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April 11, 2026Translational Psychiatry0 citationsOpen Access

Integrated clinical and postmortem profiling in schizophrenia reveals a cognitive subtype linked to cerebrovascular disease

NFN. Catie FutheyFVFidel Vila-RodriguezSSShawn J. Stochmanski

Key Points

  • The study aims to explore the relationship between neuropathology and cognitive performance in older adults with schizophrenia.
  • Investigated postmortem neuropathology and neuropsychological performance in 55 older adults.
  • Conducted clustering analysis based on cognitive testing scores to identify cognitive subgroups.
  • Assessed the prevalence of Alzheimer's and cerebrovascular disease pathologies.
  • 70% of participants exhibited cognitive impairment, with 35.1% showing Alzheimer's pathology.
  • 84.2% had cerebrovascular disease, which correlated with significantly lower MMSE scores (p < 0.001).
  • Identified three cognitive subgroups (NCOG_1, NCOG_2, NCOG_3) with distinct profiles despite similar neuropathology.

Abstract

Cognitive impairment is a core feature of schizophrenia with an unknown neuropathological basis. In older adults with schizophrenia, contributions of Alzheimer’s pathology and cerebrovascular disease (CVD) to specific neurocognitive deficits remain largely unexplored. This study investigated the relationship between postmortem neuropathology and neuropsychological performance in 55 older adults with schizophrenia (mean age 78. 2 years), providing the most detailed clinicopathologic correlation study in schizophrenia to date. Overall, 70% of the sample met criteria for cognitive impairment, but remarkably nearly half of this cognitively impaired group lacked neuropathological autopsy findings that could explain their symptoms. While the prevalence of postmortem Alzheimer’s pathology (35. 1%) was similar to rates in the general population, CVD pathology was more frequent (84. 2%) and associated with lower Mini-Mental State Examination (MMSE) scores (p < 0. 001). No other pathology-cognition relationships were observed. Clustering analysis based upon cognitive testing scores alone identified three subgroups (NCOG₁, NCOG₂, and NCOG₃) with distinct cognitive profiles despite similar postmortem neuropathology findings. NCOG₂ exhibited relatively spared cognition (mean MMSE = 26/30) and a significantly younger age at death. Interestingly, at our level of sample depth, the MMSE-CVD association was specific to only the NCOG₃ cluster, which exhibited more selective impairments, implicating vascular pathology in at least one distinct cognitive phenotype of schizophrenia. Our data suggest a novel clinicopathologic association between CVD pathology and cognitive impairment in schizophrenia and that targeted interventions to reduce cardiovascular risk may offer meaningful cognitive benefits in a specific schizophrenia patient subgroup.

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Cite This Study

Futhey et al. (2026) studied this question.

synapsesocial.com/papers/69d9e5ec78050d08c1b7622ahttps://doi.org/10.1038/s41398-026-03984-w
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