AI Article Synopsis

  • Negative symptoms (NS) in schizophrenia spectrum disorders (SSD) and bipolar disorder I (BD-I) have been linked to issues in working memory, but research on their connections to other clinical factors is limited.
  • In a study with 50 participants from SSD and 49 from BD-I, NS were evaluated using SANS scores focusing on areas like avolition-apathy and anhedonia-asociality, while relationships to symptoms and antipsychotic medication were analyzed through regression methods.
  • Results indicated that disorganization correlates with specific negative symptoms, and avolition-apathy notably predicts worse working memory across both disorders, suggesting the need for further understanding of how NS affects cognitive function in these conditions.

Article Abstract

Negative symptoms (NS) of schizophrenia spectrum disorders (SSD) are also prevalent in bipolar disorder I (BD-I) and show associations with impaired working memory (WM). However, empirical work on their relationship to other clinical factors across SSD and BD-I is sparse. Here, we characterized the associations of NS with key clinical variables and WM capacity across a combined sample of SSD and BD. We included 50 outpatients with SSD and 49 with BD-I and assessed NS domains using SANS global scores for avolition-apathy, anhedonia-asociality, alogia, and blunted affect. We assessed the transdiagnostic relationship between NS and other clinical variables, including positive symptoms, disorganization, depressive symptoms, and antipsychotic medication, using multiple regressions. The strength of these associations was further determined through dominance analyses. Finally, we used multiple regression to assess the relationship between NS domains and WM. To assess the generalizability of transdiagnostic associations, analyses were repeated in each diagnostic group separately. Across SSD and BD-I, disorganization was associated with avolition-apathy and anhedonia-asociality and depressive symptoms additionally predicted anhedonia-asociality. Antipsychotic dose was associated with blunted affect while group differences only predicted alogia. Higher avolition-apathy was related to impaired WM transdiagnostically, partially mediated by the severity of disorganization, whereas only in BD-I higher anhedonia-asociality was associated with better WM capacity. This study demonstrated transdiagnostic associations of both avolition-apathy and anhedonia-asociality with disorganization and identified avolition-apathy as a potential transdiagnostic predictor of WM impairments. Overall, our findings highlight the importance of understanding the relationship between NS domains and other clinical factors with cognitive function across SSD and BD.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11487101PMC
http://dx.doi.org/10.1093/schizbullopen/sgae024DOI Listing

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