varying Severity
quently than healthy individuals,3435 others showed

FIGURE 3 .
A Dimensional Approach to
Compulsivity and Impulsivity
Risk Aversive Impulsive

II
Illl
OCD BDO AN DEP
HYP TS

TRICH

1
1

Autisff
1
|•
Binge
KLEP
PG
SIB Sexua
Comp
BPD Anti-
socia
PD

Eating
Compulsi e Buying

OCD=obsessive-compulsive disorder; BDD=body dysmorphic disorder;


AN=anorexia nervosa; DEP=depression; HYP=hypochondriasis;TS=Tourette's
syndrome; TRICH=trichotillomania; KLEP=kleptomania; PG=pathological
gambling; BPD=borderline personality disorder; PD=personality disorder.

Hollander E, Kim S, Khanna S, Pallanti S. CNS Spectr. Vol 12, No 2 (Suppl Hollander E, Kim S, Khanna S, Pallanti S. CNS Spectr. Vol 12, No 2 (Suppl
3). 2007 3). 2007

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Obsessive-Compulsive Disorder and Obsessive-Compulsive
Spectrum Disorders: Diagnostic and Dimensional Issues

most common comorbidity was major depressive in OCD.41 OCD sufferers only had a significantly
disorder (MDD) with prevalence rates of 20.7% increased risk for lifetime MDD but not for devel-
to 22% in current diagnoses and 54% to 66% in oping any other affective or anxiety disorders.42
lifetime diagnoses.40 Social phobia, with preva- Important to note is the finding that OCD typically
lence rates of 3.6% to 26% for current diagnosis precedes depression rather than following it, sug-
and 23% to 36% for lifetime diagnosis, was the gesting that depression may occur as a result of
most common anxiety disorder comorbidity. While the OCD without having an etiological relationship
some studies found anxiety disorders were more with OCD. Thus, results are mixed in the relation-
frequent in OCD probands than matched control ship between OCD and anxiety disorders.
probands, others have found that although MDD Across OCSDs, hypochondriasis, BDD, triehotil-
was ten times more prevalent in OCD populations lomania, and compulsive shopping had the high-
than in the general public, there was no evidence est lifetime prevalence rates in patients with a
of increased prevalence rates for anxiety disorders primary diagnosis of OCD. High prevalence rates

TABLE 1 .
Clinical and Endophenotypical Factors to Evaluate the Relationships Within the OCDs
Disorders
Sydenham's/PANDAS

Schizo-obsessive
Eating Disorders
Triehotillomania

Huntington's/
Parkinson's

Addiction
Hoarding

ICD-NOS
Autism
OCPD

ICDs
BDD
OCD

Phenomenology
Endophenotype
Demographics/
gender distribution
Phenomenology/
demographics
Natural history/course
Comorbidity
Course of illness
Family history
Genetic factors
Brain circuitry/
neurocognition
Cross species
Animal models
Immune function
Pharmacologic dissection
Interventional Treatment
CBT
Culture/ethnic

OCD=obsessive-compulsive disorder; OCPD=obsessive-compulsive personality disorder; TS=Tourette's syndrome; PANDAS=pediatric autoimmune neuropsy-
chiatric disorders associated with streptococcal infections; CBT=cognitive-behavioral therapy; BDD=body dysmorphic disorder; ICD=impulse control disorders;
N0S=not otherwise specified.
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E. Hollander, S. Kim, S. Khanna, S. Pallonti

