Evidence map›Paper›PMID 26032842›Full record

ArticlePsychopharmacology2016

Inflammation and psychotropic drugs: the relationship between C-reactive protein and antipsychotic drug levels.

Gudrun Hefner, Mohamed E E Shams, Stefan Unterecker, Tanja Falter, Christoph Hiemke

Abstract read
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In one paragraph

Article in Psychopharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 20% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

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  14. E-Cigarette Use, Systemic Inflammation, and Depression.International journal of environmental research and public health · 2021
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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

5 authors at 4 institutions in 3 countries.

Gudrun HefnerDepartment of Psychiatry and Psychotherapy, University Medical Centre, Mainz, Germany. gudrun.hefner@unimedizin-mainz.de.
Mohamed E E ShamsDepartment of Pharmaceutics, Faculty of Pharmacy, University of Mansoura, Mansoura, Egypt.
Stefan UntereckerDepartment of Psychiatry, Psychosomatics, and Psychotherapy, University Hospital of Würzburg, Würzburg, Germany.
Tanja FalterInstitute of Clinical Chemistry and Laboratory Medicine, University Medical Centre, Langenbeckstrasse 1, 55131, Mainz, Germany.
Christoph HiemkeDepartment of Psychiatry and Psychotherapy, University Medical Centre, Mainz, Germany.
Johannes Gutenberg University Mainz · DEMansoura University · EGUniversitätsklinikum Würzburg · DEUniversity Medical Centre Mannheim · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationaleIn psychiatric clinical practice, there is a need to identify psychotropic drugs whose metabolisms are prone to be altered with increased inflammatory activity in an individual patient.

objectivesThe aim of this study was to find out whether elevated serum levels (≥5 mg/l) of C-reactive protein (CRP), an established laboratory marker of infection and inflammation, are associated with increased serum concentrations of the atypical antipsychotic drugs clozapine, quetiapine, and risperidone.

methodsTherapeutic drug monitoring request forms of patients whose antipsychotic drug concentrations had been measured under conditions of normal (<5 mg/l) and pathological (>5 mg/l) levels of C-reactive protein were retrospectively screened. The serum concentrations in relation to the daily doses [concentration per dose (C/D) (ng/mL/mg)] and the metabolic ratios [ratio of concentrations (metabolite/drug)] were compared intraindividually by the Wilcoxon signed rank test. To the study effects of the intensity of infections on drug concentrations, C-reactive protein and C/D levels were submitted to Spearman's correlation analysis.

resultsElevated levels of C-reactive protein were found in 105 patients. They were significantly associated with elevated values in C/D for clozapine (n = 33, P < 0.01) and risperidone (n = 40, P < 0.01). A trend for an increase was found for quetiapine (n = 32, P = 0.05). Median increases were 48.0 % (clozapine), 11.9 % (quetiapine), and 24.2 % (active moiety of risperidone), respectively.

conclusionsIn patients who exhibit signs of inflammation or infection with increased C-reactive protein values during psychopharmacological treatment, especially under clozapine and risperidone, therapeutic drug monitoring is recommendable in order to minimize the risk of intoxications due to elevated drug concentrations.

Indexed as

AgedAged, 80 and overAntipsychotic AgentsBiomarkersClozapineC-Reactive ProteinFemaleHumansInflammationMalePsychotic DisordersPsychotropic DrugsQuetiapine FumarateRisperidoneROC CurveAntipsychotic AgentsBiomarkersClozapineC-Reactive ProteinPsychotropic DrugsQuetiapine FumarateRisperidoneAntipsychoticsClozapineC-reactive proteinDrug metabolismInflammationPharmacokineticsPsychiatryQuetiapineRisperidoneTherapeutic drug monitoring

Identifiers

PMID26032842
OpenAlexW656665617

What OpenQuestion holds

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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.