Evidence map›Paper›PMID 19379125›Full record

ReviewExpert opinion on drug metabolism & toxicology2009

N-acetyltransferase SNPs: emerging concepts serve as a paradigm for understanding complexities of personalized medicine.

David W Hein

Abstract readReview
In one paragraph

Review in Expert opinion on drug metabolism & toxicology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 3 pooled it
–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

65 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. N-acetyltransferase 2 genetic variants confer the susceptibility to head and neck carcinoma: evidence from 23 case-control studies.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Pooled it
  4. Article
  5. PharmVar GeneFocus: NAT2-Genetic Variation and Updated Nomenclature.Clinical pharmacology and therapeutics · 2026
    Review
  6. Pharmacogenomic heterogeneity ofAnnals of medicine · 2025
    Observational
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. The role ofFrontiers in cellular and infection microbiology · 2023
    Review
  13. Review
  14. A Method to Determine Xenobiotic Acetylation Rate by Taq SNP rs1495741.Bulletin of experimental biology and medicine · 2022
    Article
  15. Article
  16. Article
  17. Acetyl coenzyme A kinetic studies onFrontiers in pharmacology · 2022
    Article
  18. Pharmacogenomics Informs Cardiovascular Pharmacotherapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  19. Article
  20. Article

5 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

1 author.

David W HeinUniversity of Louisville School of Medicine, James Graham Brown Cancer Center, Center for Environmental Genomics and Integrative Biology, Department of Pharmacology & Toxicology, Louisville, KY 40292, USA. d.hein@louisville.edu

Funding

Strategic Vision & Impact on Environmental HealthP30ES014443 · NIEHS · UNIVERSITY OF LOUISVILLE · PI PROUGH, RUSSELL ALLEN · 2007 to 2010
$4.4M
PHARMACOGENETICS OF DRUG &CARCINOGEN METABOLISMR01CA034627 · NCI · UNIVERSITY OF NORTH DAKOTA · PI HEIN, DAVID W · 1985 to 2009
$3.1M
Center for Pediatric Clinical Pharmacology ResearchU10HD045934 · NICHD · UNIVERSITY OF LOUISVILLE · PI SULLIVAN, JANICE E · 2004 to 2009
$2.0M
NCI NIH HHS R01 CA034627NCI NIH HHS R01-CA034627NICHD NIH HHS U10 HD045934NICHD NIH HHS U10-HD045934NIEHS NIH HHS P30 ES014443NIEHS NIH HHS P30-ES014443
6 · The paper itself

Abstract

Arylamine N-acetyltransferase 1 and 2 exhibit single nucleotide polymorphisms in human populations that modify drug and carcinogen metabolism. This paper updates the identity, location and functional effects of these single nucleotide polymorphisms and then follows with emerging concepts for understanding why pharmacogenetic findings may not be replicated consistently. Using this paradigm as an example, laboratory-based mechanistic analyses can reveal complexities such that genetic polymorphisms become biologically and medically relevant when confounding factors are more fully understood and considered. As medical care moves to a more personalized approach, the implications of these confounding factors will be important in understanding the complexities of personalized medicine.

Indexed as

Precision MedicineAnimalsArylamine N-AcetyltransferaseHumansIsoenzymesPharmacogeneticsPolymorphism, Single NucleotideArylamine N-AcetyltransferaseIsoenzymesN-acetyltransferase 1NAT2 protein, human

Identifiers

PMID19379125
PMCPMC2762189

What OpenQuestion holds

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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.