Evidence map›Paper›PMID 36364734›Full record

Trial reportNutrients2022

Oats Lower Age-Related Systemic Chronic Inflammation (iAge) in Adults at Risk for Cardiovascular Disease.

El Hadji M Dioum, Kevin L Schneider, David J Vigerust, Bryan D Cox, YiFang Chu, Jeffery J Zachwieja, David Furman

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Nutrients, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Review
  4. Review
  5. Article
  6. Article
  7. 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

7 authors at 2 institutions in 1 country.

El Hadji M DioumQuaker Oats Center of Excellence, PepsiCo Health and Nutrition Sciences, Chicago, IL 60607, USA.ORCID 0000-0001-9486-1124
Kevin L SchneiderEdifice Health Inc., San Mateo, CA 94401, USA.
David J VigerustEdifice Health Inc., San Mateo, CA 94401, USA.
Bryan D CoxEdifice Health Inc., San Mateo, CA 94401, USA.
YiFang ChuQuaker Oats Center of Excellence, PepsiCo Health and Nutrition Sciences, Chicago, IL 60607, USA.
Jeffery J ZachwiejaQuaker Oats Center of Excellence, PepsiCo Health and Nutrition Sciences, Chicago, IL 60607, USA.
David FurmanEdifice Health Inc., San Mateo, CA 94401, USA.
San Mateo County Health System · USPepsi (United States) · US

Funding

PepsiCo, Inc.
6 · The paper itself

Abstract

Despite being largely preventable, cardiovascular disease (CVD) is still the leading cause of death globally. Recent studies suggest that the immune system, particularly a form of systemic chronic inflammation (SCI), is involved in the mechanisms leading to CVD; thus, targeting SCI may help prevent or delay the onset of CVD. In a recent placebo-controlled randomized clinical trial, an oat product providing 3 g of β-Glucan improved cholesterol low-density lipoprotein (LDL) levels and lowered cardiovascular risk in adults with borderline high cholesterol. Here, we conducted a secondary measurement of the serum samples to test whether the oat product has the potential to reduce SCI and improve other clinical outcomes related to healthy aging. We investigated the effects of the oat product on a novel metric for SCI called Inflammatory Age® (iAge®), derived from the Stanford 1000 Immunomes Project. The iAge® predicts multimorbidity, frailty, immune decline, premature cardiovascular aging, and all-cause mortality on a personalized level. A beneficial effect of the oat product was observed in subjects with elevated levels of iAge® at baseline (>49.6 iAge® years) as early as two weeks post-treatment. The rice control group did not show any significant change in iAge®. Interestingly, the effects of the oat product on iAge® were largely driven by a decrease in the Eotaxin-1 protein, an aging-related chemokine, independent of a person’s gender, body mass index, or chronological age. Thus, we describe a novel anti-SCI role for oats that could have a major impact on functional, preventative, and personalized medicine.

Indexed as

AvenaCardiovascular DiseasesAdultCholesterolCholesterol, LDLDietary FiberEdible GrainHumansInflammationCholesterolCholesterol, LDLDietary Fiberbeta-glucanbiological ageoatspolyphenolssystemic chronic inflammation

Identifiers

PMID36364734
PMCPMC9656573
OpenAlexW4307350577

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.