Department of Pharmacology, Escola Paulista de Medicina (EPM), Universidade Federal de São Paulo (UNIFESP), Rua 3 de maio 100, Ed. INFAR, 3rd floor, SP CEP 04044-020, Brazil; National Institute for Translational Medicine (INCT-TM, CNPq/FAPESP/CAPES), Ribeirão Preto, Brazil.
ALCEDIAG/Sys2Diag, CNRS UMR 9005, Parc Euromédecine, 1682 rue de la Valsière, Montpellier 34184, France.
Psychiatry Res. 2023 Oct;328:115422. doi: 10.1016/j.psychres.2023.115422. Epub 2023 Aug 18.
Bipolar disorder (BD) is a worldwide leading cause of disability. Inflammation roles in this disease is well established. ADAR1-mediated RNA editing is one of the key mechanisms regulating the inflammatory response. We have identified a panel of RNA editing-based blood biomarkers which allowed to discriminate unipolar from BD depression with high accuracy. We confirmed here the diagnostic value of this panel in a new cohort of BD patients recruited in Brazil. We also identified new combinations which allow a clear discrimination of BD from healthy controls and among BD subgroups, confirming that RNA editing is a key mechanism in BD.
双相情感障碍 (BD) 是全球范围内导致残疾的主要原因。炎症在这种疾病中的作用已得到充分证实。ADAR1 介导的 RNA 编辑是调节炎症反应的关键机制之一。我们已经确定了一组基于 RNA 编辑的血液生物标志物,这些标志物可以高精度地区分单相和双相情感障碍的抑郁。我们在这里证实了该标志物在巴西新招募的双相情感障碍患者队列中的诊断价值。我们还确定了新的组合,这些组合可以清楚地区分双相情感障碍与健康对照组以及双相情感障碍亚组之间的差异,证实了 RNA 编辑是双相情感障碍的关键机制。