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Jerry Overman, Pharm.D., BCPP
Administrative Chair, 2018 Program Committee

This session can be purchased in CPNP University

Deconstructing the illness of schizophrenia is of particular interest as this heterogeneous disorder may be composed of etiologically distinct disorders with different mechanisms which could all serve as treatment targets for components of the disorder. Although the underlying pathophysiology of schizophrenia remains unknown, leading theories to date suggest it is associated with disruption of dopamine or glutamate systems. More recently, emerging evidence suggests inflammation may play a role in the illness as demonstrated by a variety of evidence. For example, increased levels of cytokines in blood and cerebrospinal fluid in schizophrenia relative to controls have been reported. Other evidence suggests that maternal infections and inflammation results in higher risk of offspring with schizophrenia. Furthermore autoimmune diseases have been associated with increased risk for schizophrenia, genes in the major histocompatibility regions are associated with increased risk for schizophrenia and some anti-inflammatory agents have shown promise in schizophrenia treatment

CPNP President Deanna Kelly presented cutting-edge research connecting gluten to schizophrenia at the 2108 CPNP Annual Meeting. Dr. Kelly is Professor of Psychiatry and Director of the Treatment Research Program at the Maryland Psychiatric Research Program (MPRC) and the University of Maryland School of Medicine in Baltimore, MD. She discussed the emerging association of inflammation and immune activity in schizophrenia, reviewed data that helps characterize subgroups of patients with antigliadin antibodies (AGA IgG) and presented ongoing work for treatment targets and mechanisms of action connecting gluten to schizophrenia. Dr. Kelly’s exciting work suggests that more personalized treatments targeting diet modulation or immune/inflammation may play future roles in schizophrenia treatment.

One specific group with elevated peripheral and central inflammatory response is those with schizophrenia having elevations in antigliadin antibodies (AGA IgG). Gliadin is a protein found in wheat, barley and rye. Research suggests that these antibodies are present in about 1/3 of the schizophrenia population, compared to about 10% of healthy controls. These antibodies are distinct and nonoverlapping with antibodies for Celiac Disease and may represent a group with gluten sensitivity. In addition to high inflammation, this subgroup with AGA IgG elevations may be distinct by having lower positive symptoms and high kynurenic acid levels. It remains unclear, however, how these elevations in AGA IgG and immune activation in this subgroup may contribute to the illness and schizophrenia psychopathology; however it may be related to gut permeability or mimicry/cross reactivity to proteins present. This population may represent a subgroup which may have personalized and targeted treatments developed.

In the past, removing the gluten antigen from the body has been shown to be effective for diminishing or eliminating schizophrenia symptoms in case reports and small clinical trials, but not consistently. The ability to screen for AGA IgG was not developed until the 1990’s, so that not a single one of the previous trials screened schizophrenia patients for AGA IgG, meaning that most participants in these studies would be unlikely to benefit from the intervention. However, an open label study and a recently completed clinical trial with a strictly controlled gluten free diet (GFD) in the subgroup of schizophrenia patients with high AGA IgG both found benefits in negative symptoms, leading the way for more robust, follow up studies to replicate these findings.

Take Home Points

  • Elevated antigliadin antibodies (AGA IgG) is present in about 30% of all people with schizophrenia
  • Elevations of AGA IgG represent a potential subgroup with high peripheral and central inflammation
  • Removing gliadin may improve negative symptoms in schizophrenia
  • Future work will focus on confirmation of original findings and on mechanistic underpinnings

References

  1. Sekar A, et al. Nature 2016;530(7589):177-183, doi: 10.1038/nature16549. Epub 2016 Jan 27
  2. Bloomfield PS, Am J of Psychiatry 2016;173(1):44-52, doi: 10.1176/appi.ajp.2015.14101358
  3. Stefansson, et al, Nature 2009, 460(7256):744-747, doi: 10.1038/nature08186
  4. Fineberg AM, et al Biol Psychiatry, 2013;73(10):951-966, doi: 10.1016/j.biopsych.2013.01.001
  5. Sapone et al. BMC Medicine 2012;10:13, doi: 10.1186/1741-7015-10-13
  6. Rowland LM, et al. Front Psychiatry 2017;8:104, doi: 10.3389/fpsyt.2017.00104
  7. Kelly DL, et al. Brain Behav Immun 2018 Mar;69:57-59, doi: 10.1016/j.bbi.2017.10.020 
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