Evidence map›Paper›PMID 32755471›Full record

Trial reportHypertension (Dallas, Tex. : 1979)2020

Effects of Oral Sodium Nitrite on Blood Pressure, Insulin Sensitivity, and Intima-Media Arterial Thickening in Adults With Hypertension and Metabolic Syndrome.

Kara S Hughan, Andrea Levine, Nicole Helbling, Steven Anthony, James P DeLany, Maja Stefanovic-Racic, Bret H Goodpaster, Mark T Gladwin

Registry-linked trialOpen access · bronzeAbstract readClinical Trial, Phase II
In one paragraph

Trial report in Hypertension (Dallas, Tex. : 1979), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01681810 (An Open-Label Study of Oral Nitrite in Adults With Metabolic Syndrome and Hypertension), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 9% 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.

NCT01681810 phase2completednot on this map

An Open-Label Study of Oral Nitrite in Adults With Metabolic Syndrome and Hypertension

TypeinterventionalSponsorGladwin, Mark, MDRan2012 to 2018Enrolled20ConditionsMetabolic Syndrome, HypertensionArms14Nitrogen Sodium Nitrite
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 32 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

8 authors at 1 institution in 1 country.

Kara S HughanFrom the Division of Pediatric Endocrinology and Diabetes, Department of Pediatrics (K.S.H.), University of Pittsburgh, PA.
Andrea LevinePittsburgh Heart, Lung, and Blood Vascular Medicine Institute (K.S.H., A.L., M.T.G.), University of Pittsburgh, PA.
Nicole HelblingDivision of Endocrinology, Department of Medicine (N.H., S.A., J.P.D., M.S.-R., B.H.G.), University of Pittsburgh, PA.
Steven AnthonyDivision of Endocrinology, Department of Medicine (N.H., S.A., J.P.D., M.S.-R., B.H.G.), University of Pittsburgh, PA.
James P DeLanyDivision of Endocrinology, Department of Medicine (N.H., S.A., J.P.D., M.S.-R., B.H.G.), University of Pittsburgh, PA.
Maja Stefanovic-RacicDivision of Endocrinology, Department of Medicine (N.H., S.A., J.P.D., M.S.-R., B.H.G.), University of Pittsburgh, PA.
Bret H GoodpasterDivision of Endocrinology, Department of Medicine (N.H., S.A., J.P.D., M.S.-R., B.H.G.), University of Pittsburgh, PA.
Mark T GladwinPittsburgh Heart, Lung, and Blood Vascular Medicine Institute (K.S.H., A.L., M.T.G.), University of Pittsburgh, PA.
University of Pittsburgh · US

Funding

Vascular Subphenotypes of Lung DiseaseP01HL103455 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI MORA, ANA LUCIA · 2011 to 2020
$26.1M
Storage Lesion in Banked Blood Due to Disruption of Nitric Oxide HomeostasisR01HL098032 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Mark T Gladwin · 2009 to 2026
$12.5M
Antidote for inhaled CO poisoning based on mutationally engineered neuroglobinR01HL125886 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Mark T Gladwin, Jesus Tejero Bravo · 2015 to 2026
$7.9M
Molecular Basis of Pediatric DiseaseK12HD052892 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TERENCE S. DERMODY · 2007 to 2026
$6.5M
Translational Pulmonary Vascular BiologyT32HL110849 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Sruti Shiva · 2012 to 2026
$5.0M
1/2 Sickle Cell Disease and CardiovAscular Risk - Red cell Exchange Trial (SCD-CARRE Trial)UG3HL143192 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GLADWIN, MARK T, TRIULZI, DARRELL J · 2019 to 2019
$1.5M
Nitrite Modulation of Hypertension, Platelet Activation and Endothelial and Mitochondrial FunctionK23HL124051 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HUGHAN, KARA S. · 2015 to 2017
$471k
NHLBI NIH HHS K23 HL124051NHLBI NIH HHS P01 HL103455NHLBI NIH HHS R01 HL098032NHLBI NIH HHS R01 HL125886NHLBI NIH HHS T32 HL110849NHLBI NIH HHS UG3 HL143192NICHD NIH HHS K12 HD052892
6 · The paper itself

Abstract

The nitrate-nitrite-NO pathway regulates NO synthase-independent vasodilation and NO signaling. Ingestion of inorganic nitrite has vasodilatory and blood pressure-lowering effects. Preclinical studies in rodent models suggest there may be a benefit of nitrite in lowering serum triglyceride levels and improving the metabolic syndrome. In a phase 2 study, we evaluated the safety and efficacy of chronic oral nitrite therapy in patients with hypertension and the metabolic syndrome. Twenty adult subjects with stage 1 or 2 hypertension and the metabolic syndrome were enrolled in an open-label safety and efficacy study. The primary efficacy end point was blood pressure reduction; secondary end points included insulin-dependent glucose disposal and endothelial function measured by flow-mediated dilation of the brachial artery and intima-media diameter of the carotid artery. Chronic oral nitrite therapy (40 mg/3× daily) was well tolerated. Oral nitrite significantly lowered systolic, diastolic, and mean arterial pressures, but tolerance was observed after 10 to 12 weeks of therapy. There was significant improvement in the intima-media thickness of the carotid artery and trends toward improvements in flow-mediated dilation of the brachial artery and insulin sensitivity. Chronic oral nitrite therapy is safe in patients with hypertension and the metabolic syndrome. Despite an apparent lack of enzymatic tolerance to nitrite, we observed tolerance after 10 weeks of chronic therapy, which requires additional mechanistic studies and possible therapeutic dose titration in clinical trials. Nitrite may be a safe therapy to concominantly improve multiple features of the metabolic syndrome including hypertension, insulin resistance, and endothelial dysfunction. Registration- URL: https://www.clinicaltrials.gov; Unique identifier: NCT01681810.

Indexed as

Brachial ArteryEndothelium, VascularHypertensionMetabolic SyndromeSodium NitriteAdultAntihypertensive AgentsBlood PressureCarotid Intima-Media ThicknessFemaleHumansInsulin ResistanceMaleTreatment OutcomeTriglyceridesVasodilationAntihypertensive AgentsSodium NitriteTriglyceridesblood pressureclinical trialhypertensionmetabolic syndromenitritevasodilation

Identifiers

PMID32755471
PMCPMC7429358
OpenAlexW3046636332

What OpenQuestion 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 OpenQuestion graph.