Evidence map›Paper›PMID 35806940›Full record

ArticleJournal of clinical medicine2022

A Metallomic Approach to Assess Associations of Plasma Metal Levels with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: An Exploratory Study.

Yu-Kai Lin, Chih-Sung Liang, Chia-Kuang Tsai, Chia-Lin Tsai, Jiunn-Tay Lee, Yueh-Feng Sung, Chung-Hsing Chou, Hung-Sheng Shang, Bing-Heng Yang, Guan-Yu Lin and 2 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
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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

12 authors at 2 institutions in 1 country.

Yu-Kai LinDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
Chih-Sung LiangGraduate Institute of Medical Sciences, National Defense Medical Center, Taipei 114, Taiwan.ORCID 0000-0003-1138-5586
Chia-Kuang TsaiDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
Chia-Lin TsaiDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
Jiunn-Tay LeeDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
Yueh-Feng SungDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
Chung-Hsing ChouDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.ORCID 0000-0001-9584-0843
Hung-Sheng ShangDivision of Clinical Pathology, Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.ORCID 0000-0002-4831-1866
Bing-Heng YangDivision of Clinical Pathology, Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.ORCID 0000-0003-2902-632X
Guan-Yu LinDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
Ming-Wei SuInstitute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan.
Fu-Chi YangDepartment of Neurology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.ORCID 0000-0001-6831-3634
Tri-Service General Hospital · TWInstitute of Biomedical Sciences, Academia Sinica · TW

Funding

Ministry of Science and Technology 108-2314-B-016-023-Ministry of Science and Technology 110-2314-B-016-036-MY2Ministry of Science and Technology MOST 108-2314-B-016-020Tri-Service General Hospital TSGH-C108-100Tri-Service General Hospital TSGH-C108-216Tri-Service General Hospital TSGH-D-109-101Tri-Service General Hospital TSGH-D-109-185Tri-Service General Hospital TSGH-D-110048
6 · The paper itself

Abstract

Alzheimer’s disease (AD) involves the abnormal activity of transition metals and metal ion dyshomeostasis; however, the potential of trace metal biomarkers in predicting cognitive decline has not been evaluated. This study aimed to assess the potential of 36 trace elements in predicting cognitive decline in patients with amnestic mild cognitive impairment (aMCI) or AD. Participants (9 controls, 23 aMCI due to AD, and 8 AD dementia) underwent comprehensive cognitive tests, including the Mini-Mental State Examination (MMSE) and trace metal analysis. The correlations between the plasma trace element levels and annual MMSE changes during follow-up were analyzed. We found that an increase in disease severity was linked to lower plasma levels of boron (B), bismuth (Bi), thorium (Th), and uranium (U) (adjusted p < 0.05). Higher baseline calcium levels (r = 0.50, p = 0.026) were associated with less annual cognitive decline; those of B (r = −0.70, p = 0.001), zirconium (r = −0.58, p = 0.007), and Th (r = −0.52, p = 0.020) with rapid annual cognitive decline in the aMCI group; and those of manganese (r = −0.91, p = 0.035) with rapid annual cognitive decline in the AD group. Overall, our exploratory study suggests that plasma metal levels have great potential as in vivo biomarkers for aMCI and AD. Larger sample studies are necessary to confirm these results.

Indexed as

Alzheimer’s diseasebiomarkersin vivo assessmentmild cognitive impairmenttrace metals

Identifiers

PMID35806940
PMCPMC9267221
OpenAlexW4283512947

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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.