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Updated: May 23, 2026

Meta-analysis of Voxel-Based Neuroimaging Studies using Seed-based d Mapping with Permutation of Subject Images (SDM-PSI)
Published on: November 27, 2019
Differences in cortical gyrification and fractional amplitude of low-frequency fluctuations between early- and
Hirofumi Tomiyama1, Keitaro Murayama1, Kiyotaka Nemoto2
1Department of Neuropsychiatry, Kyushu University Hospital, Japan.
Background:
Obsessive-compulsive disorder (OCD) is heterogeneous, and differences in age at onset may be associated with important feature of distinct subtype. However, no studies have investigated the differences between early- and late-onset OCD using structural and functional multimodal neuroimaging methods that reflect different neurobiological backgrounds.
Methods:
Structural and resting-state functional magnetic resonance imaging data were obtained from 130 participants (76 medication-free patients with OCD and 54 healthy controls (HCs)). We investigated group differences among early- and late-onset OCD and HCs in the fractional amplitude of low-frequency fluctuation (fALFF) and local gyrification index (LGI).
Results:
In the fALFF analysis, group differences were detected in the left lateral occipital cortex and bilateral thalamus (a voxel-height threshold of p < 0.001 and a cluster-level threshold of p < 0.05, with a false discovery rate correction). Both patients with early- and late-onset OCD had significantly lower fALFF in the thalamus compared to HCs (Bonferroni corrected p < 0.01). Patients with early-onset OCD exhibited significantly lower fALFF in the lateral occipital cortex than those with late-onset OCD and HCs (Bonferroni corrected p < 0.01). No significant differences were observed in the LGI analysis (a nonparametric permutation approach (10 000 iterations)), a cluster-wise threshold of p < 0.05, and a cluster-defining threshold of p < 0.001).
Limitations:
Our cross-sectional data could limit the interpretation of our results.
Conclusions:
Our results emphasize the importance of the thalamus in the pathophysiology regardless of the age-of-onset subtype of OCD. In addition, altered fALFF in the lateral occipital cortex, not accompanied by deficits of LGI, could represent a disruption of normal functional developmental processes resulting from the OCD onset at a young age. Future study should examine the relationship between the alteration of fALFF in lateral occipital cortex and clinical and treatment-refractory features of early-onset OCD, potentially improving therapeutic strategies.
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