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Confirmatory Efficacy Trial of a Gluten-Free Diet in a Subgroup of Persons With Schizophrenia Who Have High Levels of IgG Anti-Gliadin Antibodies (AGA IG)

University of Maryland Baltimore (UMB) logo

University of Maryland Baltimore (UMB)

Status

Completed

Conditions

Gluten Sensitivity
Schizophrenia
Schizo Affective Disorder

Treatments

Other: Rice Flour in Protein Shake
Other: Gluten Flour in Protein Shake

Study type

Interventional

Funder types

Other

Identifiers

NCT03183609
HP-00075175

Details and patient eligibility

About

This study purpose is to conduct a confirmatory double-blind randomized controlled trial in an inpatient setting of the effects of a tightly controlled gluten-free diet (GFD) to improve negative symptoms in people with schizophrenia or schizoaffective disorder who have antibodies to gliadin (AGA IgG). As part of the project investigators will also confirm outcomes such as cognitive symptoms, changes in peripheral and central inflammation as well as gut/blood brain barrier permeability.

Full description

This study is a randomized double blind clinical trial being funded by NIMH. Investigators will need to enroll 40 cases with AGA IgG positivity in order to present a powered and convincing result about the efficacy of gluten withdrawal in the subpopulation of persons with schizophrenia with elevated AGA IgG levels. Investigators will recruit a minimum 50 to ensure they are well powered without question, and to account for dropouts. Investigators will use a battery of measures of peripheral and central inflammation as well as gut permeability at baseline and endpoint to confirm the relationship of these outcomes to changes in AGA IgG and symptom changes in the clinical trial. Investigators will test negative symptoms as a primary outcome but will test changes in other symptom domains such as positive symptoms. After the completion of the 5 week confirmatory study, investigators will discharge participants and follow them for 8 weeks in their own environment to test the maintenance of the effect following the stringent GFD, and provide education on gluten free shopping, cooking and eating.

Enrollment

40 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. DSM-IV/DSM 5 diagnosis of schizophrenia or schizoaffective disorder
  2. Positive for antibodies to gliadin (IgG > 20 U)
  3. SANS total score ≥ 20 and the affective flattening or alogia global item ≥ 3
  4. Age 18- 64 years
  5. Same antipsychotic for at least 4 weeks
  6. Ability to consent determined by a score of 10 or greater on the Evaluation to Sign Consent.

Exclusion criteria

  1. Persons already on gluten free diets

  2. Positivity to tissue transglutaminase (tTg) antibodies or known history of Celiac Disease

  3. Pregnant or lactating females

  4. Medical condition whose pathology or treatment could alter the presentation or treatment of schizophrenia or significantly increase the risk associated with the proposed treatment protocol

  5. Meets DSM-5 criteria for alcohol or substance use disorder (other than nicotine) within the last month

  6. Gluten ataxia, as measured by the Brief Ataxia Rating Scale

    Additional exclusion for those participating in optional imaging component:

  7. Non-removable ferromagnetic metal on or within the body

  8. Current claustrophobia

  9. Inability to lie supine for 1.5 hours

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

40 participants in 2 patient groups, including a placebo group

Gluten
Active Comparator group
Description:
30 grams of gluten flour daily in protein shake
Treatment:
Other: Gluten Flour in Protein Shake
Placebo
Placebo Comparator group
Description:
30 grams of rice flour daily in protein shake
Treatment:
Other: Rice Flour in Protein Shake

Trial contacts and locations

1

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Central trial contact

Ann Keanrs, MS

Data sourced from clinicaltrials.gov

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