Evidence map›Paper›PMID 33321206›Full record

ArticleNitric oxide : biology and chemistry2021

Potential role for age as a modulator of oral nitrate reductase activity.

Khandaker Ahtesham Ahmed, Kiyoung Kim, Karina Ricart, William Van Der Pol, Xiaoping Qi, Marcas M Bamman, Christian Behrens, Gordon Fisher, Michael E Boulton, Casey Morrow and 2 more

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Nitric oxide : biology and chemistry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Trial
  2. Review
  3. ACS omega · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Khandaker Ahtesham AhmedDepartment of Pathology and Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Kiyoung KimDepartment of Pathology and Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, AL, USA; Department of Pharmacology & Experimental Therapeutics and the Whitaker Cardiovascular Institute, Boston University School of Medicine, Boston, MA, USA.
Karina RicartDepartment of Pathology and Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
William Van Der PolCenter for Clinical and Translational Science, University of Alabama at Birmingham, Birmingham, USA.
Xiaoping QiDepartment of Ophthalmology, University of Alabama at Birmingham, Birmingham, AL, USA.
Marcas M BammanDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Christian BehrensDepartment of Nutrition Sciences, University of Alabama at Birmingham, Birmingham, AL, USA.
Gordon FisherDepartment of Human Studies, University of Alabama at Birmingham, Birmingham, AL, USA.
Michael E BoultonDepartment of Ophthalmology, University of Alabama at Birmingham, Birmingham, AL, USA.
Casey MorrowDepartment of Cell, Developmental and Integrative Biology, University of Alabama at Birmingham, Birmingham, AL, USA.
Pamela V O'NealCollege of Nursing, University of Alabama in Huntsville, Huntsville, AL, USA.
Rakesh P PatelDepartment of Pathology and Center for Free Radical Biology, University of Alabama at Birmingham, Birmingham, AL, USA. Electronic address: rakeshpatel@uabmc.edu.
University of Alabama at Birmingham · USBoston University · USUniversity of Alabama in Huntsville · US

Funding

UAB Center for Clinical and Translational Science (CCTS)UL1TR001417 · NCATS · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KIMBERLY, ROBERT P. · 2015 to 2018
$31.4M
University of Alabama at Birmingham's Diabetes Research CenterP30DK079626 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Kirk Michael Habegger · 2013 to 2026
$19.5M
MECHANISMS OF HYPERTENSION AND CARDIOVASCULAR DISEASEST32HL007457 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Martin E Young · 1985 to 2026
$8.6M
Dental Academic Research Training Program (DART)T90DE022736 · NIDCR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Amjad Javed · 2012 to 2026
$6.7M
UAB Pre-Doctoral Training Program in Obesity-Related ResearchT32HL105349 · NHLBI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI BARBARA A GOWER · 2010 to 2026
$5.7M
NCATS NIH HHS UL1 TR001417NHLBI NIH HHS T32 HL007457NHLBI NIH HHS T32 HL105349NIDCR NIH HHS T90 DE022736NIDDK NIH HHS P30 DK079626
6 · The paper itself

Abstract

Reduction of salivary nitrate to nitrite by oral nitrate reductase (NR) expressing bacteria has emerged as an integral pathway in regulating nitric oxide (NO) homeostasis and signaling. The oral microbiome is critical for this pathway. Variations in this pathway may underlie variable responses in the magnitude by which dietary or therapeutic nitrate modulates NO-signaling. The relationships between oral microbes and NR activity, and the factors that affect this relationship remain unclear however. Using a cross-sectional study design, the objective of this study was to determine the relationships between oral microbes and oral NR activity using a protocol that directly measures initial NR activity. Tongue swabs were collected from 28 subjects ranging in age from 21 to 73y. Initial NR activity showed a bell-shaped dependence with age, with activity peaking at ~40-50y and being lower but similar between younger (20-30y) and older (51-73) individuals. Microbiome relative abundance and diversity analyses, using 16s sequencing, demonstrated differences across age and identified both NR expressing and non-expressing bacteria in modulating initial NR activity. Finally, initial NR activity was measured in 3mo and 13mo old C57BL/6J mice. No differences in bacterial number were observed. However initial NR activity was significantly (80%) lower in 13mo old mice. Collectively, these data suggest that age is a variable in NR activity and may modulate responsiveness to dietary nitrate.

Indexed as

AdultAgedAge FactorsAnimalsBacteriaBacterial ProteinsCross-Sectional StudiesFemaleHumansMaleMiceMice, Inbred C57BLMicrobiotaMiddle AgedNitrate ReductaseNitratesBacterial ProteinsNitrate ReductaseNitratesNitritesAgingMicrobiomeNitric oxide

Identifiers

PMID33321206
PMCPMC8085911
OpenAlexW3113214755

What OpenQuestion holds

Textmetadata
LicenceTDM
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.