Immunologic profiling in schizophrenia and rheumatoid arthritis
•The negative relationship between schizophrenia and rheumatoid arthritis has puzzled researchers for more than half a century.•There have not been studies of the immunologic and genetic structure of the two disorders in matched samples of patients with the two disorders.•This study includes study o...
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Published in | Psychiatry research Vol. 317; p. 114812 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.11.2022
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Abstract | •The negative relationship between schizophrenia and rheumatoid arthritis has puzzled researchers for more than half a century.•There have not been studies of the immunologic and genetic structure of the two disorders in matched samples of patients with the two disorders.•This study includes study of immunologic and genetic structures in samples of 40 persons with schizophrenia, 40 persons with Rheumatoid Arthritis, and 40 healthy controls.•The analyses suggests that stratification of SCZ patients by cytokine profile may enable the use of currently available cytokine-based treatment strategies.
The negative relationship between schizophrenia (SCZ) and rheumatoid arthritis (RA) has been observed for 85 years, but the mechanisms driving this association are unknown. This study analyzed differences in profiles of cytokines (IL-1β, IL-Ra, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IFNγ, TNFα), selected genes (HLA-DRB1, IL1RN, HP2), and antibodies related to gluten sensitivity (AGA-IgG, AGA-IgA), celiac disease (tTG), and systemic autoimmunity (ANA, anti-CCP, RF) in 40 subjects with SCZ, 40 with RA, and 40 healthy controls (HC). HLA-DRB1*04:01 alleles were enriched in persons with SCZ and RA compared with HC, and the HP2/HP2 genotype was 2-fold more prevalent in AGA/tTG-positive versus negative SCZ patients. Patients with SCZ demonstrated 52.5% positivity for any of the antibodies tested, compared to 90% of RA patients and 30% of HC. Cluster analysis of the cytokines revealed three clusters: one associated with SCZ marked by high levels of IL-1Ra, one associated with HC, and one associated with both SCZ and RA marked by elevated levels of IFNγ, TNFα, and IL-6. These analyses suggest that stratification of SCZ patients by cytokine profile may identify unique SCZ subgroups and enable the use of currently available cytokine-targeted treatment strategies. |
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AbstractList | •The negative relationship between schizophrenia and rheumatoid arthritis has puzzled researchers for more than half a century.•There have not been studies of the immunologic and genetic structure of the two disorders in matched samples of patients with the two disorders.•This study includes study of immunologic and genetic structures in samples of 40 persons with schizophrenia, 40 persons with Rheumatoid Arthritis, and 40 healthy controls.•The analyses suggests that stratification of SCZ patients by cytokine profile may enable the use of currently available cytokine-based treatment strategies.
The negative relationship between schizophrenia (SCZ) and rheumatoid arthritis (RA) has been observed for 85 years, but the mechanisms driving this association are unknown. This study analyzed differences in profiles of cytokines (IL-1β, IL-Ra, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IFNγ, TNFα), selected genes (HLA-DRB1, IL1RN, HP2), and antibodies related to gluten sensitivity (AGA-IgG, AGA-IgA), celiac disease (tTG), and systemic autoimmunity (ANA, anti-CCP, RF) in 40 subjects with SCZ, 40 with RA, and 40 healthy controls (HC). HLA-DRB1*04:01 alleles were enriched in persons with SCZ and RA compared with HC, and the HP2/HP2 genotype was 2-fold more prevalent in AGA/tTG-positive versus negative SCZ patients. Patients with SCZ demonstrated 52.5% positivity for any of the antibodies tested, compared to 90% of RA patients and 30% of HC. Cluster analysis of the cytokines revealed three clusters: one associated with SCZ marked by high levels of IL-1Ra, one associated with HC, and one associated with both SCZ and RA marked by elevated levels of IFNγ, TNFα, and IL-6. These analyses suggest that stratification of SCZ patients by cytokine profile may identify unique SCZ subgroups and enable the use of currently available cytokine-targeted treatment strategies. The negative relationship between schizophrenia (SCZ) and rheumatoid arthritis (RA) has been observed for 85 years, but the mechanisms driving this association are unknown. This study analyzed differences in profiles of cytokines (IL-1β, IL-Ra, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IFNγ, TNFα), selected genes ( HLA-DRB1, IL1RN, HP2 ), and antibodies related to gluten sensitivity (AGA-IgG, AGA-IgA), celiac disease (tTG), and systemic autoimmunity (ANA, anti-CCP, RF) in 40 subjects with SCZ, 40 with RA, and 40 healthy controls (HC). HLA-DRB1 * 04:01 alleles were enriched in persons with SCZ and RA compared with HC, and the HP2/HP2 genotype was 2-fold more prevalent in AGA/tTG-positive versus negative SCZ patients. Patients with SCZ demonstrated 52.5% positivity for any of the antibodies tested, compared to 90% of RA patients and 30% of HC. Cluster analysis of the cytokines revealed three clusters: one associated with SCZ marked by high levels of IL-1Ra, one associated with HC, and one associated with both SCZ and RA marked by elevated levels of IFNγ, TNFα, and IL-6. These analyses suggest that stratification of SCZ patients by cytokine profile may identify unique SCZ subgroups and enable the use of currently available cytokine-targeted treatment strategies. The negative relationship between schizophrenia (SCZ) and rheumatoid arthritis (RA) has been observed for 85 years, but the mechanisms driving this association are unknown. This study analyzed differences in profiles of cytokines (IL-1β, IL-Ra, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IFNγ, TNFα), selected genes (HLA-DRB1, IL1RN, HP2), and antibodies related to gluten sensitivity (AGA-IgG, AGA-IgA), celiac disease (tTG), and systemic autoimmunity (ANA, anti-CCP, RF) in 40 subjects with SCZ, 40 with RA, and 40 healthy controls (HC). HLA-DRB1*04:01 alleles were enriched in persons with SCZ and RA compared with HC, and the HP2/HP2 genotype was 2-fold more prevalent in AGA/tTG-positive versus negative SCZ patients. Patients with SCZ demonstrated 52.5% positivity for any of the antibodies tested, compared to 90% of RA patients and 30% of HC. Cluster analysis of the cytokines revealed three clusters: one associated with SCZ marked by high levels of IL-1Ra, one associated with HC, and one associated with both SCZ and RA marked by elevated levels of IFNγ, TNFα, and IL-6. These analyses suggest that stratification of SCZ patients by cytokine profile may identify unique SCZ subgroups and enable the use of currently available cytokine-targeted treatment strategies. The negative relationship between schizophrenia (SCZ) and rheumatoid arthritis (RA) has been observed for 85 years, but the mechanisms driving this association are unknown. This study analyzed differences in profiles of cytokines (IL-1β, IL-Ra, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IFNγ, TNFα), selected genes (HLA-DRB1, IL1RN, HP2), and antibodies related to gluten sensitivity (AGA-IgG, AGA-IgA), celiac disease (tTG), and systemic autoimmunity (ANA, anti-CCP, RF) in 40 subjects with SCZ, 40 with RA, and 40 healthy controls (HC). HLA-DRB1*04:01 alleles were enriched in persons with SCZ and RA compared with HC, and the HP2/HP2 genotype was 2-fold more prevalent in AGA/tTG-positive versus negative SCZ patients. Patients with SCZ demonstrated 52.5% positivity for any of the antibodies tested, compared to 90% of RA patients and 30% of HC. Cluster analysis of the cytokines revealed three clusters: one associated with SCZ marked by high levels of IL-1Ra, one associated with HC, and one associated with both SCZ and RA marked by elevated levels of IFNγ, TNFα, and IL-6. These analyses suggest that stratification of SCZ patients by cytokine profile may identify unique SCZ subgroups and enable the use of currently available cytokine-targeted treatment strategies.The negative relationship between schizophrenia (SCZ) and rheumatoid arthritis (RA) has been observed for 85 years, but the mechanisms driving this association are unknown. This study analyzed differences in profiles of cytokines (IL-1β, IL-Ra, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12p70, IFNγ, TNFα), selected genes (HLA-DRB1, IL1RN, HP2), and antibodies related to gluten sensitivity (AGA-IgG, AGA-IgA), celiac disease (tTG), and systemic autoimmunity (ANA, anti-CCP, RF) in 40 subjects with SCZ, 40 with RA, and 40 healthy controls (HC). HLA-DRB1*04:01 alleles were enriched in persons with SCZ and RA compared with HC, and the HP2/HP2 genotype was 2-fold more prevalent in AGA/tTG-positive versus negative SCZ patients. Patients with SCZ demonstrated 52.5% positivity for any of the antibodies tested, compared to 90% of RA patients and 30% of HC. Cluster analysis of the cytokines revealed three clusters: one associated with SCZ marked by high levels of IL-1Ra, one associated with HC, and one associated with both SCZ and RA marked by elevated levels of IFNγ, TNFα, and IL-6. These analyses suggest that stratification of SCZ patients by cytokine profile may identify unique SCZ subgroups and enable the use of currently available cytokine-targeted treatment strategies. |
