Evidence map›Paper›PMID 33669176›Full record

ArticleJournal of personalized medicine2021

Common Treatment, Common Variant: Evolutionary Prediction of Functional Pharmacogenomic Variants.

Laura B Scheinfeldt, Andrew Brangan, Dara M Kusic, Sudhir Kumar, Neda Gharani

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Overcoming Barriers to Discovery and Implementation of Equitable Pharmacogenomic Testing in Oncology.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2024
    Review
  5. Article
  6. Article
  7. Article
  8. 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

5 authors at 2 institutions in 2 countries.

Laura B ScheinfeldtCoriell Institute for Medical Research, Camden, NJ 08003, USA.ORCID 0000-0001-6529-6701
Andrew BranganCoriell Institute for Medical Research, Camden, NJ 08003, USA.
Dara M KusicCoriell Institute for Medical Research, Camden, NJ 08003, USA.
Sudhir KumarInstitute for Genomics and Evolutionary Medicine, Temple University, Philadelphia, PA 19122, USA.ORCID 0000-0002-9918-8212
Neda GharaniCoriell Institute for Medical Research, Camden, NJ 08003, USA.
Coriell Institute For Medical Research · USKing Abdulaziz University · SA

Funding

Sample Repository for Human Genetic ResearchU41HG008736 · NHGRI · CORIELL INSTITUTE FOR MEDICAL RESEARCH · PI RESCH, ALISSA MARIE · 2016 to 2020
$4.3M
Methods For Evolutionary Genomics AnalysisR35GM139540 · NIGMS · TEMPLE UNIV OF THE COMMONWEALTH · PI Sudhir Kumar · 2021 to 2026
$2.9M
Bioinformatics of metastatic migration historiesR01LM013385 · NLM · TEMPLE UNIV OF THE COMMONWEALTH · PI KUMAR, SUDHIR · 2020 to 2023
$1.4M
NHGRI NIH HHS U41 HG008736NIGMS NIH HHS R35 GM139540NLM NIH HHS R01 LM013385
6 · The paper itself

Abstract

Pharmacogenomics holds the promise of personalized drug efficacy optimization and drug toxicity minimization. Much of the research conducted to date, however, suffers from an ascertainment bias towards European participants. Here, we leverage publicly available, whole genome sequencing data collected from global populations, evolutionary characteristics, and annotated protein features to construct a new in silico machine learning pharmacogenetic identification method called XGB-PGX. When applied to pharmacogenetic data, XGB-PGX outperformed all existing prediction methods and identified over 2000 new pharmacogenetic variants. While there are modest pharmacogenetic allele frequency distribution differences across global population samples, the most striking distinction is between the relatively rare putatively neutral pharmacogene variants and the relatively common established and newly predicted functional pharamacogenetic variants. Our findings therefore support a focus on individual patient pharmacogenetic testing rather than on clinical presumptions about patient race, ethnicity, or ancestral geographic residence. We further encourage more attention be given to the impact of common variation on drug response and propose a new 'common treatment, common variant' perspective for pharmacogenetic prediction that is distinct from the types of variation that underlie complex and Mendelian disease. XGB-PGX has identified many new pharmacovariants that are present across all global communities; however, communities that have been underrepresented in genomic research are likely to benefit the most from XGB-PGX's in silico predictions.

Indexed as

adaptationhuman evolutionmachine learningpharmacogenomic

Identifiers

PMID33669176
PMCPMC7919641
OpenAlexW3132668965

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.