Evidence map›Paper›PMID 26791477›Full record

Trial reportJournal of human hypertension2016

The effects of genes implicated in cardiovascular disease on blood pressure response to treatment among treatment-naive hypertensive African Americans in the GenHAT study.

A N Do, A I Lynch, S A Claas, E Boerwinkle, B R Davis, C E Ford, J H Eckfeldt, H K Tiwari, D K Arnett, M R Irvin

Open access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Journal of human hypertension, 2016. 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
1.6field-weighted citation impact, top 16% 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, 21 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

A N DoDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
A I LynchDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
S A ClaasDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
E BoerwinkleHuman Genetics Center, University of Texas Health Science Center at Houston, Houston, TX, USA.
B R DavisSchool of Public Health, University of Texas Health Science Center at Houston, Houston, TX, USA.
C E FordSchool of Public Health, University of Texas Health Science Center at Houston, Houston, TX, USA.
J H EckfeldtDepartment of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA.
H K TiwariDepartment of Biostatistics, University of Alabama at Birmingham, Birmingham, AL, USA.
D K ArnettDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
M R IrvinDepartment of Epidemiology, University of Alabama at Birmingham, Birmingham, AL, USA.
University of Alabama at Birmingham · USThe University of Texas Health Science Center at Houston · USUniversity of Minnesota · US

Funding

CLINICAL TRIALS CENTER FOR ALLHAT-N01HC35130-268035130N01HC035130 · HC · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · 1993 to 2005
$6.3M
GENHAT-GENETICS OF HYPERTENSION ASSOCIATED TREATMENTSR01HL063082 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ARNETT, DONNA K · 1999 to 2009
$5.1M
NHLBI NIH HHS N01 HC035130NHLBI NIH HHS R01 HL063082
6 · The paper itself

Abstract

African Americans have the highest prevalence of hypertension in the United States. Blood pressure (BP) control is important to reduce cardiovascular disease-related morbidity and mortality in this ethnic group. Genetic variants have been found to be associated with BP response to treatment. Previous pharmacogenetic studies of BP response to treatment in African Americans suffer limitations of small sample size as well as a limited number of candidate genes, and often focused on one antihypertensive treatment. Using 1131 African-American treatment-naive participants from the Genetics of Hypertension Associated Treatment Study, we examined whether variants in 35 candidate genes might modulate BP response to four different antihypertensive medications, including an angiotensin-converting enzyme inhibitor (lisinopril), a calcium channel blocker (amlodipine), and an a-adrenergic blocker (doxazosin) as compared with a thiazide diuretic (chlorthalidone) after 6 months of follow-up. Several suggestive gene by treatment interactions were identified. For example, among participants with two minor alleles of renin rs6681776, diastolic BP response was much improved on doxazosin compared with chlorthalidone (on average -9.49 mm Hg vs -1.70 mm Hg) (P=0.007). Although several suggestive loci were identified, none of the findings passed significance criteria after correction for multiple testing. Given the impact of hypertension and its sequelae in this population, this research highlights the potential for genetic factors to contribute to BP response to treatment. Continued concerted research efforts focused on genetics are needed to improve treatment response in this high-risk group.

Indexed as

Pharmacogenomic VariantsAdrenergic alpha-1 Receptor AntagonistsAgedAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsBlack or African AmericanBlood PressureCalcium Channel BlockersDiureticsDouble-Blind MethodFemaleGenetic Predisposition to DiseaseHumansHypertensionMaleMiddle AgedAdrenergic alpha-1 Receptor AntagonistsAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsCalcium Channel BlockersDiuretics

Identifiers

PMID26791477
PMCPMC4956602
OpenAlexW2337573400

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.