Dissociable computational markers of semantic search and verbal retrieval drive across the psychosis spectrum
Discuss this preprint
Start a discussion What are Sciety discussions?Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
Formal thought disorder (FTD) is a core psychosis feature. Disentangling its dimensions requires tasks simple enough for formal modeling yet sensitive enough to capture individual variation across the psychosis spectrum. The semantic verbal fluency task offers precisely this: a structured behavioral trace of semantic memory sampling, amenable to computational analysis using distributed word embeddings. We hypothesized that this sampling process is governed by two dissociable mechanisms mapping onto FTD dimensions: initial retrieval drive ( d 0 ), quantifying the motivational resource sustaining production, and semantic search precision ( α ), quantifying how strongly similarity to the preceding word constrains each retrieval step from near-random to highly structured. We hypothesized that reduced d 0 would track negative psychosis symptoms and alogia, while degraded α would track language disorganization and left inferior longitudinal fasciculus (ILF) fractional anisotropy. We tested these predictions in a primary ( N = 120) and an independent replication sample ( N = 249) of German-speaking individuals across the psychosis spectrum. Both parameters decreased with greater psychosis severity and, in the primary sample, they dissociated regarding their clinical correlates. d 0 correlated negatively with negative symptoms, general psychopathology, and poverty of speech, consistent with a computational signature of alogia. α correlated negatively with positive symptoms and cognitive flexibility, and, in individuals with psychosis, positively with left ILF fractional anisotropy. The association between d 0 and negative symptoms was replicated in the independent sample. These findings pave the way for mechanistic, automatically derived FTD markers capturing subclinical variation across the psychosis spectrum and mapping onto underlying cognitive and neural processes.