Evidence map›Paper›PMID 39521974›Full record

ArticleParasites & vectors2024

Changes in lipid abundance are associated with disease progression and treatment response in chronic Trypanosoma cruzi infection.

Juan Carlos Gabaldón-Figueira, Albert Ros-Lucas, Nieves Martínez-Peinado, Gavin Blackburn, Irene Losada-Galvan, Elizabeth Posada, Cristina Ballart, Elisa Escabia, Jordi Capellades, Oscar Yanes and 3 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Alterations in Cardiac Metabolism byACS infectious diseases · 2025
    Article
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.

Juan Carlos Gabaldón-Figueira *ISGlobal, Barcelona, Spain. juancarlos.gabaldon@isglobal.org.
Albert Ros-Lucas *ISGlobal, Barcelona, Spain.
Nieves Martínez-PeinadoISGlobal, Barcelona, Spain.
Gavin BlackburnMVLS Shared Research Facilities, University of Glasgow, Glasgow, G12 8QQ, Scotland.
Irene Losada-GalvanISGlobal, Barcelona, Spain.
Elizabeth PosadaISGlobal, Barcelona, Spain.
Cristina BallartISGlobal, Barcelona, Spain.
Elisa EscabiaISGlobal, Barcelona, Spain.
Jordi CapelladesInstitut d'Investigació Sanitària Pere Virgili (IISPV), Metabolomics Platform, Reus, Spain.
Oscar YanesInstitut d'Investigació Sanitària Pere Virgili (IISPV), Metabolomics Platform, Reus, Spain.
María-Jesús PinazoCIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III (CIBERINFEC, ISCIII), Madrid, Spain.
Joaquim GascónISGlobal, Barcelona, Spain.
Julio Alonso-PadillaISGlobal, Barcelona, Spain. julio.a.padilla@isglobal.org.

Funding

Generalitat de Catalunya CERCA programInstituto de Salud Carlos III PI18/01054'la Caixa' Foundation LCF/BQ/DI21/11860037Ministerio de Ciencia e Innovación CEX2023-0001290-S
6 · The paper itself

Abstract

backgroundChagas disease, caused by the parasite Trypanosoma cruzi, is a zoonosis that affects more than seven million people. Current limitations on the diagnosis of the disease hinder the prognosis of patients and the evaluation of treatment efficacy, slowing the development of new therapeutic options. The infection is known to disrupt several host metabolic pathways, providing an opportunity for the identification of biomarkers.

methodsThe metabolomic and lipidomic profiles of a cohort of symptomatic and asymptomatic patients with T. cruzi infection and a group of uninfected controls were analysed using liquid chromatography/mass spectrometry. Differences among all groups and changes before and after receiving anti-parasitic treatment across those with T. cruzi infection were explored.

resultsThree lipids were found to differentiate between symptomatic and asymptomatic participants: 10-hydroxydecanoic acid and phosphatidylethanolamines PE(18:0/20:4) and PE(18:1/20:4). Additionally, sphinganine, 4-hydroxysphinganine, hexadecasphinganine, and other sphingolipids showed post-treatment abundance similar to that in non-infected controls.

conclusionsThese molecules hold promise as potentially useful biomarkers for monitoring disease progression and treatment response in patients with chronic T. cruzi infection.

Indexed as

Chagas DiseaseDisease ProgressionTrypanosoma cruziAdultBiomarkersChromatography, LiquidChronic DiseaseFemaleHumansLipidomicsLipidsMaleMass SpectrometryMetabolomicsMiddle AgedTreatment OutcomeBiomarkersLipidsChagas diseaseHydroxydecanoic acidLipidomicsMetabolomicsPhosphatidylethanolamineSphingolipidsTreatment responseTrypanosoma cruzi

Identifiers

PMID39521974
PMCPMC11549750

What OpenQuestion holds

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Registered trials

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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.