ArticleTranslational psychiatry2025
Differential trajectories of corticostriatal structural connectivity in individuals at clinical high risk for psychosis according to functional outcome.
Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- From synapse to system: mechanistic pathways of neural signaling dysfunction in psychiatric disorders.Frontiers in cell and developmental biology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Dysconnectivity in the corticostriatal pathway, which is central to psychosis pathophysiology, is also known to be present in individuals at clinical high risk for psychosis (CHR-P). Considering that the corticostriatal pathway actively matures until adulthood and that neuroanatomical maturation is suggested to be related to functional outcomes in individuals at CHR-P, longitudinal studies on the corticostriatal structural pathway in individuals at CHR-P are warranted. To characterize the longitudinal trajectory of corticostriatal structural connectivity, diffusion-weighted images were collected from 23 individuals at CHR-P and 20 healthy controls (HCs) at baseline and at a 2-year follow-up visit. Probabilistic tractography was performed to segment the pathways between seven cortical regions and the striatum. The relative connectivity between each cortical region and associated striatal subregion was calculated. The CHR-P group was divided into subgroups according to the functional outcome of the modified Global Assessment of Functioning score at follow-up. A significant group‒time interaction between the left orbitofrontal cortex and its associated striatal subregion was found, with a negative slope in the CHR-P group and positive slope in the HC group. In the left orbitofrontal corticostriatal relative connectivity, the group‒time interaction between HCs and individuals at CHR-P with poor functional outcomes at follow-up was statistically significant, whereas that between HCs and individuals at CHR-P with good functional outcomes at follow-up was not. These findings indicate abnormal white matter maturation of the orbitofrontal corticostriatal pathway in individuals at CHR-P. Abnormal neuroanatomical maturation of the orbitofrontal corticostriatal pathway may reflect prognosis for functional outcomes in these individuals.
Indexed as
Identifiers
What OpenQuestion holds
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.