TY - JOUR
T1 - Blood microRNA changes in depressed patients during antidepressant treatment
AU - Bocchio-Chiavetto, Luisella
AU - Maffioletti, Elisabetta
AU - Bettinsoli, Paola
AU - Giovannini, Caterina
AU - Bignotti, Stefano
AU - Tardito, Daniela
AU - Corrada, Dario
AU - Milanesi, Luciano
AU - Gennarelli, Massimo
PY - 2013/7
Y1 - 2013/7
N2 - MicroRNAs (miRNAs) are potent modulators of protein expression that play key roles in brain pathways regulating neurogenesis and synaptic plasticity. These small RNAs may be critical for the pathophysiology of mental disorders and may influence the effectiveness of psychotropic drugs. To investigate the possible involvement of miRNAs in the mechanism of action of antidepressants (AD), we conducted a whole-miRNome quantitative analysis with qRT-PCR of the changes in the blood of 10 depressed subjects after 12 weeks of treatment with escitalopram. Thirty miRNAs were differentially expressed after the AD treatment: 28 miRNAs were up-regulated, and 2 miRNAs were strongly down-regulated. miRNA target gene prediction and functional annotation analysis showed that there was a significant enrichment in several pathways associated with neuronal brain function (such as neuroactive ligand-receptor interaction, axon guidance, long-term potentiation and depression), supporting the hypothesis that the differentially regulated miRNAs may be involved in the AD mechanism.
AB - MicroRNAs (miRNAs) are potent modulators of protein expression that play key roles in brain pathways regulating neurogenesis and synaptic plasticity. These small RNAs may be critical for the pathophysiology of mental disorders and may influence the effectiveness of psychotropic drugs. To investigate the possible involvement of miRNAs in the mechanism of action of antidepressants (AD), we conducted a whole-miRNome quantitative analysis with qRT-PCR of the changes in the blood of 10 depressed subjects after 12 weeks of treatment with escitalopram. Thirty miRNAs were differentially expressed after the AD treatment: 28 miRNAs were up-regulated, and 2 miRNAs were strongly down-regulated. miRNA target gene prediction and functional annotation analysis showed that there was a significant enrichment in several pathways associated with neuronal brain function (such as neuroactive ligand-receptor interaction, axon guidance, long-term potentiation and depression), supporting the hypothesis that the differentially regulated miRNAs may be involved in the AD mechanism.
KW - Antidepressant
KW - Blood
KW - Escitalopram
KW - Major depression
KW - MicroRNA
KW - MiRNA
UR - http://www.scopus.com/inward/record.url?scp=84878881944&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84878881944&partnerID=8YFLogxK
U2 - 10.1016/j.euroneuro.2012.06.013
DO - 10.1016/j.euroneuro.2012.06.013
M3 - Article
C2 - 22925464
AN - SCOPUS:84878881944
VL - 23
SP - 602
EP - 611
JO - European Neuropsychopharmacology
JF - European Neuropsychopharmacology
SN - 0924-977X
IS - 7
ER -