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Published on: June 25, 2014
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Structural neuroimaging of skin-picking disorder
Anne Schienle1, Albert Wabnegger1
1Clinical Psychology, University of Graz, BioTechMed Graz, Austria.
Summary
This study found that individuals with skin-picking disorder (SPD) have reduced grey matter volume in several brain regions. Early symptom onset in SPD is linked to more severe picking and distinct brain differences.
Area of Science:
- Neuroscience
- Psychiatry
- Radiology
Background:
- Skin-picking disorder (SPD) is classified as an obsessive-compulsive and related disorder (OCRD).
- SPD is characterized by repetitive skin manipulation, leading to physical and psychological harm.
- The underlying neuroanatomy of SPD remains largely unexplored.
Purpose of the Study:
- To investigate the neuroanatomical differences in patients with SPD compared to healthy controls.
- To explore how age of symptom onset influences brain structure in SPD.
- To identify potential brain regions associated with SPD pathophysiology.
Main Methods:
- A voxel-based morphometry (VBM) study was conducted on 220 participants (123 with SPD, 97 controls).
- Grey matter volume (GMV) was compared between SPD patients and controls.
- SPD patients were subgrouped by age of symptom onset (before puberty, during puberty, adulthood) for further analysis.
Main Results:
- Patients with SPD exhibited significantly reduced GMV in the insula, orbitofrontal cortex, pallidum, cerebellum, supramarginal gyrus, frontal pole, and occipital regions compared to controls.
- Early onset SPD (before puberty) was associated with more focused skin-picking behavior.
- Early onset was also linked to reduced GMV in the insula, orbitofrontal cortex, paracingulate, and superior temporal regions.
Conclusions:
- SPD is associated with grey matter volume reductions in brain areas crucial for interoception, emotional regulation, and motor control.
- Findings suggest a partial overlap in neuroanatomical characteristics between SPD and obsessive-compulsive disorder (OCD).
- The distinct clinical and morphometric profiles across age-of-onset groups highlight the heterogeneity of SPD, necessitating further research.

