4.4 Review

Autonomic nervous system dysfunction in schizophrenia: impact on cognitive and metabolic health

Journal

NPJ SCHIZOPHRENIA
Volume 7, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41537-021-00151-6

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Funding

  1. CIHR Canada Graduate Scholarship Master's Program (CGS-M)
  2. Banting and Best Diabetes Centre (BBDC) Novo-Nordisk Graduate Studentship
  3. Department of Psychiatry, University of Toronto
  4. Canadian Institutes of Health Research
  5. CAMH Discovery Fund
  6. Banting and Best Diabetes Center (BBDC)
  7. Canadian Institutes of Health Research (CIHR) [PJT-153262]
  8. PSI Foundation, Ontario
  9. Kelly and Michael Meighen Chair in Psychosis Prevention
  10. PSI Foundation

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Autonomic dysfunction is closely related to the pathophysiology of schizophrenia, including symptom severity, cognitive impairment, and cardiometabolic comorbidities. Studies have shown that the strongest association of low heart rate variability is noted among patients receiving antipsychotic treatment with high-affinity muscarinic antagonism.
Schizophrenia (SCZ) is a psychiatric disorder characterized by a wide range of positive, negative and cognitive symptoms, along with an increased risk of metabolic syndrome and cardiovascular disease that contribute to a 15-20-year reduced life expectancy. Autonomic dysfunction, in the form of increased sympathetic activity and decreased parasympathetic activity, is postulated to be implicated in SCZ and its treatment. The aim of this narrative review is to view SCZ through an autonomic lens and synthesize the evidence relating autonomic dysfunction to different domains of SCZ. Using various methods of assessing autonomic activity, autonomic dysfunction was found to be associated with multiple aspects of SCZ pathophysiology, including symptom severity, cognitive impairment, and the development of cardiometabolic comorbidities, such as metabolic syndrome and high BMI. The strongest association of low heart rate variability was noted among patients on antipsychotic treatment with high-affinity muscarinic antagonism (i.e., clozapine, olanzapine and quetiapine). The review will also suggest ways in which studying autonomic dysfunction can help reduce morbidity and mortality associated with SCZ and its treatment.

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