Evidence map›Paper›PMID 29955151›Full record

Trial reportNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2018

Pretreatment and early-treatment cortical thickness is associated with SSRI treatment response in major depressive disorder.

Elizabeth A Bartlett, Christine DeLorenzo, Priya Sharma, Jie Yang, Mengru Zhang, Eva Petkova, Myrna Weissman, Patrick J McGrath, Maurizio Fava, R Todd Ogden and 10 more

Open access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 4 pooled it
4.9field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 4 syntheses or guidelines pooled it, 77 citations in OpenAlex.

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  6. Acute neurofunctional effects of escitalopram during emotional processing in pediatric anxiety: a double-blind, placebo-controlled trial.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 9 institutions in 1 country.

Elizabeth A BartlettDepartment of Biomedical Engineering, Stony Brook University, Stony Brook, NY, USA. Elizabeth.Bartlett@stonybrook.edu.
Christine DeLorenzoDepartment of Psychiatry, Stony Brook University, Stony Brook, NY, USA.
Priya SharmaDepartment of Psychiatry, Stony Brook University, Stony Brook, NY, USA.
Jie YangDepartment of Family, Population, and Preventive Medicine, Stony Brook University, Stony Brook, NY, USA.
Mengru ZhangDepartment of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY, USA.
Eva PetkovaDepartment of Child & Adolescent Psychiatry, Department of Population Health, New York University Langone Medical Center, NY, NY, USA.
Myrna WeissmanDepartment of Psychiatry, Columbia University College of Physicians & Surgeons and New York State Psychiatric Institute, NY, NY, USA.
Patrick J McGrathDepartment of Psychiatry, Columbia University College of Physicians & Surgeons and New York State Psychiatric Institute, NY, NY, USA.
Maurizio FavaDepartment of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
R Todd OgdenDepartment of Biostatistics, Columbia University, NY, NY, USA.
Benji T KurianDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Ashley MalchowDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Crystal M CooperDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Joseph M TrombelloDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Melvin McInnisDepartment of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
Phillip AdamsDepartment of Psychiatry, Columbia University College of Physicians & Surgeons and New York State Psychiatric Institute, NY, NY, USA.
Maria A OquendoDepartment of Psychiatry, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Diego A PizzagalliDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
Madhukar TrivediDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, TX, USA.ORCID http://orcid.org/0000-0002-2983-1110
Ramin V ParseyDepartment of Psychiatry, Stony Brook University, Stony Brook, NY, USA.
Stony Brook University · USThe University of Texas Southwestern Medical Center · USNew York State Psychiatric InstituteColumbia University · USHarvard University · USMassachusetts General Hospital · USNYU Langone Health · USUniversity of Michigan · USUniversity of Pennsylvania · US

Funding

Establishing Moderators/Biosignatures of Antidepressant Response- Clinical CareU01MH092221 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · PI TRIVEDI, MADHUKAR H. · 2010 to 2015
$9.7M
Biosignatures of Treatment Remission in Major DepressionU01MH092250 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MCGRATH, PATRICK J, PARSEY, RAMIN V. · 2010 to 2015
$8.9M
NIMH NIH HHS U01 MH092221NIMH NIH HHS U01 MH092250U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) U01MH092221U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) U01MH092250
6 · The paper itself

Abstract

To date, there are no biomarkers for major depressive disorder (MDD) treatment response in clinical use. Such biomarkers could allow for individualized treatment selection, reducing time spent on ineffective treatments and the burden of MDD. In search of such a biomarker, multisite pretreatment and early-treatment (1 week into treatment) structural magnetic resonance (MR) images were acquired from 184 patients with MDD randomized to an 8-week trial of the selective serotonin reuptake inhibitor (SSRI) sertraline or placebo. This study represents a large, multisite, placebo-controlled effort to examine the association between pretreatment differences or early-treatment changes in cortical thickness and treatment-specific outcomes. For standardization, a novel, robust site harmonization procedure was applied to structural measures in a priori regions (rostral and caudal anterior cingulate, lateral orbitofrontal, rostral middle frontal, and hippocampus), chosen based on previously published reports. Pretreatment cortical thickness or volume did not significantly associate with SSRI response. Thickening of the rostral anterior cingulate cortex in the first week of treatment was associated with better 8-week responses to SSRI (p = 0.010). These findings indicate that frontal lobe structural alterations in the first week of treatment may be associated with long-term treatment efficacy. While these associational findings may help to elucidate the specific neural targets of SSRIs, the predictive accuracy of pretreatment or early-treatment structural alterations in classifying treatment remitters from nonremitters was limited to 63.9%. Therefore, in this large sample of adults with MDD, structural MR imaging measures were not found to be clinically translatable biomarkers of treatment response to SSRI or placebo.

Indexed as

AdultCerebral CortexDouble-Blind MethodFemaleHumansMachine LearningMajor Depressive DisorderMaleMiddle AgedOrgan SizeSelective Serotonin Reuptake InhibitorsTreatment OutcomeYoung AdultSelective Serotonin Reuptake Inhibitors

Identifiers

PMID29955151
PMCPMC6135779
OpenAlexW2808444231

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.