TY - JOUR
T1 - Validation study of microRNAs previously associated with antidepressant response in older adults treated for late-life depression with venlafaxine
AU - Marshe, Victoria S.
AU - Islam, Farhana
AU - Maciukiewicz, Malgorzata
AU - Fiori, Laura M.
AU - Yerko, Volodymyr
AU - Yang, Jennie
AU - Turecki, Gustavo
AU - Foster, Jane A.
AU - Kennedy, Sidney H.
AU - Blumberger, Daniel M.
AU - Karp, Jordan F.
AU - Kennedy, James L.
AU - Mulsant, Benoit H.
AU - Reynolds, Charles F.
AU - Lenze, Eric J.
AU - Müller, Daniel J.
N1 - Funding Information:
Ms. Marshe is supported through the Frederick Banting and Charles Best Canada Graduate Doctoral Research Award from the Canadian Institutes for Health Research (#394160)During the time of writing, Dr. Maciukiewicz was supported by a Postdoctoral Fellowship from the Canadian Institute of Health Research (#81655).Dr. Lenze is supported by funding from NIH and from the Taylor Family Institute for Innovative Psychiatric Research and the Center for Brain Research in Mood Disorders at Washington University.Dr. Mulsant receives compensation from the Department of Psychiatry, University of Toronto, Toronto, Ontario; the Centre for Addiction and Mental Health (CAMH), Toronto, Ontario; and the University of Pittsburgh, Pittsburgh, Pennsylvania. Dr. Mulsant belongs to the following Boards: Member, Board of Trustees, Centre for Addiction and Mental Health, Toronto, OntarioDr. Lenze has received funding from Takeda, Lundbeck, Janssen, Alkermes, Aptynx, and PCORI, and is a consultant for Janssen and Jazz Pharmaceuticals.Dr. Mulsant currently receives research support from Brain Canada, the Canadian Institutes of Health Research, the CAMH Foundation, the Patient-Centered Outcomes Research Institute (PCORI), the US National Institute of Health (NIH), Capital Solution Design LLC (software used in a study founded by CAMH Foundation), and HAPPYneuron (software used in a study founded by Brain Canada). He directly owns stocks of General Electric (less than $5000). Within the past three years, he has also received research support from Eli Lilly (medications for an NIH-funded clinical trial) and Pfizer (medications for an NIH-funded clinical trial).
Publisher Copyright:
© 2020
PY - 2020/6/8
Y1 - 2020/6/8
N2 - Background: MicroRNAs (miRNAs) are small 22 nucleotides long, non-coding RNAs that are potential biomarkers for antidepressant treatment response. We aimed to replicate previous associations of miRNAs with antidepressant treatment response in a sample of older adults diagnosed with late-life depression. Methods: Our sample included 184 older adults diagnosed with moderately severe depression that received open-label venlafaxine (up to 300 mg/day) for approximately 12 weeks. We quantified miRNA expression levels at baseline and week 12 for miRNAs miR-1202, miR-135a-5p, miR-16-5p, miR-146a-5p, miR-146b-5p, miR-425-3p, and miR-24-3p to explore their association with remission status, response trajectories, and time-to-remission. Results: At T0 and T12, there were no differences in miRNA expression levels between remitters and non-remitters. However, remitters showed a trend toward higher baseline miR-135a-5p (Median = 11.3 [9.9, 15.7], p = .083). Prior to correction, baseline miR-135a-5p expression levels showed an association with remission status (OR = 1.8 [1.0, 3.3], p = .037). Individuals with higher baseline miR-135a-5p showed better response trajectories (F = 4.5, FDR-corrected p = 4.4 × 10−4), particularly at weeks 10 and 12 (p <. 05). In addition, individuals with higher miR-135a-5p expression reached remission faster than those with lower expression (HR = 0.6 [0.4, 0.9], FDR-corrected p = .055). Limitations: Although the sample size was relatively modest, our findings are consistent with the literature suggesting that higher miR-135a-5p levels may be associated with better antidepressant treatment response. Conclusions: However, the miRNA signature of antidepressant response in older adults may be different as compared to younger adults.
AB - Background: MicroRNAs (miRNAs) are small 22 nucleotides long, non-coding RNAs that are potential biomarkers for antidepressant treatment response. We aimed to replicate previous associations of miRNAs with antidepressant treatment response in a sample of older adults diagnosed with late-life depression. Methods: Our sample included 184 older adults diagnosed with moderately severe depression that received open-label venlafaxine (up to 300 mg/day) for approximately 12 weeks. We quantified miRNA expression levels at baseline and week 12 for miRNAs miR-1202, miR-135a-5p, miR-16-5p, miR-146a-5p, miR-146b-5p, miR-425-3p, and miR-24-3p to explore their association with remission status, response trajectories, and time-to-remission. Results: At T0 and T12, there were no differences in miRNA expression levels between remitters and non-remitters. However, remitters showed a trend toward higher baseline miR-135a-5p (Median = 11.3 [9.9, 15.7], p = .083). Prior to correction, baseline miR-135a-5p expression levels showed an association with remission status (OR = 1.8 [1.0, 3.3], p = .037). Individuals with higher baseline miR-135a-5p showed better response trajectories (F = 4.5, FDR-corrected p = 4.4 × 10−4), particularly at weeks 10 and 12 (p <. 05). In addition, individuals with higher miR-135a-5p expression reached remission faster than those with lower expression (HR = 0.6 [0.4, 0.9], FDR-corrected p = .055). Limitations: Although the sample size was relatively modest, our findings are consistent with the literature suggesting that higher miR-135a-5p levels may be associated with better antidepressant treatment response. Conclusions: However, the miRNA signature of antidepressant response in older adults may be different as compared to younger adults.
KW - Late-life depression
KW - Pharmacogenetics
KW - Treatment response
KW - Venlafaxine
KW - miRNA
UR - http://www.scopus.com/inward/record.url?scp=85078974805&partnerID=8YFLogxK
U2 - 10.1016/j.pnpbp.2020.109867
DO - 10.1016/j.pnpbp.2020.109867
M3 - Article
C2 - 31954757
AN - SCOPUS:85078974805
SN - 0278-5846
VL - 100
JO - Progress in Neuro-Psychopharmacology and Biological Psychiatry
JF - Progress in Neuro-Psychopharmacology and Biological Psychiatry
M1 - 109867
ER -