Golimbet V E, Korovaĭtseva G I, Gabaeva M V, Velikaia N V, Snegireva A A, Kasparov S V, Kolesina N Iu, Ganisheva T K, Savel'eva T M
Zh Nevrol Psikhiatr Im S S Korsakova. 2014;114(5):46-9.
Neurotoxic metabolites of the kynurenine pathway are thought to be implicated in the pathogenesis of schizophrenia. The enzyme indoleamine 2,3-dioxygenase (IDO) catalyzes the initial step of the kynurenine pathway that converts tryptophan to kynurenine metabolites. IDO is induced by proinflammatory cytokines. We studied IL-1Β T-511C (rs16944), IL-1Β C3954T (rs1143634), IDO VNTR and IDO rs9657182 polymorphisms in patients with schizophrenia and controls.
Genotyping was performed in 296 patients with schizophrenia (ICD-10 F20.0) and 355 healthy controls.
The multiple dimension reduction (MDR) analysis revealed a combination included alleles С (T-511C), Т (C3954T), V1 (VNTR) and С (rs9657182), which was associated with schizophrenia (OR 3,3 CI 95% 2,3-4,8).
This is the first report of the interaction between IL-1Β and IDO genes. Further research into genes of the kynurenine pathway is needed.
犬尿氨酸途径的神经毒性代谢产物被认为与精神分裂症的发病机制有关。吲哚胺2,3-双加氧酶(IDO)催化犬尿氨酸途径的第一步,该步骤将色氨酸转化为犬尿氨酸代谢产物。IDO由促炎细胞因子诱导。我们研究了精神分裂症患者和对照组中白细胞介素-1β T-511C(rs16944)、白细胞介素-1β C3954T(rs1143634)、IDO可变数目串联重复序列(VNTR)以及IDO rs9657182基因多态性。
对296例精神分裂症患者(国际疾病分类第十版F20.0)和355名健康对照者进行基因分型。
多维度约简(MDR)分析显示,一个包含等位基因C(T-511C)、T(C3954T)、V1(VNTR)和C(rs9657182)的组合与精神分裂症相关(比值比3.3,95%置信区间2.3 - 4.8)。
这是白细胞介素-1β和IDO基因之间相互作用的首次报道。需要对犬尿氨酸途径的基因进行进一步研究。