ArticleBiological psychiatry global open science2026
Developmental Alterations in the Diffusion Tensor Imaging Analysis Along the Perivascular Space Index Suggest Possible Glymphatic-Related Mechanisms Underlying Excitation/Inhibition Imbalance and Psychosis Vulnerability in 22q11.2 Deletion Syndrome.
Article in Biological psychiatry global open science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
Background: Impairment of the glymphatic system may contribute to atypical brain development and increased vulnerability to psychiatric conditions such as psychosis. In particular, disrupted glymphatic efficiency may affect neurochemical homeostasis during critical maturational windows, leading to structural and circuit-level alterations. However, its role in early neurodevelopmental trajectories remains largely unexplored. Methods: We combined longitudinal diffusion tensor imaging (DTI) in 85 individuals with 22q11.2 deletion syndrome (22q11DS), a neurodevelopmental condition associated with elevated psychosis risk (143 scans), with cross-sectional magnetic resonance spectroscopy in a subset of 39 individuals with 22q11DS. Glymphatic function was estimated indirectly using the DTI analysis along the perivascular space (ALPS) index, a diffusion-based proxy derived from manual and automated region of interest placement. Excitation/inhibition ratio was assessed in the right hippocampus via cerebrospinal fluid-corrected combined glutamate-glutamine signal (Glx) and GABA (gamma-aminobutyric acid) levels. Results: The ALPS index was significantly reduced in individuals with 22q11DS compared with control participants ( Conclusions: These findings provide in vivo evidence that glymphatic-related dysfunction, as indexed by the DTI-ALPS proxy, emerges early and follows atypical developmental trajectories in individuals at risk for psychosis. An impaired ALPS index is also associated with excitatory/inhibitory imbalance. This dysfunction may represent a novel pathway contributing to psychosis vulnerability and a potential target for early intervention.
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