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微小RNA在监测抗抑郁药治疗反应中的潜在应用

Potential Use of MicroRNA for Monitoring Therapeutic Response to Antidepressants.

作者信息

Belzeaux Raoul, Lin Rixing, Turecki Gustavo

机构信息

McGill Group for Suicide Studies, Douglas Mental Health University Institute, McGill University, 6875 boulevard LaSalle, Montreal, QC, H4H 1R3, Canada.

出版信息

CNS Drugs. 2017 Apr;31(4):253-262. doi: 10.1007/s40263-017-0418-z.

DOI:10.1007/s40263-017-0418-z
PMID:28290081
Abstract

Major depressive disorder (MDD) is a serious and common psychiatric disorder that affects millions of people worldwide. The most common treatment methods for MDD are antidepressant drugs, many of which act by regulating monoamines by inhibiting pre-synaptic reuptake and/or by modulating monoamine receptors. Despite advances in antidepressants and other treatment options, therapy is often based on subjective decisions made by the physician. Moreover, it requires time to determine treatment outcome and to define whether the prescribed treatment is effective. Biomarkers may help identify individuals with MDD who are more likely to respond to specific antidepressant treatment and may thus provide more objectivity in treatment decision making. MicroRNA as biomarkers of antidepressant response has engendered substantial enthusiasm. In this review, we give a detailed overview of biomarkers, particularly the major studies that have investigated microRNA in relationship to antidepressant treatment response.

摘要

重度抑郁症(MDD)是一种严重且常见的精神疾病,影响着全球数百万人。MDD最常见的治疗方法是抗抑郁药物,其中许多药物通过抑制突触前再摄取和/或调节单胺受体来调节单胺起作用。尽管抗抑郁药和其他治疗选择取得了进展,但治疗往往基于医生做出的主观决定。此外,确定治疗结果并定义所开处方的治疗是否有效需要时间。生物标志物可能有助于识别更有可能对特定抗抑郁治疗产生反应的MDD患者,从而在治疗决策中提供更多客观性。作为抗抑郁反应生物标志物的微小RNA引起了广泛关注。在本综述中,我们详细概述了生物标志物,特别是研究微小RNA与抗抑郁治疗反应关系的主要研究。

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本文引用的文献

1
Co-Variation of Peripheral Levels of miR-1202 and Brain Activity and Connectivity During Antidepressant Treatment.抗抑郁治疗期间外周血 miR-1202 水平与脑活动及脑连接的共同变化
Neuropsychopharmacology. 2017 Sep;42(10):2043-2051. doi: 10.1038/npp.2017.9. Epub 2017 Jan 12.
2
A genetic variant in miRNA binding site of glutamate receptor 4, metabotropic (GRM4) is associated with increased risk of major depressive disorder.代谢型谷氨酸受体4(GRM4)的微小RNA结合位点中的一种基因变异与重度抑郁症风险增加有关。
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DCC Confers Susceptibility to Depression-like Behaviors in Humans and Mice and Is Regulated by miR-218.
逃离压力:运动诱导的小细胞外囊泡对重度抑郁症患者潜在益处的视角
Front Mol Biosci. 2023 Jun 15;10:1154872. doi: 10.3389/fmolb.2023.1154872. eCollection 2023.
4
Habenula as a Possible Target for Treatment-Resistant Depression Phenotype in Wistar Kyoto Rats.缰核作为 Wistar Kyoto 大鼠治疗抵抗性抑郁表型的可能靶点。
Mol Neurobiol. 2023 Feb;60(2):643-654. doi: 10.1007/s12035-022-03103-y. Epub 2022 Nov 8.
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miRNAs as potential diagnostic biomarkers and pharmacogenomic indicators in psychiatric disorders.miRNAs 作为精神障碍的潜在诊断生物标志物和药物基因组学指标。
Pharmacogenomics J. 2022 Jul;22(4):211-222. doi: 10.1038/s41397-022-00283-7. Epub 2022 Jun 20.
6
MicroRNA Let-7e in the Mouse Prefrontal Cortex Differentiates Restraint-Stress-Resilient Genotypes from Susceptible Genotype.小鼠前额皮质中的 microRNA Let-7e 将应激易感性基因型与应激抗性基因型区分开来。
Int J Mol Sci. 2021 Aug 30;22(17):9439. doi: 10.3390/ijms22179439.
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Cells. 2021 Jun 29;10(7):1630. doi: 10.3390/cells10071630.
8
The Importance of Epigenetics in Diagnostics and Treatment of Major Depressive Disorder.表观遗传学在重度抑郁症诊断与治疗中的重要性
J Pers Med. 2021 Mar 1;11(3):167. doi: 10.3390/jpm11030167.
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Identification of MicroRNA-124-3p as a Putative Epigenetic Signature of Major Depressive Disorder.鉴定MicroRNA-124-3p作为重度抑郁症的一种潜在表观遗传特征
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J Psychiatr Res. 2016 Nov;82:58-67. doi: 10.1016/j.jpsychires.2016.07.012. Epub 2016 Jul 18.