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Associations between SNPs and immune-related circulating proteins in schizophrenia
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| Veröffentlicht in: | Scientific reports 7(2017) Artikel-Nummer 12586, 11 Seiten |
|---|---|
| Personen und Körperschaften: | , |
| Titel: | Associations between SNPs and immune-related circulating proteins in schizophrenia/ Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel and Sabine Bahn |
| Format: | E-Book-Kapitel |
| Sprache: | Englisch |
| veröffentlicht: |
03 October 2017
|
| Gesamtaufnahme: |
: Scientific reports, 7(2017) Artikel-Nummer 12586, 11 Seiten
, volume:7 |
| Quelle: | Verbunddaten SWB Lizenzfreie Online-Ressourcen |
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| 245 | 1 | 0 | |a Associations between SNPs and immune-related circulating proteins in schizophrenia |c Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel and Sabine Bahn |
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| 520 | |a Genome-wide association studies (GWAS) and proteomic studies have provided convincing evidence implicating alterations in immune/inflammatory processes in schizophrenia. However, despite the convergence of evidence, direct links between the genetic and proteomic findings are still lacking for schizophrenia. We investigated associations between single nucleotide polymorphisms (SNPs) from the custom-made PsychArray and the expression levels of 190 multiplex immunoassay profiled serum proteins in 149 schizophrenia patients and 198 matched controls. We identified associations between 81 SNPs and 29 proteins, primarily involved in immune/inflammation responses. Significant SNPxDiagnosis interactions were identified for eight serum proteins including Factor-VII[rs555212], Alpha-1-Antitrypsin[rs11846959], Interferon-Gamma Induced Protein 10[rs4256246] and von-Willebrand-Factor[rs12829220] in the control group; Chromogranin-A[rs9658644], Cystatin-C[rs2424577] and Vitamin K-Dependent Protein S[rs6123] in the schizophrenia group; Interleukin-6 receptor[rs7553796] in both the control and schizophrenia groups. These results suggested that the effect of these SNPs on expression of the respective proteins varies with diagnosis. The combination of patient-specific genetic information with blood biomarker data opens a novel approach to investigate disease mechanisms in schizophrenia and other psychiatric disorders. Our findings not only suggest that blood protein expression is influenced by polymorphisms in the corresponding gene, but also that the effect of certain SNPs on expression of proteins can vary with diagnosis. | ||
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| contents | Genome-wide association studies (GWAS) and proteomic studies have provided convincing evidence implicating alterations in immune/inflammatory processes in schizophrenia. However, despite the convergence of evidence, direct links between the genetic and proteomic findings are still lacking for schizophrenia. We investigated associations between single nucleotide polymorphisms (SNPs) from the custom-made PsychArray and the expression levels of 190 multiplex immunoassay profiled serum proteins in 149 schizophrenia patients and 198 matched controls. We identified associations between 81 SNPs and 29 proteins, primarily involved in immune/inflammation responses. Significant SNPxDiagnosis interactions were identified for eight serum proteins including Factor-VII[rs555212], Alpha-1-Antitrypsin[rs11846959], Interferon-Gamma Induced Protein 10[rs4256246] and von-Willebrand-Factor[rs12829220] in the control group; Chromogranin-A[rs9658644], Cystatin-C[rs2424577] and Vitamin K-Dependent Protein S[rs6123] in the schizophrenia group; Interleukin-6 receptor[rs7553796] in both the control and schizophrenia groups. These results suggested that the effect of these SNPs on expression of the respective proteins varies with diagnosis. The combination of patient-specific genetic information with blood biomarker data opens a novel approach to investigate disease mechanisms in schizophrenia and other psychiatric disorders. Our findings not only suggest that blood protein expression is influenced by polymorphisms in the corresponding gene, but also that the effect of certain SNPs on expression of proteins can vary with diagnosis. |
