bioRxivNeurosciencePreprint
Mapping Higher-Order Topology in OCD Brain Networks with Hodge Laplacian
Hanyang RuaniD, Moo K Chung, Willem B. BruiniD, Nadža DžinalijaiD, Yoshinari AbeiD, P. AlonsoiD, Alan AnticeviciD, Srinivas BalachanderiD, Marcelo C. BatistuzzoiD, Francesco BenedettiiD, Sara BertolíniD, Silvia BremiD, Youngsun ChoiD, Federica ColomboiD, Beatriz CoutoiD, Goi Khia EngiD, Sónia Rio FerreiraiD, Jamie D. FeusneriD, Rachael G. GraziopleneiD, Patricia GruneriD, Kristen HageniD, Bjarne K. A. HanseniD, Yoshiyuki HiranoiD, Marcelo Q. HoexteriD, Jonathan IpseriD, , Kathrin KochiD
Abstract
Brain disorders are increasingly understood as disorders of distributed brain circuits, yet functional connectivity (FC), the dominant framework for mapping them, treats the brain as a collection of pairwise relationships between regions and cannot represent pathology distributed across coordinated sets of connections. We introduce a Hodge-Laplacian topological framework that localizes higher-order "loop" (1-cycle) organization within functional connectome, maps each loop to specific edges and networks, and yields a subject-level measure of loop expression. Applied to resting-state fMRI from the ENIGMA-OCD consortium (1,024 patients and 1,028 controls across 28 sites), the framework identified 93 loop-level abnormalities in obsessive-compulsive disorder (OCD), concentrated in frontoparietal and somatomotor systems. The edges forming these loops largely showed no significant differences between groups, indicating that the abnormalities were invisible to conventional FC analysis. The frontoparietal and somatomotor loop clusters recurred across the clinical subgroups, suggesting convergence on a shared higher-order phenotype. Robustness analyses showed the loop signal reflected higher-order organization rather than an artifact of individual edges, the network backbone, or any single site. These results indicate that coordinated, multi-edge pathology exists and can be localized even when pairwise analyses fail to detect it, positioning higher-order topology as a generalizable axis for mapping circuit pathology across psychiatric and neurological disorders.
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