Individual atrophy patterns clarify latent neural subtypes in addiction.
Addiction is a brain disorder marked by profound inter-individual heterogeneity, a factor that limits the clinical utility of group-level neuroimaging findings.
To address this, we constructed a precision neuroimaging framework to capture individual variability. We quantified gray matter volume (GMV) deviations in 464 individuals with five substance-related and addictive disorders using a normative model derived from over 1000 healthy controls. Subsequently, we applied a dimensionality reduction technique to decompose these individual deviations into distinct spatial patterns.
We observe a shared pattern involving the insula and prefrontal cortex that reflects common underlying biology across different addictions. In contrast, a pattern centered on the basal ganglia captures the differences between specific addiction types. Importantly, only transdiagnostic factors correlated with clinical measures, whereas the heterogeneity factor did not.
By resolving neurobiological heterogeneity into distinct, structural atrophy subtypes, this framework offers insights into understanding structural heterogeneity as a local effect of common networks.
To address this, we constructed a precision neuroimaging framework to capture individual variability. We quantified gray matter volume (GMV) deviations in 464 individuals with five substance-related and addictive disorders using a normative model derived from over 1000 healthy controls. Subsequently, we applied a dimensionality reduction technique to decompose these individual deviations into distinct spatial patterns.
We observe a shared pattern involving the insula and prefrontal cortex that reflects common underlying biology across different addictions. In contrast, a pattern centered on the basal ganglia captures the differences between specific addiction types. Importantly, only transdiagnostic factors correlated with clinical measures, whereas the heterogeneity factor did not.
By resolving neurobiological heterogeneity into distinct, structural atrophy subtypes, this framework offers insights into understanding structural heterogeneity as a local effect of common networks.
Authors
Wang Wang, Guo Guo, Zeng Zeng, Wu Wu, Huang Huang, Chen Chen, Chen Chen, Wang Wang, Hu Hu, Dong Dong, Yin Yin, Su Su, Zheng Zheng
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