Evidence map›Paper›PMID 38877455›Full record

ArticleBMC psychiatry2024

Effect of duloxetine on changes in serum proinflammatory cytokine levels in patients with major depressive disorder.

Wenfan Gao, Yejun Gao, Yayun Xu, Jun Liang, Yanhong Sun, Yuanyuan Zhang, Feng Shan, Jinfang Ge, Qingrong Xia

Abstract read
In one paragraph

Article in BMC psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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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

9 authors.

Wenfan GaoAffiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Yejun GaoSchool of Pharmacy, Anhui Medical University, 81 Meishan Road, Hefei, 230000, PR China.
Yayun XuAffiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Jun LiangAffiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Yanhong SunAffiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Yuanyuan ZhangAffiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Feng ShanAffiliated Psychological Hospital of Anhui Medical University, Hefei, China.
Jinfang GeInflammation and Immune Mediated Diseases Laboratory of Anhui Province, Anhui Institute of Innovative Drugs, Anhui Medical University, Hefei, China. gejinfang@ahmu.edu.cn.
Qingrong XiaSchool of Pharmacy, Anhui Medical University, 81 Meishan Road, Hefei, 230000, PR China. ahmcxqr@163.com.

Funding

Key Research and Development Program of Anhui Province 202004j07020001
6 · The paper itself

Abstract

objectiveAccumulating evidence supports the idea that inflammation may contribute to the pathophysiology of major depressive disorder (MDD). Duloxetine, a serotonin-norepinephrine reuptake inhibitor, exhibits anti-inflammatory effects both in vitro and in vivo. In this study, we investigated the impact of duloxetine on changes in serum proinflammatory cytokine levels among individuals diagnosed with MDD.

methodsA cohort of 23 drug-naïve individuals diagnosed with MDD and 23 healthy controls were included in this study. The severity of depressive symptoms was evaluated using the 24-item Hamilton Depression Scale (HAMD-24). A panel of 7 proinflammatory cytokines, including interleukin-1β (IL-1β), IL-2, IL-6, IL-8, IL-12, tumor necrosis factor-α (TNF-α), and interferon-γ (IFN-γ), were quantified using multiplex Luminex assays. The levels of serum cytokines in healthy controls and patients with MDD were compared at baseline. All patients received duloxetine at a dosage range of 40-60 mg/day for a duration of 4 weeks. The HAMD-24 scores and serum cytokine levels were compared before and after duloxetine treatment.

resultsCompared with healthy controls, patients with MDD had significantly greater levels of IL-2, IL-6, IL-8, IL-12, TNF-α, and IFN-γ (P < 0.05). Moreover, there was a significant decrease in HAMD-24 scores observed pre- and post-treatment (t = 13.161, P < 0.001). Furthermore, after 4 weeks of treatment, the serum levels of IL-8 (t = 3.605, P = 0.002), IL-12 (t = 2.559, P = 0.018), and IFN-γ (t = 3.567, P = 0.002) decreased significantly. However, there were no significant differences in other cytokines, including IL-1β, IL-2, IL-6, and TNF-α, before and after treatment (P > 0.05).

conclusionsThese findings present compelling evidence, potentially for the first time, indicating that duloxetine treatment may effectively reduce the serum concentrations of IL-8, IL-12, and IFN-γ in individuals diagnosed with MDD. However, the precise mechanisms underlying this effect remain unclear and warrant further investigation.

Indexed as

CytokinesDuloxetine HydrochlorideMajor Depressive DisorderAdultAntidepressive AgentsCase-Control StudiesFemaleHumansInflammationMaleMiddle AgedAntidepressive AgentsCytokinesDuloxetine HydrochlorideDuloxetineMajor depressive disorderPatientsPro-inflammatory cytokinesSerum

Identifiers

PMID38877455
PMCPMC11179362

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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.