TY - JOUR
T1 - Transcriptional biomarkers of response to pharmacological treatments in severe mental disorders
T2 - A systematic review
AU - Pisanu, Claudia
AU - Severino, Giovanni
AU - De Toma, Ilario
AU - Dierssen, Mara
AU - Fusar-Poli, Paolo
AU - Gennarelli, Massimo
AU - Lio, Pietro
AU - Maffioletti, Elisabetta
AU - Maron, Eduard
AU - Mehta, Divya
AU - Minelli, Alessandra
AU - Potier, Marie-Claude
AU - Serretti, Alessandro
AU - Stacey, David
AU - van Westrhenen, Roos
AU - Xicota, Laura
AU - Baune, Bernhard T
AU - Squassina, Alessio
AU - European College of Neuropsychopharmacology (ECNP) Pharmacogenomics & Transcriptomics Network
N1 - Copyright © 2021. Published by Elsevier B.V.
PY - 2022/2
Y1 - 2022/2
N2 - Variation in the expression level and activity of genes involved in drug disposition and action in tissues of pharmacological importance have been increasingly investigated in patients treated with psychotropic drugs. Findings are promising, but reliable predictive biomarkers of response have yet to be identified. Here we conducted a PRISMA-compliant systematic search of PubMed, Scopus and PsycInfo up to 12 September 2020 for studies investigating RNA expression levels in cells or biofluids from patients with major depressive disorder, schizophrenia or bipolar disorder characterized for response to psychotropic drugs (antidepressants, antipsychotics or mood stabilizers) or adverse effects. Among 5497 retrieved studies, 123 (63 on antidepressants, 33 on antipsychotics and 27 on mood stabilizers) met inclusion criteria. Studies were either focused on mRNAs (n = 96), microRNAs (n = 19) or long non-coding RNAs (n = 1), with only a minority investigating both mRNAs and microRNAs levels (n = 7). The most replicated results include genes playing a role in inflammation (antidepressants), neurotransmission (antidepressants and antipsychotics) or mitochondrial function (mood stabilizers). Compared to those investigating response to antidepressants, studies focused on antipsychotics or mood stabilizers more often showed lower sample size and lacked replication. Strengths and limitations of available studies are presented and discussed in light of the specific designs, methodology and clinical characterization of included patients for transcriptomic compared to DNA-based studies. Finally, future directions of transcriptomics of psychopharmacological interventions in psychiatric disorders are discussed.
AB - Variation in the expression level and activity of genes involved in drug disposition and action in tissues of pharmacological importance have been increasingly investigated in patients treated with psychotropic drugs. Findings are promising, but reliable predictive biomarkers of response have yet to be identified. Here we conducted a PRISMA-compliant systematic search of PubMed, Scopus and PsycInfo up to 12 September 2020 for studies investigating RNA expression levels in cells or biofluids from patients with major depressive disorder, schizophrenia or bipolar disorder characterized for response to psychotropic drugs (antidepressants, antipsychotics or mood stabilizers) or adverse effects. Among 5497 retrieved studies, 123 (63 on antidepressants, 33 on antipsychotics and 27 on mood stabilizers) met inclusion criteria. Studies were either focused on mRNAs (n = 96), microRNAs (n = 19) or long non-coding RNAs (n = 1), with only a minority investigating both mRNAs and microRNAs levels (n = 7). The most replicated results include genes playing a role in inflammation (antidepressants), neurotransmission (antidepressants and antipsychotics) or mitochondrial function (mood stabilizers). Compared to those investigating response to antidepressants, studies focused on antipsychotics or mood stabilizers more often showed lower sample size and lacked replication. Strengths and limitations of available studies are presented and discussed in light of the specific designs, methodology and clinical characterization of included patients for transcriptomic compared to DNA-based studies. Finally, future directions of transcriptomics of psychopharmacological interventions in psychiatric disorders are discussed.
KW - ANTIDEPRESSANT TREATMENT
KW - Antidepressants
KW - Antipsychotics
KW - BIPOLAR DISORDER
KW - Bipolar disorder
KW - LITHIUM RESPONSE
KW - LYMPHOBLASTOID CELL-LINES
KW - Lithium
KW - MAJOR DEPRESSIVE DISORDER
KW - MESSENGER-RNA EXPRESSION
KW - Major depressive disorder
KW - NEUROTRANSMITTER RECEPTOR
KW - PERIPHERAL-BLOOD
KW - Psychiatric disorders
KW - Schizophrenia
KW - TRANSPORTER GENE-EXPRESSION
KW - TUMOR-NECROSIS-FACTOR
U2 - 10.1016/j.euroneuro.2021.12.005
DO - 10.1016/j.euroneuro.2021.12.005
M3 - (Systematic) Review article
C2 - 35016057
SN - 0924-977X
VL - 55
SP - 112
EP - 157
JO - European Neuropsychopharmacology
JF - European Neuropsychopharmacology
ER -