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| spelling | Chan, Man K. VerfasserIn (DE-588)1150994169 (DE-627)1011214237 (DE-576)497358697 aut, Associations between SNPs and immune-related circulating proteins in schizophrenia Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel and Sabine Bahn, 03 October 2017, 11, Text txt rdacontent, Computermedien c rdamedia, Online-Ressource cr rdacarrier, Gesehen am 21.08.2018, Genome-wide association studies (GWAS) and proteomic studies have provided convincing evidence implicating alterations in immune/inflammatory processes in schizophrenia. However, despite the convergence of evidence, direct links between the genetic and proteomic findings are still lacking for schizophrenia. We investigated associations between single nucleotide polymorphisms (SNPs) from the custom-made PsychArray and the expression levels of 190 multiplex immunoassay profiled serum proteins in 149 schizophrenia patients and 198 matched controls. We identified associations between 81 SNPs and 29 proteins, primarily involved in immune/inflammation responses. Significant SNPxDiagnosis interactions were identified for eight serum proteins including Factor-VII[rs555212], Alpha-1-Antitrypsin[rs11846959], Interferon-Gamma Induced Protein 10[rs4256246] and von-Willebrand-Factor[rs12829220] in the control group; Chromogranin-A[rs9658644], Cystatin-C[rs2424577] and Vitamin K-Dependent Protein S[rs6123] in the schizophrenia group; Interleukin-6 receptor[rs7553796] in both the control and schizophrenia groups. These results suggested that the effect of these SNPs on expression of the respective proteins varies with diagnosis. The combination of patient-specific genetic information with blood biomarker data opens a novel approach to investigate disease mechanisms in schizophrenia and other psychiatric disorders. Our findings not only suggest that blood protein expression is influenced by polymorphisms in the corresponding gene, but also that the effect of certain SNPs on expression of proteins can vary with diagnosis., Rietschel, Marcella 1957- VerfasserIn (DE-588)112785751 (DE-627)505574020 (DE-576)289742307 aut, Enthalten in Scientific reports [London] : Macmillan Publishers Limited, part of Springer Nature, 2011 7(2017) Artikel-Nummer 12586, 11 Seiten Online-Ressource (DE-627)663366712 (DE-600)2615211-3 (DE-576)346641179 2045-2322 nnns, volume:7 year:2017 extent:11, http://dx.doi.org/10.1038/s41598-017-12986-0 Verlag Resolving-System kostenfrei Volltext, https://www.nature.com/articles/s41598-017-12986-0 Verlag kostenfrei Volltext, http://dx.doi.org/10.1038/s41598-017-12986-0 LFER, LFER 2018-09-13T00:00:00Z |
| spellingShingle | Chan, Man K., Rietschel, Marcella, Associations between SNPs and immune-related circulating proteins in schizophrenia, Genome-wide association studies (GWAS) and proteomic studies have provided convincing evidence implicating alterations in immune/inflammatory processes in schizophrenia. However, despite the convergence of evidence, direct links between the genetic and proteomic findings are still lacking for schizophrenia. We investigated associations between single nucleotide polymorphisms (SNPs) from the custom-made PsychArray and the expression levels of 190 multiplex immunoassay profiled serum proteins in 149 schizophrenia patients and 198 matched controls. We identified associations between 81 SNPs and 29 proteins, primarily involved in immune/inflammation responses. Significant SNPxDiagnosis interactions were identified for eight serum proteins including Factor-VII[rs555212], Alpha-1-Antitrypsin[rs11846959], Interferon-Gamma Induced Protein 10[rs4256246] and von-Willebrand-Factor[rs12829220] in the control group; Chromogranin-A[rs9658644], Cystatin-C[rs2424577] and Vitamin K-Dependent Protein S[rs6123] in the schizophrenia group; Interleukin-6 receptor[rs7553796] in both the control and schizophrenia groups. These results suggested that the effect of these SNPs on expression of the respective proteins varies with diagnosis. The combination of patient-specific genetic information with blood biomarker data opens a novel approach to investigate disease mechanisms in schizophrenia and other psychiatric disorders. Our findings not only suggest that blood protein expression is influenced by polymorphisms in the corresponding gene, but also that the effect of certain SNPs on expression of proteins can vary with diagnosis. |
| swb_id_str | 510260632 |
| title | Associations between SNPs and immune-related circulating proteins in schizophrenia |
| title_auth | Associations between SNPs and immune-related circulating proteins in schizophrenia |
| title_full | Associations between SNPs and immune-related circulating proteins in schizophrenia Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel and Sabine Bahn |
| title_fullStr | Associations between SNPs and immune-related circulating proteins in schizophrenia Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel and Sabine Bahn |
| title_full_unstemmed | Associations between SNPs and immune-related circulating proteins in schizophrenia Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel and Sabine Bahn |
| title_in_hierarchy | Associations between SNPs and immune-related circulating proteins in schizophrenia / Man K. Chan, Jason D. Cooper, Stefanie Heilmann-Heimbach, Josef Frank, Stephanie H. Witt, Markus M. Nöthen, Johann Steiner, Marcella Rietschel and Sabine Bahn, |
| title_short | Associations between SNPs and immune-related circulating proteins in schizophrenia |
| title_sort | associations between snps and immune related circulating proteins in schizophrenia |
| url | http://dx.doi.org/10.1038/s41598-017-12986-0, https://www.nature.com/articles/s41598-017-12986-0 |