Evidence map›Paper›PMID 32927458›Full record

ReviewAmerican journal of nephrology2020

Genotype-Guided Hydralazine Therapy.

Kimberly S Collins, Anthony L J Raviele, Amanda L Elchynski, Alexander M Woodcock, Yang Zhao, Rhonda M Cooper-DeHoff, Michael T Eadon

Open access · bronzeAbstract readReview
In one paragraph

Review in American journal of nephrology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 2 pooled it
3.7field-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

18 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

  1. Guideline
  2. Pooled it
  3. Article
  4. Article
  5. PharmVar GeneFocus: NAT2-Genetic Variation and Updated Nomenclature.Clinical pharmacology and therapeutics · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Pharmacogenomics Informs Cardiovascular Pharmacotherapy.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. 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 at 3 institutions in 1 country.

Kimberly S CollinsDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Anthony L J RavieleDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Amanda L ElchynskiDepartment of Pharmacotherapy and Translational Research, University of Florida, Gainesville, Florida, USA.
Alexander M WoodcockDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA.
Yang ZhaoDepartment of Pharmacotherapy and Translational Research, University of Florida, Gainesville, Florida, USA.
Rhonda M Cooper-DeHoffDepartment of Pharmacotherapy and Translational Research, University of Florida, Gainesville, Florida, USA.
Michael T EadonDepartment of Medicine, Indiana University School of Medicine, Indianapolis, Indiana, USA, meadon@iupui.edu.
Indiana University – Purdue University Indianapolis · USUniversity of Florida · USIndiana University School of Medicine

Funding

Sparking Advancements in Genomic MedicineU01HG007269 · NHGRI · UNIVERSITY OF FLORIDA · PI CAVALLARI, LARISA HUMMA, JOHNSON, JULIE A. · 2013 to 2024
$17.0M
Implementing genomic medicine through pragmatic trials in diverse and underserved populations across Indiana.U01HG010245 · NHGRI · INDIANA UNIVERSITY INDIANAPOLIS · PI DEXTER, PAUL, SKAAR, TODD C. · 2018 to 2024
$9.4M
Indiana University Comprehensive Training in Clinical PharmacologyT32GM008425 · NIGMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI Zeruesenay Desta, Michael Thomas Eadon · 1992 to 2026
$7.7M
Acute inhibition of renal gene expression to prevent nephrotoxicity.K08DK107864 · NIDDK · INDIANA UNIVERSITY INDIANAPOLIS · PI EADON, MICHAEL THOMAS · 2016 to 2020
$772k
NHGRI NIH HHS U01 HG007269NHGRI NIH HHS U01 HG010245NIDDK NIH HHS K08 DK107864NIGMS NIH HHS T32 GM008425
6 · The paper itself

Abstract

backgroundDespite its approval in 1953, hydralazine hydrochloride continues to be used in the management of resistant hypertension, a condition frequently managed by nephrologists and other clinicians. Hydralazine hydrochloride undergoes metabolism by the N-acetyltransferase 2 (NAT2) enzyme. NAT2 is highly polymorphic as approximately 50% of the general population are slow acetylators. In this review, we first evaluate the link between NAT2 genotype and phenotype. We then assess the evidence available for genotype-guided therapy of hydralazine, specifically addressing associations of NAT2 acetylator status with hydralazine pharmacokinetics, antihypertensive efficacy, and toxicity. SUMMARY: There is a critical need to use hydralazine in some patients with resistant hypertension. Available evidence supports a significant link between genotype and NAT2 enzyme activity as 29 studies were identified with an overall concordance between genotype and phenotype of 92%. The literature also supports an association between acetylator status and hydralazine concentration, as fourteen of fifteen identified studies revealed significant relationships with a consistent direction of effect. Although fewer studies are available to directly link acetylator status with hydralazine antihypertensive efficacy, the evidence from this smaller set of studies is significant in 7 of 9 studies identified. Finally, 5 studies were identified which support the association of acetylator status with hydralazine-induced lupus. Clinicians should maintain vigilance when prescribing maximum doses of hydralazine. Key Messages: NAT2 slow acetylator status predicts increased hydralazine levels, which may lead to increased efficacy and adverse effects. Caution should be exercised in slow acetylators with total daily hydralazine doses of 200 mg or more. Fast acetylators are at risk for inefficacy at lower doses of hydralazine. With appropriate guidance on the usage of NAT2 genotype, clinicians can adopt a personalized approach to hydralazine dosing and prescription, enabling more efficient and safe treatment of resistant hypertension.

Indexed as

Antihypertensive AgentsArylamine N-AcetyltransferaseDose-Response Relationship, DrugDrug ResistanceHumansHydralazineHypertensionNephrologyPharmacogenomic TestingPharmacogenomic VariantsPractice Guidelines as TopicPrecision MedicineTreatment OutcomeAntihypertensive AgentsArylamine N-AcetyltransferaseHydralazineNAT2 protein, humanHydralazineN-acetyltransferase 2PharmacogeneticsResistant hypertension

Identifiers

PMID32927458
PMCPMC7606720
OpenAlexW3085419331

What OpenQuestion holds

Textmetadata
LicenceTDM
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.