Evidence map›Paper›PMID 35707037›Full record

ArticleFrontiers in neurology2022

A Set of Reliable Samples for the Study of Biomarkers for the Early Diagnosis of Parkinson's Disease.

Marcela Konjevod, Jorge Sáiz, Coral Barbas, Alberto Bergareche, Eva Ardanaz, José Ma Huerta, Ana Vinagre-Aragón, Ma Elena Erro, Ma Dolores Chirlaque, Eunate Abilleira and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

12 authors at 7 institutions in 2 countries.

Marcela KonjevodDivision of Molecular Medicine, Rudjer Boskovic Institute, Zagreb, Croatia.
Jorge SáizFacultad de Farmacia, Centro de Metabolómica y Bioanálisis, Universidad San Pablo-CEU, CEU Universities, Madrid, Spain.
Coral BarbasFacultad de Farmacia, Centro de Metabolómica y Bioanálisis, Universidad San Pablo-CEU, CEU Universities, Madrid, Spain.
Alberto BergarecheDepartment of Neurology, University Hospital Donostia, San Sebastián, Spain.
Eva ArdanazNavarra Public Health Institute, Pamplona, Spain.
José Ma HuertaSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Instituto de Salud Carlos III, Madrid, Spain.
Ana Vinagre-AragónDepartment of Neurology, University Hospital Donostia, San Sebastián, Spain.
Ma Elena ErroNavarra Institute for Health Research (IdiSNA), Pamplona, Spain.
Ma Dolores ChirlaqueSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Instituto de Salud Carlos III, Madrid, Spain.
Eunate AbilleiraMinistry of Health of the Basque Government, Public Health Laboratory in Gipuzkoa, San Sebastián, Spain.
Jesús Ma IbarluzeaSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Instituto de Salud Carlos III, Madrid, Spain.
Pilar AmianoSpanish Consortium for Research on Epidemiology and Public Health (CIBERESP), Instituto de Salud Carlos III, Madrid, Spain.
Biogipuzkoa Health Research Institute · ESInstituto Murciano de Investigación Biosanitaria · ESMinistry of Health · ESUniversidad San Pablo CEU · ESCentro de Investigación Biomédica en Red de Epidemiología y Salud Pública · ESNavarre Institute of Health Research · ESRudjer Boskovic Institute · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Parkinson's disease (PD) is a progressive neurodegenerative disorder, diagnosed according to the clinical criteria that occur in already advanced stages of PD. The definition of biomarkers for the early diagnosis of PD represents a challenge that might improve treatment and avoid complications in this disease. Therefore, we propose a set of reliable samples for the identification of altered metabolites to find potential prognostic biomarkers for early PD. Methods: This case-control study included plasma samples of 12 patients with PD and 21 control subjects, from the Spanish European Prospective Investigation into Cancer and Nutrition (EPIC)-Navarra cohort, part of the EPIC-Spain study. All the case samples were provided by healthy volunteers who were followed-up for 15.9 (±4.1) years and developed PD disease later on, after the sample collection. Liquid chromatography coupled to tandem mass spectrometry was used for the analysis of samples. Results: Out of 40 that were selected and studied due to their involvement in established cases of PD, seven significantly different metabolites between PD cases and healthy control subjects were obtained in this study (benzoic acid, palmitic acid, oleic acid, stearic acid, myo-inositol, sorbitol, and quinolinic acid). These metabolites are related to mitochondrial dysfunction, the oxidative stress, and the mechanisms of energy production. Conclusion: We propose the samples from the EPIC study as reliable and invaluable samples for the search of early biomarkers of PD. Likewise, this study might also be a starting point in the establishment of a well-founded panel of metabolites that can be used for the early detection of this disease.

Indexed as

biomarkersEPIC-Navarrafatty acidsmetabolomicsParkinson's disease

Identifiers

PMID35707037
PMCPMC9189395
OpenAlexW4281723529

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.