Association between psychiatric admissions in patients with schizophrenia and IL-6 plasma levels polygenic score

被引:4
作者
Facal, Fernando [1 ,2 ]
Arrojo, Manuel [1 ,2 ]
Paramo, Mario [1 ,2 ]
Costas, Javier [1 ]
机构
[1] Complexo Hosp Univ Santiago de Compostela CHUS, Inst Invest Sanitaria IDIS Santiago de Compostela, Serv Galego Saude SERGAS, Hosp Clin Univ, Edificio Consultas,Andar 2, Santiago De Compostela 15706, Galicia, Spain
[2] Complexo Hosp Univ Santiago de Compostela, Serv Galego Saude SERGAS, Serv Psiquiatria, Santiago De Compostela, Galicia, Spain
关键词
Psychosis; Chronicity; Cytokines; Inflammation; Immunity; SERUM CYTOKINE LEVELS; C-REACTIVE PROTEIN; 1ST-EPISODE PSYCHOSIS; INTERLEUKIN-6; RISK; METAANALYSIS; TOCILIZUMAB; SYMPTOMS; INSIGHTS; RECEPTOR;
D O I
10.1007/s00406-024-01786-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Schizophrenia diagnosis and admission history were associated with a polygenic score (PGS) for schizophrenia based on a subset of variants that act by modifying the expression of genes whose expression is also modified by antipsychotics. This gene set was enriched in cytokine production. Interleukin-6 (IL-6) is the only cytokine whose plasma levels were associated both with schizophrenia diagnosis and with acute decompensations in the largest meta-analysis. Therefore, we hypothesized that an IL-6 PGS, but not other cytokines PGSs, would be associated with schizophrenia chronicity/psychiatric admissions. Using the IL-6 PGS model from The PGS Catalog, IL-6 PGS was calculated in 427 patients with schizophrenia and data regarding admission history. Association between IL-6 PGS and chronicity, measured as number and duration of psychiatric admissions, or ever readmission was analyzed by multivariate ordinal and logistic regression, respectively. Specificity of results was assessed by analysis of PGSs from the other cytokines at The PGS Catalog with meta-analytic evidence of association with schizophrenia diagnosis or acute decompensations, IL-1RA, IL-4, IL-8, and IL-12. IL-6 PGS was associated with schizophrenia chronicity, explaining 1.51% of variability (OR = 1.29, 95% CI 1.07-1.55, P = 0.007). There was no association with ever readmission. Other cytokines PGSs were not associated with chronicity. Association with IL-6 PGS was independent of association with schizophrenia PGS. Our results provide evidence that genetically regulated higher levels of IL-6 are involved in schizophrenia chronicity, highlighting the relevance of immunity processes for a subgroup of patients.
引用
收藏
页码:1671 / 1679
页数:9
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