were also seen for anorexia, bulimia,Tourette's concurrent anxiety disorders being a consequence
syndrome, and trichotillomania in an OCD popu- of the OCD.These findings were also mixed as
lation.43 Eating disorders were notably eight times Carter and colleagues51 reported that although
more common in OCD patients than in the general OCD occurred more frequently in case relatives
populace.41 Reciprocally, higher OCD prevalence compared to control relatives, there were no differ-
rates were also found in patients with primary ences between these two groups in terms of other
diagnoses of OCSDs such as BDD (30%)44 and anxiety disorders and MDD frequencies. When
anorexia (37%).45 Mixed results were also seen in the case relative had clinical or subclinical OCD,
these studies as Jasisoorya and colleagues46 failed panic disorder, MDD, and GAD rates increased,
to find evidence of greater prevalence rates for and this trend may suggest that the latter disor-
impulse-control and eating disorders in patients ders occurred as a consequence of the OCD.
with primary diagnoses of OCD. Diverging results Family studies suggest a relationship between
in these studies may be due to methodology, OCD and OCSDs as well. In one OCD family
sampling, cross-cultural issues or, more broadly, study, case probands had greater occurrences
the heterogeneous quality of OCD. OCD subtypes of hypochondriasis, BDD, anorexia, bulimia, and
may have distinct comorbidity trends such as excessive grooming disorders. However, the co-
in the case ofTS. In one study, 50% of 101 chil- occurrence of disorders may be due to a com-
dren with Tourette's syndrome had an additional mon latent vulnerability, that in and of itself may
diagnosis of OCD, and an another 8% developed be nonspecific to either condition. For example,
OCD during the observation period of the study.47 neuroticism may be a risk factor for OCD and
There may indeed be some similar genetic vul- OCSDs, but neither is necessary nor sufficient for
nerability in both childhood OCD (possibly a tic- either group of disorders. Such was the case in
related subtype) andTS.48 Moreover, a distinct first-degree relatives when compared with con-
OCD subtype with comorbid attention deficit dis- trol proband relatives with the exception of eating
order with hyperactivity may have greater risk of disorders. Additionally, these OCSDs occurred
pathological gambling or other impulse control even if the OCD proband did not have these disor-
disorders compared to other OCD subtypes.5 ders.52 Although this study and a previous study53
Comorbidity studies are more telling when con- did not find evidence of a higher prevalence of
ducted with matched healthy controls, and results eating disorders and impulse disorder, such as
indicate that not only are OCD and OCSDs highly pathological gambling in first-degree relatives
correlated but that OCSDs should be more related of OCD probands, some other studies suggest a
to OCD than any other anxiety disorder. In compar- familial association between OCD or obsessive-
ing patients with lifetime diagnoses of OCD, panic compulsive personality disorder and eating dis-
disorder, or social phobia, Richter and colleagues49 orders, but results are also mixed. First-degree
found that the OCD population had a greater prev- relatives of probands diagnosed with an eating
alence (37%) of lifetime OCSD as compared with disorder had greater risk of an OCSD, and it was
the panic disorder and social phobia groups.Those independent of whether the probands were diag-
with OCD showed a greater number of spectrum nosed with the OCSD, suggesting that these dis-
conditions, and more individuals in this group than orders share similar etiology.54 In another study,
in the panic and social phobia groups had multiple there was no apparent link between OCD diag-
lifetime spectrum disorders. nosis and eating disorders among relatives, but
there was a greater risk of obsessive-compulsive
personality disorder in relatives of anorexic pro-
Family Studies
bands, which may suggest a familial component
In a family study of OCD, anxiety, and affective
to the diffusion of these disorders.55
disorders, Nestadt and colleagues50 found that in
families where a relative was diagnosed with OCD, Some studies also show a familial link
there was a greater prevalence of panic disorder, between OCD and neurologically based OCSDs.
recurrent MDD, and separation anxiety disorder. Relatives of OCD patients compared to relatives
On the other hand, GAD and agoraphobia occur- of controls exhibited greater lifetime prevalence
rences were more frequent in case relatives irre- of Tourette's syndrome and tic disorders, includ-
spective of OCD diagnoses.The deduction arrived ing chronic motor and vocal tics.66 Moreover,
from this study was a possible familial relationship parents of autistic children who scored higher
between OCD, GAD, and agoraphobia with other on repetitive behavior domains were also more

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Obsessive-Compulsive Disorder and Obsessive-Compulsive
Spectrum Disorders: Diagnostic and Dimensional Issues

