Evidence map›Paper›PMID 33755736›Full record

ArticleEuropean journal of clinical pharmacology2021

Evaluation of the effects of atazanavir-ritonavir on the pharmacokinetics of lumefantrine in patients living with HIV in Lagos University Teaching Hospital, South-Western Nigeria.

Sikiru Olatunji Usman, Ibrahim Adekunle Oreagba, Michael Rotimi Kadri, Ololade Oluwatosin Adewumi, Akinwumi Akinyede, Esther Oluwatoyin Agbaje, Ganiyu Abideen, AbdulWasiu Adeniyi Busari, Olayinka Olaiwola Hassan, Moshood Olusola Akinleye and 1 more

Registry-linked trialAbstract read
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In one paragraph

Article in European journal of clinical pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04531072 (Effect of Atazanavir-ritonavir on the Pharmacokinetics and Toxicity of Lumefantrine in People Living With HIV Attending Lagos University Teaching Hospital), which is not on this map. Cited by 3 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 2 pooled it
0.1field-weighted citation impact, top 60% 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.

NCT04531072 phase4completednot on this map

Effect of Atazanavir-ritonavir on the Pharmacokinetics and Toxicity of Lumefantrine in People Living With HIV Attending Lagos University Teaching Hospital

TypeinterventionalSponsorFogarty International Center of the National Institute of HealthRan2018 to 2019Enrolled20ConditionsDrug InteractionArmsArtemether-lumefantrine, Atazanavir-ritonavir 300/100 mg
3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 2 syntheses or guidelines pooled it, 4 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. 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

11 authors at 3 institutions in 1 country.

Sikiru Olatunji UsmanDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria. osusman1967@gmail.com.ORCID http://orcid.org/0000-0001-7860-0442
Ibrahim Adekunle OreagbaDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
Michael Rotimi KadriDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
Ololade Oluwatosin AdewumiDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
Akinwumi AkinyedeDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
Esther Oluwatoyin AgbajeDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
Ganiyu AbideenDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
AbdulWasiu Adeniyi BusariDepartment of Pharmacology, Therapeutics and Toxicology, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
Olayinka Olaiwola HassanLagos University Teaching Hospital, Lagos, Nigeria.
Moshood Olusola AkinleyeDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
Alani Sulaimon AkanmuDepartment of Haematology and Blood Transfusion, Faculty of Clinical Science, College of Medicine of the University of Lagos, Idi-Araba, Lagos State, Nigeria.
University of Lagos · NGLagos State University · NGLagos University Teaching Hospital · NG

Funding

Building Research And Innovation in Nigeria's Science - (BRAINS)D43TW010134 · FIC · COLLEGE OF MEDICINE, UNIVERSITY OF LAGOS · PI OGUNSOLA, FOLASADE TOLULOPE · 2015 to 2020
$3.2M
FIC NIH HHS D43 TW010134FIC NIH HHS D43TW010134
6 · The paper itself

Abstract

purposeAtazanavir-ritonavir (ATVr)-based antiretroviral therapy and artemether-lumefantrine (AL) are commonly used drugs for the treatment of human immune deficiency virus (HIV) infection and malaria respectively. However, interaction of both drugs, with Cytochrome P 3A4 (CYP 3A4) isoenzyme, may spawn clinically significant pharmacokinetic interactions. This study evaluated the effects of atazanavir-ritonavir on the pharmacokinetics of lumefantrine.

methodIn a case-control study, twenty participants having Plasmodium falciparum malaria were recruited and divided into two groups (ATVr-arm, n=10; and control-arm, n= 10). All the participants were administered six oral doses of AL 80-480 mg (Coartem). Thereafter, their blood samples were collected at different time intervals over seven days. The concentration of lumefantrine in each sample was quantified with high-performance liquid chromatography (HPLC) and used to determine its pharmacokinetic parameters which were compared between the test and control groups.

resultsATVr increased the mean day 7 concentration of lumefantrine (ATVr 3847.09 ± 893.35 ng/mL, control 1374.53 ± 265.55 ng/mL, p = 0.016) and the area under its plasma concentration-time curve (ATVr 670529.57 ± 157172.93 ng.h/mL, control 447976.28 ± 80886.99 ng.h/mL, p = 0.224) by 179.88 % and 49.68 %, respectively, but decreased its mean maximum plasma drug concentration (Cmax) (ATVr 13725.70 ± 2658.44 ng/mL, control 15380.48 ± 2332.62 ng/mL, p = 0.645) by 10.76 %.

conclusionATVr increased drug exposure and day 7 plasma concentration of lumefantrine. AL is therefore considered effective for the treatment of malaria in patients taking ATVr-based regimen. However, the safety associated with the interaction requires further elucidation.

trial registrationClin ClinicalTrials.gov Identifier: NCT04531072, August 27, 2020. "Retrospectively registered".

Indexed as

AdultAntimalarialsAnti-Retroviral AgentsArtemether, Lumefantrine Drug CombinationAtazanavir SulfateCase-Control StudiesChromatography, High Pressure LiquidDrug CombinationsFemaleHIV InfectionsHospitals, TeachingHumansMalariaMaleMiddle AgedNigeriaalpha-methylacyl-CoA racemaseAntimalarialsAnti-Retroviral AgentsArtemether, Lumefantrine Drug CombinationAtazanavir SulfateDrug CombinationsRacemases and EpimerasesRitonavirAtazanavir-ritonavirHIVInteractionLumefantrinePharmacokinetic

Identifiers

PMID33755736
OpenAlexW3139452807

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.