Evidence map›Paper›PMID 32978302›Full record

ArticleRMD open2020

Introduction and switching of biologic agents are associated with antidepressant and anxiolytic medication use: data on 42 815 real-world patients with inflammatory rheumatic disease.

Vasiliki-Kalliopi Bournia, Maria G Tektonidou, Dimitrios Vassilopoulos, Katerina Laskari, Stylianos Panopoulos, Kalliopi Fragiadaki, Konstantinos Mathioudakis, Anastasios Tsolakidis, Panagiota Mitrou, Petros P Sfikakis

Open access · goldAbstract read
In one paragraph

Article in RMD open, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 15 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

10 authors at 3 institutions in 1 country.

Vasiliki-Kalliopi BourniaJoint Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece lily_bournia@hotmail.com psfikakis@med.uoa.gr.ORCID http://orcid.org/0000-0002-2162-1362
Maria G TektonidouJoint Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece.ORCID http://orcid.org/0000-0003-2238-0975
Dimitrios VassilopoulosJoint Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Katerina LaskariJoint Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Stylianos PanopoulosJoint Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Kalliopi FragiadakiJoint Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
Konstantinos MathioudakisIDIKA SA - e-Government Center for Social Security Services, Athens, Greece.
Anastasios TsolakidisIDIKA SA - e-Government Center for Social Security Services, Athens, Greece.
Panagiota MitrouHellenic Republic Ministry of Health, Athens, Greece.
Petros P SfikakisJoint Rheumatology Program, Medical School, National and Kapodistrian University of Athens, Athens, Greece.
National and Kapodistrian University of Athens · GRCenter for Security Studies · GRMinistry of Health · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesDepression and anxiety are linked bi-directionally with inflammatory rheumatic diseases (IRDs) activity, which in turn, depends on subjective patient reported outcomes that can be distorted by comorbid mood disorders. We tested the hypothesis that introduction and/or switching of biologic agents for IRDs are associated with treatment for depression and/or anxiety, by analysing real-world data.

methodsUsing a country-wide electronic prescription database (10 012 604 registered, 99% population coverage), we captured almost all patients with rheumatoid arthritis (n=12 002), psoriatic arthritis (n=5465) and ankylosing spondylitis (n=6423) who received biologic disease modifying anti-rheumatic drugs (bDMARDs) during a 2-year period (8/2016-7/2018). Concomitant antidepressant/anxiolytic medication use was documented in patients who started or switched bDMARDs and compared with those who remained on conventional synthetic (cs)DMARDs or the same bDMARD, respectively, by multivariate regression analysis.

resultsTwo-year data analysis on 42 815 patients revealed that bDMARD introduction was associated with both antidepressant [OR: 1.248, 95% CI 1.153 to 1.350, p<0.0001] and anxiolytic medication use [OR: 1.178, 95% CI 1.099 to 1.263, p<0.0001]. Moreover, bDMARD switching was also associated with antidepressant [OR: 1.502, 95% CI 1.370 to 1.646, p<0.0001] and anxiolytic medication use [OR: 1.161, 95% CI 1.067 to 1.264, p=0.001]. Notably, all these associations were independent of age, gender, underlying disease diagnosis and concomitant glucocorticoid or csDMARD medication use.

conclusionIn real-world settings, both introduction and switching of bDMARDs in patients with IRDs were associated with the presence of mood disorders. Although a causal relationship is uncertain, the impact of depression and anxiety should always be considered by physicians facing the decision to introduce or switch bDMARDs in patients with active IRDs.

Indexed as

Anti-Anxiety AgentsAntirheumatic AgentsArthritis, RheumatoidBiological ProductsAntidepressive AgentsBiological FactorsHumansAnti-Anxiety AgentsAntidepressive AgentsAntirheumatic AgentsBiological FactorsBiological ProductsAnkylosingArthritisBiological TherapyPsoriaticRheumatoidSpondylitis

Identifiers

PMID32978302
PMCPMC7539856
OpenAlexW3088675319

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.