Evidence map›Paper›PMID 30489456›Full record

ArticlePharmacogenetics and genomics2019

Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy.

Kimberly S Collins, Victoria M Pratt, Wesley M Stansberry, Elizabeth B Medeiros, Karthik Kannegolla, Marelize Swart, Todd C Skaar, Arlene B Chapman, Brian S Decker, Ranjani N Moorthi and 1 more

Abstract read
In one paragraph

Article in Pharmacogenetics and genomics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Oxidative medicine and cellular longevity · 2019
    Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Pharmacogenomic and Statistical Analysis.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  7. Article
  8. Article
  9. Article
  10. Genotype-Guided Hydralazine Therapy.American journal of nephrology · 2020
    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

11 authors at 4 institutions in 1 country.

Kimberly S CollinsDepartments of Medicine.
Victoria M PrattMedical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Wesley M StansberryMedical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Elizabeth B MedeirosMedical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, Indiana.
Karthik KannegollaDepartments of Medicine.
Marelize SwartDepartments of Medicine.
Todd C SkaarDepartments of Medicine.
Arlene B ChapmanDepartment of Medicine, University of Chicago, Illinois, USA.
Brian S DeckerDepartments of Medicine.
Ranjani N MoorthiDepartments of Medicine.
Michael T EadonDepartments of Medicine.
Indiana University – Purdue University Indianapolis · USGTx (United States) · USIndiana University School of MedicineUniversity of Chicago · US

Funding

Embedding Pharmacogenotyping in an Integrated Health System for the UnderservedU01HG007762 · NHGRI · INDIANA UNIVERSITY INDIANAPOLIS · PI DEXTER, PAUL, SKAAR, TODD C. · 2014 to 2018
$4.4M
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 HG007762NIDDK NIH HHS K08 DK107864
6 · The paper itself

Abstract

Hypertension and chronic kidney disease are inextricably linked. Hypertension is a well-recognized contributor to chronic kidney disease progression and, in turn, renal disease potentiates hypertension. A generalized approach to drug selection and dosage has not proven effective in managing these conditions, in part, because patients with heterogeneous kidney disease and hypertension etiologies are frequently grouped according to functional or severity classifications. Genetic testing may serve as an important tool in the armamentarium of clinicians who embrace precision medicine. Increasing scientific evidence has supported the utilization of genomic information to select efficacious antihypertensive therapy and understand hereditary contributors to chronic kidney disease progression. Given the wide array of antihypertensive agents available and diversity of genetic renal disease predictors, a panel-based approach to genotyping may be an efficient and economic means of establishing an individualized blood pressure response profile for patients with various forms of chronic kidney disease and hypertension. In this manuscript, we discuss the validation process of a Clinical Laboratory Improvement Amendments-approved genetic test to relay information on 72 genetic variants associated with kidney disease progression and hypertension therapy. These genomic-based interventions, in addition to routine clinical data, may help inform physicians to provide personalized therapy.

Indexed as

Pharmacogenomic VariantsAntihypertensive AgentsGenotyping TechniquesHumansHypertensionPatient-Centered CarePrecision MedicineRenal Insufficiency, ChronicAntihypertensive Agents

Identifiers

PMID30489456
PMCPMC6358457
OpenAlexW2902122622

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.