likely to be diagnosed with OCD or OCSDs than The limbic activity found in this study was much
parents of those who scored lower.57 A possible more prominent than in other studies.
genetic association between OCD and OCSDs The pathophysiology of anxiety disorders is
was found in a study observing multiplex autism centered around a fear neurocircuitry involving
families that showed a linked locus on chro- the amygdala.63-64 The amygdala's role in assess-
mosome 1 in a subset of families who exhib- ing the fear stimuli for emotional significance
ited severe obsessive compulsive behaviors.58 and forming memories of the emotion suggests
Furthermore, in an animal study conducted by its function in provoking appropriate automatic
Greer and Capecchi,59 mutations found on the and behavioral responses to fear. Multiple pre-
hoxb8 gene in mice were linked with the com- frontal cortical structures may modulate anxiety
pulsive grooming and hair pulling characteristic by sending feedback to the amygdala and alert-
of trichotillomania. Because the hoxb8 gene can ing it when the danger is no longer present or
be located in areas of the central nervous system relegating the importance of the fear stimulus.66
called the OCD circuit, trichotillomania and OCD Because of its role in situational fear condition-
may share similar neurobiological bases. ing, the hippocampus may also be implicated in
anxiety disorders
NEUROLOGICAL STUDIES IN OCD, The neurocircuitry of OCD and anxiety disor-
ANXIETY DISORDERS, AND OCSDS ders differs in that OCD demonstrates dysfunc-
Saxena and Rauch60 proposed a pathophysiol- tion in the frontal-striatal circuitry while anxi-
ogy model of OCD that suggests dysfunction in ety disorders involve the amygdala and a fear
the orbitofrontal-subcortical circuitry composed response. While there are also possible anoma-
of direct and indirect pathways originating in the lies with the hippocampus and medial prefrontal
frontal cortex and projecting into the striatum. cortex, other abnormalities exhibited in OCD are
The direct pathway projects from the striatum to in the caudate nuclei, thalamus, and orbitofrontal
the globus pallidus interna/substantia nigra, pars cortex. However, some research indicate possible
reticulate (Gpi/SHr) complex (the primary output amydala involvement in OCD, orbitofrontal cortex
location of the basal ganglia) and back to the cor- activation in simple phobia, and prefrontal and
tex, which activates the thalamic system that in thalamo-striatal regions in GAD.
turn assists in complex motor activities.The indi-
rect pathway follows a route from the striatum NEUROCIRCUITRY OF OBSESSIVE
to the globus pallidus externa, the subthalamic COMPULSIVE SPECTRUM DISORDERS
nucleus, globus pallidus-substantia nigra pars Research on the neurocircuitry of OCSDs is
reticula, thalamus, and then returns to the cortex. more limited but suggests dysfunction in the
By inhibiting the thalamus, this pathway stymies basal ganglia, specifically in autism, BDD, some
complex motor activities. While there is a balance eating disorders, andTS. Enlarged caudate vol-
between these two pathways in healthy individu- ume,19 increased right caudate and putamen vol-
als, OCD sufferers show preference for the direct umes65 were found in autism. Ritualistic behavior
pathway, thereby increasing activity in the orbito- but not communication or social behavior
frontal cortex, ventromedial caudate, and medial were implicated with caudate volume. In BDD,
dorsal thalamus, which results in obsessions and enlarged white matter volume and a leftward
compulsions. 60 Although previous research in shift in the caudate nucleus asymmetry were
functional imaging supports this corticostriatal- observed when compared to healthy controls.66
thalamocortical neurocircuity of OCD, a meta- Anorexia also displayed increased antiputamen
anaylysis of 13 functional neuroimaging studies in antibody levels.67 Finally, decreased volumes
OCD found no consistent differences in the orbi- in caudate, putamen, and globus pallidus were
tofrontal cortex, caudate nucleus, or other previ- found in aTS population.18
ously mentioned regions between OCD patients
and healthy controls.61 Some research also sug-
gest limbic system activation in OCD in that after CONCLUSION
symptom arousal, OCD patients displayed sig- Although results are mixed in comorbity, fam-
nificant activation in the amygdala, the medial ily, and neuroimaging studies in establishing the
orbitofrontal, lateral, frontal, anterior temporal, relationships between OCD and anxiety disorders
anterior cingulate insular cortex, and caudate.62 and OCSDs, there is growing evidence that sup-

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E. Hollander, S. Kim, S. Khanna, S. Pollanti

