Evidence map›Paper›PMID 35829770›Full record

ArticleAnalytical and bioanalytical chemistry2022

Studying the Parkinson's disease metabolome and exposome in biological samples through different analytical and cheminformatics approaches: a pilot study.

Begoña Talavera Andújar, Dagny Aurich, Velma T E Aho, Randolph R Singh, Tiejun Cheng, Leonid Zaslavsky, Evan E Bolton, Brit Mollenhauer, Paul Wilmes, Emma L Schymanski

Open access · hybridAbstract read
In one paragraph

Article in Analytical and bioanalytical chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 7% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Parkinson's Disease is Predominantly a Genetic Disease.Journal of Parkinson's disease · 2024
    Review
  17. Article
  18. 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

10 authors at 4 institutions in 4 countries.

Begoña Talavera AndújarLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Avenue du Swing 6, 4367, Belvaux, Luxembourg. begona.talavera@uni.lu.ORCID http://orcid.org/0000-0002-3430-9255
Dagny AurichLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Avenue du Swing 6, 4367, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0001-8823-0596
Velma T E AhoLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Avenue du Swing 6, 4367, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0003-2916-7018
Randolph R SinghLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Avenue du Swing 6, 4367, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0003-4500-3400
Tiejun ChengNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20894, USA.ORCID http://orcid.org/0000-0002-4486-3356
Leonid ZaslavskyNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20894, USA.ORCID http://orcid.org/0000-0001-5873-4873
Evan E BoltonNational Center for Biotechnology Information, National Library of Medicine, National Institutes of Health, Bethesda, MD, 20894, USA.ORCID http://orcid.org/0000-0002-5959-6190
Brit MollenhauerDepartment of Neurology, University Medical Center Göttingen, Göttingen, Germany.
Paul WilmesLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Avenue du Swing 6, 4367, Belvaux, Luxembourg.ORCID http://orcid.org/0000-0002-6478-2924
Emma L SchymanskiLuxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Avenue du Swing 6, 4367, Belvaux, Luxembourg. emma.schymanski@uni.lu.ORCID http://orcid.org/0000-0001-6868-8145
University of Luxembourg · LUNational Institutes of Health · USIfremer · FRUniversitätsmedizin Göttingen · DE

Funding

National Biomedical Information ServicesZIHLM200888 · NLM · NATIONAL LIBRARY OF MEDICINE · PI PALTOO, DINA · 2009 to 2025
$5200.7M
European Union's Horizon 2020 research and innovation programme Grant agreement No. 863664Luxembourg National Research Fund (FNR) FNR; CORE/16/BM/11333923Luxembourg National Research Fund (FNR) MiBiPaLuxembourg National Research Fund (FNR) Project A18/BM/12341006Michael J. Fox Foundation for Parkinson's Research 14701 (MiBiPa-PLUS)Michael J. Fox Foundation for Parkinson's Research MJFF-019228 (PARKdiet)Parkinson's Foundation MiBiPa Saliva
6 · The paper itself

Abstract

Parkinson's disease (PD) is the second most prevalent neurodegenerative disease, with an increasing incidence in recent years due to the aging population. Genetic mutations alone only explain <10% of PD cases, while environmental factors, including small molecules, may play a significant role in PD. In the present work, 22 plasma (11 PD, 11 control) and 19 feces samples (10 PD, 9 control) were analyzed by non-target high-resolution mass spectrometry (NT-HRMS) coupled to two liquid chromatography (LC) methods (reversed-phase (RP) and hydrophilic interaction liquid chromatography (HILIC)). A cheminformatics workflow was optimized using open software (MS-DIAL and patRoon) and open databases (all public MSP-formatted spectral libraries for MS-DIAL, PubChemLite for Exposomics, and the LITMINEDNEURO list for patRoon). Furthermore, five disease-specific databases and three suspect lists (on PD and related disorders) were developed, using PubChem functionality to identifying relevant unknown chemicals. The results showed that non-target screening with the larger databases generally provided better results compared with smaller suspect lists. However, two suspect screening approaches with patRoon were also good options to study specific chemicals in PD. The combination of chromatographic methods (RP and HILIC) as well as two ionization modes (positive and negative) enhanced the coverage of chemicals in the biological samples. While most metabolomics studies in PD have focused on blood and cerebrospinal fluid, we found a higher number of relevant features in feces, such as alanine betaine or nicotinamide, which can be directly metabolized by gut microbiota. This highlights the potential role of gut dysbiosis in PD development.

Indexed as

ExposomeNeurodegenerative DiseasesParkinson DiseaseAgedAlanineBetaineCheminformaticsHumansMetabolomeMetabolomicsNiacinamidePilot ProjectsAlanineBetaineNiacinamideExposomicsGut dysbiosisLiquid chromatography (LC)MetabolomicsNon-target high-resolution mass spectrometry (NT-HRMS)Parkinson’s disease

Identifiers

PMID35829770
PMCPMC9482909
OpenAlexW4285084981

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.