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. 2019 Jul 26;126(9):1241–1258. doi: 10.1007/s00702-019-02048-2

Table 4.

Summary of miRNAs modulated by antidepressant drugs in human samples

miRNAs Samples/tissue Antidepressant drug Results References

miR-16

miR-30

miR-34

miR-128

miR-132

miR-134

miR-182

miR-183

miR-185

miR-212

Serum Different SSRI and SNRI (4 weeks of treatment) In patients treated with SSRI, miR-16, miR-183, and miR-212 levels increased significantly after 4 weeks of antidepressant treatment Lin et al. (2018)

miR-451a

miR-34a-5p

miR-221-3p

Serum Paroxetine (8 weeks of treatment) Depressed patients had lower serum miRNA-451a, and higher serum miRNA-34a-5p and miRNA-221-3p as compared to controls; miRNA-34a-5p and miRNA-221-3p decreased, whereas miRNA-451a increased after paroxetine treatment Kuang et al. (2018)

miR-151a-3p

miR-221/222

In silico study SSRI (paroxetine) miR-151a-3p, miR-221/222, and their respective target genes, CHL1 and ITGB3, are implicated in the response to SSRI Oved et al. (2017)

miR-130b

miR-26a/26b

let-7f

miR-770-5p

miR-34c-5p

Human U87 glioblastoma cells Escitalopram (24, 48, 72 h) Significant increase in let-7f, after both 48 h and 72 h and of miR-26a after 48 h of treatment Maffioletti et al. (2017)

miR-146a-5p

miR-146b-5p

miR-425-3p

miR-24-3p

Blood cells Duloxetine (8 weeks of treatment) Differential expression of miR-146a-5p, miR-146b-5p, miR-425-3p, and miR-24-3p according to treatment response Lopez et al. (2017)

miR-1202

miR-135a

miR-16

Blood cells Escitalopram or Desvenlafaxine or Duloxetine (8 weeks of treatment) In two different cohorts, responders displayed lower baseline miR-1202 levels compared with non-responders; miR-1202 levels increased after 8 weeks of antidepressant treatment Fiori et al. (2017)
miR-1202 Blood cells Desvenlafaxine (8 weeks of treatment) Changes in peripheral miR-1202 levels were associated with changes in brain regions associated with depression and antidepressant response Lopez et al. (2017)

miR-572

miR-663a

Neuroblastoma cell lines Fluoxetine (24 h) Fluoxetine increased the expression of both miR-572 and miR-663a Mundalil Vasu et al. (2016)
414 miRNAs Blood cells and PBMC Citalopram (8 weeks of treatment) 414 miRNAs modulated highly correlated set of genes (modules) which are associated with clinical improvements. Belzeaux et al. (2016)
222 miRNAs RNA from plasma Escitalopram (12 weeks of treatment) Of 222 miRNAs, 40 miRNAs were differently expressed after treatment; 23 significantly over-expressed and 17 down-regulated Enatescu et al. (2016)
miR-124 PBMC Different antidepressant drugs (8 weeks of treatment) The expression level of miR-124 was significantly down-regulated after antidepressant drug treatment He et al. (2016)
miR-355 Blood cells Citalopram (4 weeks of treatment) Citalopram up-regulated miR-335 expression and down-regulated GRM4 mRNA levels Li et al. (2015)
miR-135 Blood cells Escitalopram (12 weeks of treatment) Trend for higher expression after CBT vs escitalopram Issler et al. (2014)
miR-1202 Human Neural Progenitor cells (NPCs) and blood cells Citalopram or Imipramine (24 h or 15 days for NPCs; 8 weeks of treatment for depressed subjects) MiR-1202 was up-regulated in NPCs after acute treatment with both citalopram and imipramine. Moreover, remitter depressed patients showed an up-regulation of miR-1202 after citalopram treatment Lopez et al. (2014)

miR-221

miR-222

Human Lymphoblastoid cell lines Paroxetine (21 days of treatment) Decreased expression of miR-221 and miR-222 after paroxetine treatment Oved et al. (2013)
30 miRNAs Blood cells Escitalopram (12 weeks of treatment) Identification of 30 miRNAs modulated by antidepressant treatment: 28 miRNAs were up-regulated, and 2 miRNAs were down-regulated Bocchio-Chiavetto et al. (2013)
42 miRNAs Human Lymphoblastoid cell lines Paroxetine (3 days of treatment) Of the 42 miRNAs, 19 had higher expression levels in the LCLs with high sensitivity to paroxetine Oved et al. (2012)

miR-145

miR-20b

PBMC Different antidepressant drugs (8 weeks of treatment) Increased miRNAs levels during treatment only in responder patients Belzeaux et al. (2012)