ports the latter; there appears to be more phe- belong in this new category of OCSDs?; (3) Could
nomenological similarities between OCD and a common endophenotype (mediating factors
OCSD than with anxiety disorders.The Obsessive between genes and observable behaviors) across
Compulsive Disorder Consensus Group was the OCSDs be established?; (4) How would the
assembled in 2005 to discuss a reorganization of endophenotypes be defined?; and (5) what stud-
the DSM in its 5th edition and future international ies are needed?
classification systems to address these concerns. In addressing these issues in future research,
The objectives of this collaborative effort is to we should: (1) examine evidence for the relation-
update the current data on OCD and OCSDs, dis- ship between OCD and OCSD in a comprehensive
cuss the controversies surrounding these issues, manner and across various methods, which is cur-
engage experts from around the world, and dis- rently underway as the research planning agenda
seminate the conclusions via symposia consisting for DSM-V; (2) Reexamine the existing data-
bases to answer the aforementioned questions;
of workgroup discussions and presentations.The
(3) Define a common endophenotype battery,
breadth of topics covered in areas of diagnosis,
neurocognitive aspects, genotyping, functional
specific topics and cross-cutting issues are dis-
magnetic resonance imaging, symptom scales,
played inTable 1 with the ultimate goal of defin-
structured assessment for comorbidity, and treat-
ing OCSDs based on endophenotypical features.
ment response; and (4) Allow for multicenter tri-
The main unresolved issues and future direc- als that include an endophenotyping project.
tions of this topic are: (1) Should OCD be clas-
A reclassification of OCD as an OCSD would
sified as an anxiety disorder; (2) If not, does it allow for better scrutiny of distinct obsessive-
compulsive symptoms, as currently this disorder
TABLE 2 . often goes undetected in patients who complain
Reasons to Establish OCSDs of a broad symptom of anxiety.Table 2 outlines
the advantages and disadvantages to establishing
Advantages
OCSDs and its implications on diagnosis, treat-
I Classification is a better fit with the scientific data ment, medication and research. Not only will this
Compatible with ICD-10 reclassification bolster more accurate diagnoses
Help screening - clinic samples and epidemiological and appropriate treatment for OCD, it will also
surveys give way to determining the biological underpin-
Enhance treatment
nings of the repetitive thoughts and compulsions
characteristic of OCSD. CNS
Access to insurance - a serious and persistent disor-
der - increased resources for specialist services
Influence research funding agencies REFERENCES
1. Diagnostic and Statistical Manual of Mental Disorders. 4th ed text rev. Washington,
• Enhance endophenotyping and neurological efforts DC: American Psychiatric Association; 2000.
2. Tynes LL, White K, Steketee GS. Toward a new nosology of obsessive compulsive
Facilitate drug development (larger market) disorder. Compr Psychiatry. 1990:31:465-480.
3. Marks IM. Fears, Phobias and Rituals: Panic, Anxiety and their Disorders. New York,
Decrease concerns regarding off-label prescribing NY: Oxford University Press; 1987.
4. Hollander E. Obsessive-Compulsive Related Disorders. American Psychiatric Press:
Disadvantages Washington, DC; 1993.
5. Hollander E, Friedberg JP, Wasserman S, Yeh CC, lyengar R. The case for the OCD
Anxiety is a target for CBT. However, could lead to the spectrum. In: Abramowitz JS, Houts AC, eds. Handbook of Controversial Issues in
development of CBT strategies that are more specific Obsessive-Compulsive Disorder. Kluwer Academic Press; 2005.
to OCDs 6. Jenike MA. Illnesses related to obsessive-compulsive disorder. In: Jenike MA, Baer
LB, Minichiello WE, eds. Obsessive Compulsive Disorders: Theory and Management.
Against a long-standing tradition of classifying OCD as 2nd ed. Year Book Medical; 1990:39-60.
part of anxiety disorders 7. McElroy SL, Phillips KA, Keck PE. Obsessive compulsive spectrum disorder. J Clin
Psychiatry. 1994;55(suppl 10):33-51.
Fragmentation of anxiety clinics 8. Stein DJ. Neurobiology of the obsessive-compulsive spectrum disorders. Biol
Psychiatry. 2002,47:296-304.
Decrease use of benzodiazepines and SGAs for OCD 9. Leckman JF, Zhang H, Alsobrook JP, Pauls DL. Symptom dimensions in obsessive-com-
(minor versus major tranquillizers) pulsive disorder Toward Quantitative phenotypes. Am J Med Gen. 2001 ;105:28-30.
10. Baer L. Factor analysis of symptom subtypes of obsessive compulsive disorder and
their relation to personality and tic disorders. J Clin Psychiatry. 1994;55:18-23.
OCSD=obsessive-compulsive spectrum disorders; ICD-Mklnternational
11. Samuels J, Bienvenu 0J, Riddle MA, et al. Hoarding in obsessive compulsive disor-
Classification of Diseases, Tenth Edition; CBT=cognitive-behavioral therapy; der: results from a case-control study. BehavRes Ther. 2002;40(5):517-528.
OCD=obsessive-compulsive disorder; SGA=second-generation antipsychotics. 12. Mataix-Cols D, Conceicao do Rosario-Campos M, Leckman JF. A multidimensional
Hollander E, Kim S, Khanna S, Pallanti S. CNS Spectr. Vol 12, No 2 (Suppl model of obsessive-compulsive disorder. Am J Psychiatry. 2005:162:228-238.
3). 2007. 13. Pauls DL, Alsobrook J, Goodman W, Rasmussen S, Leckman JF. A family study of
obsessive-compulsive disorder. Am J Psychiatry. 1995:152:76-84.

