Evidence map›Paper›PMID 32714143›Full record

ArticleFrontiers in molecular neuroscience2020

Integrated Metabolomics and Proteomics Analysis Reveals Plasma Lipid Metabolic Disturbance in Patients With Parkinson's Disease.

Ling Hu, Mei-Xue Dong, Yan-Ling Huang, Chang-Qi Lu, Qian Qian, Chun-Cheng Zhang, Xiao-Min Xu, Yang Liu, Guang-Hui Chen, You-Dong Wei

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular neuroscience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 3 pooled it
3.6field-weighted citation impact, top 5% 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

45 citing papers in PubMed, 3 syntheses or guidelines pooled it, 76 citations in OpenAlex.

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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

10 authors at 6 institutions in 1 country.

Ling HuDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Mei-Xue DongDepartment of Neurology, Renmin Hospital of Wuhan University, Hubei General Hospital, Wuhan, China.
Yan-Ling HuangDepartment of Neurology, Chongqing University Central Hospital, Chongqing Emergency Medical Center, Chongqing, China.
Chang-Qi LuDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Qian QianDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Chun-Cheng ZhangDepartment of Neurology, The People's Hospital of Tongliang District, Chongqing, China.
Xiao-Min XuDepartment of Neurology, The Affiliated Hospital of Southwest Medical University, Luzhou, China.
Yang LiuDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Guang-Hui ChenDepartment of Neurology, Renmin Hospital of Wuhan University, Hubei General Hospital, Wuhan, China.
You-Dong WeiDepartment of Neurology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Chongqing Medical University · CNFirst Affiliated Hospital of Chongqing Medical University · CNWuhan University · CNAffiliated Hospital of Southwest Medical University · CNChongqing Emergency Medical Center · CNThe People's Hospital Tongling · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a common neurodegenerative disease in the elderly with a pathogenesis that remains unclear. We aimed to explore its pathogenesis through plasma integrated metabolomics and proteomics analysis. The clinical data of consecutively recruited PD patients and healthy controls were assessed. Fasting plasma samples were obtained and analyzed using metabolomics and proteomics methods. After that, differentially expressed metabolites and proteins were identified for further bioinformatics analysis. No significant difference was found in the clinical data between these two groups. Eighty-three metabolites were differentially expressed in PD patients identified by metabolomics analysis. These metabolites were predominately lipid and lipid-like molecules (63%), among which 25% were sphingolipids. The sphingolipid metabolism pathway was enriched and tended to be activated in the following KEGG pathway analysis. According to the proteomics analysis, forty proteins were identified to be differentially expressed, seven of which were apolipoproteins. Furthermore, five of the six top ranking Gene Ontology terms from cellular components and eleven of the other fourteen Gene Ontology terms from biological processes were directly associated with lipid metabolism. In KEGG pathway analysis, the five enriched pathways were also significantly related with lipid metabolism (

Indexed as

apolipoproteinlipidmetabolomicsParkinson’s diseaseproteomicssphingolipid metabolism

Identifiers

PMID32714143
PMCPMC7344253
OpenAlexW3038793460

What OpenQuestion holds

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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.