Allostatic load index and its clinical correlates at various stages of psychosis

Schizophr Res. 2019 Aug:210:73-80. doi: 10.1016/j.schres.2019.06.009. Epub 2019 Jun 28.

Abstract

Accumulating evidence indicates systemic biological dysregulations in patients with psychosis that have been conceptualized as the "allostatic load" (AL) index. We aimed to investigate the AL index in 37 subjects at familial high risk of psychosis (FHRP), 42 first-episode psychosis (FEP) patients, 25 acutely relapsed schizophrenia (SCZ-AR) patients and 42 healthy controls (HCs), taking into account psychopathology and cognitive impairment. The AL index was calculated based on 15 biomarkers (cardiovascular markers, anthropometric measures, inflammatory markers, glucose homeostasis parameters, lipids and steroids). Cognition was assessed using the Repeatable Battery for the Assessment of Neuropsychological Status (RBANS). The AL index was significantly higher in patients with psychosis and FHR-P individuals compared to HCs. Patients with FEP and FHR-P individuals had similar AL index. Moreover, the AL index was significantly higher in SCZ-AR patients compared to other groups of participants. Higher AL index was associated with more severe general psychopathology and depressive symptoms, lower scores of attention (total score, digit span and digit coding tasks) and semantic fluency, as well as worse general functioning in patients with psychosis. There was a significant negative correlation between the AL index and the scores of attention (total score and digit coding task) in FHR-P individuals. No significant correlations between the AL index and cognition were found in HCs. Our results indicate that biological dysregulations, captured by the AL index, appear already in FHR-P individuals and progress with psychotic exacerbations. Elevated AL index might contribute to cognitive impairments in FHR-P individuals and patients with psychosis.

Keywords: Processing speed; Schizophrenia; Trauma; Working memory.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Allostasis / physiology*
  • Attention / physiology*
  • Biomarkers / blood
  • Cognitive Dysfunction / etiology
  • Cognitive Dysfunction / physiopathology*
  • Depression / etiology
  • Depression / physiopathology*
  • Disease Progression*
  • Female
  • Humans
  • Male
  • Psychotic Disorders / blood*
  • Psychotic Disorders / complications
  • Psychotic Disorders / physiopathology*
  • Schizophrenia / blood*
  • Schizophrenia / complications
  • Schizophrenia / physiopathology*
  • Symptom Flare Up*
  • Young Adult

Substances

  • Biomarkers