Evidence mapPaperPMID 18728266Full record

Trial reportJAMA2008

Effect of allopurinol on blood pressure of adolescents with newly diagnosed essential hypertension: a randomized trial.

Daniel I Feig, Beth Soletsky, Richard J Johnson

4 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in JAMA, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 392 papers, 11 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
392citing papers in PubMed, 11 pooled it
31.0field-weighted citation impact, top 1% 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.

NCT00288184 phase2completednot on this map

Randomized Double-blinded, Placebo-controlled, Cross-over Trial of Allopurinol for the Treatment of Newly Diagnosed Essential Hypertension in Adolescents

TypeinterventionalSponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)Ran2004 to 2007Enrolled30ConditionsEssential HypertensionArmsAllopurinol, Placebo
NCT03305562 terminatednot on this mapstarted 2017, after this paper: background citation

Pediatric Hypertension Registry (PHREG)

Typeobservational_patient_registrySponsorWake Forest University Health SciencesRan2017 to 2021Enrolled179ConditionsHypertension, Pediatric Disorder
NCT03310684 completednot on this mapstarted 2018, after this paper: background citation

The Role of the Renin-Angiotensin System in Pediatric Primary Hypertension (PHRAS)

TypeobservationalSponsorWake Forest University Health SciencesRan2018 to 2023Enrolled35ConditionsPediatric Disorder, Pediatric Obesity, Primary Hypertension
NCT04752293 recruitingnot on this mapstarted 2021, after this paper: background citation

Pediatric Hypertension and the Renin-Angiotensin SystEm (PHRASE): The Role of Angiotensin-(1-7) in Hypertension and Hypertension-Induced Heart and Kidney Damage

TypeobservationalSponsorWake Forest University Health SciencesRan2021 to 2026Enrolled125ConditionsHypertension, Left Ventricular Hypertrophy, Left Ventricular Dysfunction, Left Atrial Dilatation
3 · Its place in the literature

Who cites it

392 citing papers in PubMed, 11 syntheses or guidelines pooled it, 915 citations in OpenAlex.

  1. Guideline
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  8. Pharmacotherapy for hyperuricaemia in hypertensive patients.The Cochrane database of systematic reviews · 2020
    Pooled it
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  10. Pharmacotherapy for hyperuricemia in hypertensive patients.The Cochrane database of systematic reviews · 2017
    Pooled it
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  20. Vascular Function and Uric Acid-Lowering in Stage 3 CKD.Journal of the American Society of Nephrology : JASN · 2017
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332 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Daniel I FeigDepartment of Pediatrics, Renal Section, Baylor College of Medicine, Houston, TX 77030, USA. dfeig@bcm.tmc.edu
Beth Soletsky
Richard J Johnson
Baylor College of Medicine · USUniversity of Florida · US

Funding

Role of Uric Acid in Hypertension and Renal DiseaseR01HL068607 · UNIVERSITY OF FLORIDA · 2002 to 2005
$1.5M
Uric Acid in Childhood HypertensionK23DK064587 · BAYLOR COLLEGE OF MEDICINE · 2003 to 2005
$411k
NHLBI NIH HHS HL-68607NHLBI NIH HHS R01 HL068607NIDDK NIH HHS 5 K23 DK064587NIDDK NIH HHS K23 DK064587
6 · The paper itself

Abstract

contextHyperuricemia is a predictor for the development of hypertension and is commonly present in new-onset essential hypertension. Experimentally increasing uric acid levels using a uricase inhibitor causes systemic hypertension in animal models.

objectiveTo determine whether lowering uric acid lowers blood pressure (BP) in hyperuricemic adolescents with newly diagnosed hypertension. DESIGN, SETTING, AND PATIENTS: Randomized, double-blind, placebo-controlled, crossover trial (September 2004-March 2007) involving 30 adolescents (aged 11-17 years) who had newly diagnosed, never-treated stage 1 essential hypertension and serum uric acid levels > or = 6 mg/dL. Participants were treated at the Pediatric Hypertension Clinic at Texas Children's Hospital in Houston. Patients were excluded if they had stage 2 hypertension or known renal, cardiovascular, gastrointestinal tract, hepatic, or endocrine disease.

interventionAllopurinol, 200 mg twice daily for 4 weeks, and placebo, twice daily for 4 weeks, with a 2-week washout period between treatments. The order of the treatments was randomized.

main outcome measuresChange in casual and ambulatory blood pressure.

resultsFor casual BP, the mean change in systolic BP for allopurinol was -6.9 mm Hg (95% confidence interval [CI], -4.5 to -9.3 mm Hg) vs -2.0 mm Hg (95% CI, 0.3 to -4.3 mm Hg; P = .009) for placebo, and the mean change in diastolic BP for allopurinol was -5.1 mm Hg (95% CI, -2.5 to -7.8 mm Hg) vs -2.4 (95% CI, 0.2 to -4.1; P = .05) for placebo. Mean change in mean 24-hour ambulatory systolic BP for allopurinol was -6.3 mm Hg (95% CI, -3.8 to -8.9 mm Hg) vs 0.8 mm Hg (95% CI, 3.4 to -2.9 mm Hg; P = .001) for placebo and mean 24-hour ambulatory diastolic BP for allopurinol was -4.6 mm Hg (-2.4 to -6.8 mm Hg) vs -0.3 mm Hg (95% CI, 2.3 to -2.1 mm Hg; P = .004) for placebo. Twenty of the 30 participants achieved normal BP by casual and ambulatory criteria while taking allopurinol vs 1 participant while taking placebo (P < .001).

conclusionsIn this short-term, crossover study of adolescents with newly diagnosed hypertension, treatment with allopurinol resulted in reduction of BP. The results represent a new potential therapeutic approach, although not a fully developed therapeutic strategy due to potential adverse effects. These preliminary findings require confirmation in larger clinical trials.

trial registrationclinicaltrials.gov Identifier: NCT00288184.

Indexed as

AdolescentAllopurinolBlood PressureCross-Over StudiesDouble-Blind MethodEnzyme InhibitorsFemaleHumansHypertensionHyperuricemiaMaleUric AcidXanthine OxidaseAllopurinolEnzyme InhibitorsUric AcidXanthine Oxidase

Identifiers

PMID18728266
PMCPMC2684336
OpenAlexW2031005241

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.