Evidence map›Paper›PMID 36329260›Full record

ReviewNature reviews. Nephrology2023

Oxalate homeostasis.

Theresa Ermer, Lama Nazzal, Maria Clarissa Tio, Sushrut Waikar, Peter S Aronson, Felix Knauf

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Nephrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
13.1field-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.

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

57 citing papers in PubMed, 95 citations in OpenAlex.

  1. Review
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  10. Observational
  11. Histology and histopathology · 2026
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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

6 authors at 4 institutions in 2 countries.

Theresa ErmerDepartment of Surgery, Division of Thoracic Surgery, Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0001-8483-5758
Lama NazzalDepartment of Medicine, NYU Grossman School of Medicine, New York, NY, USA.
Maria Clarissa TioDivision of Nephrology, University of Mississippi Medical Center, Jackson, MS, USA.
Sushrut WaikarDepartment of Medicine, Section of Nephrology, Boston University, Boston, MA, USA.ORCID 0000-0003-4004-326X
Peter S AronsonDepartment of Internal Medicine, Section of Nephrology, Yale School of Medicine, New Haven, CT, USA.ORCID 0000-0002-1860-2419
Felix KnaufDepartment of Internal Medicine, Section of Nephrology, Yale School of Medicine, New Haven, CT, USA. felix.knauf@charite.de.ORCID 0000-0001-5762-1404
Yale University · USBoston University · USJackson Memorial Hospital · USNew York University · US

Funding

Tracking and Evaluation CoreU54GM115428 · NIGMS · UNIVERSITY OF MISSISSIPPI MED CTR · PI COMPRETTA, CAROLINE E. · 2016 to 2025
$38.2M
NIGMS NIH HHS U54 GM115428
6 · The paper itself

Abstract

Oxalate homeostasis is maintained through a delicate balance between endogenous sources, exogenous supply and excretion from the body. Novel studies have shed light on the essential roles of metabolic pathways, the microbiome, epithelial oxalate transporters, and adequate oxalate excretion to maintain oxalate homeostasis. In patients with primary or secondary hyperoxaluria, nephrolithiasis, acute or chronic oxalate nephropathy, or chronic kidney disease irrespective of aetiology, one or more of these elements are disrupted. The consequent impairment in oxalate homeostasis can trigger localized and systemic inflammation, progressive kidney disease and cardiovascular complications, including sudden cardiac death. Although kidney replacement therapy is the standard method for controlling elevated plasma oxalate concentrations in patients with kidney failure requiring dialysis, more research is needed to define effective elimination strategies at earlier stages of kidney disease. Beyond well-known interventions (such as dietary modifications), novel therapeutics (such as small interfering RNA gene silencers, recombinant oxalate-degrading enzymes and oxalate-degrading bacterial strains) hold promise to improve the outlook of patients with oxalate-related diseases. In addition, experimental evidence suggests that anti-inflammatory medications might represent another approach to mitigating or resolving oxalate-induced conditions.

Indexed as

HyperoxaluriaRenal InsufficiencyRenal Insufficiency, ChronicHomeostasisHumansKidneyOxalatesRenal DialysisOxalates

Identifiers

PMID36329260
PMCPMC10278040
OpenAlexW4308258337

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.