Evidence map›Paper›PMID 18080812›Full record

ArticleEuropean journal of clinical pharmacology2008

The association of ABCB1 polymorphisms and elevated serum digitoxin concentrations in geriatric patients.

Charalampos Dragonas, Jan T Wagner, Hans J Heppner, Thomas Bertsch, Wolfgang Muhlberg, Susanne Wicklein, Andreas Pahl, Christine Diewald, Iouri Bachmakov, Cornel C Sieber and 1 more

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Article in European journal of clinical pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Charalampos DragonasInstitute for Biomedicine of Aging, Department of Internal Medicine V (Geriatrics), University of Erlangen-Nuremberg, Nuremberg, Germany. c.dragonas@gmx.net
Jan T Wagner
Hans J Heppner
Thomas Bertsch
Wolfgang Muhlberg
Susanne Wicklein
Andreas Pahl
Christine Diewald
Iouri Bachmakov
Cornel C Sieber
Martin F Fromm
Friedrich-Alexander-Universität Erlangen-Nürnberg · DENuremberg Hospital · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveDigitoxin is a known substrate of the efflux pump P-glycoprotein (gene name: ABCB1). P-glycoprotein expression was shown to be modulated by single nucleotide polymorphisms in the ABCB1 gene, but it remains unclear whether these polymorphisms influence digitoxin blood levels. Our objective was to examine the association of ABCB1 C3435T genotype and elevated serum digitoxin concentrations (SDC) in a cohort of 77 geriatric patients consecutively admitted to a geriatric department over a 12-month period.

methodsThe impact of ABCB1 3435 CC, CT, and TT genotypes on SDC and SDC normalized for daily digitoxin dosage and body weight was assessed by multivariate regression analysis.

resultsAmong participants, 18 (23%) had the CC, 36 (47%) the CT, and 23 (30%) the TT genotype. Adjusting for relevant covariates, no significant association of ABCB1 C3435T genotype and SDC or normalized SDC was detected. Mean SDC was 22.4 ng/ml (95% CI 18.9-25.9) for the TT, 21.8 ng/ml (95% CI 18.1-25.5) for the CT, and 25.7 ng/ml (95% CI 20.6-30.8) for the CC genotype. The means for normalized SDC were 5.2 kg.l(-1) (95% CI 4.3-6.1) for the TT, 6.1 kg.l(-1) (95% CI 4.7-7.5) for the CT, and 6.2 kg.l(-1) (95% CI 4.6-7.7) for the CC genotype.

conclusionIn this sample of frail geriatric patients, the impact of ABCB1 C3435T genotype on serum digitoxin concentration was not of major relevance. Regular monitoring of digitoxin blood levels and surveillance of appropriate drug use remain the best ways to prevent digitoxin intoxications in the elderly.

Indexed as

AgedAnalysis of VarianceATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily B, Member 1Cardiotonic AgentsDigitoxinFemaleGenotypeHumansMalePolymorphism, GeneticReverse Transcriptase Polymerase Chain ReactionTreatment OutcomeABCB1 protein, humanATP Binding Cassette Transporter, Subfamily BATP Binding Cassette Transporter, Subfamily B, Member 1Cardiotonic AgentsDigitoxin

Identifiers

PMID18080812
OpenAlexW1975211016

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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.