ReviewMedComm2026
Obsessive-Compulsive Disorder: Comorbidity, Biomarkers, Circuits, and Treatment Strategies.
Review in MedComm, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Obsessive-compulsive disorder (OCD), characterized by intrusive thoughts and repetitive behaviors, frequently co-occurs with anxiety disorders, contributing to greater diagnostic complexity, more severe symptoms, and poorer treatment outcomes. In this review, we consider OCD in the context of its comorbidity with anxiety and examine evidence that the two conditions may share genetic, neurochemical, and circuit-level vulnerabilities. Particular attention is given to the cortico-striato-thalamo-cortical, frontoparietal, and frontolimbic networks, which may interact to form a self-reinforcing cycle in which anxiety intensifies OCD symptoms, while compulsive behaviors provide transient relief but may ultimately maintain pathological patterns of brain activity. We also discuss how these shared mechanisms may shape current and emerging treatment strategies, including pharmacological approaches targeting serotonergic, glutamatergic, dopaminergic, and histaminergic systems, cognitive-behavioral interventions, and neuromodulation techniques such as deep brain stimulation, repetitive transcranial magnetic stimulation, transcranial direct current stimulation, and focused ultrasound. We further consider major depressive disorder and posttraumatic stress disorder as additional examples of psychiatric comorbidity, with overlapping neural substrates and clinical features. Taken together, these findings suggest that considering comorbidity alongside core OCD symptoms may improve our understanding of its pathophysiology, help identify clinically relevant biomarkers, and support individualized treatment, while providing a broader transdiagnostic perspective on psychiatric disorders.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.