Downloaded from https:/www.cambridge.org/core. University of Arizona, on 02 May 2017 at 17:01:59, subject to the Cambridge Core terms of use, available at
CNS Spectr 12:2 (Suppl
https:/www.cambridge.org/core/terms. 3)
https://doi.org/10.1017/S1092852900002467 12 February 2007
Obsessive-Compulsive Disorder and Obsessive-Compulsive
Spectrum Disorders: Diagnostic and Dimensional Issues

14. Holzer JC, Goodman WK, McDougle CJ, et al. Obsessive-compulsive disorder with 41. Denys D, Tenney N, van Megen HJ, de Geus F Westenberg HG. Axis I and II comor-
and without a chronic tic disorder. A comparison of symptoms in 70 patients. Br J bidity in a large sample of patients with obsessive-compulsive disorder. J Affect
Psychiatry. 1994; 164:469-473. Disord 2004:80:155-162.
15. Hollander E, Wong CM. Obsessive-compulsive spectrum disorders. J Clin Psychiatry. 42. Brown TA, Campbell LA, Lehman CL, Grisham JR, Mancill RB. Current and lifetime
1995; 56(suppl 4):3-6. comorbidity of the DSM-IV anxiety and mood disorders in a large clinical sample. J
16. Blaszczynski A. Pathological gambling and obsessive-compulsive spectrum disorders. Abnorm Psychol. 2001:110:585-599.
Psychol /?ep. 1999:84:107-113. 43. du Toit PL, van Kradenburg J, Niehaus D, Stein DJ. Comparison of obsessive-compulsive
17. Dale RC. Autoimmunity and the basal ganglia: new insights into old diseases. QJM. disorder patients with and without comorbid putative obsessive-compulsive spectrum
2003:96:183-191. disorders using a structured clinical interview. ComprPsychiatry. 2001:42:291-300.
18. Peterson BS, Thomas P, Kane MJ, Scahill L, Zhang H, Bronen R. Basal Ganglia volumes 44. Gunstad J, Phillips KA. Axis I comorbidity in body dysmorphic disorder. Compr
in patients with Gilles de la Tourette syndrome. Arch Gen Psychiatry. 2003:60:415-424. Psychiatry. 2003:44:270-276.
19. Sears LL, Vest C, Mohamed S, Bailey J, Ranson BJ, Piven J. An MRI study of the basal 45. Thornton C, Russell J. Obsessive compulsive comorbidity in the dieting disorders. Int
ganglia in autism. Prog Neuropsychopharmacol Biol Psychiatry. 1999:23:673-624. J Eat Disord. 1997:21:83-87.
20. Cath DC, Spinhoven R Hoogduin CA, Landman AD, van Woerkom TC, van de Wetering 46. Jaisoorya TS, Reddy YC, Srinath S. The relationship of obsessive-compulsive disorder
BJ. Repetitive behaviors in Tourette's syndrome and OCD with and without tics: what to putative spectrum disorders: results from an Indian study. Compr Psychiatry.
are the differences? Psychiatry Res. 2001:101:171-185. 2003:44:317-323.
21. McDougle CJ, Kresch LE, Goodman WK, Naylor ST, Volkmar FR, Cohen DJ. A case- 47. Park S, Como PG, Cui L, Kurlan R. The early course of the Tourette's syndrome clinical
controlled study of repetitive thoughts and behavior in adults with autistic disorder spectrum. Neurology. 1993:43:1712-1715.
and obsessive-compulsive disorder. Am J Psychiatry. 1995:152:772-777. 48. Grados MA, Walkup J, Walford S. Genetics of obsessive-compulsive disorders: new
22. World Health Organization G. The ICD-W Classification of Mental and Behavioral findings and challenges. Brain Dev. 2003;25(suppl):S55-S61
Disorders—Diagnostic Criteria for Research. Geneva, Switzerland: World Health 49. Richter MA, Summerfeldt LJ, Antony MM, Swinson RR Obsessive-compulsive
Organization; 1993. spectrum conditions in obsessive-compulsive disorder and other anxiety disorders.
23. Robins LN, Helzer JE, Croughan J, Ratcliff KS. National Institute of Mental Health Depress Anxiety. 2003; 18:118-127.
