Research Unit of Molecular Epidemiology, Helmholtz Zentrum München, Neuherberg, Germany.
Transl Psychiatry. 2012 Aug 14;2(8):e149. doi: 10.1038/tp.2012.76.
Schizophrenia is a severe complex mental disorder affecting 0.5-1% of the world population. To date, diagnosis of the disease is mainly based on personal and thus subjective interviews. The underlying molecular mechanism of schizophrenia is poorly understood. Using targeted metabolomics we quantified and compared 103 metabolites in plasma samples from 216 healthy controls and 265 schizophrenic patients, including 52 cases that do not take antipsychotic medication. Compared with healthy controls, levels of five metabolites were found significantly altered in schizophrenic patients (P-values ranged from 2.9 × 10(-8) to 2.5 × 10(-4)) and in neuroleptics-free probands (P-values ranging between 0.006 and 0.03), respectively. These metabolites include four amino acids (arginine, glutamine, histidine and ornithine) and one lipid (PC ae C38:6) and are suggested as candidate biomarkers for schizophrenia. To explore the genetic susceptibility on the associated metabolic pathways, we constructed a molecular network connecting these five aberrant metabolites with 13 schizophrenia risk genes. Our result implicated aberrations in biosynthetic pathways linked to glutamine and arginine metabolism and associated signaling pathways as genetic risk factors, which may contribute to patho-mechanisms and memory deficits associated with schizophrenia. This study illustrated that the metabolic deviations detected in plasma may serve as potential biomarkers to aid diagnosis of schizophrenia.
精神分裂症是一种严重的复杂精神障碍,影响全球 0.5-1%的人口。迄今为止,该疾病的诊断主要基于个人,因此是主观的访谈。精神分裂症的潜在分子机制尚未完全了解。使用靶向代谢组学,我们定量比较了 216 名健康对照者和 265 名精神分裂症患者的血浆样本中的 103 种代谢物,其中包括 52 名未服用抗精神病药物的患者。与健康对照者相比,在精神分裂症患者(P 值范围从 2.9×10(-8)到 2.5×10(-4)) 和未服用抗精神病药物的患者(P 值范围从 0.006 到 0.03)中,发现五种代谢物的水平显著改变。这些代谢物包括四种氨基酸(精氨酸、谷氨酰胺、组氨酸和鸟氨酸)和一种脂质(PC ae C38:6),并被认为是精神分裂症的候选生物标志物。为了探索相关代谢途径的遗传易感性,我们构建了一个分子网络,将这五种异常代谢物与 13 个精神分裂症风险基因连接起来。我们的结果表明,与谷氨酰胺和精氨酸代谢以及相关信号通路相关的生物合成途径的异常可能是遗传风险因素,这些因素可能导致与精神分裂症相关的病理机制和记忆缺陷。本研究表明,血浆中检测到的代谢偏差可作为辅助精神分裂症诊断的潜在生物标志物。