Evidence map›Paper›PMID 12439737›Full record

ArticleThe pharmacogenomics journal2002

Pharmacogenetic approaches to hypertension therapy: design and rationale for the Genetics of Hypertension Associated Treatment (GenHAT) study.

D K Arnett, E Boerwinkle, B R Davis, J Eckfeldt, C E Ford, H Black

2 registry-linked trialsAbstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
1.1field-weighted citation impact, top 23% 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.

NCT00006294 completednot on this map

Pharmacological Association of the Angiotensin-Converting Enzyme Insertion/Deletion Polymorphism on Blood Pressure and Cardiovascular Risk in Relation to Anti-hypertensive Treatment

TypeobservationalSponsorDonna Arnett, 257-5678Ran1999 to 2005Enrolled37,939ConditionsCardiovascular Diseases, Heart Diseases, Hypertension, Coronary DiseaseArmsChlorthalidone, Lisinopril, Amlodipine, Doxazosin
NCT00563901 completednot on this map

GenHAT - Genetics of Hypertension Associated Treatments - Ancillary to ALLHAT

TypeobservationalSponsorUniversity of Alabama at BirminghamRan2000 to 2004Enrolled37,939ConditionsHypertension, Coronary Disease, Cerebrovascular Accident
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 58 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Frontiers in medicine · 2022
    Article
  19. Hypertension genomics and cardiovascular prevention.Annals of translational medicine · 2018
    Review
  20. 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

6 authors at 4 institutions in 1 country.

D K ArnettUniversity of Minnesota, Division of Epidemiology, Minneapolis, 55454-1015, USA. arnett@epi.umn.edu
E Boerwinkle
B R Davis
J Eckfeldt
C E Ford
H Black
The University of Texas Health Science Center at Houston · USRush University Medical Center · USUniversity of Minnesota · USUniversity of Minnesota Medical Center · US

Funding

GENHAT-GENETICS OF HYPERTENSION ASSOCIATED TREATMENTSR01HL063082 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ARNETT, DONNA K · 1999 to 2009
$5.1M
Genetics of Hypertension Associated Treatment "GenHAT"R01HL083498 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BOERWINKLE, ERIC A. · 2007 to 2009
$1.4M
NHLBI NIH HHS R01 HL063082NHLBI NIH HHS R01 HL083498
6 · The paper itself

Abstract

The Genetics of Hypertension Associated Treatment (GenHAT) study will determine whether variants in hypertension susceptibility genes interact with antihypertensive medication to modify coronary heart disease (CHD) risk in hypertensives. GenHAT is an ancillary study of the Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial, ALLHAT, a double-blind, randomized trial of 42 418 hypertensives, 55 years of age or older, with systolic or diastolic hypertension and one or more risk factors for cardiovascular disease. About 50% are non-white, and about half are female. ALLHAT completes follow-up in March 2002. GenHAT is typing variants in hypertension genes; completion of genotyping is scheduled for 2003. Analysis of gene-treatment interactions in relation to outcomes include CHD, stroke, heart failure, and blood pressure lowering. To our knowledge, GenHAT is the largest pharmacogenetic study ever conducted. An added strength is its ability to link gene-treatment interactions with important clinical outcomes across diverse ethnic and gender groups.

Indexed as

HumansHypertensionPharmacogeneticsRandomized Controlled Trials as Topic

Identifiers

PMID12439737
OpenAlexW2045580470

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.