Diagnostic Interview Schedule: Its history, characteristics, and validity. Arch Gen 50. Nestadt G, Samuels J, Riddle MA, Liang KY, Bienvenu OJ, Hoehn-Saric R. The rela-
Psychiatry. 1981:38:381-389. tionship between obsessive-compulsive disorder and anxiety and affective disorders:
24. Robins LN, Helzer JE, Orvaschel H, Anthony JS, Blazer DG, Burnham A. The diagnostic results from the Johns Hopkins OCD Family Study. Psychol Med 2001 ;31:481 -487.
interview schedule. In: Eaton WW, Kessler LG, eds. Epiderniologic Field Methods in 51. Carter AS, Pollock RA, Suvak MK, Pauls DL. Anxiety and major depression comorbidity in
Psychiatry: The NIMH Epidemiologic Catchment Area Program. Orlando, FL: Academic a family study of obsessive-compulsive disorder. Depress Anxiety. 2004:20:165-174.
Press;1985:143-168. 52. Bienvenu OJ, Samuels JF, Riddle MA, Hoehn-Saric R, Liang KY, Cullen BA. The
25. Robins LN, Wing J, Wittchen HU, Helzer JE, Babor TF, Burke J. The composite interna- relationship of obsessive-compulsive disorder to possible spectrum disorders: results
tional diagnostic interview An epidemiologic instrument suitable for use in conjunc- from a family study. Biol Psychiatry. 2000:48:287-293.
tion with different diagnostic systems and in different cultures. Arch Gen Psychiatry. 53. Black DW, Goldstein RB, Noyes R, Blum N. Compulsive behaviors and obsessive-
1988:45:1069-1077. compulsive disorder (OCD): lack of a relationship between OCD, eating disorders, and
26. Robins L, Helzer J, Cottier L, Goldring E. NIMH Diagnostic Interview Schedule. 3rd ed gambling. Compr Psychiatry. 1994:35:145-148.
rev. St Louis, MO: Washington; 1988. 54. Bellodi L, Cavallini MC, Bertelli S, Chiapparino D, Riboldi C, Smeraldi E. Morbidity risk
27. Endicott J, Spitzer RL. A diagnostic interview: the schedule for affective disorders and for obsessive-compulsive spectrum disorders in first-degree relatives of patients with
schizophrenia. Arch Gen Psychiatry. 1978:35:837-844. eating disorders. Am J Psychiatry. 2001:158:563-569.
28. Lewis G, Pelosi AJ, Araya R, Dunn G. Measuring psychiatry disorder in the community: a 55. Lilenfeld LR, Kaye WH, Greeno CG, Merikangas KR, Plotnicov K, Pollice C. A controlled
standardized assessment for use by lay interviewers. Psychol Med. 1992:22:465-486. family study of anorexia nervosa and bulimia nervosa: psychiatric disorders in first-degree
29. Weissman MM, Bland RC, Camino GJ, Greenwald S, Hwu HG, Lee CK. The cross epi- relatives and effects of proband comorbidity. Arch Gen Psychiatry. 1998:55:603-610.
demiology of obsessive compulsive disorder The Cross National Collaborative Group. 56. Grados MA, Riddle MA, Samuels JF, Liang KY, Hoehn-Saric R, Bienvenu OJ. The
J Clin Psychiatry. 1994;55(suppl):5-10. familial phenotype of obsessive-compulsive disorder in relation to tic disorders: the
30. Andrade L, Walters EE, Gentil V, Laurenti R. Prevalence of ICD-10 mental disorders Hopkins OCD family study. 8/0/ftyc/i/afty. 2001:50:559-565.
in a catchment area in the city of Sao Paulo, Brazil. Soc Psychiatry Epidemiol. 57. Hollander E, King A, Delaney K, Smith CJ, Silverman JM. Obsessive-compulsive
2002:37:316-325. behaviors in parents of multiplex autism families. Psychiatry Res. 2003:117:11-16.
31. Stein MB, Forde DR, Anderson G, Walker JR. Obsessive-compulsive disorder in 58. Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E, Ramoz N. Linkage
the community: an epidemiologic survey with clinical reappraisal. Am J Psychiatry. analysis for autism in a subset of families with obsessive-compulsive behaviors:
