Evidence map›Paper›PMID 26357585›Full record

ArticleBrain and behavior2015

Inflammation and depression: combined use of selective serotonin reuptake inhibitors and NSAIDs or paracetamol and psychiatric outcomes.

Ole Köhler, Liselotte Petersen, Ole Mors, Christiane Gasse

Abstract read
In one paragraph

Article in Brain and behavior, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–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

24 citing papers in PubMed.

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  3. Effect of Ibuprofen on BrainAGE: A Randomized, Placebo-Controlled, Dose-Response Exploratory Study.Biological psychiatry. Cognitive neuroscience and neuroimaging · 2018
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  14. Inflaming sex differences in mood disorders.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2019
    Review
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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

4 authors.

Ole KöhlerDepartment P, Research Unit, Aarhus University Hospital Risskov Risskov, Denmark ; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH Aarhus, Denmark.
Liselotte PetersenThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH Aarhus, Denmark ; National Centre for Register-based Research, Aarhus University Aarhus, Denmark.
Ole MorsDepartment P, Research Unit, Aarhus University Hospital Risskov Risskov, Denmark ; The Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH Aarhus, Denmark.
Christiane GasseNational Centre for Register-based Research, Aarhus University Aarhus, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNonsteroidal anti-inflammatory drugs (NSAIDs) and paracetamol have been shown to yield the potential of adjunctive antidepressant treatment effects to selective serotonin reuptake inhibitors (SSRIs); however, when investigating treatment effects of concomitant use, simultaneous evaluation of potential adverse events is important. The objective was thus to investigate treatment effectiveness and safety aspects of concomitant SSRI use with NSAIDs or paracetamol.

methodsWithin a 25% random sample of the Danish population, we identified all incident SSRI users between 1997 and 2006 (N = 123,351). Effectiveness and safety measures were compared between periods of SSRI use only and periods of combined SSRI and NSAID or paracetamol use by applying Cox regression.

resultsAmong 123,351 SSRI users (follow-up: 53,697.8 person-years), 21,666 (17.5%) used NSAIDs and 10,232 (8.3%) paracetamol concomitantly. Concomitant NSAID use increased the risk of any psychiatric contact [Hazard rate ratio (95%-confidence interval): 1.22 (1.07; 1.38)] and with depression [1.31 (1.11; 1.55)]. Low-dose acetylsalicylic acid reduced the risk of psychiatric contact in general [0.74 (0.56; 0.98)] and with depression [0.71 (0.50; 1.01)]. Ibuprofen reduced the risk of psychiatric contacts [0.76 (0.60; 0.98)]. Concerning safety, paracetamol was associated with increased mortality [3.18 (2.83; 3.58)], especially cardiovascular [2.51 (1.93; 3.28)]. Diclofenac [1.77 (1.22; 2.55)] and the selective COX-2 inhibitors [1.75 (1.21; 2.53)] increased mortality risks.

conclusionsConcomitant use of SSRIs and NSAIDs occurred frequently, and effectiveness and safety outcomes varied across individual NSAIDs. Especially low-dose acetylsalicylic acid may represent an adjunctive antidepressant treatment option. The increased mortality risk of concomitant use of paracetamol needs further investigation.

Indexed as

AcetaminophenAdolescentAdultAgedAged, 80 and overAnti-Inflammatory Agents, Non-SteroidalChildDenmarkDepressionDrug Therapy, CombinationFemaleHumansInflammationMaleMiddle AgedSelective Serotonin Reuptake InhibitorsAcetaminophenAnti-Inflammatory Agents, Non-SteroidalSelective Serotonin Reuptake InhibitorsAntidepressantsdepressionepidemiologymood disorderspharmacoepidemiologypharmacotherapy

Identifiers

PMID26357585
PMCPMC4559013

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Registered trials

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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.