Evidence map›Paper›PMID 39283831›Full record

ArticleThe international journal of neuropsychopharmacology2024

Distinct Effects of Major Affective Disorder Diagnoses and Suicidal Symptom Severity on Inhibitory Control Function and Proinflammatory Cytokines: Single-Site Analysis of 800 Adolescents and Adults.

Ya-Mei Bai, Mu-Hong Chen, Ju-Wei Hsu, Hsiang-Hsuan Huang, Jia-Shyun Jeng, Shih-Jen Tsai

Abstract read
In one paragraph

Article in The international journal of neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Ya-Mei BaiInstitute of Brain Science, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Mu-Hong ChenInstitute of Brain Science, National Yang Ming Chiao Tung University, Taipei, Taiwan.ORCID 0000-0001-6516-1073
Ju-Wei HsuDepartment of Psychiatry, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Hsiang-Hsuan HuangDepartment of Psychiatry, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Jia-Shyun JengDepartment of Psychiatry, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Shih-Jen TsaiInstitute of Brain Science, National Yang Ming Chiao Tung University, Taipei, Taiwan.

Funding

Academia Sinica Joint Research Program VTA112-V1-6-1Kaohsiung Veterans General HospitalMinistry of Science and TechnologyTaichungTaipeiTaipei Veterans General Hospital V111C-010Taiwan MOST110-2314-B-075-026Tri-Service General HospitalVeterans General Hospitals and University System of Taiwan Joint Research Program VGHUST112-G1-8-1Yen Tjing Ling Medical Foundation CI-109-21
6 · The paper itself

Abstract

backgroundInhibitory control function and proinflammatory cytokines play a role in the pathomechanisms underlying major affective disorders and suicidal behavior. However, the distinct or interactive effects of major affective disorders and suicidal symptom severity on inhibitory control function and proinflammatory cytokines remain unclear.

methodsThis study included 287 patients with bipolar disorder, 344 with major depressive disorder, and 169 healthy controls. We categorized the participants into 3 groups based on Montgomery-Åsberg Depression Rating Scale (MADRS) item 10 (suicidal symptoms) score: 0, 2 or 3, and ≥4. The participants completed the go/no-go task and the measurements for C-reactive protein (CRP) and tumor necrosis factor-α (TNF-α) levels.

resultsErrors in the go/no-go task were associated with suicidality (P = .040), regardless of the severity of suicidal symptoms and diagnosis. An elevated CRP level was especially associated with a Montgomery-Åsberg Depression Rating Scale item 10 score ≥4 (P = .001). An increased TNF-α level could distinguish bipolar disorder from major depressive disorder (P < .001). DISCUSSION: Our study indicated the distinct effects of major affective disorder diagnosis and suicide symptom severity on inhibitory control function and CRP and TNF-α levels. Importantly, individuals with the poorest inhibitory control function and highest CRP levels had more severe suicidal symptoms.

Indexed as

Bipolar DisorderC-Reactive ProteinMajor Depressive DisorderSuicidal IdeationTumor Necrosis Factor-alphaAdolescentAdultCytokinesFemaleHumansInhibition, PsychologicalMaleMiddle AgedPsychiatric Status Rating ScalesSeverity of Illness IndexYoung AdultC-Reactive ProteinCytokinesTumor Necrosis Factor-alphabipolar disorderCRPinhibitory controlmajor depressive disorderSuicide

Identifiers

PMID39283831
PMCPMC11450626

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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.