Evidence map›Paper›PMID 37761859›Full record

ReviewGenes2023

Oxalate (dys)Metabolism: Person-to-Person Variability, Kidney and Cardiometabolic Toxicity.

Pedro Baltazar, Antonio Ferreira de Melo Junior, Nuno Moreira Fonseca, Miguel Brito Lança, Ana Faria, Catarina O Sequeira, Luísa Teixeira-Santos, Emilia C Monteiro, Luís Campos Pinheiro, Joaquim Calado and 3 more

Open access · goldAbstract readReview
In one paragraph

Review in Genes, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
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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

13 authors at 2 institutions in 1 country.

Pedro BaltazarCentro Hospitalar Universitário de Lisboa Central, E.P.E, 1150-199 Lisboa, Portugal.
Antonio Ferreira de Melo JunioriNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.ORCID 0000-0001-6831-1823
Nuno Moreira FonsecaCentro Hospitalar Universitário de Lisboa Central, E.P.E, 1150-199 Lisboa, Portugal.ORCID 0000-0003-0821-2764
Miguel Brito LançaCentro Hospitalar Universitário de Lisboa Central, E.P.E, 1150-199 Lisboa, Portugal.ORCID 0000-0002-9801-849X
Ana FariaCHRC, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.ORCID 0000-0002-5165-9513
Catarina O SequeiraiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.
Luísa Teixeira-SantosiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.ORCID 0000-0001-7729-9010
Emilia C MonteiroiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.
Luís Campos PinheiroCentro Hospitalar Universitário de Lisboa Central, E.P.E, 1150-199 Lisboa, Portugal.
Joaquim CaladoCentro Hospitalar Universitário de Lisboa Central, E.P.E, 1150-199 Lisboa, Portugal.
Cátia SousaiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.
Judit MorelloiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.
Sofia A PereiraiNOVA4Health, NOVA Medical School|Faculdade de Ciências Médicas, NMS|FCM, Universidade NOVA de Lisboa, 1150-082 Lisboa, Portugal.ORCID 0000-0002-8456-9995
Unidade Local de Saúde de São José · PTUniversidade Nova de Lisboa · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxalate is a metabolic end-product whose systemic concentrations are highly variable among individuals. Genetic (primary hyperoxaluria) and non-genetic (e.g., diet, microbiota, renal and metabolic disease) reasons underlie elevated plasma concentrations and tissue accumulation of oxalate, which is toxic to the body. A classic example is the triad of primary hyperoxaluria, nephrolithiasis, and kidney injury. Lessons learned from this example suggest further investigation of other putative factors associated with oxalate dysmetabolism, namely the identification of precursors (glyoxylate, aromatic amino acids, glyoxal and vitamin C), the regulation of the endogenous pathways that produce oxalate, or the microbiota's contribution to oxalate systemic availability. The association between secondary nephrolithiasis and cardiovascular and metabolic diseases (hypertension, type 2 diabetes, and obesity) inspired the authors to perform this comprehensive review about oxalate dysmetabolism and its relation to cardiometabolic toxicity. This perspective may offer something substantial that helps advance understanding of effective management and draws attention to the novel class of treatments available in clinical practice.

Indexed as

Diabetes Mellitus, Type 2Hyperoxaluria, PrimaryHypertensionNephrolithiasisHumansKidneyOxalatesOxalatescardiovascular diseasehyperoxaluriahypertensionkidney diseasekidney stonesmetabolic diseasemicrobiotanephrolithiasisobstructive sleep apneapharmacologysystemic inflammation

Identifiers

PMID37761859
PMCPMC10530622
OpenAlexW4386255708

What OpenQuestion 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 OpenQuestion graph.