Faculty of Science, Centre for Neuroscience, Department of Molecular Animal Physiology, Donders Institute for Brain, Cognition and Behavior, Radboud University Nijmegen, Geert Grooteplein Zuid 26-28, 6525 GA, Nijmegen, The Netherlands.
Sorbonne Université, Paris Brain Institute - ICM, Inserm U1127, CNRS UMR 7225, Hôpital Pitié-Salpêtrière, Paris, France.
Transl Psychiatry. 2020 Nov 12;10(1):399. doi: 10.1038/s41398-020-01084-x.
Schizophrenia (SZ) is a psychiatric disorder with a convoluted etiology that includes cognitive symptoms, which arise from among others a dysfunctional dorsolateral prefrontal cortex (dlPFC). In our search for the molecular underpinnings of the cognitive deficits in SZ, we here performed RNA sequencing of gray matter from the dlPFC of SZ patients and controls. We found that the differentially expressed RNAs were enriched for mRNAs involved in the Liver X Receptor/Retinoid X Receptor (LXR/RXR) lipid metabolism pathway. Components of the LXR/RXR pathway were upregulated in gray matter but not in white matter of SZ dlPFC. Intriguingly, an analysis for shared genetic etiology, using two SZ genome-wide association studies (GWASs) and GWAS data for 514 metabolites, revealed genetic overlap between SZ and acylcarnitines, VLDL lipids, and fatty acid metabolites, which are all linked to the LXR/RXR signaling pathway. Furthermore, analysis of structural T-weighted magnetic resonance imaging in combination with cognitive behavioral data showed that the lipid content of dlPFC gray matter is lower in SZ patients than in controls and correlates with a tendency towards reduced accuracy in the dlPFC-dependent task-switching test. We conclude that aberrations in LXR/RXR-regulated lipid metabolism lead to a decreased lipid content in SZ dlPFC that correlates with reduced cognitive performance.
精神分裂症(SZ)是一种具有复杂病因的精神疾病,包括认知症状,这些症状源自功能失调的背外侧前额叶皮层(dlPFC)等。在我们寻找 SZ 认知缺陷的分子基础的过程中,我们对 SZ 患者和对照组的 dlPFC 灰质进行了 RNA 测序。我们发现差异表达的 RNA 富集了参与肝 X 受体/视黄醇 X 受体(LXR/RXR)脂质代谢途径的 mRNAs。LXR/RXR 途径的成分在 SZ dlPFC 的灰质中上调,但在白质中没有上调。有趣的是,使用两项 SZ 全基因组关联研究(GWAS)和 514 种代谢物的 GWAS 数据进行的共享遗传病因分析显示,SZ 与酰基辅酶 A、VLDL 脂质和脂肪酸代谢物之间存在遗传重叠,这些都与 LXR/RXR 信号通路有关。此外,对结构 T1 加权磁共振成像与认知行为数据的分析表明,SZ 患者 dlPFC 灰质中的脂质含量低于对照组,并且与 dlPFC 依赖的任务转换测试中准确性降低的趋势相关。我们得出结论,LXR/RXR 调节的脂质代谢异常导致 SZ dlPFC 中的脂质含量降低,这与认知表现下降有关。