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Immunologic profiling in schizophrenia and rheumatoid arthritis
William W Eaton1, Katrina M Rodriguez1, Mekha A Thomas2
1Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, US.
Psychiatry Research
|September 4, 2022
Summary
This study investigated biomarkers linking schizophrenia (SCZ) and rheumatoid arthritis (RA), finding distinct cytokine profiles. Stratifying SCZ patients by these profiles may reveal subgroups for targeted treatments.
Area of Science:
- Immunology
- Psychiatry
- Genetics
Background:
- An 85-year observed negative association exists between schizophrenia (SCZ) and rheumatoid arthritis (RA).
- The underlying biological mechanisms for this SCZ-RA relationship remain largely unknown.
- Understanding shared or distinct immunological pathways is crucial for both conditions.
Purpose of the Study:
- To analyze differences in cytokine profiles, gene variants, and autoantibodies between SCZ, RA patients, and healthy controls (HC).
- To explore potential biomarkers that could explain the observed association between SCZ and RA.
- To investigate if cytokine profiles can stratify SCZ patients for potential targeted therapies.
Main Methods:
- Analyzed cytokine levels (e.g., IL-1β, IFNγ, TNFα), gene polymorphisms (e.g., HLA-DRB1, HP2), and autoantibodies (e.g., AGA, tTG, ANA, anti-CCP, RF).
- Included 40 SCZ patients, 40 RA patients, and 40 healthy controls.
- Employed cluster analysis to group cytokine profiles.
Main Results:
- HLA-DRB1*04:01 alleles were more common in SCZ and RA patients compared to HC.
- SCZ patients showed 52.5% positivity for tested antibodies, versus 90% for RA patients and 30% for HC.
- Cytokine cluster analysis identified profiles associated with SCZ (high IL-1Ra) and shared SCZ/RA (elevated IFNγ, TNFα, IL-6).
Conclusions:
- Cytokine profiles differ significantly across SCZ, RA, and HC groups.
- Specific genetic and antibody markers may be relevant to SCZ and RA pathophysiology.
- Stratifying SCZ patients based on cytokine profiles could identify distinct subgroups amenable to cytokine-targeted treatments.
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