Evidence map›Paper›PMID 34681563›Full record

ArticleInternational journal of molecular sciences2021

Discovery of a Metabolic Signature Predisposing High Risk Patients with Mild Cognitive Impairment to Converting to Alzheimer's Disease.

Yi-Long Huang, Chao-Hsiung Lin, Tsung-Hsien Tsai, Chen-Hua Huang, Jie-Ling Li, Liang-Kung Chen, Chun-Hsien Li, Ting-Fen Tsai, Pei-Ning Wang

Open access · goldAbstract readComparative Study
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

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  8. Gut microbial metabolism in Alzheimer's disease and related dementias.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
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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

9 authors at 1 institution in 1 country.

Yi-Long HuangAging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.ORCID 0000-0002-0980-4828
Chao-Hsiung LinAging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.ORCID 0000-0001-6344-271X
Tsung-Hsien TsaiAdvanced Tech BU, Acer Inc., New Taipei City 221, Taiwan.
Chen-Hua HuangDepartment of Life Sciences and Institute of Genome Sciences, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Jie-Ling LiAging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Liang-Kung ChenAging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.ORCID 0000-0002-2387-8508
Chun-Hsien LiAdvanced Tech BU, Acer Inc., New Taipei City 221, Taiwan.
Ting-Fen TsaiAging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
Pei-Ning WangAging and Health Research Center, National Yang Ming Chiao Tung University, Taipei 112, Taiwan.
National Yang Ming Chiao Tung University · TW

Funding

Ministry of Science and Technology MOST 108-2321-B-010-013-MY2Ministry of Science and Technology MOST 110-2321-B-010-007Ministry of Science and Technology MOST 110-2634-F-010-004
6 · The paper itself

Abstract

Assessing dementia conversion in patients with mild cognitive impairment (MCI) remains challenging owing to pathological heterogeneity. While many MCI patients ultimately proceed to Alzheimer's disease (AD), a subset of patients remain stable for various times. Our aim was to characterize the plasma metabolites of nineteen MCI patients proceeding to AD (P-MCI) and twenty-nine stable MCI (S-MCI) patients by untargeted metabolomics profiling. Alterations in the plasma metabolites between the P-MCI and S-MCI groups, as well as between the P-MCI and AD groups, were compared over the observation period. With the help of machine learning-based stratification, a 20-metabolite signature panel was identified that was associated with the presence and progression of AD. Furthermore, when the metabolic signature panel was used for classification of the three patient groups, this gave an accuracy of 73.5% using the panel. Moreover, when specifically classifying the P-MCI and S-MCI subjects, a fivefold cross-validation accuracy of 80.3% was obtained using the random forest model. Importantly, indole-3-propionic acid, a bacteria-generated metabolite from tryptophan, was identified as a predictor of AD progression, suggesting a role for gut microbiota in AD pathophysiology. Our study establishes a metabolite panel to assist in the stratification of MCI patients and to predict conversion to AD.

Indexed as

AgedAged, 80 and overAlzheimer DiseaseBiomarkersCognitive DysfunctionDisease ProgressionFemaleHumansMachine LearningMaleMetabolomicsMiddle AgedPropionatesBiomarkersPropionatesAlzheimer’s diseasefeature selectionmild cognitive impairmentplasmauntargeted metabolomics

Identifiers

PMID34681563
PMCPMC8535253
OpenAlexW3205394101

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.