首页> 外文期刊>Schizophrenia research >Association study of functional polymorphisms in interleukins and interleukin receptors genes: IL1A, IL1B, IL1RN, IL6, IL6R, IL10, IL10RA and TGFB1 in schizophrenia in Polish population
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Association study of functional polymorphisms in interleukins and interleukin receptors genes: IL1A, IL1B, IL1RN, IL6, IL6R, IL10, IL10RA and TGFB1 in schizophrenia in Polish population

机译:波兰人群精神分裂症中白介素和白介素受体基因功能基因多态性的关联研究:IL1A,IL1B,IL1RN,IL6,IL6R,IL10,IL10RA和TGFB1

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Schizophrenia has been associated with a large range of autoimmune diseases, with a history of any autoimmune disease being associated with a 45% increase in risk for the illness. The inflammatory system may trigger or modulate the course of schizophrenia through complex mechanisms influencing neurodevelopment, neuroplasticity and neurotransmission. In particular, increases or imbalance in cytokine before birth or during the early stages of life may affect neurodevelopment and produce vulnerability to the disease. A total of 27 polymorphisms of IL1N gene: rs1800587, rs17561; IL1B gene: rs1143634, rs1143643, rs16944, rs4848306, rs1143623, rs1143633, rs1143627; IL1RN gene: rs419598, rs315952, rs9005, rs4251961; IL6 gene: rs1800795, rs1800797; IL6R gene: rs4537545, rs4845617, rs2228145, IL10 gene: rs1800896, rs1800871, rs1800872, rs1800890, rs6676671; IL10RA gene: rs2229113, rs3135932; TGF1B gene: rs1800469, rs1800470; each selected on the basis of molecular evidence for functionality, were investigated in this study. Analysis was performed on a group of 621 patients with diagnosis of schizophrenia and 531 healthy controls in Polish population. An association of rs4848306 in IL1B gene, rs4251961 in IL1RN gene, rs2228145 and rs4537545 in IL6R with schizophrenia have been observed. rs6676671 in IL10 was associated with early age of onset. Strong linkage disequilibrium was observed between analyzed polymorphisms in each gene, except of IL10RA. We observed that haplotypes composed of rs4537545 and rs2228145 in IL6R gene were associated with schizophrenia. Analyses with family history of schizophrenia, other psychiatric disorders and alcohol abuse/dependence did not show any positive findings. Further studies on larger groups along with correlation with circulating protein levels are needed. (C) 2015 Elsevier B.V. All rights reserved.
机译:精神分裂症与多种自身免疫性疾病有关,任何自身免疫性疾病的病史都与患该疾病的风险增加45%有关。炎症系统可能通过影响神经发育,神经可塑性和神经传递的复杂机制触发或调节精神分裂症的病程。特别是,在出生前或生命的早期阶段,细胞因子的增加或失衡可能会影响神经发育并产生对该疾病的脆弱性。 IL1N基因共有27个多态性:rs1800587,rs17561; IL1B基因:rs1143634,rs1143643,rs16944,rs4848306,rs1143623,rs1143633,rs1143627; IL1RN基因:rs419598,rs315952,rs9005,rs4251961; IL6基因:rs1800795,rs1800797; IL6R基因:rs4537545,rs4845617,rs2228145,IL10基因:rs1800896,rs1800871,rs1800872,rs1800890,rs6676671; IL10RA基因:rs2229113,rs3135932; TGF1B基因:rs1800469,rs1800470;在这项研究中对每种均基于功能性的分子证据进行选择。在波兰人群中,对诊断为精神分裂症的621例患者和531名健康对照者进行了分析。已经观察到IL1B基因中的rs4848306,IL1RN基因中的rs4251961,IL6R中的rs2228145和rs4537545与精神分裂症的关联。 IL10中的rs6676671与发病初期有关。除IL10RA外,每个基因的分析多态性之间均观察到强连锁不平衡。我们观察到IL6R基因中由rs4537545和rs2228145组成的单倍型与精神分裂症有关。对精神分裂症,其他精神疾病和酗酒/依赖性的家族病史进行的分析未显示任何阳性结果。需要对更大的群体进行进一步研究,并与循环蛋白水平相关。 (C)2015 Elsevier B.V.保留所有权利。

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