Evidence map›Paper›PMID 30452466›Full record

ArticlePloS one2018

Characterization of ADME genes variation in Roma and 20 populations worldwide.

Tatjana Škarić-Jurić, Željka Tomas, Matea Zajc Petranović, Nada Božina, Nina Smolej Narančić, Branka Janićijević, Marijana Peričić Salihović

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. From Croatian Roma to 1000 Genomes: The Story of theJournal of personalized medicine · 2022
    Article
  4. Untangling SNP Variations withinJournal of personalized medicine · 2022
    Article
  5. Article
  6. 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

7 authors.

Tatjana Škarić-JurićInstitute for Anthropological Research, Zagreb, Croatia.
Željka TomasInstitute for Anthropological Research, Zagreb, Croatia.
Matea Zajc PetranovićInstitute for Anthropological Research, Zagreb, Croatia.
Nada BožinaDepartment for Pharmacogenomics and Therapy Individualization, University Hospital Center Zagreb, Department of Pharmacology, University of Zagreb School of Medicine, Zagreb, Croatia.
Nina Smolej NarančićInstitute for Anthropological Research, Zagreb, Croatia.
Branka JanićijevićInstitute for Anthropological Research, Zagreb, Croatia.ORCID 0000-0002-2466-4392
Marijana Peričić SalihovićInstitute for Anthropological Research, Zagreb, Croatia.ORCID 0000-0001-6860-3316

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The products of the polymorphic ADME genes are involved in Absorption, Distribution, Metabolism, and Excretion of drugs. The pharmacogenetic data have been studied extensively due to their clinical importance in the appropriate drug prescription, but such data from the isolated populations are rather scarce. We analyzed the distribution of 95 polymorphisms in 31 core ADME genes in 20 populations worldwide and in newly genotyped samples from the Roma (Gypsy) population living in Croatia. Global distribution of ADME core gene loci differentiated three major clusters; (1) African, (2) East Asian, and (3) joint European, South Asian and South American cluster. The SLCO1B3 (rs4149117) and CYP3A4 (rs2242480) genes differentiated at the highest level the African group of populations, while NAT2 gene loci (rs1208, rs1801280, and rs1799929) and VKORC1 (rs9923231) differentiated East Asian populations. The VKORC1 rs9923231 was among the investigated loci the one with the largest global minor allele frequency (MAF) range; its MAF ranged from 0.027 in Nigeria to 0.924 in Han Chinese. The distribution of the investigated gene loci positions Roma population within the joined European and South Asian clusters, suggesting that their ADME gene pool is a combination of ancestral (Indian) and more recent (European) surrounding, as it was already implied by other genetic markers. However, when compared to the populations worldwide, the Croatian Roma have extreme MAF values in 10 out of the 95 investigated ADME core gene loci. Among loci which have extraordinary MAFs in Roma population two have strong proof of clinical importance: rs1799853 (CYP2C9) for warfarin dosage, and rs12248560 (CYP2C19) for clopidogrel dosage, efficacy and toxicity. This finding confirms the importance of taking the Roma as well as the other isolated populations`genetic profiles into account in pharmaco-therapeutic practice.

Indexed as

Pharmacogenomic VariantsAfricaArylamine N-AcetyltransferaseAsiaClopidogrelCroatiaCytochrome P-450 CYP2C19Cytochrome P-450 CYP3AGene FrequencyGenetics, PopulationHuman MigrationHumansPolymorphism, Single NucleotidePrincipal Component AnalysisRomani PeopleSolute Carrier Organic Anion Transporter Family Member 1B3Arylamine N-AcetyltransferaseClopidogrelCYP2C19 protein, humanCYP3A4 protein, humanCytochrome P-450 CYP2C19Cytochrome P-450 CYP3ANAT2 protein, humanSLCO1B3 protein, humanSolute Carrier Organic Anion Transporter Family Member 1B3Vitamin K Epoxide ReductasesVKORC1 protein, humanWarfarin

Identifiers

PMID30452466
PMCPMC6242375

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.