Evidence map›Paper›PMID 42075003›Full record

ReviewNutrients2026

Oxalate as an Emerging Contributor to Cardiovascular Disease: Links to Inflammation, Immunity, and Oxidative Stress.

Mary A E M Doamekpor, Vivek Verma, Christine M Wright, Breanna Young, Diksha S Saini, Gregory A Payne, Clintoria R Williams, Tanecia Mitchell

Abstract readReview
In one paragraph

Review in Nutrients, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Mary A E M DoamekporDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.ORCID 0000-0002-1015-0091
Vivek VermaDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.ORCID 0000-0002-1202-5972
Christine M WrightDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Breanna YoungDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Diksha S SainiDepartment of Cell Biology, Neuroscience and Physiology, Wright State University, Dayton, OH 45435, USA.
Gregory A PayneDepartment of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.ORCID 0000-0002-8525-8603
Clintoria R WilliamsDepartment of Cell Biology, Neuroscience and Physiology, Wright State University, Dayton, OH 45435, USA.
Tanecia MitchellDepartment of Urology, University of Alabama at Birmingham, Birmingham, AL 35294, USA.ORCID 0000-0002-4032-913X

Funding

Oxalate-Driven Host Responses in Kidney Stone DiseaseR01DK129885 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Tanecia R Mitchell · 2022 to 2026
$2.7M
Mechanisms of the Renoprotective Properties of Zinc Supplementation in Mouse Models of Chronic Kidney DiseaseR01DK133698 · NIDDK · WRIGHT STATE UNIVERSITY · PI WILLIAMS, CLINTORIA RICHARDS · 2022 to 2025
$1.9M
NIDDK NIH HHS R01 DK129885NIDDK NIH HHS R01 DK133698NIH HHS R01DK129885NIH HHS R01DK133698
6 · The paper itself

Abstract

Cardiovascular disease (CVD) is the world's leading cause of death and continues to rise in prevalence, contributing to healthcare and economic costs. Following diagnosis, patients are advised to adopt medication regimens, increase physical activity, and modify dietary intake to reduce disease progression and prevent additional comorbidities. Oxalate is a small molecule in plant-derived foods such as spinach, potatoes, almonds, and peanuts and is also produced endogenously. Although oxalate is traditionally studied in the context of kidney stone disease, recent evidence suggests that it may be a dietary contributor to inflammation and oxidative stress in CVD. Elevated systemic oxalate levels promote reactive oxygen species (ROS) generation and activate inflammatory pathways such as nuclear factor-kappa B (NF-κB), mitogen-activated protein kinase (MAPK), and the NLRP3 inflammasome, which are key players in CVD. In this narrative review, we discuss the current literature describing the role of inflammation in CVD and evaluate emerging evidence that dietary oxalate may influence immune, oxidative, and vascular mechanisms contributing to CVD development and progression. In addition, we highlight populations that may be most vulnerable to oxalate-mediated vascular effects. We conclude by describing existing gaps in knowledge and potential future directions for the field. Understanding these mechanisms further may guide dietary recommendations and delineate oxalate's potential role as a modifiable risk factor for CVD.

Indexed as

Cardiovascular DiseasesImmunityInflammationOxalatesOxidative StressAnimalsDietHumansReactive Oxygen SpeciesOxalatesReactive Oxygen Speciesatherosclerosiscalcium oxalatecardiovascular diseaseimmunityinflammationmetabolismoxalatereactive oxygen species

Identifiers

PMID42075003
PMCPMC13119074

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.