Evidence map›Paper›PMID 37997330›Full record

ArticlePsychiatry investigation2023

Elevated Brain-Derived Neurotrophic Factor Levels During Depressive Mixed States.

Naoaki Otsuka, Yoshikazu Takaesu, Yu Zamami, Kazuki Ota, Kazuhiro Kurihara, Hotaka Shinzato, Tsuyoshi Kondo

Open access · diamondAbstract read
In one paragraph

Article in Psychiatry investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 57% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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 2 institutions in 1 country.

Naoaki OtsukaDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Yoshikazu TakaesuDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Yu ZamamiDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Kazuki OtaDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Kazuhiro KuriharaDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Hotaka ShinzatoDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
Tsuyoshi KondoDepartment of Neuropsychiatry, Graduate School of Medicine, University of the Ryukyus, Okinawa, Japan.
University of the Ryukyus · JPHiroshima University · JP

Funding

JSPS KAKENHI JP17K10311JSPS KAKENHI JP21K07504
6 · The paper itself

Abstract

objectiveNeurotrophin-like brain-derived neurotrophic factor (BDNF) and pro-inflammatory cytokines may modulate the pathophysiology of mood disorders. Although several studies show alterations in these biomarkers during the depressive, manic, and euthymic states of mood disorders, evidence is lacking for those in a mixed state. Therefore, this study aimed to investigate the relationship between the depressive mixed state (DMX) and peripheral neurobiological factors.

methodsWe enrolled 136 patients with major depressive episodes. Depressive symptoms were assessed using the Quick Inventory of Depressive Symptomatology Self-Report Japanese version (QIDS-SR-J). The severity of DMX was assessed using the self-administered 12-item questionnaire (DMX-12). Categorical screening as DMX-positive (n=54) was determined by a cutoff score of 13 or more in the specific eight symptoms from the DMX-12; the remaining were DMX-negative (n=82). Serum BDNF, tumor necrosis factor-α, highsensitivity C-reactive protein, and interleukin-6 levels were measured.

resultsWhen comparing biomarkers between the DMX-positive and DMX-negative groups, higher serum BDNF concentration in the DMX-positive group than in the DMX-negative group was the only significant finding (p=0.009). A positive correlation existed between the total score of the eight specific symptoms of DMX-12 and the BDNF concentration (r=0.190, p=0.027). After adjustment for confounders, logistic regression analysis revealed that BDNF (odds ratio [OR]=1.07, 95% confidence interval [CI]=1.00-1.14, p=0.045), bipolar diagnosis (OR=3.43, 95% CI=1.36-8.66, p=0.009), and total QIDS-SR-J score (OR=1.29, 95% CI=1.15-1.43, p<0.001) were significantly associated with DMX positivity.

conclusionBDNF was positively associated with DMX severity, suggesting that higher BDNF concentrations may be involved in the pathophysiology of DMX.

Indexed as

Brain-derived neurotrophic factorInterleukin-6Mood disorders

Identifiers

PMID37997330
PMCPMC10678153
OpenAlexW4388879857

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.