1997:154:1120-1126. evidence for an autism susceptibility gene on chromosome 1 and further support for
32. Fontenelle LF, Mendlowicz MV, Versiani M. The descriptive epidemiology of obsessive- susceptibility genes on chromosome 6 and 19. MolPsychiatry. 2004:9:144-150.
compulsive disorder. Prog Neuropsychopharmacol Biol Psychiatry. 2006:30(1 ):327-337. 59. Greer JM, Capecchi MR. Hoxb8 is required for normal grooming behavior in mice.
33. Mohammad MR, Ghanizadeh A, Rahgozar M, Noorbala AA, Davidian H, Afzali HM. Neuron. 2002:33:23-34.
Prevalence of obsessive-compulsive disorder in Iran. BMC Psychaitr. 2004;4:2. 60. Saxena S, Rauch SL. Functional neuroimaging and the neuroanatomy of obses-
34. Karno M, Golding JM, Dorenson SB, Burnam MA. The epidemiology of obsessive-com- sive-compulsive disorder. Psychiatr Clin North Am. 2000:23:563-586.
pulsive disorder in five US communities. Arch Gen Psychiatry. 1988:45:1094-1099. 61. Whiteside SP, Port JD, Abramowitz JS. A meta-analysis of functional neuroimaging in
35. Guerrero AP, Hishinuma ES, Andrade NN, Bell CK, Kurahara DK, Lee TG. Demographic obsessive-compulsive disorder. Psychiatry Res. 2004:132:69-79.
and clinical characteristics of adolescents in Hawaii with obsessive-compulsive 62. Breiter HC, Rauch SL, Kwong KK, Baker JR, Weisskoff RM, Kennedy DN. Functional
disoder. Arch PediatrAdolesc Med. 2003:157:665-670. magnetic resonance imaging of symptom provocation in obsessive-compulsive disor-
36. Nestadt G, Samuels JF Romanoski AJ, Folstein MF, McHugh PR. Obsessions and der. Arch Gen Psychiatry. 1996:53:595-606.
compulsions in the community. Ada Psychiatr Scand. 1994:89:219-224. 63. Charney DS. Neuroanatomical circuits modulating fear and anxiety behaviors. Ada
37. Nestadt G, Bienvenu OJ, Cai G, Samuels J, Eaton WW. Incidence of obsessive-com- Psychiatr Scand. 2003;417(suppl):38-50.
pulsive disorder in adults. J Nerv Ment Dis. 1998:186:401-406. 64. Kent JM, Rauch SL. Neurocircuitry of anxiety disorders. Curr Psychiatry Rep.
38. Fireman B, Koran LM, Leventhal JL, Jacobson A. The prevalence of clinically recog- 2003:5:266-273.
nized obsessive-compulsive disorder in a large health maintenance organization. Am 65. Hollander E, Anagnoustou E, Chaplin W, Esposito K, Haznedar MM, Licalzi E et al.
J Psychiatry. 2001; 158:1904-1910. Striatal volume on magnetic resonance imagine and repetitive behaviors in autism.
39. Fontenelle LF, Mendlowicz MV, Marques C, Versiani M. Trans-cultural aspects of Biol Psychiatry. 2005:58:226-232.
obsessive-compulsive disorder: a description of a Brazillian sample and a systemic 66. Rauch SL, Phillips KA, Segal E, Makris N, Shin LM, Whalen PJ. A preliminary
review of international clinical studies. J Psychiatr Res. 2004:38:403-411. morphometric magnetic resonance imaging study of regional brain volumes in body
40. LaSalle VH, Cramer KR, Nelson KN, Kazuba D, Justement L, Murphy DL. Diagnostic dysmorphic disorder. Psychiatry Res. 2003:122:13-19.
interview assessed neuropsychiatric disorder comorbidity in 334 individuals with 67. Harel Z, Hallett J, Riggs S, Vaz R, Kiessling L. Antibodies against human putamen in
obsessive-compulsive disorder. Depress Anxiety. 2004:19:163-173. adolescents with anorexia nervosa. Int J Eat Disord. 2001:29:463-469.

Downloaded from https:/www.cambridge.org/core. University of Arizona, on 02 May 2017 at 17:01:59, subject to the Cambridge Core terms of use, available at
CNS Spectr 12:2 (Suppl
https:/www.cambridge.org/core/terms. 3)
https://doi.org/10.1017/S1092852900002467 13 February 2007

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