Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Obsessive-compulsive disorder (OCD) is a chronic and severe psychiatric disorder for which effective treatment options are limited. Structural and functional neuroimaging studies have consistently implicated the orbitofrontal cortex (OFC) and striatum in the pathophysiology of the disorder. Recent genetic evidence points to involvement of components of the excitatory synapse in the etiology of OCD. However, the transcriptional alterations that could link genetic risk to known structural and functional abnormalities remain mostly unknown. To assess potential transcriptional changes in the OFC and two striatal regions (caudate nucleus and nucleus accumbens) of OCD subjects relative to unaffected comparison subjects, we sequenced messenger RNA transcripts from these brain regions. In a joint analysis of all three regions, 904 transcripts were differentially expressed between 7 OCD versus 8 unaffected comparison subjects. Region-specific analyses highlighted a smaller number of differences, which concentrated in caudate and nucleus accumbens. Pathway analyses of the 904 differentially expressed transcripts showed enrichment for genes involved in synaptic signaling, with these synapse-associated genes displaying lower expression in OCD subjects relative to unaffected comparison subjects. Finally, we estimated that cell type fractions of medium spiny neurons were lower whereas vascular cells and astrocyte fractions were higher in tissue of OCD subjects. Together, these data provide the first unbiased examination of differentially expressed transcripts in both OFC and striatum of OCD subjects. These transcripts encoded synaptic proteins more often than expected by chance, and thus implicate the synapse as a vulnerable molecular compartment for OCD.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961029PMC
http://dx.doi.org/10.1038/s41398-021-01290-1DOI Listing

Publication Analysis

Top Keywords

ocd subjects
16
unaffected comparison
12
comparison subjects
12
differentially expressed
12
synapse-associated genes
8
subjects
8
obsessive-compulsive disorder
8
ocd
8
structural functional
8
ofc striatum
8

Similar Publications

Purpose: To validate a custom FIJI (ImageJ) program for more reproducible, faster curvilinear periorbital measurements, as compared with 2 custom artificial intelligence-based tools.

Design: Combined technical validation and method comparison study.

Subjects: Front-facing photographs of 45 cleft palate syndromic patients.

View Article and Find Full Text PDF

Background Mitochondrial-related genes (MRGs) and programmed cell death-related genes (PCD-RGs) have been proven to play important roles in obsessive-compulsive disorder (OCD), and identifying their shared biomarkers is conducive to the diagnosis and research of OCD. Methods Differentially expressed genes (DEGs) between OCD and control samples were identified from the GSE78104 dataset. Differentially expressed MRGs (DE MRGs) and PCD-RGs (DE-PCD-RGs) were derived by intersecting with MRG and PCD-RG gene sets, respectively, resulting in DE mitochondrial-related PCD (DE-MPCD) genes.

View Article and Find Full Text PDF

Disruption of consciousness depends on insight in obsessive-compulsive disorder and on positive symptoms in schizophrenia.

Neurosci Conscious

August 2025

Institut de Neuromodulation, GHU Paris, Psychiatrie et Neurosciences, Centre Hospitalier Sainte-Anne, Pôle Hospitalo-universitaire 15, Université Paris Cité, 12 rue Cabanis, 75014 Paris, France.

Disruption of conscious access contributes to the advent of psychotic symptoms in schizophrenia and could also explain lack of insight in other psychiatric disorders. In this study, we explored how insight and psychotic symptoms related to disruption of consciousness in obsessive-compulsive disorder (OCD) and schizophrenia, respectively. Patients with schizophrenia, and patients with OCD with good versus poor insight and matched controls underwent clinical assessments and performed a visual masking task.

View Article and Find Full Text PDF

The majority of patients with chronic tic disorders suffer from psychiatric comorbidities, most frequently attention-deficit/hyperactivity disorder (ADHD), obsessive-compulsive disorder (OCD), depression, and anxiety. While characteristics of these psychiatric disorders are widely known, other comorbidities including self-injurious behaviors (SIB) and body focused repetitive behaviors (BFRB) are still under-investigated. Currently, there is a controversial discussion whether BFRB and SIB belong to the same spectrum because of clinical similarities or they represent distinct entities.

View Article and Find Full Text PDF

The 15q11.2 microdeletion syndrome, also known as Burnside-Butler syndrome (BBS), is a rare genetic disorder involving a deletion in the breakpoint 1 to breakpoint 2 (BP1-BP2) on the long arm of chromosome 15, often associated with growth retardation and delayed speech development. In contrast, rare manifestations consist of dysmorphic traits, seizures, and neurodevelopmental or psychiatric conditions such as epilepsy, autism spectrum disorder (ASD), and schizophrenia.

View Article and Find Full Text PDF