Evidence map›Paper›PMID 28330509›Full record

ArticleAlzheimer's research & therapy2017

Chemically treated plasma Aβ is a potential blood-based biomarker for screening cerebral amyloid deposition.

Jong-Chan Park, Sun-Ho Han, Hyun Jin Cho, Min Soo Byun, Dahyun Yi, Young Min Choe, Seokjo Kang, Eun Sun Jung, Su Jin Won, Eun Hye Kim and 3 more

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.5field-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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

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  15. Application of QPLEXExperimental & molecular medicine · 2022
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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

13 authors at 4 institutions in 1 country.

Jong-Chan ParkDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Sun-Ho HanDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Hyun Jin ChoDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Min Soo ByunInstitute of Human Behavioral Medicine, Medical Research Center Seoul National University, Seoul, 110-799, South Korea.
Dahyun YiInstitute of Human Behavioral Medicine, Medical Research Center Seoul National University, Seoul, 110-799, South Korea.
Young Min ChoeDepartment of Neuropsychiatry, University of Ulsan College of Medicine, Ulsan University Hospital, Ulsan, 682-714, South Korea.
Seokjo KangDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Eun Sun JungDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Su Jin WonDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Eun Hye KimDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea.
Yu Kyeong KimDepartment of Nuclear Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, 156-707, South Korea.
Dong Young LeeDepartment of Neuropsychiatry, Seoul National University Hospital, 101 Daehak-ro, Jongno-gu, Seoul, 110-744, South Korea. selfpsy@snu.ac.kr.
Inhee Mook-JungDepartment of Biochemistry and Biomedical Sciences, Seoul National University, College of Medicine, 103 Daehak-ro, Jongno-gu, Seoul, 110-799, South Korea. inhee@snu.ac.kr.
Seoul National University · KRSeoul National University Hospital · KRSNUH SMG-SNU Boramae Medical Center · KRUlsan University Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPlasma β-amyloid (Aβ) is a potential candidate for an Alzheimer's disease (AD) biomarker because blood is an easily accessible bio-fluid, which can be collected routinely, and Aβ is one of the major hallmarks of AD pathogenesis in the brain. However, the association between plasma Aβ levels and AD diagnosis is still unclear due to the instability and inaccurate measurements of plasma Aβ levels in the blood of patients with AD. If a consistent value of plasma Aβ from the blood can be obtained, this might help determine whether plasma Aβ is a potential biomarker for AD diagnosis.

methodsWe predicted the brain amyloid deposit by measuring the plasma Aβ levels. This cross-sectional study included 353 participants (215 cognitively normal, 79 with mild cognitive impairment, and 59 with AD dementia) who underwent Pittsburgh-compound B positron emission tomography (PiB-PET) scans. We treated a mixture of protease inhibitors and phosphatase inhibitors (MPP) and detected plasma Aβ42 and Aβ40 (MPP-Aβ42 and MPP-Aβ40) in a stable manner using xMAP technology.

resultsMPP-Aβ40 and MPP-Aβ42/40 (MPP-Aβs) were significantly different between subjects with positive amyloid deposition (PiB+) and those with negative amyloid deposition (PiB-) (P < 0.0001). Furthermore, MPP-Aβ40 (P < 0.0001, r = 0.23) and MPP-Aβ42/40 ratio (P < 0.0001, r = -0.23) showed significant correlation with global PiB deposition (standardized uptake value ratio). In addition, our integrated multivariable (MPP-Aβ42/40, gender, age, and apolipoprotein E genotypes) logistic regression model proposes a new standard for the prediction of cerebral amyloid deposition.

conclusionsMPP-Aβ might be one of the potential blood biomarkers for the prediction of PiB-PET positivity in the brain.

Indexed as

AgedAlzheimer DiseaseAmyloid beta-PeptidesAniline CompoundsBiomarkersBrainCognitive DysfunctionCross-Sectional StudiesFemaleHumansMalePeptide FragmentsPlaque, AmyloidPositron-Emission TomographyProspective StudiesRadiopharmaceuticals2-(4'-(methylamino)phenyl)-6-hydroxybenzothiazoleAmyloid beta-Peptidesamyloid beta-protein (1-40)amyloid beta-protein (1-42)Aniline CompoundsBiomarkersPeptide FragmentsRadiopharmaceuticalsThiazolesAlzheimer’s diseaseBlood-based biomarkerMPPPittsburgh-compound B positron emission tomographyPlasma Aββ-amyloid

Identifiers

PMID28330509
PMCPMC5361707
OpenAlexW2599951549

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.