Effects of antipsychotic medication on functional connectivity in major depressive disorder with psychotic features

被引:3
|
作者
Neufeld, Nicholas H. [1 ,2 ]
Oliver, Lindsay D. [2 ]
Mulsant, Benoit H. [1 ,2 ]
Alexopoulos, George S. [3 ]
Hoptman, Matthew J. [4 ,5 ]
Tani, Hideaki [2 ,6 ]
Marino, Patricia [3 ]
Meyers, Barnett S. [3 ]
Rothschild, Anthony J. [7 ,8 ]
Whyte, Ellen M. [9 ,10 ]
Bingham, Kathleen S. [1 ,11 ]
Flint, Alastair J. [1 ,11 ]
Voineskos, Aristotle N. [1 ,2 ]
机构
[1] Univ Toronto, Temerty Fac Med, Dept Psychiat, Toronto, ON, Canada
[2] Ctr Addict & Mental Hlth, Toronto, ON, Canada
[3] Weill Cornell Med Coll, Weill Cornell Med, Westchester Behav Hlth Ctr, Dept Psychiat, White Plains, NY USA
[4] Nathan S Kline Inst Psychiat Res, Div Clin Res, Orangeburg, NY USA
[5] NYU, Dept Psychiat, Grossman Sch Med, New York, NY USA
[6] Keio Univ, Dept Neuropsychiat, Sch Med, Tokyo, Japan
[7] Univ Massachusetts, Chan Med Sch, Dept Psychiat, Worcester, MA USA
[8] UMass Mem Hlth Care, Worcester, MA USA
[9] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA USA
[10] UPMC Western Psychiat Hosp, Pittsburgh, PA USA
[11] Univ Hlth Network, Ctr Mental Hlth, Toronto, ON, Canada
关键词
CONTROLLED-TRIAL; BRAIN; SCHIZOPHRENIA; PLACEBO; CORTEX; ANTIDEPRESSANT; METAANALYSIS; METABOLISM; OLANZAPINE; ASTROCYTE;
D O I
10.1038/s41380-023-02118-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The effect of antipsychotic medication on resting state functional connectivity in major depressive disorder (MDD) is currently unknown. To address this gap, we examined patients with MDD with psychotic features (MDDPsy) participating in the Study of the Pharmacotherapy of Psychotic Depression II. All participants were treated with sertraline plus olanzapine and were subsequently randomized to continue sertraline plus olanzapine or be switched to sertraline plus placebo. Participants completed an MRI at randomization and at study endpoint (study completion at Week 36, relapse, or early termination). The primary outcome was change in functional connectivity measured within and between specified networks and the rest of the brain. The secondary outcome was change in network topology measured by graph metrics. Eighty-eight participants completed a baseline scan; 73 completed a follow-up scan, of which 58 were usable for analyses. There was a significant treatment X time interaction for functional connectivity between the secondary visual network and rest of the brain (t = -3.684; p = 0.0004; pFDR = 0.0111). There was no significant treatment X time interaction for graph metrics. Overall, functional connectivity between the secondary visual network and the rest of the brain did not change in participants who stayed on olanzapine but decreased in those switched to placebo. There were no differences in changes in network topology measures when patients stayed on olanzapine or switched to placebo. This suggests that olanzapine may stabilize functional connectivity, particularly between the secondary visual network and the rest of the brain.
引用
收藏
页码:3305 / 3313
页数:9
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