Evidence map›Paper›PMID 37272562›Full record

ArticleJournal of Korean medical science2023

Population Pharmacokinetic-Pharmacodynamic Modeling of Carvedilol to Evaluate the Effect of Cytochrome P450 2D6 Genotype on the Heart Rate Reduction.

Sejung Hwang, Soyoung Lee, Jangsoo Yoon, Jae-Yong Chung

Open access · goldAbstract read
In one paragraph

Article in Journal of Korean medical science, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 35% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Article
  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

4 authors at 1 institution in 1 country.

Sejung HwangDepartment of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-0154-5777
Soyoung LeeDepartment of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0001-5799-4489
Jangsoo YoonDepartment of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0002-3946-2718
Jae-Yong ChungDepartment of Clinical Pharmacology and Therapeutics, Seoul National University College of Medicine, Seoul, Korea.ORCID https://orcid.org/0000-0003-4188-2786
Seoul National University · KR

Funding

Ministry of Food and Drug Safety 14181MFDS532
6 · The paper itself

Abstract

backgroundCarvedilol is a beta-adrenergic receptor antagonist primarily metabolized by cytochromes P450 (CYP) 2D6. This study established a carvedilol population pharmacokinetic (PK)-pharmacodynamic (PD) model to describe the effects of

methodsThe PK-PD model was developed from a clinical study conducted on 21 healthy subjects divided into three CYP2D6 phenotype groups, with six subjects in the extensive metabolizer (EM,

resultsThe carvedilol PK was well described by a two-compartment model with zero-order absorption, lag time, and first-order elimination. The carvedilol clearance in the

conclusionThe PK-PD model revealed that the

Indexed as

Cytochrome P-450 CYP2D6PropanolaminesCarbazolesCarvedilolGenotypeHeart RateCarbazolesCarvedilolCytochrome P-450 CYP2D6PropanolaminesCarvedilolCytochrome P-450 Enzyme SystemGenetic VariationPharmacodynamicsPharmacokinetics

Identifiers

PMID37272562
PMCPMC10244018
OpenAlexW4379376101

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.