Evidence map›Paper›PMID 38396309›Full record

ArticleEuropean journal of clinical pharmacology2024

Dose-dependent effect of lamotrigine on quetiapine serum concentration in patients using instant release tablets.

Kristine Hole, Silje K Lorentsen, Karoline L Nordby, Marie Slettvik, Ida Tg Sørum, Espen Molden, Tore Haslemo

Open access · hybridAbstract read
In one paragraph

Article in European journal of clinical pharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
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

7 authors at 3 institutions in 2 countries.

Kristine HoleCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway. kristine.hole@diakonsyk.no.ORCID http://orcid.org/0000-0001-7300-5329
Silje K LorentsenCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.
Karoline L NordbyCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.
Marie SlettvikCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.
Ida Tg SørumCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.
Espen MoldenCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0001-6190-2751
Tore HaslemoCenter for Psychopharmacology, Diakonhjemmet Hospital, Oslo, Norway.ORCID http://orcid.org/0000-0003-3888-5919
OsloMet – Oslo Metropolitan University · NODiakonhjemmet Hospital · NOUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLamotrigine was previously reported to reduce serum concentration of quetiapine. The aim of this study was to investigate whether lamotrigine dose or quetiapine formulation was of importance for the drug interaction.

methodsPatients combining lamotrigine with quetiapine (cases) were included retrospectively from a routine therapeutic drug monitoring (TDM) service, as were a control group of patients using quetiapine without any interacting drugs. The case and control groups were divided into groups using immediate release (IR) and extended release (XR) quetiapine. The case group was further split into high-dose (> 200 mg/day) and low-dose (≤ 200 mg/day) lamotrigine users. Quetiapine concentration-to-dose (C/D) ratio and metabolite-to-parent ratio (MPR) were compared between the control group and dose-separated case groups using ANOVA test and t-tests.

resultsIn total, 406 patients were included. The mean C/D ratio of IR quetiapine was 46% lower in the high-dose lamotrigine group compared with the control group (P < 0.001), while no interaction effect was present in the low dose lamotrigine group (P = 0.7). Regardless of lamotrigine dose, there was no difference in quetiapine C/D ratio for patients using the XR formulation (P = 0.4). The quetiapine MPR was unaffected regardless of formulation and lamotrigine dose (P ≥ 0.06).

conclusionThe effect of lamotrigine in reducing quetiapine concentration is only significant for patients using quetiapine IR tablets who are treated with lamotrigine doses > 200 mg/day. Because of high variability in the interaction effect, TDM of quetiapine should be recommended during co-prescription of high-dose lamotrigine.

Indexed as

Antipsychotic AgentsDelayed-Action PreparationsDose-Response Relationship, DrugDrug InteractionsLamotrigineQuetiapine FumarateTabletsAdultAgedDrug MonitoringFemaleHumansMaleMiddle AgedRetrospective StudiesTriazinesAntipsychotic AgentsDelayed-Action PreparationsLamotrigineQuetiapine FumarateTabletsTriazinesDrug-drug-interactionLamotriginePharmacokinetic variabilityQuetiapine

Identifiers

PMID38396309
PMCPMC11098907
OpenAlexW4392111532

What OpenQuestion holds

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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.