Evidence map›Paper›PMID 35780191›Full record

ArticleThe pharmacogenomics journal2022

The clinically relevant CYP2C8*3 and CYP2C9*2 haplotype is inherited from Neandertals.

Sigrid Haeggström, Magnus Ingelman-Sundberg, Svante Pääbo, Hugo Zeberg

Open access · hybridAbstract read
In one paragraph

Article in The pharmacogenomics journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
26.0field-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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
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 2 institutions in 3 countries.

Sigrid HaeggströmDepartment of Neuroscience, Karolinska Institutet, SE-17177, Stockholm, Sweden.
Magnus Ingelman-SundbergDepartment of Physiology and Pharmacology, Karolinska Institutet, SE-17177, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-7255-9079
Svante PääboDepartment of Evolutionary Genetics, Max Planck Institute for Evolutionary Anthropology, D-04103, Leipzig, Germany.
Hugo ZebergDepartment of Neuroscience, Karolinska Institutet, SE-17177, Stockholm, Sweden. hugo.zeberg@ki.se.ORCID http://orcid.org/0000-0001-7118-1249
Karolinska Institutet · SEOkinawa Institute of Science and Technology Graduate University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic variation in genes encoding cytochrome P450 enzymes influences the metabolism of drugs and endogenous compounds. The locus containing the cytochrome genes CYP2C8 and CYP2C9 on chromosome 10 exhibits linkage disequilibrium between the CYP2C8*3 and CYP2C9*2 alleles, forming a haplotype of ~300 kilobases. This haplotype is associated with altered metabolism of several drugs, most notably reduced metabolism of warfarin and phenytoin, leading to toxicity at otherwise therapeutic doses. Here we show that this haplotype is inherited from Neandertals.

Indexed as

Aryl Hydrocarbon HydroxylasesNeanderthalsAnimalsCytochrome P-450 CYP2C8Cytochrome P-450 CYP2C9Gene FrequencyHaplotypesHumansAryl Hydrocarbon HydroxylasesCYP2C8 protein, humanCYP2C9 protein, humanCytochrome P-450 CYP2C8Cytochrome P-450 CYP2C9

Identifiers

PMID35780191
PMCPMC9363273
OpenAlexW4283784471

What OpenQuestion 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 OpenQuestion graph.