scholarly journals Diagnostic Issues in Early-Onset Obsessive-Compulsive Disorder and their Treatment Implications

2019 ◽  
Vol 17 (8) ◽  
pp. 672-680 ◽  
Author(s):  
Elisabetta Burchi ◽  
Stefano Pallanti

Background: The lifespan approach and recent shift in the conceptualization of Obsessive- Compulsive Disorder (OCD) promoted by the Diagnostic and Statistical Manual of Mental Disorders Fifth Edition (DSM5) along with novel insights into the pathogenesis of this heterogeneous disorder are driving the development of new outcome measures and new treatments for a disease that, on the other hand, is characterized by high rates of refractoriness. Objective and Methods: The aim of this review is to provide a discussion of the translational evidence about Early Onset OCD (EO) in compliance with a neurodevelopmental and RdoC perspective. Results and Conclusion: O might be considered the neurodevelopmental subtype of OCD. Indeed there is evidence that different clusters of symptoms and dimensions at an early stage predict different trajectories in phenotype and that distinct neurocircuit pathways underpin the progression of the disorder. Despite the development of high refractoriness in the course of the disorder, evidence suggests that EO may be particularly treatment responsive in the early stages, thus showing the need for early recognition and additional recovery oriented studies in this subgroup. : Consistent with the neurodevelopmental perspective, immunity and glutamate neurotransmission are emerging as novel pathways for parsing out the neurobiology of OCD, the EO form, in particular, supporting the implementation of new multisystemic models of the OCD phenotype. Brain connectivity patterns, immune and microbiome profiles are standing out as promising areas for biomarkers with the potential for targeted personalized therapies in EO.

CNS Spectrums ◽  
2009 ◽  
Vol 14 (7) ◽  
pp. 362-370 ◽  
Author(s):  
Maria Alice de Mathis ◽  
Juliana B. Diniz ◽  
Roseli G. Shavitt ◽  
Albina R. Torres ◽  
Ygor A. Ferrão ◽  
...  

ABSTRACTIntroduction: Research suggests that obsessive-compulsive disorder (OCD) is not a unitary entity, but rather a highly heterogeneous condition, with complex and variable clinical manifestations.Objective: The aims of this study were to compare clinical and demographic characteristics of OCD patients with early and late age of onset of obsessive-compulsive symptoms (OCS); and to compare the same features in early onset OCD with and without tics. The independent impact of age at onset and presence of tics on comorbidity patterns was investigated.Methods: Three hundred and thirty consecutive outpatients meeting Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition criteria for OCD were evaluated: 160 patients belonged to the “early onset” group (EOG): before 11 years of age, 75 patients hadResults: The EOG had a predominance of males, higher frequency of family history of OCS, higher mean scores on the “aggression/violence” and “miscellaneous” dimensions, and higher mean global DY-BOCS scores. Patients with EOG without tic disorders presented higher mean global DY-BOCS scores and higher mean scores in the “contamination/cleaning” dimension.Conclusion: The current results disentangle some of the clinical overlap between early onset OCD with and without tics.


CNS Spectrums ◽  
2021 ◽  
pp. 1-7
Author(s):  
Giacomo Grassi ◽  
Chiara Cecchelli ◽  
Gloria Mazzocato ◽  
Luisa Vignozzi

Abstract Moving from a behavioral-based to a biological-based classification of mental disorders is a crucial step toward a precision-medicine approach in psychiatry. In the last decade, a big effort has been made in order to stratify genetic, immunological, neurobiological, cognitive, and clinical profiles of patients. Making the case of obsessive–compulsive disorder (OCD), a lot have been made in this direction. Indeed, while the Diagnostic and Statistical Manual of Mental Disorders (DSM) diagnosis of OCD aimed to delineate a homogeneous group of patients, it is now clear that OCD is instead an heterogeneous disorders both in terms of neural networks, immunological, genetic, and clinical profiles. In this view, a convergent amount of literature, in the last years, indicated that OCD patients with an early age at onset seem to have a specific clinical and biological profile, suggesting it as a neurodevelopmental disorder. Also, these patients tend to have a worse outcome respect to adult-onset patients and there is growing evidence that early-interventions could potentially improve their prognosis. Therefore, the aim of the present paper is to review the current available genetic, immunological, neurobiological, cognitive, and clinical data in favor of a more biologically precise subtype of OCD: the early-onset subtype. We also briefly resume current available recommendations for the clinical management of this specific population.


2010 ◽  
Vol 19 (3) ◽  
pp. 227-235 ◽  
Author(s):  
Susanne Walitza ◽  
Jens R. Wendland ◽  
Edna Gruenblatt ◽  
Andreas Warnke ◽  
Thomas A. Sontag ◽  
...  

2005 ◽  
Vol 57 (8) ◽  
pp. 895-900 ◽  
Author(s):  
Gregory L. Hanna ◽  
Daniel J. Fischer ◽  
Kristin R. Chadha ◽  
Joseph A. Himle ◽  
Michelle Van Etten

2007 ◽  
Vol 61 (3) ◽  
pp. 322-329 ◽  
Author(s):  
Diane E. Dickel ◽  
Jeremy Veenstra-VanderWeele ◽  
Nancy Chiu Bivens ◽  
Xiaolin Wu ◽  
Daniel J. Fischer ◽  
...  

2017 ◽  
Author(s):  
Christine Lochner ◽  
Dan Stein ◽  
Eileen Thomas

Hoarding disorder is characterized by an obsessive need to acquire, collect, or keep possessions and difficulty in organizing and discarding, resulting in accumulation of clutter, which elicits great concern from family and friends. Functioning is usually impaired in a variety of domains. Obsessive-compulsive disorder is the disorder most closely associated with hoarding. Overvalued ideation regarding the value or usefulness of possessions may make it impossible for individuals to discard items. This review contains 1 table, and 22 references. Key words: clutter, diagnostic and statistical manual, etiology, hoarding, obsessive-compulsive and related disorder


2007 ◽  
Vol 62 (8) ◽  
pp. 856-862 ◽  
Author(s):  
Gregory L. Hanna ◽  
Jeremy Veenstra-VanderWeele ◽  
Nancy J. Cox ◽  
Michelle Van Etten ◽  
Daniel J. Fischer ◽  
...  

2000 ◽  
Vol 47 (8) ◽  
pp. S135-S136
Author(s):  
G.L. Hanna ◽  
G.C. Curtis ◽  
J.A. Himle ◽  
D.Q. Koram ◽  
K.R. Chadha ◽  
...  

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