Evidence map›Paper›PMID 26503820›Full record

ReviewThe pharmacogenomics journal2016

Interethnic variation of CYP2C19 alleles, 'predicted' phenotypes and 'measured' metabolic phenotypes across world populations.

I Fricke-Galindo, C Céspedes-Garro, F Rodrigues-Soares, M E G Naranjo, Á Delgado, F de Andrés, M López-López, E Peñas-Lledó, A LLerena

Abstract readReview
PubMed Publisher
In one paragraph

Review in The pharmacogenomics journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 4 pooled it
19.6field-weighted citation impact, top 1% 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

72 citing papers in PubMed, 4 syntheses or guidelines pooled it, 166 citations in OpenAlex.

  1. Pooled it
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  4. The Effect of CYP2C19 and Nongenetic Factors on Clopidogrel Responsiveness in the MENA Region: A Systematic Review.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Pooled it
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  14. Influence ofPharmaceuticals (Basel, Switzerland) · 2026
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  16. Distribution ofFrontiers in genetics · 2026
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12 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 4 countries.

I Fricke-GalindoCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.
C Céspedes-GarroCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.
F Rodrigues-SoaresCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.ORCID http://orcid.org/0000-0002-2559-3223
M E G NaranjoCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.
Á DelgadoCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.
F de AndrésCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.
M López-LópezDepartment of Biological Systems, Metropolitan Autonomous University, Mexico City, Mexico.
E Peñas-LledóCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.
A LLerenaCICAB Clinical Research Centre, Extremadura University Hospital and Medical School, Badajoz, Spain.
Universidad de Extremadura · ESUniversidad Autónoma Metropolitana · MXUniversidad de Costa Rica · CRUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study evaluates the worldwide frequency distribution of CYP2C19 alleles and CYP2C19 metabolic phenotypes ('predicted' from genotypes and 'measured' with a probe drug) among healthy volunteers from different ethnic groups and geographic regions, as well as the relationship between the 'predicted' and 'measured' CYP2C19 metabolic phenotypes. A total of 52 181 healthy volunteers were studied within 138 selected original research papers. CYP2C19*17 was 42- and 24-fold more frequent in Mediterranean-South Europeans and Middle Easterns than in East Asians (P<0.001, in both cases). Contrarily, CYP2C19*2 and CYP2C19*3 alleles were more frequent in East Asians (30.26% and 6.89%, respectively), and even a twofold higher frequency of these alleles was found in Native populations from Oceania (61.30% and 14.42%, respectively; P<0.001, in all cases), which may be a consequence of genetic drift process in the Pacific Islands. Regarding CYP2C19 metabolic phenotype, poor metabolizers (PMs) were more frequent among Asians than in Europeans, contrarily to the phenomenon reported for CYP2D6. A correlation has been found between the frequencies of CYP2C19 poor metabolism 'predicted' from CYP2C19 genotypes (gPMs) and the poor metabolic phenotype 'measured' with a probe drug (mPMs) when subjects are either classified by ethnicity (r=0.94, P<0.001) or geographic region (r=0.99, P=0.002). Nevertheless, further research is needed in African and Asian populations, which are under-represented, and additional CYP2C19 variants and the 'measured' phenotype should be studied.

Indexed as

Racial GroupsCytochrome P-450 CYP2C19Gene FrequencyGenotypeGeographyHumansPhenotypePolymorphism, Single NucleotideCytochrome P-450 CYP2C19

Identifiers

PMID26503820
OpenAlexW2333696311

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.