Evidence map›Paper›PMID 32956213›Full record

ArticleNeuroreport2020

Peripheral vascular endothelial growth factor changes after transcranial magnetic stimulation in treatment-resistant depression.

Andrew M Fukuda, Lauren E Hindley, Jee Won Diane Kang, Eric Tirrell, Audrey R Tyrka, Alfred Ayala, Linda L Carpenter

Open access · greenAbstract read
In one paragraph

Article in Neuroreport, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 2 pooled it
1.0field-weighted citation impact, top 23% 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

11 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

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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

7 authors at 3 institutions in 1 country.

Andrew M FukudaButler Hospital TMS Clinic and Neuromodulation Research Facility.
Lauren E HindleyButler Hospital TMS Clinic and Neuromodulation Research Facility.
Jee Won Diane KangButler Hospital TMS Clinic and Neuromodulation Research Facility.
Eric TirrellButler Hospital TMS Clinic and Neuromodulation Research Facility.
Audrey R TyrkaButler Hospital TMS Clinic and Neuromodulation Research Facility.
Alfred AyalaDivision of Surgical Research/Department of Surgery, Rhode Island Hospital/Brown University School of Medicine, Providence, Rhode Island, USA.
Linda L CarpenterButler Hospital TMS Clinic and Neuromodulation Research Facility.
Butler Hospital · USBrown University · USRhode Island Hospital · US

Funding

Neuroimaging and Neuromodulation CoreP20GM130452 · NIGMS · BUTLER HOSPITAL (PROVIDENCE, RI) · PI GREENBERG, BENJAMIN D · 2019 to 2023
$11.3M
Mechanisms of Immune Dysfunction and Morbid Outcome in Response to Shock/SepsisR35GM118097 · NIGMS · RHODE ISLAND HOSPITAL · PI AYALA, ALFRED · 2016 to 2025
$6.3M
Promoting Research Training During Psychiatry ResidencyR25MH101076 · NIMH · BROWN UNIVERSITY · PI AUDREY TYRKA · 2013 to 2026
$2.8M
NIGMS NIH HHS P20 GM130452NIGMS NIH HHS R35 GM118097NIMH NIH HHS R25 MH101076
6 · The paper itself

Abstract

objectivesTo determine if vascular endothelial growth factor (VEGF) changes with transcranial magnetic stimulation (TMS) in treatment-resistant major depressive disorder (MDD).

methodsSerum from a naturalistic population of 15 patients with MDD was collected at baseline and after standard TMS treatment. VEGF concentration was determined via ELISA. Inventory of Depressive Symptomatology Self Report and Patient Health Questionnaire were used as a measure of depression symptom severity, clinical response and remission. Mann-Whitney U and Kendall's Tau Correlation were used for continuous variables.

resultsVEGF increased from pre- to post-TMS (+30.3%) in remitters whereas VEGF decreased in non-remitters (-9.87%) (P < 0.05). This same pattern was observed when comparing mean %change in VEGF between responders (+14.7%) and non-responders (-14.9%) (P = 0.054). Correlation was present between change in VEGF concentration (baseline to post) and change in Inventory of Depressive Symptomatology-Self Report at Tx30 (r = -0.371, P < 0.054), reflecting greater increases in VEGF linked to greater improvement in depressive symptoms following the standard 6-week course of TMS.

conclusionPatients with a successful treatment with TMS had significantly greater increase in VEGF from baseline to after treatment compared to non-responders/non-remitters and a larger increase in VEGF was associated with greater improvement in depressive symptoms after TMS. This is the first report examining VEGF levels in depressed patients receiving TMS. This study provides correlative data supporting further investigation into VEGF's role as an important mediator in the processes underpinning TMS' antidepressant effects and as a potential biomarker of clinical outcomes.

Indexed as

AdolescentAdultBiomarkersDepressive Disorder, Treatment-ResistantFemaleHumansMajor Depressive DisorderMaleProspective StudiesTranscranial Magnetic StimulationVascular Endothelial Growth Factor AYoung AdultBiomarkersVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID32956213
PMCPMC7541741
OpenAlexW3087322744

What Socratic holds

Textmetadata
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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 Socratic graph.