Evidence map›Paper›PMID 38230293›Full record

ReviewACS pharmacology & translational science2024

Gender Differences in Pharmacokinetics: A Perspective on Contrast Agents.

Myriam Courchesne, Gabriela Manrique, Laurie Bernier, Leen Moussa, Jeanne Cresson, Andreas Gutzeit, Johannes M Froehlich, Dow-Mu Koh, Carl Chartrand-Lefebvre, Simon Matoori

Open access · greenAbstract readReview
In one paragraph

Review in ACS pharmacology & translational science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
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  9. A PopPBPK-RL approach for precision dosing of benazepril in renal impaired patients.Journal of pharmacokinetics and pharmacodynamics · 2024
    Article
  10. Review
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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 4 institutions in 4 countries.

Myriam CourchesneFaculté de Pharmacie, Université de Montréal, 2940 Chemin de Polytechnique, Montreal, Quebec H3T 1J4, Canada.ORCID https://orcid.org/0009-0003-4396-4854
Gabriela ManriqueFaculté de Pharmacie, Université de Montréal, 2940 Chemin de Polytechnique, Montreal, Quebec H3T 1J4, Canada.
Laurie BernierFaculté de Pharmacie, Université de Montréal, 2940 Chemin de Polytechnique, Montreal, Quebec H3T 1J4, Canada.
Leen MoussaFaculté de Pharmacie, Université de Montréal, 2940 Chemin de Polytechnique, Montreal, Quebec H3T 1J4, Canada.
Jeanne CressonClinical Research Group, Klus Apotheke Zurich, 8032 Zurich, Switzerland.ORCID https://orcid.org/0009-0009-9157-0570
Andreas GutzeitDepartment of Health Sciences and Medicine, University of Lucerne, Frohburgstaße 3, 6002 Luzern, Switzerland.
Johannes M FroehlichClinical Research Group, Klus Apotheke Zurich, 8032 Zurich, Switzerland.
Dow-Mu KohCancer Research UK Clinical Magnetic Resonance Research Group, Institute of Cancer Research, Sutton, Surrey SM2 5NG, United Kingdom.
Carl Chartrand-LefebvreRadiology Department, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec H2X 3E4, Canada.
Simon MatooriFaculté de Pharmacie, Université de Montréal, 2940 Chemin de Polytechnique, Montreal, Quebec H3T 1J4, Canada.ORCID https://orcid.org/0000-0002-1559-0950
Université de Montréal · CACentre Hospitalier de l’Université de Montréal · CAInstitute of Cancer Research · GBUniversity of Lucerne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gender is an important risk factor for adverse drug reactions. Women report significantly more adverse drug reactions than men. There is a growing consensus that gender differences in drug PK is a main contributor to higher drug toxicity in women. These differences stem from physiological differences (body composition, plasma protein concentrations, and liver and kidney function), drug interactions, and comorbidities. Contrast agents are widely used to enhance diagnostic performance in computed tomography and magnetic resonance imaging. Despite their broad use, these contrast agents can lead to important adverse reactions including hypersensitivity reactions, nephropathy, and hyperthyroidism. Importantly, female gender is one of the main risk factors for contrast agent toxicity. As these adverse reactions may be related to gender differences in PK, this perspective aims to describe distribution and elimination pathways of commonly used contrast agents and to critically discuss gender differences in these processes.

Identifiers

PMID38230293
PMCPMC10789139
OpenAlexW4389616597

What OpenQuestion holds

Textmetadata
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.