PBMC telomerase activity in depression and the response to electroconvulsive therapy.
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Authors
Ryan, Karen M
Finnegan, Martha
Harkin, Andrew
McLoughlin, Declan M
Issue Date
2021-07-15
Type
Journal Article
Randomized Controlled Trial
Randomized Controlled Trial
Language
en
Keywords
Depression , Electroconvulsive therapy , HAM-D24 , PBMC , Telomerase
Alternative Title
Abstract
Telomerase, the DNA polymerase responsible for maintaining telomere length, has previously been implicated in depression and the response to antidepressant drugs. In this study, we aimed to compare telomerase activity in peripheral blood mononuclear cells between patients with severe depression recruited as part of the KEEP-WELL Trial (Ketamine for Depression Relapse Prevention Following ECT; NCT02414932) and age- and sex-matched healthy volunteers both at baseline/pre-ECT and at follow-up 1 month later for controls or in patients after a course of ECT. We found no differences in telomerase activity between patients with depression (nā=ā20) compared to healthy controls (nā=ā33) at baseline/pre-ECT, or between patients treated with ECT compared to controls at follow-up. In patients, telomerase activity was not associated with mood, as assessed by the 24-item Hamilton Rating Scale for Depression, or the duration of the current depressive episode. Additionally, we found no significant relationship between telomerase activity and exposure to recent or childhood adversity in either the patient or control groups. Overall, our results suggest that telomerase activity is not associated with depression, the therapeutic response to ECT, or exposure to adversity.
Description
Citation
Ryan, K. M., Finnegan, M., Harkin, A., & McLoughlin, D. M. (2021). PBMC telomerase activity in depression and the response to electroconvulsive therapy. European archives of psychiatry and clinical neuroscience, 271(7), 1297ā1307. https://doi.org/10.1007/s00406-021-01294-4
Publisher
License
Ā© 2021. The Author(s).
Journal
European archives of psychiatry and clinical neuroscience
Volume
271
Issue
7
PubMed ID
DOI
10.1007/s00406-021-01294-4
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10.1016/j.psyneuen.2005.08.011
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10.1016/j.jpsychires.2016.01.015
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10.1017/S0033291719002228
10.31887/DCNS.2011.13.1/owolkowitz
10.1101/cshperspect.a032383
10.9758/cpn.2019.17.3.343
10.1016/j.arr.2013.12.006
10.1016/j.psyneuen.2018.10.019
10.1016/j.psyneuen.2011.10.008
10.1016/j.bbi.2019.06.015
10.1371/journal.pone.0138904
10.1155/2017/5958429
10.4049/jimmunol.174.9.5261
10.1016/j.bbrc.2004.02.080
10.1101/gad.313460.118
10.1042/CBI20110308
10.1523/JNEUROSCI.0805-11.2011
10.1098/rsbl.2012.0747
10.1093/ijnp/pyv002
10.1016/j.lfs.2017.08.020
10.1038/mp.2010.133
10.1016/j.pscychresns.2015.01.007
10.1016/j.psyneuen.2015.04.004
10.1016/j.psyneuen.2015.11.017
10.1016/j.jad.2014.07.035
10.1136/bmj.l1079
10.1111/acps.12951
10.1001/jama.2013.281053
10.1097/YCT.0000000000000560
10.1176/appi.ajp.2015.15030372
10.4088/JCP.08m04309
10.1016/0277-9536(88)90397-8
10.1007/s004390050711
10.1080/14653240902887267
10.1517/14728222.2015.1016500
10.3390/genes7090058
10.1016/j.psyneuen.2005.08.011
10.3758/BF03193146
10.1016/j.bbrc.2014.07.138
10.1002/da.22351
10.1016/j.jpsychires.2016.01.015
10.1016/j.jad.2015.11.052
10.1017/S0033291719002228
ISSN
1433-8491