4.7 Article

Circulating microRNA 134 sheds light on the diagnosis of major depressive disorder

期刊

TRANSLATIONAL PSYCHIATRY
卷 10, 期 1, 页码 -

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NATURE PUBLISHING GROUP
DOI: 10.1038/s41398-020-0773-2

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资金

  1. National Key R&D Program of China [2017YFA0505700]
  2. Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences [2019PT320002]
  3. Natural Science Foundation Project of China [81820108015, 81701360, 81601208, 81601207]
  4. Chongqing Science & Technology Commission [cstc2017jcyjAX0377]
  5. Chongqing Yuzhong District Science & Technology Commission [20190115]
  6. Joint International Research Laboratory of Reproduction & Development, Institute of Life Sciences, Chongqing Medical University, Chongqing, China
  7. Scientific Research and Innovation Experiment Project of Chongqing Medical University [CXSY201862, CXSY201863]

向作者/读者索取更多资源

Major depressive disorder (MDD) is a prevalent and debilitating psychiatric mood disorder that lacks objective laboratory-based tests to support its diagnosis. A class of microRNAs (miRNAs) has been found to be centrally involved in regulating many molecular processes fundamental to central nervous system function. Among these miRNAs, miRNA-134 (miR-134) has been reported to be related to neurogenesis and synaptic plasticity. In this study, the hypothesis that plasma miR-134 can be used to diagnose MDD was tested. Perturbation of peripheral and central miR-134 in a depressive-like rat model was also examined. By reverse-transcription quantitative PCR, miR-134 was comparatively measured in a small set of plasma samples from MDD and healthy control (HC) subjects. To determine its diagnostic efficacy, plasma miR-134 levels were assessed in 100 MDD, 50 bipolar disorder (BD), 50 schizophrenic (SCZ), and 100 HC subjects. A chronic unpredictable mild stress (CUMS) rat model was also developed to evaluate miR-134 expression in plasma, hippocampus (HIP), prefrontal cortex (PFC), and olfactory bulb. We found that plasma miR-134 was significantly downregulated in MDD subjects. Diagnostically, plasma miR-134 levels could effectively distinguish MDD from HC with 79% sensitivity and 84% specificity, while distinguishing MDD from HC, BD, and SCZ subjects with 79% sensitivity and 76.5% specificity. Congruent with these clinical findings, CUMS significantly reduced miR-134 levels in the rat plasma, HIP, and PFC. Although limited by the relatively small sample size, these results demonstrated that plasma miR-134 displays potential ability as a biomarker for MDD.

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