Evidence map›Paper›PMID 30590387›Full record

Trial reportAmerican journal of hypertension2019

The Interaction of a Diabetes Gene Risk Score With 3 Different Antihypertensive Medications for Incident Glucose-level Elevation.

Joshua I Barzilay, Dejian Lai, Barry R Davis, Sara Pressel, Hannah E Previn, Donna K Arnett

Registry-linked trialOpen access · bronzeAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in American journal of hypertension, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT00000542. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact, top 84% 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.

NCT00000542 phase3completed

Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT)

Ran1993Registered outcomes0Posted comparisons0ConditionsCardiovascular Diseases, Coronary Disease, Diabetes Mellitus, Heart DiseasesArmsamlodipine, chlorthalidone, diet, fat-restricted, doxazosin, Inhibitors, ACE
Open the trial in the graph
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 3 institutions in 1 country.

Joshua I BarzilayDivision of Endocrinology, Kaiser Permanente of Georgia and Division of Endocrinology, Emory University School of Medicine, Atlanta, Georgia, USA.
Dejian LaiDepartment of Biostatistics, University of Texas School of Public Health, Houston, Texas, USA.
Barry R DavisClinical Trial Center, University of Texas School of Public Health, Houston, Texas, USA.
Sara PresselClinical Trial Center, University of Texas School of Public Health, Houston, Texas, USA.
Hannah E PrevinDepartment of Biostatistics, University of Texas School of Public Health, Houston, Texas, USA.
Donna K ArnettDepartment of Epidemiology, University of Kentucky College of Public Health, Lexington, Kentucky, USA.
The University of Texas Health Science Center at Houston · USKaiser Permanente · USUniversity of Kentucky · US

Funding

NHLBI NIH HHS HHSN268201100036C
6 · The paper itself

Abstract

backgroundElevations of fasting glucose (FG) levels are frequently encountered in people treated with thiazide diuretics. The risk is lower in people treated with ACE inhibitors (ACEi). To determine if genetic factors play a role in FG elevation, we examined the interaction of a diabetes gene risk score (GRS) with the use of 3 different antihypertensive medications.

methodsWe examined 376 nondiabetic hypertensive individuals with baseline FG <100 mg/dl who were genotyped for 24 genes associated with risk of elevated glucose levels. All participants had ≥1 follow-up FG level over 6 years of follow-up. Participants were randomized to treatment with a thiazide-like diuretic (chlorthalidone), a calcium channel blocker (CCB; amlodipine), or an ACEi (lisinopril). Outcomes were an FG increase of ≥13 or ≥27 mg/dl, the upper 75% and 90% FG increase in the parent cohort from which the present cohort was obtained. Odds ratios were adjusted for factors that increase FG levels.

resultsFor every 1 allele increase in GRS, the adjusted odds ratios (ORs) were 1.06 (95% confidence interval (CI): 0.99, 1.14; P = 0.06) and 1.09 (95% CI: 0.99, 1.20; P = 0.08). When results were examined by randomized medications, participants randomized to amlodipine had statistically significant odds for either outcome (OR: 1.23; 95% CI: 1.03, 1.48; P = 0.01 and OR: 1.31; 95% CI: 1.06, 1.62; P = 0.01). No such risk increase was found in participants randomized to the other 2 medications.

conclusionsA diabetes GRS predicts FG elevation in people treated with a CCB, but not with an ACEi or diuretic. These findings require confirmation. CLINICAL TRIALS REGISTRATION: Trial number NCT00000542.

Indexed as

Polymorphism, Single NucleotideAlkadienesAmlodipineAngiotensin-Converting Enzyme InhibitorsBlood GlucoseCalcium Channel BlockersChlorthalidoneDiabetes MellitusFemaleGene FrequencyGenetic TestingGenotypeHumansHypertensionLisinoprilMaleAlkadienesAmlodipineAngiotensin-Converting Enzyme InhibitorsBlood GlucoseCalcium Channel BlockersChlorthalidoneLisinoprilpropadieneSodium Chloride Symporter Inhibitorsarea under curveblood pressurediabetesfasting glucosegene risk scorehypertensionnet reclassification improvement

Identifiers

PMID30590387
PMCPMC6420683
OpenAlexW2906172322

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.