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Perturbations of Circulating miRNAs in Irritable Bowel Syndrome Detected Using a Multiplexed High-throughput Gene Expression Platform
Published on: November 30, 2016
Circulating microRNA 134 sheds light on the diagnosis of major depressive disorder
Han-Ping Zhang1,2, Xiao-Lei Liu3, Jian-Jun Chen4
1Department of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, 400016, China.
Abstract:
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.
Insights
Plasma miR-134 levels are significantly lower in major depressive disorder (MDD) patients. This microRNA shows potential as a diagnostic biomarker for MDD, distinguishing it from healthy controls and other psychiatric disorders.
Area of Science:
- Neuroscience
- Molecular Biology
- Psychiatry
Background:
- Major Depressive Disorder (MDD) lacks objective diagnostic tests.
- MicroRNAs (miRNAs), including miRNA-134 (miR-134), are involved in central nervous system regulation.
- miR-134 is linked to neurogenesis and synaptic plasticity.
Purpose of the Study:
- To investigate plasma miR-134 as a diagnostic biomarker for MDD.
- To examine miR-134 perturbations in a rat model of depression.
Main Methods:
- Reverse-transcription quantitative PCR (RT-qPCR) to measure plasma miR-134.
- Analysis of plasma samples from MDD, healthy controls (HC), bipolar disorder (BD), and schizophrenia (SCZ) patients.
- Utilized a chronic unpredictable mild stress (CUMS) rat model to assess miR-134 in plasma and brain regions (hippocampus, prefrontal cortex).
Main Results:
- Plasma miR-134 was significantly downregulated in MDD patients compared to HC.
- Plasma miR-134 distinguished MDD from HC with 79% sensitivity and 84% specificity.
- Plasma miR-134 differentiated MDD from HC, BD, and SCZ with 79% sensitivity and 76.5% specificity.
- CUMS significantly reduced miR-134 levels in rat plasma, hippocampus, and prefrontal cortex.
Conclusions:
- Plasma miR-134 demonstrates potential as a biomarker for diagnosing MDD.
- miR-134 dysregulation in plasma and brain correlates with depressive-like states.
- Further research with larger sample sizes is warranted to validate these findings.
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