ArticleNumber | 114812 |
Author | Thomas, Mekha A. Musci, Rashelle Rodriguez, Katrina M. Dohan, Curtis Eaton, William W. Cihakova, Daniela Kelly, Deanna L. Roth, Kimberly Darrah, Erika Talor, Monica V. Johnson, Jeanette Bingham, Clifton O. |
AuthorAffiliation | d Department of Pathology and Laboratory Medicine, University of Tennessee Health Science Center, US b Department of Medicine, Division of Rheumatology, Johns Hopkins School of Medicine, US c Department of Pathology, Johns Hopkins School of Medicine, US f Maryland Psychiatric Research Center (MPRC), University of Maryland School of Medicine, US e Department of Community Medicine, Mercer University School of Medicine, US a Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, US |
AuthorAffiliation_xml | – name: d Department of Pathology and Laboratory Medicine, University of Tennessee Health Science Center, US – name: f Maryland Psychiatric Research Center (MPRC), University of Maryland School of Medicine, US – name: a Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, US – name: b Department of Medicine, Division of Rheumatology, Johns Hopkins School of Medicine, US – name: c Department of Pathology, Johns Hopkins School of Medicine, US – name: e Department of Community Medicine, Mercer University School of Medicine, US |
Author_xml | – sequence: 1 givenname: William W. surname: Eaton fullname: Eaton, William W. email: weaton@jhsph.edu organization: Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, US – sequence: 2 givenname: Katrina M. surname: Rodriguez fullname: Rodriguez, Katrina M. organization: Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, US – sequence: 3 givenname: Mekha A. orcidid: 0000-0002-5169-6568 surname: Thomas fullname: Thomas, Mekha A. organization: Department of Medicine, Division of Rheumatology, Johns Hopkins School of Medicine, US – sequence: 4 givenname: Jeanette surname: Johnson fullname: Johnson, Jeanette organization: Department of Medicine, Division of Rheumatology, Johns Hopkins School of Medicine, US – sequence: 5 givenname: Monica V. surname: Talor fullname: Talor, Monica V. organization: Department of Pathology, Johns Hopkins School of Medicine, US – sequence: 6 givenname: Curtis surname: Dohan fullname: Dohan, Curtis organization: Department of Pathology and Laboratory Medicine, University of Tennessee Health Science Center, US – sequence: 7 givenname: Clifton O. orcidid: 0000-0002-4752-5029 surname: Bingham fullname: Bingham, Clifton O. organization: Department of Medicine, Division of Rheumatology, Johns Hopkins School of Medicine, US – sequence: 8 givenname: Rashelle surname: Musci fullname: Musci, Rashelle organization: Department of Mental Health, Johns Hopkins Bloomberg School of Public Health, US – sequence: 9 givenname: Kimberly orcidid: 0000-0001-5006-9362 surname: Roth fullname: Roth, Kimberly organization: Department of Community Medicine, Mercer University School of Medicine, US – sequence: 10 givenname: Deanna L. surname: Kelly fullname: Kelly, Deanna L. organization: Maryland Psychiatric Research Center (MPRC), University of Maryland School of Medicine, US – sequence: 11 givenname: Daniela surname: Cihakova fullname: Cihakova, Daniela organization: Department of Pathology, Johns Hopkins School of Medicine, US – sequence: 12 givenname: Erika surname: Darrah fullname: Darrah, Erika organization: Department of Medicine, Division of Rheumatology, Johns Hopkins School of Medicine, US |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/36058039$$D View this record in MEDLINE/PubMed |
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Snippet | •The negative relationship between schizophrenia and rheumatoid arthritis has puzzled researchers for more than half a century.•There have not been studies of... The negative relationship between schizophrenia (SCZ) and rheumatoid arthritis (RA) has been observed for 85 years, but the mechanisms driving this association... |
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SubjectTerms | Antibodies Arthritis, Rheumatoid - genetics Arthritis, Rheumatoid - immunology Autoantibodies Cytokines Epidemiology Genes HLA-DRB1 Chains - genetics HLA-DRB1 Chains - immunology Humans Immunology Interleukin-6 Peptides, Cyclic Schizophrenia - genetics Schizophrenia - immunology Tumor Necrosis Factor-alpha |
Title | Immunologic profiling in schizophrenia and rheumatoid arthritis |
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